Chemicals

Showing 13951–14100 of 41137 results

  • Cyclin-dependent kinase 5 (Cdk5) is a serine/threonine kinase that is predominantly active in neuronal tissues. With p25 or p35, Cdk5 phosphorylates a range of proteins, including histone H1 and tau.{28590} Cdk5 substrate is a synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1. It is phosphorylated by Cdk5 with a Km value of 5 µM.{28589,28591}  

     

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  • Cyclin-dependent kinase 5 (Cdk5) is a serine/threonine kinase that is predominantly active in neuronal tissues. With p25 or p35, Cdk5 phosphorylates a range of proteins, including histone H1 and tau.{28590} Cdk5 substrate is a synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1. It is phosphorylated by Cdk5 with a Km value of 5 µM.{28589,28591}  

     

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  • Cyclin-dependent kinase 5 (Cdk5) is a serine/threonine kinase that is predominantly active in neuronal tissues. With p25 or p35, Cdk5 phosphorylates a range of proteins, including histone H1 and tau.{28590} Cdk5 substrate is a synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1. It is phosphorylated by Cdk5 with a Km value of 5 µM.{28589,28591}  

     

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  • Cyclin-dependent kinase 5 (Cdk5) is a serine/threonine kinase that is predominantly active in neuronal tissues. With p25 or p35, Cdk5 phosphorylates a range of proteins, including histone H1 and tau.{28590} Cdk5 substrate is a synthetic peptide (PKTPKKAKKL) corresponding to a sequence of histone H1. It is phosphorylated by Cdk5 with a Km value of 5 µM.{28589,28591}  

     

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    Cayman
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  • CDN1163 is an allosteric activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2 (SERCA2) that enhances calcium uptake in endoplasmic reticulum (ER) vesicles when used at concentrations ranging from 1 to 10 µM.{57074} It decreases peroxide-induced cell death in HEK293 cells. CDN1163 (50 mg/kg) increases calcium uptake in ER microsomes isolated from obese mouse liver. It decreases blood glucose levels, plasma and hepatic triglyceride levels, and plasma cholesterol and malondialdehyde (MDA) levels in obese mice. CDN1163 (50 mg/kg) restores SERCA activity, prevents gastrocnemius muscle loss and contractile dysfunction, and reduces mitochondrial production of reactive oxygen species (ROS) in the CuZnSOD-deficient (Sod-/-) mouse model of oxidative stress-related muscle atrophy and weakness.{57075} It also improves motor deficits in the initiation time (IT), stepping, and cylinder tests for akinesia in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57076}  

     

    Brand:
    Cayman
    SKU:31123 - 1 mg

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  • CDN1163 is an allosteric activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2 (SERCA2) that enhances calcium uptake in endoplasmic reticulum (ER) vesicles when used at concentrations ranging from 1 to 10 µM.{57074} It decreases peroxide-induced cell death in HEK293 cells. CDN1163 (50 mg/kg) increases calcium uptake in ER microsomes isolated from obese mouse liver. It decreases blood glucose levels, plasma and hepatic triglyceride levels, and plasma cholesterol and malondialdehyde (MDA) levels in obese mice. CDN1163 (50 mg/kg) restores SERCA activity, prevents gastrocnemius muscle loss and contractile dysfunction, and reduces mitochondrial production of reactive oxygen species (ROS) in the CuZnSOD-deficient (Sod-/-) mouse model of oxidative stress-related muscle atrophy and weakness.{57075} It also improves motor deficits in the initiation time (IT), stepping, and cylinder tests for akinesia in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57076}  

     

    Brand:
    Cayman
    SKU:31123 - 10 mg

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  • CDN1163 is an allosteric activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2 (SERCA2) that enhances calcium uptake in endoplasmic reticulum (ER) vesicles when used at concentrations ranging from 1 to 10 µM.{57074} It decreases peroxide-induced cell death in HEK293 cells. CDN1163 (50 mg/kg) increases calcium uptake in ER microsomes isolated from obese mouse liver. It decreases blood glucose levels, plasma and hepatic triglyceride levels, and plasma cholesterol and malondialdehyde (MDA) levels in obese mice. CDN1163 (50 mg/kg) restores SERCA activity, prevents gastrocnemius muscle loss and contractile dysfunction, and reduces mitochondrial production of reactive oxygen species (ROS) in the CuZnSOD-deficient (Sod-/-) mouse model of oxidative stress-related muscle atrophy and weakness.{57075} It also improves motor deficits in the initiation time (IT), stepping, and cylinder tests for akinesia in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57076}  

     

    Brand:
    Cayman
    SKU:31123 - 25 mg

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  • CDN1163 is an allosteric activator of sarcoplasmic/endoplasmic reticulum Ca2+-ATPase 2 (SERCA2) that enhances calcium uptake in endoplasmic reticulum (ER) vesicles when used at concentrations ranging from 1 to 10 µM.{57074} It decreases peroxide-induced cell death in HEK293 cells. CDN1163 (50 mg/kg) increases calcium uptake in ER microsomes isolated from obese mouse liver. It decreases blood glucose levels, plasma and hepatic triglyceride levels, and plasma cholesterol and malondialdehyde (MDA) levels in obese mice. CDN1163 (50 mg/kg) restores SERCA activity, prevents gastrocnemius muscle loss and contractile dysfunction, and reduces mitochondrial production of reactive oxygen species (ROS) in the CuZnSOD-deficient (Sod-/-) mouse model of oxidative stress-related muscle atrophy and weakness.{57075} It also improves motor deficits in the initiation time (IT), stepping, and cylinder tests for akinesia in a rat model of Parkinson’s disease induced by 6-OHDA (Item No. 25330).{57076}  

     

    Brand:
    Cayman
    SKU:31123 - 5 mg

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  • Exchange protein activated by cAMP (Epac) proteins mediate cAMP signaling independent of protein kinase A (PKA). CE3F4 is an uncompetitive inhibitor of Epac1 activity toward its effector Rap1 in vitro (IC50 = 23 µM) and in cells.{29533,29532}. It has no effect on PKA activity. CE3F4 blocks Epac1-induced autophagy in cardiomyocytes stimulated with isoprenaline and blocks the activation of transient receptor potential canonical (TRPC) channels by the Epac activator 8-pCPT.{29535,29534}  

     

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  • Exchange protein activated by cAMP (Epac) proteins mediate cAMP signaling independent of protein kinase A (PKA). CE3F4 is an uncompetitive inhibitor of Epac1 activity toward its effector Rap1 in vitro (IC50 = 23 µM) and in cells.{29533,29532}. It has no effect on PKA activity. CE3F4 blocks Epac1-induced autophagy in cardiomyocytes stimulated with isoprenaline and blocks the activation of transient receptor potential canonical (TRPC) channels by the Epac activator 8-pCPT.{29535,29534}  

     

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  • Exchange protein activated by cAMP (Epac) proteins mediate cAMP signaling independent of protein kinase A (PKA). CE3F4 is an uncompetitive inhibitor of Epac1 activity toward its effector Rap1 in vitro (IC50 = 23 µM) and in cells.{29533,29532}. It has no effect on PKA activity. CE3F4 blocks Epac1-induced autophagy in cardiomyocytes stimulated with isoprenaline and blocks the activation of transient receptor potential canonical (TRPC) channels by the Epac activator 8-pCPT.{29535,29534}  

     

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  • Cebranopadol is an agonist of nociceptin-, µ-, ĸ-, and δ-opioid receptors (Kis = 0.9, 0.7, 2.6, and 18 nM, respectively).{52240} It is greater than 100-fold selective for these receptors over a panel of more than 100 ion channels, neurotransmitter transporters, receptors, and enzymes, but does bind to the serotonin (5-HT) receptor subtype 5-HT5A with a Ki value of 8.7 nM. Cebranopadol inhibits nociceptin-, DAMGO-, and SNC 80-induced GTPɣS binding in CHO cells expressing nociceptin-, µ-, and δ-opioid receptors, respectively (EC50s = 13, 1.2, and 110 nM, respectively), as well as U69,593-induced GTPɣS binding in HEK293 cells expressing the ĸ-opioid receptor (EC50 = 17 nM). It increases the paw withdrawal threshold in rat models of bone cancer pain and streptozotocin-induced diabetic neuropathy (ED50s = 3.6 and 0.5 µg/kg, respectively, i.v.). Cebranopadol also increases paw weight bearing on the ipsilateral side in a rat model of arthritis induced by complete Freund’s adjuvant (CFA) and M. tuberculosis (ED50 = 5.5 µg/kg, i.v.).  

     

    Brand:
    Cayman
    SKU:29500 - 10 mg

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  • Cebranopadol is an agonist of nociceptin-, µ-, ĸ-, and δ-opioid receptors (Kis = 0.9, 0.7, 2.6, and 18 nM, respectively).{52240} It is greater than 100-fold selective for these receptors over a panel of more than 100 ion channels, neurotransmitter transporters, receptors, and enzymes, but does bind to the serotonin (5-HT) receptor subtype 5-HT5A with a Ki value of 8.7 nM. Cebranopadol inhibits nociceptin-, DAMGO-, and SNC 80-induced GTPɣS binding in CHO cells expressing nociceptin-, µ-, and δ-opioid receptors, respectively (EC50s = 13, 1.2, and 110 nM, respectively), as well as U69,593-induced GTPɣS binding in HEK293 cells expressing the ĸ-opioid receptor (EC50 = 17 nM). It increases the paw withdrawal threshold in rat models of bone cancer pain and streptozotocin-induced diabetic neuropathy (ED50s = 3.6 and 0.5 µg/kg, respectively, i.v.). Cebranopadol also increases paw weight bearing on the ipsilateral side in a rat model of arthritis induced by complete Freund’s adjuvant (CFA) and M. tuberculosis (ED50 = 5.5 µg/kg, i.v.).  

     

    Brand:
    Cayman
    SKU:29500 - 25 mg

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  • Cebranopadol is an agonist of nociceptin-, µ-, ĸ-, and δ-opioid receptors (Kis = 0.9, 0.7, 2.6, and 18 nM, respectively).{52240} It is greater than 100-fold selective for these receptors over a panel of more than 100 ion channels, neurotransmitter transporters, receptors, and enzymes, but does bind to the serotonin (5-HT) receptor subtype 5-HT5A with a Ki value of 8.7 nM. Cebranopadol inhibits nociceptin-, DAMGO-, and SNC 80-induced GTPɣS binding in CHO cells expressing nociceptin-, µ-, and δ-opioid receptors, respectively (EC50s = 13, 1.2, and 110 nM, respectively), as well as U69,593-induced GTPɣS binding in HEK293 cells expressing the ĸ-opioid receptor (EC50 = 17 nM). It increases the paw withdrawal threshold in rat models of bone cancer pain and streptozotocin-induced diabetic neuropathy (ED50s = 3.6 and 0.5 µg/kg, respectively, i.v.). Cebranopadol also increases paw weight bearing on the ipsilateral side in a rat model of arthritis induced by complete Freund’s adjuvant (CFA) and M. tuberculosis (ED50 = 5.5 µg/kg, i.v.).  

     

    Brand:
    Cayman
    SKU:29500 - 5 mg

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  • Receptors for VEGF have central roles in vasculogenesis and angiogenesis and thus serve as targets for cancer therapy.{18368,20203} Cediranib is a potent inhibitor of VEGF receptor tyrosine kinases, including VEGFR1, 2, and 3 (IC50s = 5, 1, and 3 nM, respectively).{24157} It also potently inhibits a variety of other receptor and non-receptor tyrosine kinases, including several in the platelet-derived growth factor, fibroblast growth factor, and endothelial growth factor receptor families.{24157,24156} Cediranib blocks tubule formation by human umbilical vein endothelial cells in vitro and prevents angiogenesis as well as xenograft tumor growth in vivo.{24157} Because of these effects, cediranib has potential use in a range of cancers.{19939,24159,24155}  

     

    Brand:
    Cayman
    SKU:11495 - 10 mg

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  • Receptors for VEGF have central roles in vasculogenesis and angiogenesis and thus serve as targets for cancer therapy.{18368,20203} Cediranib is a potent inhibitor of VEGF receptor tyrosine kinases, including VEGFR1, 2, and 3 (IC50s = 5, 1, and 3 nM, respectively).{24157} It also potently inhibits a variety of other receptor and non-receptor tyrosine kinases, including several in the platelet-derived growth factor, fibroblast growth factor, and endothelial growth factor receptor families.{24157,24156} Cediranib blocks tubule formation by human umbilical vein endothelial cells in vitro and prevents angiogenesis as well as xenograft tumor growth in vivo.{24157} Because of these effects, cediranib has potential use in a range of cancers.{19939,24159,24155}  

     

    Brand:
    Cayman
    SKU:11495 - 25 mg

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  • Receptors for VEGF have central roles in vasculogenesis and angiogenesis and thus serve as targets for cancer therapy.{18368,20203} Cediranib is a potent inhibitor of VEGF receptor tyrosine kinases, including VEGFR1, 2, and 3 (IC50s = 5, 1, and 3 nM, respectively).{24157} It also potently inhibits a variety of other receptor and non-receptor tyrosine kinases, including several in the platelet-derived growth factor, fibroblast growth factor, and endothelial growth factor receptor families.{24157,24156} Cediranib blocks tubule formation by human umbilical vein endothelial cells in vitro and prevents angiogenesis as well as xenograft tumor growth in vivo.{24157} Because of these effects, cediranib has potential use in a range of cancers.{19939,24159,24155}  

     

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    Cayman
    SKU:11495 - 5 mg

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  • Cefaclor is a cephalosporin antibiotic that is active against S. pyogenes, S. pneumoniae, S. aureus, P. mirabilis, S. typhi, E. coli, and H. influenzae (MICs = 0.25, 0.25-2, 1-2, 1, 0.5, 1, and 2-4 μg/ml, respectively).{48414} It is protective against S. pyogenes, S. pneumoniae, S. aureus, P. mirabilis, S. typhi, E. coli, and H. influenzae infections in mice (ED50s = 0.08-30.2 mg/kg). Formulations containing cefaclor have been used in the treatment of various bacterial infections.  

     

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    Cayman
    SKU:23626 - 100 mg

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  • Cefaclor is a cephalosporin antibiotic that is active against S. pyogenes, S. pneumoniae, S. aureus, P. mirabilis, S. typhi, E. coli, and H. influenzae (MICs = 0.25, 0.25-2, 1-2, 1, 0.5, 1, and 2-4 μg/ml, respectively).{48414} It is protective against S. pyogenes, S. pneumoniae, S. aureus, P. mirabilis, S. typhi, E. coli, and H. influenzae infections in mice (ED50s = 0.08-30.2 mg/kg). Formulations containing cefaclor have been used in the treatment of various bacterial infections.  

     

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    Cayman
    SKU:23626 - 250 mg

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  • Cefadroxil is a semisynthetic cephalosporin antibiotic.{42841} It is active against the bacteria B. anthracis, V. cholerae, and P. multocida (MICs = 1, 2, and 4 µg/ml, respectively) among others. Cefadroxil is protective against systemic infections by S. pyogenes, S. pneumoniae, and S. aureus strains in mice with 50% protective dose values (PC50s) of 0.6-2.4, 18-24, and 0.3-29 mg/kg, respectively. Formulations containing cefadroxil have been used in the treatment of a variety of bacterial infections.  

     

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    SKU:20365 -

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  • Cefadroxil is a semisynthetic cephalosporin antibiotic.{42841} It is active against the bacteria B. anthracis, V. cholerae, and P. multocida (MICs = 1, 2, and 4 µg/ml, respectively) among others. Cefadroxil is protective against systemic infections by S. pyogenes, S. pneumoniae, and S. aureus strains in mice with 50% protective dose values (PC50s) of 0.6-2.4, 18-24, and 0.3-29 mg/kg, respectively. Formulations containing cefadroxil have been used in the treatment of a variety of bacterial infections.  

     

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    Cayman
    SKU:20365 -

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  • Cefadroxil is a semisynthetic cephalosporin antibiotic.{42841} It is active against the bacteria B. anthracis, V. cholerae, and P. multocida (MICs = 1, 2, and 4 µg/ml, respectively) among others. Cefadroxil is protective against systemic infections by S. pyogenes, S. pneumoniae, and S. aureus strains in mice with 50% protective dose values (PC50s) of 0.6-2.4, 18-24, and 0.3-29 mg/kg, respectively. Formulations containing cefadroxil have been used in the treatment of a variety of bacterial infections.  

     

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    Cayman
    SKU:20365 -

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  • Cefadroxil is a semisynthetic cephalosporin antibiotic.{42841} It is active against the bacteria B. anthracis, V. cholerae, and P. multocida (MICs = 1, 2, and 4 µg/ml, respectively) among others. Cefadroxil is protective against systemic infections by S. pyogenes, S. pneumoniae, and S. aureus strains in mice with 50% protective dose values (PC50s) of 0.6-2.4, 18-24, and 0.3-29 mg/kg, respectively. Formulations containing cefadroxil have been used in the treatment of a variety of bacterial infections.  

     

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    Cayman
    SKU:20365 -

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  • Cefalothin is a β-lactam cephalosporin antibiotic.{48055,48056} It inhibits the growth of various Gram-positive and Gram-negative bacteria, including several strains of S. pyogenes, S. aureus, C. tetani, N. gonorrhoeae, Salmonella, and Shigella (MICs = 0.1-0.2, 0.312-0.625, 0.078, 1.25, 1.56-6.25, and 3.12-12.5 μg/ml, respectively).{48055} Cefalothin binds to E. coli penicillin-binding proteins (PBPs; IC50s = S. pyogenes, D. pneumoniae, and S. aureus.{48055} Formulations containing cefalothin were previously used in the prophylaxis and treatment of bacterial infections.  

     

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    Cayman
    SKU:26063 - 1 g

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  • Cefalothin is a β-lactam cephalosporin antibiotic.{48055,48056} It inhibits the growth of various Gram-positive and Gram-negative bacteria, including several strains of S. pyogenes, S. aureus, C. tetani, N. gonorrhoeae, Salmonella, and Shigella (MICs = 0.1-0.2, 0.312-0.625, 0.078, 1.25, 1.56-6.25, and 3.12-12.5 μg/ml, respectively).{48055} Cefalothin binds to E. coli penicillin-binding proteins (PBPs; IC50s = S. pyogenes, D. pneumoniae, and S. aureus.{48055} Formulations containing cefalothin were previously used in the prophylaxis and treatment of bacterial infections.  

     

    Brand:
    Cayman
    SKU:26063 - 250 mg

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  • Cefalothin is a β-lactam cephalosporin antibiotic.{48055,48056} It inhibits the growth of various Gram-positive and Gram-negative bacteria, including several strains of S. pyogenes, S. aureus, C. tetani, N. gonorrhoeae, Salmonella, and Shigella (MICs = 0.1-0.2, 0.312-0.625, 0.078, 1.25, 1.56-6.25, and 3.12-12.5 μg/ml, respectively).{48055} Cefalothin binds to E. coli penicillin-binding proteins (PBPs; IC50s = S. pyogenes, D. pneumoniae, and S. aureus.{48055} Formulations containing cefalothin were previously used in the prophylaxis and treatment of bacterial infections.  

     

    Brand:
    Cayman
    SKU:26063 - 5 g

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  • Cefalothin is a β-lactam cephalosporin antibiotic.{48055,48056} It inhibits the growth of various Gram-positive and Gram-negative bacteria, including several strains of S. pyogenes, S. aureus, C. tetani, N. gonorrhoeae, Salmonella, and Shigella (MICs = 0.1-0.2, 0.312-0.625, 0.078, 1.25, 1.56-6.25, and 3.12-12.5 μg/ml, respectively).{48055} Cefalothin binds to E. coli penicillin-binding proteins (PBPs; IC50s = S. pyogenes, D. pneumoniae, and S. aureus.{48055} Formulations containing cefalothin were previously used in the prophylaxis and treatment of bacterial infections.  

     

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    Cayman
    SKU:26063 - 500 mg

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  • Cefamandole is a cephalosporin antibiotic that is effective against E. coli (MIC values range from 0.25-2 mg/L depending on strain) as well as H. influenza, S. pneumoniae, and S. aureus.{26293,29387} It has been used to study the expression and inhibition of penicillin-binding proteins on bacterial cell walls and to study antibiotic resistance.{26293}  

     

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  • Cefamandole is a cephalosporin antibiotic that is effective against E. coli (MIC values range from 0.25-2 mg/L depending on strain) as well as H. influenza, S. pneumoniae, and S. aureus.{26293,29387} It has been used to study the expression and inhibition of penicillin-binding proteins on bacterial cell walls and to study antibiotic resistance.{26293}  

     

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    Cayman
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  • Cefamandole is a cephalosporin antibiotic that is effective against E. coli (MIC values range from 0.25-2 mg/L depending on strain) as well as H. influenza, S. pneumoniae, and S. aureus.{26293,29387} It has been used to study the expression and inhibition of penicillin-binding proteins on bacterial cell walls and to study antibiotic resistance.{26293}  

     

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    Cayman
    SKU:-

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  • Cefamandole is a cephalosporin antibiotic that is effective against E. coli (MIC values range from 0.25-2 mg/L depending on strain) as well as H. influenza, S. pneumoniae, and S. aureus.{26293,29387} It has been used to study the expression and inhibition of penicillin-binding proteins on bacterial cell walls and to study antibiotic resistance.{26293}  

     

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    Cayman
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  • Cefamandole nafate is a formate ester prodrug form of the cephalosporin antibiotic cefamandole (Item No. 18138).{43407} Cefamandole nafate inhibits the growth of E. cloacae, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. aureus, and S. pyogenes in vitro (MICs = 0.1-50 μg/ml). In vivo, cefamanadole nafate protects against E. cloacae, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. aureus, and S. pyogenes infection in mice (ED50s = 0.3-334 mg/kg). Cefamandole (500 mg/kg) also protects against nephrotoxicity induced by the aminoglycoside antibiotic tobramycin (Item No. 14596) in rats.{43408}  

     

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    Cayman
    SKU:23988 - 1 g

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  • Cefamandole nafate is a formate ester prodrug form of the cephalosporin antibiotic cefamandole (Item No. 18138).{43407} Cefamandole nafate inhibits the growth of E. cloacae, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. aureus, and S. pyogenes in vitro (MICs = 0.1-50 μg/ml). In vivo, cefamanadole nafate protects against E. cloacae, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. aureus, and S. pyogenes infection in mice (ED50s = 0.3-334 mg/kg). Cefamandole (500 mg/kg) also protects against nephrotoxicity induced by the aminoglycoside antibiotic tobramycin (Item No. 14596) in rats.{43408}  

     

    Brand:
    Cayman
    SKU:23988 - 5 g

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  • Cefamandole nafate is a formate ester prodrug form of the cephalosporin antibiotic cefamandole (Item No. 18138).{43407} Cefamandole nafate inhibits the growth of E. cloacae, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. aureus, and S. pyogenes in vitro (MICs = 0.1-50 μg/ml). In vivo, cefamanadole nafate protects against E. cloacae, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. aureus, and S. pyogenes infection in mice (ED50s = 0.3-334 mg/kg). Cefamandole (500 mg/kg) also protects against nephrotoxicity induced by the aminoglycoside antibiotic tobramycin (Item No. 14596) in rats.{43408}  

     

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    Cayman
    SKU:23988 - 500 mg

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  • Cefapirin is a first generation cephalosporin antibiotic that is broadly effective against gram-negative and gram-positive bacteria.{28405,28406} The bactericidal action of cefapirin results from inhibition of cell-wall synthesis, mediated by its binding to penicillin binding proteins. It is mainly used in veterinary medicine for intramammary treatment of mastitis and intrauterine treatment of endometritis in cattle.{28405,28406}  

     

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  • Cefapirin is a first generation cephalosporin antibiotic that is broadly effective against gram-negative and gram-positive bacteria.{28405,28406} The bactericidal action of cefapirin results from inhibition of cell-wall synthesis, mediated by its binding to penicillin binding proteins. It is mainly used in veterinary medicine for intramammary treatment of mastitis and intrauterine treatment of endometritis in cattle.{28405,28406}  

     

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    Cayman
    SKU:-

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  • Cefapirin is a first generation cephalosporin antibiotic that is broadly effective against gram-negative and gram-positive bacteria.{28405,28406} The bactericidal action of cefapirin results from inhibition of cell-wall synthesis, mediated by its binding to penicillin binding proteins. It is mainly used in veterinary medicine for intramammary treatment of mastitis and intrauterine treatment of endometritis in cattle.{28405,28406}  

     

    Brand:
    Cayman
    SKU:-

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  • Cefapirin is a first generation cephalosporin antibiotic that is broadly effective against gram-negative and gram-positive bacteria.{28405,28406} The bactericidal action of cefapirin results from inhibition of cell-wall synthesis, mediated by its binding to penicillin binding proteins. It is mainly used in veterinary medicine for intramammary treatment of mastitis and intrauterine treatment of endometritis in cattle.{28405,28406}  

     

    Brand:
    Cayman
    SKU:-

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  • Cefazolin is a broad-spectrum cephalosporin antibiotic that is active in vitro against various Gram-positive and Gram-negative bacteria (MICs = 0.2-12.5 μg/ml).{25759} It also inhibits the growth of clinical isolates of S. aureus, E. coli, P. mirabilis, and K. pneumoniae (MICs = 0.1-25 μg/ml). In vivo, cefazolin protects against S. aureus, E. coli, and P. mirabilis infection in mice (ED50s = <0.09-1.78, 0.44-3.63, and 2.31-5.2 mg/animal, respectively). Formulations containing cefazolin have been used to treat a variety of bacterial infections.  

     

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  • Cefazolin is a broad-spectrum cephalosporin antibiotic that is active in vitro against various Gram-positive and Gram-negative bacteria (MICs = 0.2-12.5 μg/ml).{25759} It also inhibits the growth of clinical isolates of S. aureus, E. coli, P. mirabilis, and K. pneumoniae (MICs = 0.1-25 μg/ml). In vivo, cefazolin protects against S. aureus, E. coli, and P. mirabilis infection in mice (ED50s = <0.09-1.78, 0.44-3.63, and 2.31-5.2 mg/animal, respectively). Formulations containing cefazolin have been used to treat a variety of bacterial infections.  

     

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    Cayman
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  • Cefazolin is a broad-spectrum cephalosporin antibiotic that is active in vitro against various Gram-positive and Gram-negative bacteria (MICs = 0.2-12.5 μg/ml).{25759} It also inhibits the growth of clinical isolates of S. aureus, E. coli, P. mirabilis, and K. pneumoniae (MICs = 0.1-25 μg/ml). In vivo, cefazolin protects against S. aureus, E. coli, and P. mirabilis infection in mice (ED50s = <0.09-1.78, 0.44-3.63, and 2.31-5.2 mg/animal, respectively). Formulations containing cefazolin have been used to treat a variety of bacterial infections.  

     

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    Cayman
    SKU:-
  • Cefazolin is a broad-spectrum cephalosporin antibiotic that is active in vitro against various Gram-positive and Gram-negative bacteria (MICs = 0.2-12.5 μg/ml).{25759} It also inhibits the growth of clinical isolates of S. aureus, E. coli, P. mirabilis, and K. pneumoniae (MICs = 0.1-25 μg/ml). In vivo, cefazolin protects against S. aureus, E. coli, and P. mirabilis infection in mice (ED50s = <0.09-1.78, 0.44-3.63, and 2.31-5.2 mg/animal, respectively). Formulations containing cefazolin have been used to treat a variety of bacterial infections.  

     

    Brand:
    Cayman
    SKU:-
  • Cefazolin-13C2,15N is intended for use as an internal standard for the quantification of cefazolin (Item No. 15776) by GC- or LC-MS. Cefazolin is a broad-spectrum cephalosporin antibiotic that is active in vitro against various Gram-positive and Gram-negative bacteria (MICs = 0.2-12.5 μg/ml).{25759} It also inhibits the growth of clinical isolates of S. aureus, E. coli, P. mirabilis, and K. pneumoniae (MICs = 0.1-25 µg/ml). In vivo, cefazolin protects against S. aureus, E. coli, and P. mirabilis infection in mice (ED50s = <0.09-1.78, 0.44-3.63, and 2.31-5.2 mg/animal, respectively). Formulations containing cefazolin have been used to treat a variety of bacterial infections.  

     

    Brand:
    Cayman
    SKU:25319 - 1 mg

    Available on backorder

  • Cefdinir is a broad-spectrum β-lactam antibiotic of the cephalosporin class that inhibits cell wall synthesis in Gram-positive and Gram-negative bacteria.{33830} Formulations containing cefdinir are used for bacterial infections of the respiratory system, ear, throat, and skin.{33829} Children with severe acute malnutrition treated with a formulation containing cefnidir (14 mg/kg twice daily for seven days) had a 90.9% recovery rate and a significantly reduced mortality rate.{33831}  

     

    Brand:
    Cayman
    SKU:21521 -

    Out of stock

  • Cefdinir is a broad-spectrum β-lactam antibiotic of the cephalosporin class that inhibits cell wall synthesis in Gram-positive and Gram-negative bacteria.{33830} Formulations containing cefdinir are used for bacterial infections of the respiratory system, ear, throat, and skin.{33829} Children with severe acute malnutrition treated with a formulation containing cefnidir (14 mg/kg twice daily for seven days) had a 90.9% recovery rate and a significantly reduced mortality rate.{33831}  

     

    Brand:
    Cayman
    SKU:21521 -

    Out of stock

  • Cefdinir is a broad-spectrum β-lactam antibiotic of the cephalosporin class that inhibits cell wall synthesis in Gram-positive and Gram-negative bacteria.{33830} Formulations containing cefdinir are used for bacterial infections of the respiratory system, ear, throat, and skin.{33829} Children with severe acute malnutrition treated with a formulation containing cefnidir (14 mg/kg twice daily for seven days) had a 90.9% recovery rate and a significantly reduced mortality rate.{33831}  

     

    Brand:
    Cayman
    SKU:21521 -

    Out of stock

  • Cefditoren pivoxil is an orally bioavailable prodrug form of the broad-spectrum cephalosporin antibiotic cefditoren.{53674} Cefditoren pivoxil is hydrolyzed by intestinal wall esterases to form cefditoren. Cefditoren pivoxil is effective against systemic S. aureus, E. coli, K. pneumoniae, P. mirabilis, or S. marcescens infections in mice with ED50 values of 10, 2.5, 11, 4.4, and 11 mg/kg, respectively.{53675} Formulations containing cefditoren pivoxil were previously used in the treatment of acute bacterial exacerbations of chronic bronchitis and community-acquired pneumonia.  

     

    Brand:
    Cayman
    SKU:30315 - 10 mg

    Available on backorder

  • Cefditoren pivoxil is an orally bioavailable prodrug form of the broad-spectrum cephalosporin antibiotic cefditoren.{53674} Cefditoren pivoxil is hydrolyzed by intestinal wall esterases to form cefditoren. Cefditoren pivoxil is effective against systemic S. aureus, E. coli, K. pneumoniae, P. mirabilis, or S. marcescens infections in mice with ED50 values of 10, 2.5, 11, 4.4, and 11 mg/kg, respectively.{53675} Formulations containing cefditoren pivoxil were previously used in the treatment of acute bacterial exacerbations of chronic bronchitis and community-acquired pneumonia.  

     

    Brand:
    Cayman
    SKU:30315 - 100 mg

    Available on backorder

  • Cefditoren pivoxil is an orally bioavailable prodrug form of the broad-spectrum cephalosporin antibiotic cefditoren.{53674} Cefditoren pivoxil is hydrolyzed by intestinal wall esterases to form cefditoren. Cefditoren pivoxil is effective against systemic S. aureus, E. coli, K. pneumoniae, P. mirabilis, or S. marcescens infections in mice with ED50 values of 10, 2.5, 11, 4.4, and 11 mg/kg, respectively.{53675} Formulations containing cefditoren pivoxil were previously used in the treatment of acute bacterial exacerbations of chronic bronchitis and community-acquired pneumonia.  

     

    Brand:
    Cayman
    SKU:30315 - 5 mg

    Available on backorder

  • Cefditoren pivoxil is an orally bioavailable prodrug form of the broad-spectrum cephalosporin antibiotic cefditoren.{53674} Cefditoren pivoxil is hydrolyzed by intestinal wall esterases to form cefditoren. Cefditoren pivoxil is effective against systemic S. aureus, E. coli, K. pneumoniae, P. mirabilis, or S. marcescens infections in mice with ED50 values of 10, 2.5, 11, 4.4, and 11 mg/kg, respectively.{53675} Formulations containing cefditoren pivoxil were previously used in the treatment of acute bacterial exacerbations of chronic bronchitis and community-acquired pneumonia.  

     

    Brand:
    Cayman
    SKU:30315 - 50 mg

    Available on backorder

  • Cefepime is a broad-spectrum cephalosporin antibiotic that inhibits the growth of Gram-positive and Gram-negative bacteria.{38779,38780} It inhibits the growth of some clinical isolates of Corynebacterium, Streptococcus, and Staphylococcus (MIC90s = 0.03-8 μg/ml), but does not inhibit the growth of methicillin-resistant S. aureus (MRSA) or S. haemolyticus (MIC50s = >128 μg/ml).{38779} Cefepime inhibits the growth of some Citrobacter, Enterobacter, Klebsiella, Salmonella, Serratia, Shigella, and enteric bacilli species in addition to P. mirabilis and E. coli clinical isolates (MIC90s = ≤0.12-2 μg/ml).{38780} It also inhibits the growth of E. coli and Klebsiella strains that produce extended-spectrum β-lactamase (ESBL; MIC90s = 4 and 8 μg/mL, respectively) and of indole-positive Proteae (MIC90 = 0.25 μg/ml). Cefepime inhibits the growth of pneumococci strains (MICs = 0.5-2 mg/l) in vitro and in vivo in a mouse model of peritonitis (ED50s = 0.6-1.14 mg/kg).{38781} Formulations containing cefepime have been used in the treatment of a variety of bacterial infections.  

     

    Brand:
    Cayman
    SKU:23633 - 1 g

    Available on backorder

  • Cefepime is a broad-spectrum cephalosporin antibiotic that inhibits the growth of Gram-positive and Gram-negative bacteria.{38779,38780} It inhibits the growth of some clinical isolates of Corynebacterium, Streptococcus, and Staphylococcus (MIC90s = 0.03-8 μg/ml), but does not inhibit the growth of methicillin-resistant S. aureus (MRSA) or S. haemolyticus (MIC50s = >128 μg/ml).{38779} Cefepime inhibits the growth of some Citrobacter, Enterobacter, Klebsiella, Salmonella, Serratia, Shigella, and enteric bacilli species in addition to P. mirabilis and E. coli clinical isolates (MIC90s = ≤0.12-2 μg/ml).{38780} It also inhibits the growth of E. coli and Klebsiella strains that produce extended-spectrum β-lactamase (ESBL; MIC90s = 4 and 8 μg/mL, respectively) and of indole-positive Proteae (MIC90 = 0.25 μg/ml). Cefepime inhibits the growth of pneumococci strains (MICs = 0.5-2 mg/l) in vitro and in vivo in a mouse model of peritonitis (ED50s = 0.6-1.14 mg/kg).{38781} Formulations containing cefepime have been used in the treatment of a variety of bacterial infections.  

     

    Brand:
    Cayman
    SKU:23633 - 250 mg

    Available on backorder

  • Cefepime is a broad-spectrum cephalosporin antibiotic that inhibits the growth of Gram-positive and Gram-negative bacteria.{38779,38780} It inhibits the growth of some clinical isolates of Corynebacterium, Streptococcus, and Staphylococcus (MIC90s = 0.03-8 μg/ml), but does not inhibit the growth of methicillin-resistant S. aureus (MRSA) or S. haemolyticus (MIC50s = >128 μg/ml).{38779} Cefepime inhibits the growth of some Citrobacter, Enterobacter, Klebsiella, Salmonella, Serratia, Shigella, and enteric bacilli species in addition to P. mirabilis and E. coli clinical isolates (MIC90s = ≤0.12-2 μg/ml).{38780} It also inhibits the growth of E. coli and Klebsiella strains that produce extended-spectrum β-lactamase (ESBL; MIC90s = 4 and 8 μg/mL, respectively) and of indole-positive Proteae (MIC90 = 0.25 μg/ml). Cefepime inhibits the growth of pneumococci strains (MICs = 0.5-2 mg/l) in vitro and in vivo in a mouse model of peritonitis (ED50s = 0.6-1.14 mg/kg).{38781} Formulations containing cefepime have been used in the treatment of a variety of bacterial infections.  

     

    Brand:
    Cayman
    SKU:23633 - 5 g

    Available on backorder

  • Cefepime is a broad-spectrum cephalosporin antibiotic that inhibits the growth of Gram-positive and Gram-negative bacteria.{38779,38780} It inhibits the growth of some clinical isolates of Corynebacterium, Streptococcus, and Staphylococcus (MIC90s = 0.03-8 μg/ml), but does not inhibit the growth of methicillin-resistant S. aureus (MRSA) or S. haemolyticus (MIC50s = >128 μg/ml).{38779} Cefepime inhibits the growth of some Citrobacter, Enterobacter, Klebsiella, Salmonella, Serratia, Shigella, and enteric bacilli species in addition to P. mirabilis and E. coli clinical isolates (MIC90s = ≤0.12-2 μg/ml).{38780} It also inhibits the growth of E. coli and Klebsiella strains that produce extended-spectrum β-lactamase (ESBL; MIC90s = 4 and 8 μg/mL, respectively) and of indole-positive Proteae (MIC90 = 0.25 μg/ml). Cefepime inhibits the growth of pneumococci strains (MICs = 0.5-2 mg/l) in vitro and in vivo in a mouse model of peritonitis (ED50s = 0.6-1.14 mg/kg).{38781} Formulations containing cefepime have been used in the treatment of a variety of bacterial infections.  

     

    Brand:
    Cayman
    SKU:23633 - 500 mg

    Available on backorder

  • Cefixime is a third generation cephalosporin antibiotic. It is effective against a variety of Gram-negative bacteria, including E. coli, K. pneumoniae, and H. influenzae (MIC values range from <0.025 to 25 µg/ml).{28223} Cefixime binds penicillin-binding proteins and is stable to many penicillinases and β-lactamases.{28221,28225} It is an effective, orally-active cephalosporin with applications in acute otitis media, respiratory tract infections, and urinary tract infections.{28222,28224}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Cefixime is a third generation cephalosporin antibiotic. It is effective against a variety of Gram-negative bacteria, including E. coli, K. pneumoniae, and H. influenzae (MIC values range from <0.025 to 25 µg/ml).{28223} Cefixime binds penicillin-binding proteins and is stable to many penicillinases and β-lactamases.{28221,28225} It is an effective, orally-active cephalosporin with applications in acute otitis media, respiratory tract infections, and urinary tract infections.{28222,28224}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Cefixime is a third generation cephalosporin antibiotic. It is effective against a variety of Gram-negative bacteria, including E. coli, K. pneumoniae, and H. influenzae (MIC values range from <0.025 to 25 µg/ml).{28223} Cefixime binds penicillin-binding proteins and is stable to many penicillinases and β-lactamases.{28221,28225} It is an effective, orally-active cephalosporin with applications in acute otitis media, respiratory tract infections, and urinary tract infections.{28222,28224}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Cefixime is a third generation cephalosporin antibiotic. It is effective against a variety of Gram-negative bacteria, including E. coli, K. pneumoniae, and H. influenzae (MIC values range from <0.025 to 25 µg/ml).{28223} Cefixime binds penicillin-binding proteins and is stable to many penicillinases and β-lactamases.{28221,28225} It is an effective, orally-active cephalosporin with applications in acute otitis media, respiratory tract infections, and urinary tract infections.{28222,28224}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Cefmenoxime is a broad-spectrum cephalosporin antibiotic.{45158} It is active against clinical isolates of S. aureus, S. epidermidis, S. pyogenes, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. marcescens, and E. cloacae in vitro (MICs = 0.013-6.25 μg/ml). It is active against various Gram-positive and Gram-negative bacterial infections in mice (ED50s = 0.016-66 mg/kg). It increases survival in a mouse model of K. pneumoniae infection with a 50% survival dose (SD50) value of 7.6 mg/kg. Cefmenoxime is curative in a mouse model of P. mirabilis urinary tract infection with curative dose (CD50) values ranging from 0.4 to 0.75 mg/kg. Formulations containing cefmenoxime have been used to treat various bacterial infections.  

     

    Brand:
    Cayman
    SKU:26440 - 1 g

    Available on backorder

  • Cefmenoxime is a broad-spectrum cephalosporin antibiotic.{45158} It is active against clinical isolates of S. aureus, S. epidermidis, S. pyogenes, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. marcescens, and E. cloacae in vitro (MICs = 0.013-6.25 μg/ml). It is active against various Gram-positive and Gram-negative bacterial infections in mice (ED50s = 0.016-66 mg/kg). It increases survival in a mouse model of K. pneumoniae infection with a 50% survival dose (SD50) value of 7.6 mg/kg. Cefmenoxime is curative in a mouse model of P. mirabilis urinary tract infection with curative dose (CD50) values ranging from 0.4 to 0.75 mg/kg. Formulations containing cefmenoxime have been used to treat various bacterial infections.  

     

    Brand:
    Cayman
    SKU:26440 - 100 mg

    Available on backorder

  • Cefmenoxime is a broad-spectrum cephalosporin antibiotic.{45158} It is active against clinical isolates of S. aureus, S. epidermidis, S. pyogenes, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. marcescens, and E. cloacae in vitro (MICs = 0.013-6.25 μg/ml). It is active against various Gram-positive and Gram-negative bacterial infections in mice (ED50s = 0.016-66 mg/kg). It increases survival in a mouse model of K. pneumoniae infection with a 50% survival dose (SD50) value of 7.6 mg/kg. Cefmenoxime is curative in a mouse model of P. mirabilis urinary tract infection with curative dose (CD50) values ranging from 0.4 to 0.75 mg/kg. Formulations containing cefmenoxime have been used to treat various bacterial infections.  

     

    Brand:
    Cayman
    SKU:26440 - 50 mg

    Available on backorder

  • Cefmenoxime is a broad-spectrum cephalosporin antibiotic.{45158} It is active against clinical isolates of S. aureus, S. epidermidis, S. pyogenes, E. coli, K. pneumoniae, P. mirabilis, P. vulgaris, P. morganii, S. marcescens, and E. cloacae in vitro (MICs = 0.013-6.25 μg/ml). It is active against various Gram-positive and Gram-negative bacterial infections in mice (ED50s = 0.016-66 mg/kg). It increases survival in a mouse model of K. pneumoniae infection with a 50% survival dose (SD50) value of 7.6 mg/kg. Cefmenoxime is curative in a mouse model of P. mirabilis urinary tract infection with curative dose (CD50) values ranging from 0.4 to 0.75 mg/kg. Formulations containing cefmenoxime have been used to treat various bacterial infections.  

     

    Brand:
    Cayman
    SKU:26440 - 500 mg

    Available on backorder

  • Cefmetazole is a cephamycin antibiotic.{55066} It is active against E. coli, P. mirabilis, H. influenzae, N. gonorrhoeae, S. pneumoniae, and S. pyogenes (MIC50s = 0.25-2 μg/ml). Cefmetazole (20 and 40 mg/kg per day) decreases the lesion size and the number of ulcerative lesions in a rabbit model of active syphilis.{55067}  

     

    Brand:
    Cayman
    SKU:30269 - 10 mg

    Available on backorder

  • Cefmetazole is a cephamycin antibiotic.{55066} It is active against E. coli, P. mirabilis, H. influenzae, N. gonorrhoeae, S. pneumoniae, and S. pyogenes (MIC50s = 0.25-2 μg/ml). Cefmetazole (20 and 40 mg/kg per day) decreases the lesion size and the number of ulcerative lesions in a rabbit model of active syphilis.{55067}  

     

    Brand:
    Cayman
    SKU:30269 - 100 mg

    Available on backorder

  • Cefmetazole is a cephamycin antibiotic.{55066} It is active against E. coli, P. mirabilis, H. influenzae, N. gonorrhoeae, S. pneumoniae, and S. pyogenes (MIC50s = 0.25-2 μg/ml). Cefmetazole (20 and 40 mg/kg per day) decreases the lesion size and the number of ulcerative lesions in a rabbit model of active syphilis.{55067}  

     

    Brand:
    Cayman
    SKU:30269 - 25 mg

    Available on backorder

  • Cefmetazole is a cephamycin antibiotic.{55066} It is active against E. coli, P. mirabilis, H. influenzae, N. gonorrhoeae, S. pneumoniae, and S. pyogenes (MIC50s = 0.25-2 μg/ml). Cefmetazole (20 and 40 mg/kg per day) decreases the lesion size and the number of ulcerative lesions in a rabbit model of active syphilis.{55067}  

     

    Brand:
    Cayman
    SKU:30269 - 50 mg

    Available on backorder

  • Cefonicid is a second-generation cephalosporin antibiotic.{29387} Like other cephalosporins, cefonicid interferes with cell wall biosynthesis in bacteria, leading to lysis of the infectious organism. It is a broad-spectrum antibiotic and has a prolonged serum elimination half-life in animals.{29387}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cefonicid is a second-generation cephalosporin antibiotic.{29387} Like other cephalosporins, cefonicid interferes with cell wall biosynthesis in bacteria, leading to lysis of the infectious organism. It is a broad-spectrum antibiotic and has a prolonged serum elimination half-life in animals.{29387}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cefonicid is a second-generation cephalosporin antibiotic.{29387} Like other cephalosporins, cefonicid interferes with cell wall biosynthesis in bacteria, leading to lysis of the infectious organism. It is a broad-spectrum antibiotic and has a prolonged serum elimination half-life in animals.{29387}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cefoperazone is a cephalosporin antibiotic that is active in vitro against most Gram-positive and Gram-negative bacteria, including β-lactamase strains (3-4 µg/ml inhibits 90% of S. aureus growth).{25856} It has been studied in the treatment of upper and lower respiratory tract infections, urinary tract infections, gynecological infections, skin infections, as well as bacteremia.{25856}  

     

    Brand:
    Cayman
    SKU:-
  • Cefoperazone is a cephalosporin antibiotic that is active in vitro against most Gram-positive and Gram-negative bacteria, including β-lactamase strains (3-4 µg/ml inhibits 90% of S. aureus growth).{25856} It has been studied in the treatment of upper and lower respiratory tract infections, urinary tract infections, gynecological infections, skin infections, as well as bacteremia.{25856}  

     

    Brand:
    Cayman
    SKU:-
  • Cefoperazone is a cephalosporin antibiotic that is active in vitro against most Gram-positive and Gram-negative bacteria, including β-lactamase strains (3-4 µg/ml inhibits 90% of S. aureus growth).{25856} It has been studied in the treatment of upper and lower respiratory tract infections, urinary tract infections, gynecological infections, skin infections, as well as bacteremia.{25856}  

     

    Brand:
    Cayman
    SKU:-
  • Cefotaxime is a cephalosporin antibiotic with potent in vitro activity against streptococcal species, including S. aureus (IC50 = 2 µg/ml) and penicillin-resistant S. pneumoniae.{25856} It is also effective against a wide range of other β-lactamase-producing bacterial species (MIC90s = 0.01 – 130 µg/ml).{25856} Cefotaxime acts by interfering with bacterial cell wall synthesis and has also been shown to be a competitive inhibitor of β-lactamase.{25971}  

     

    Brand:
    Cayman
    SKU:-
  • Cefotaxime is a cephalosporin antibiotic with potent in vitro activity against streptococcal species, including S. aureus (IC50 = 2 µg/ml) and penicillin-resistant S. pneumoniae.{25856} It is also effective against a wide range of other β-lactamase-producing bacterial species (MIC90s = 0.01 – 130 µg/ml).{25856} Cefotaxime acts by interfering with bacterial cell wall synthesis and has also been shown to be a competitive inhibitor of β-lactamase.{25971}  

     

    Brand:
    Cayman
    SKU:-
  • Cefotaxime is a cephalosporin antibiotic with potent in vitro activity against streptococcal species, including S. aureus (IC50 = 2 µg/ml) and penicillin-resistant S. pneumoniae.{25856} It is also effective against a wide range of other β-lactamase-producing bacterial species (MIC90s = 0.01 – 130 µg/ml).{25856} Cefotaxime acts by interfering with bacterial cell wall synthesis and has also been shown to be a competitive inhibitor of β-lactamase.{25971}  

     

    Brand:
    Cayman
    SKU:-
  • Cefotaxime is a cephalosporin antibiotic with potent in vitro activity against streptococcal species, including S. aureus (IC50 = 2 µg/ml) and penicillin-resistant S. pneumoniae.{25856} It is also effective against a wide range of other β-lactamase-producing bacterial species (MIC90s = 0.01 – 130 µg/ml).{25856} Cefotaxime acts by interfering with bacterial cell wall synthesis and has also been shown to be a competitive inhibitor of β-lactamase.{25971}  

     

    Brand:
    Cayman
    SKU:-
  • Cefotetan is a cephamycin antibiotic that is active against both Gram-positive and Gram-negative bacteria including isolates of E. coli, S. aureus, K. pneumoniae, and P. maltophilia (MICs = 0.03-32 mg/ml).{36577} It reduces mortality by 50% in a rabbit model of fecal peritonitis when administered at a dose of 25 mg/kg twice daily.{36578} Formulations containing cefotetan have been used in the treatment of various bacterial infections.  

     

    Brand:
    Cayman
    SKU:23624 - 100 mg

    Available on backorder

  • Cefotetan is a cephamycin antibiotic that is active against both Gram-positive and Gram-negative bacteria including isolates of E. coli, S. aureus, K. pneumoniae, and P. maltophilia (MICs = 0.03-32 mg/ml).{36577} It reduces mortality by 50% in a rabbit model of fecal peritonitis when administered at a dose of 25 mg/kg twice daily.{36578} Formulations containing cefotetan have been used in the treatment of various bacterial infections.  

     

    Brand:
    Cayman
    SKU:23624 - 250 mg

    Available on backorder

  • Cefotetan is a cephamycin antibiotic that is active against both Gram-positive and Gram-negative bacteria including isolates of E. coli, S. aureus, K. pneumoniae, and P. maltophilia (MICs = 0.03-32 mg/ml).{36577} It reduces mortality by 50% in a rabbit model of fecal peritonitis when administered at a dose of 25 mg/kg twice daily.{36578} Formulations containing cefotetan have been used in the treatment of various bacterial infections.  

     

    Brand:
    Cayman
    SKU:23624 - 50 mg

    Available on backorder

  • Cefoxitin is a second generation cephalosporin antibiotic that has been used to treat a wide range of gram-negative and gram-positive bacteria including anaerobes.{25972} It acts by interfering with bacterial cell wall synthesis and has also been shown to induce β-lactamase synthesis.{25971}  

     

    Brand:
    Cayman
    SKU:-
  • Cefoxitin is a second generation cephalosporin antibiotic that has been used to treat a wide range of gram-negative and gram-positive bacteria including anaerobes.{25972} It acts by interfering with bacterial cell wall synthesis and has also been shown to induce β-lactamase synthesis.{25971}  

     

    Brand:
    Cayman
    SKU:-
  • Cefoxitin is a second generation cephalosporin antibiotic that has been used to treat a wide range of gram-negative and gram-positive bacteria including anaerobes.{25972} It acts by interfering with bacterial cell wall synthesis and has also been shown to induce β-lactamase synthesis.{25971}  

     

    Brand:
    Cayman
    SKU:-
  • Cefpodoxime is a metabolite of cefpodoxime proxetil, a third generation cephalosporin antibiotic, that is active against both Gram-positive and Gram-negative bacteria (MIC90s = 0.015-8 µg/ml).{26281}  

     

    Brand:
    Cayman
    SKU:-
  • Cefpodoxime is a metabolite of cefpodoxime proxetil, a third generation cephalosporin antibiotic, that is active against both Gram-positive and Gram-negative bacteria (MIC90s = 0.015-8 µg/ml).{26281}  

     

    Brand:
    Cayman
    SKU:-
  • Cefpodoxime is a metabolite of cefpodoxime proxetil, a third generation cephalosporin antibiotic, that is active against both Gram-positive and Gram-negative bacteria (MIC90s = 0.015-8 µg/ml).{26281}  

     

    Brand:
    Cayman
    SKU:-
  • Cefpodoxime is a metabolite of cefpodoxime proxetil, a third generation cephalosporin antibiotic, that is active against both Gram-positive and Gram-negative bacteria (MIC90s = 0.015-8 µg/ml).{26281}  

     

    Brand:
    Cayman
    SKU:-
  • Cefprozil is an orally bioavailable, second generation, broad-spectrum cephalosporin antibiotic that inhibits the growth of both Gram-positive and Gram-negative bacteria.{43139,43140} It inhibits the growth of E. coli, E. faecalis, E. faecium, N. gonorrhoeae, N. meningitidis, P. mirabilis, S. aureus, S. pyogenes, and S. pneumoniae strains (MICs = 0.013-25 μg/ml) and clinical isolates of penicillin-susceptible, -intermediate, and -resistant S. pneumoniae and methicillin-sensitive S. aureus (MIC90s = 0.12-16 μg/ml). In vivo, cefprozil protects mice challenged with E. coli, S. aureus, S. pyogenes, and P. mirabilis strains with protective doses (PD50s) ranging from 0.07 to 1.3 mg/kg.{43139} Cefprozil binds to penicillin-binding proteins (PBPs), which disrupts their ability to cross-link peptidoglycan and leads to weakened bacterial cell walls.{43141} Formulations containing cefprozil have been used in the treatment of respiratory tract, skin, and other bacterial infections.  

     

    Brand:
    Cayman
    SKU:23840 - 10 mg

    Available on backorder

  • Cefprozil is an orally bioavailable, second generation, broad-spectrum cephalosporin antibiotic that inhibits the growth of both Gram-positive and Gram-negative bacteria.{43139,43140} It inhibits the growth of E. coli, E. faecalis, E. faecium, N. gonorrhoeae, N. meningitidis, P. mirabilis, S. aureus, S. pyogenes, and S. pneumoniae strains (MICs = 0.013-25 μg/ml) and clinical isolates of penicillin-susceptible, -intermediate, and -resistant S. pneumoniae and methicillin-sensitive S. aureus (MIC90s = 0.12-16 μg/ml). In vivo, cefprozil protects mice challenged with E. coli, S. aureus, S. pyogenes, and P. mirabilis strains with protective doses (PD50s) ranging from 0.07 to 1.3 mg/kg.{43139} Cefprozil binds to penicillin-binding proteins (PBPs), which disrupts their ability to cross-link peptidoglycan and leads to weakened bacterial cell walls.{43141} Formulations containing cefprozil have been used in the treatment of respiratory tract, skin, and other bacterial infections.  

     

    Brand:
    Cayman
    SKU:23840 - 25 mg

    Available on backorder

  • Cefprozil is an orally bioavailable, second generation, broad-spectrum cephalosporin antibiotic that inhibits the growth of both Gram-positive and Gram-negative bacteria.{43139,43140} It inhibits the growth of E. coli, E. faecalis, E. faecium, N. gonorrhoeae, N. meningitidis, P. mirabilis, S. aureus, S. pyogenes, and S. pneumoniae strains (MICs = 0.013-25 μg/ml) and clinical isolates of penicillin-susceptible, -intermediate, and -resistant S. pneumoniae and methicillin-sensitive S. aureus (MIC90s = 0.12-16 μg/ml). In vivo, cefprozil protects mice challenged with E. coli, S. aureus, S. pyogenes, and P. mirabilis strains with protective doses (PD50s) ranging from 0.07 to 1.3 mg/kg.{43139} Cefprozil binds to penicillin-binding proteins (PBPs), which disrupts their ability to cross-link peptidoglycan and leads to weakened bacterial cell walls.{43141} Formulations containing cefprozil have been used in the treatment of respiratory tract, skin, and other bacterial infections.  

     

    Brand:
    Cayman
    SKU:23840 - 5 mg

    Available on backorder

  • Cefprozil is an orally bioavailable, second generation, broad-spectrum cephalosporin antibiotic that inhibits the growth of both Gram-positive and Gram-negative bacteria.{43139,43140} It inhibits the growth of E. coli, E. faecalis, E. faecium, N. gonorrhoeae, N. meningitidis, P. mirabilis, S. aureus, S. pyogenes, and S. pneumoniae strains (MICs = 0.013-25 μg/ml) and clinical isolates of penicillin-susceptible, -intermediate, and -resistant S. pneumoniae and methicillin-sensitive S. aureus (MIC90s = 0.12-16 μg/ml). In vivo, cefprozil protects mice challenged with E. coli, S. aureus, S. pyogenes, and P. mirabilis strains with protective doses (PD50s) ranging from 0.07 to 1.3 mg/kg.{43139} Cefprozil binds to penicillin-binding proteins (PBPs), which disrupts their ability to cross-link peptidoglycan and leads to weakened bacterial cell walls.{43141} Formulations containing cefprozil have been used in the treatment of respiratory tract, skin, and other bacterial infections.  

     

    Brand:
    Cayman
    SKU:23840 - 50 mg

    Available on backorder

  • Cefradine is an orally bioavailable β-lactam cephalosporin antibiotic.{42982} It is active against S. pyogenes, E. coli, K. pneumoniae, and E. cloacae (MICs = 0.04, 9.4, 9.4, and 6.3 μg/ml, respectively). Cefradine is also active against clinical isolates of S. aureus (MICs = 0.8-6 μg/ml) and S. pyogenes (MICs = 0.1-0.4 μg/ml), as well as H. influenzae, E. coli, and K. pneumoniae (MICs = 6.2-12.5 μg/ml).{42983} It increases survival in mouse models of systemic lethal infection by S. pyogenes, E. coli, K. pneumoniae, or E. cloacae (ED50s = 5, 37, 122, and 50 mg/kg, respectively), as well as by penicillin-susceptible or -resistant strains of S. aureus (ED50s = 18 and 91 mg/kg, respectively).{42982} Formulations containing cefradine have previously been used in the treatment of respiratory and urinary tract infections, skin infections, and otitis media.  

     

    Brand:
    Cayman
    SKU:26060 - 1 g

    Available on backorder

  • Cefradine is an orally bioavailable β-lactam cephalosporin antibiotic.{42982} It is active against S. pyogenes, E. coli, K. pneumoniae, and E. cloacae (MICs = 0.04, 9.4, 9.4, and 6.3 μg/ml, respectively). Cefradine is also active against clinical isolates of S. aureus (MICs = 0.8-6 μg/ml) and S. pyogenes (MICs = 0.1-0.4 μg/ml), as well as H. influenzae, E. coli, and K. pneumoniae (MICs = 6.2-12.5 μg/ml).{42983} It increases survival in mouse models of systemic lethal infection by S. pyogenes, E. coli, K. pneumoniae, or E. cloacae (ED50s = 5, 37, 122, and 50 mg/kg, respectively), as well as by penicillin-susceptible or -resistant strains of S. aureus (ED50s = 18 and 91 mg/kg, respectively).{42982} Formulations containing cefradine have previously been used in the treatment of respiratory and urinary tract infections, skin infections, and otitis media.  

     

    Brand:
    Cayman
    SKU:26060 - 10 g

    Available on backorder

  • Cefradine is an orally bioavailable β-lactam cephalosporin antibiotic.{42982} It is active against S. pyogenes, E. coli, K. pneumoniae, and E. cloacae (MICs = 0.04, 9.4, 9.4, and 6.3 μg/ml, respectively). Cefradine is also active against clinical isolates of S. aureus (MICs = 0.8-6 μg/ml) and S. pyogenes (MICs = 0.1-0.4 μg/ml), as well as H. influenzae, E. coli, and K. pneumoniae (MICs = 6.2-12.5 μg/ml).{42983} It increases survival in mouse models of systemic lethal infection by S. pyogenes, E. coli, K. pneumoniae, or E. cloacae (ED50s = 5, 37, 122, and 50 mg/kg, respectively), as well as by penicillin-susceptible or -resistant strains of S. aureus (ED50s = 18 and 91 mg/kg, respectively).{42982} Formulations containing cefradine have previously been used in the treatment of respiratory and urinary tract infections, skin infections, and otitis media.  

     

    Brand:
    Cayman
    SKU:26060 - 5 g

    Available on backorder

  • Cefradine is an orally bioavailable β-lactam cephalosporin antibiotic.{42982} It is active against S. pyogenes, E. coli, K. pneumoniae, and E. cloacae (MICs = 0.04, 9.4, 9.4, and 6.3 μg/ml, respectively). Cefradine is also active against clinical isolates of S. aureus (MICs = 0.8-6 μg/ml) and S. pyogenes (MICs = 0.1-0.4 μg/ml), as well as H. influenzae, E. coli, and K. pneumoniae (MICs = 6.2-12.5 μg/ml).{42983} It increases survival in mouse models of systemic lethal infection by S. pyogenes, E. coli, K. pneumoniae, or E. cloacae (ED50s = 5, 37, 122, and 50 mg/kg, respectively), as well as by penicillin-susceptible or -resistant strains of S. aureus (ED50s = 18 and 91 mg/kg, respectively).{42982} Formulations containing cefradine have previously been used in the treatment of respiratory and urinary tract infections, skin infections, and otitis media.  

     

    Brand:
    Cayman
    SKU:26060 - 500 mg

    Available on backorder

  • Cefsulodin is a β-lactam antibiotic that lyses actively-growing E. coli by binding specifically to the intermembrane proteins, penicillin-binding proteins 1a and b, whose transglycosylase and transpeptidase activities are involved in cell elongation and septation.{26292} Cefsulodin has been used in combination with other β-lactam antibiotics, such as cefazolin (Item No. 15776) as a strategy to circumvent drug resistance.{26293}  

     

    Brand:
    Cayman
    SKU:-
  • Cefsulodin is a β-lactam antibiotic that lyses actively-growing E. coli by binding specifically to the intermembrane proteins, penicillin-binding proteins 1a and b, whose transglycosylase and transpeptidase activities are involved in cell elongation and septation.{26292} Cefsulodin has been used in combination with other β-lactam antibiotics, such as cefazolin (Item No. 15776) as a strategy to circumvent drug resistance.{26293}  

     

    Brand:
    Cayman
    SKU:-
  • Cefsulodin is a β-lactam antibiotic that lyses actively-growing E. coli by binding specifically to the intermembrane proteins, penicillin-binding proteins 1a and b, whose transglycosylase and transpeptidase activities are involved in cell elongation and septation.{26292} Cefsulodin has been used in combination with other β-lactam antibiotics, such as cefazolin (Item No. 15776) as a strategy to circumvent drug resistance.{26293}  

     

    Brand:
    Cayman
    SKU:-
  • Cefsulodin is a β-lactam antibiotic that lyses actively-growing E. coli by binding specifically to the intermembrane proteins, penicillin-binding proteins 1a and b, whose transglycosylase and transpeptidase activities are involved in cell elongation and septation.{26292} Cefsulodin has been used in combination with other β-lactam antibiotics, such as cefazolin (Item No. 15776) as a strategy to circumvent drug resistance.{26293}  

     

    Brand:
    Cayman
    SKU:-
  • Ceftazidime is a broad-spectrum β-lactam antibiotic used for parenteral administration.{23618} It is a cephalosporin antibiotic that works by stopping the growth of bacteria.{23618} It is used in many types of bacterial infections.{23617,23616,23618}  

     

    Brand:
    Cayman
    SKU:-
  • Ceftazidime is a broad-spectrum β-lactam antibiotic used for parenteral administration.{23618} It is a cephalosporin antibiotic that works by stopping the growth of bacteria.{23618} It is used in many types of bacterial infections.{23617,23616,23618}  

     

    Brand:
    Cayman
    SKU:-
  • Ceftazidime is a broad-spectrum β-lactam antibiotic used for parenteral administration.{23618} It is a cephalosporin antibiotic that works by stopping the growth of bacteria.{23618} It is used in many types of bacterial infections.{23617,23616,23618}  

     

    Brand:
    Cayman
    SKU:-
  • Ceftazidime is a broad-spectrum β-lactam antibiotic used for parenteral administration.{23618} It is a cephalosporin antibiotic that works by stopping the growth of bacteria.{23618} It is used in many types of bacterial infections.{23617,23616,23618}  

     

    Brand:
    Cayman
    SKU:-
  • Ceftibuten is an orally bioavailable broad-spectrum cephalosporin antibiotic that inhibits the growth of B. catarrhalis, H. influenzae, pathogenic Neisseria, Streptococcus, penicillin-susceptible S. pneumoniae, and eleven Enterobacteriaceae strains (MICs = 0.25, ≤0.06, ≤0.06, 0.5-1, 4, and ≤0.06-0.5 μg/ml, respectively).{42366,42365} Ceftibuten is also active against E. coli expressing β-lactamase type I, III, and V and K. oxytoca expressing β-lactamase type IV (MICs = 8, 0.25, 0.5, and ≤0.06 μg/ml, respectively) as well as a panel of eight bacterial stains expressing plasmid-encoded extended spectrum β-lactamases, including E. coli CTX-M and K. pneumoniae SHV-2 (MICs = 1 and 0.25 μg/ml, respectively). In vivo, ceftibuten reduces the number of mice killed within 6 days of a K. pneumoniae, E. coli, S. pneumoniae, or S. aureus infection by 50% when administered subcutaneously at doses of 0.125, 2, 1,024, and >512 mg/kg, respectively.{42367} Formulations containing ceftibuten have been used in the treatment of bacterial infections including bronchitis, pneumonia, and enteritis.  

     

    Brand:
    Cayman
    SKU:25334 - 10 mg

    Available on backorder

  • Ceftibuten is an orally bioavailable broad-spectrum cephalosporin antibiotic that inhibits the growth of B. catarrhalis, H. influenzae, pathogenic Neisseria, Streptococcus, penicillin-susceptible S. pneumoniae, and eleven Enterobacteriaceae strains (MICs = 0.25, ≤0.06, ≤0.06, 0.5-1, 4, and ≤0.06-0.5 μg/ml, respectively).{42366,42365} Ceftibuten is also active against E. coli expressing β-lactamase type I, III, and V and K. oxytoca expressing β-lactamase type IV (MICs = 8, 0.25, 0.5, and ≤0.06 μg/ml, respectively) as well as a panel of eight bacterial stains expressing plasmid-encoded extended spectrum β-lactamases, including E. coli CTX-M and K. pneumoniae SHV-2 (MICs = 1 and 0.25 μg/ml, respectively). In vivo, ceftibuten reduces the number of mice killed within 6 days of a K. pneumoniae, E. coli, S. pneumoniae, or S. aureus infection by 50% when administered subcutaneously at doses of 0.125, 2, 1,024, and >512 mg/kg, respectively.{42367} Formulations containing ceftibuten have been used in the treatment of bacterial infections including bronchitis, pneumonia, and enteritis.  

     

    Brand:
    Cayman
    SKU:25334 - 100 mg

    Available on backorder

  • Ceftibuten is an orally bioavailable broad-spectrum cephalosporin antibiotic that inhibits the growth of B. catarrhalis, H. influenzae, pathogenic Neisseria, Streptococcus, penicillin-susceptible S. pneumoniae, and eleven Enterobacteriaceae strains (MICs = 0.25, ≤0.06, ≤0.06, 0.5-1, 4, and ≤0.06-0.5 μg/ml, respectively).{42366,42365} Ceftibuten is also active against E. coli expressing β-lactamase type I, III, and V and K. oxytoca expressing β-lactamase type IV (MICs = 8, 0.25, 0.5, and ≤0.06 μg/ml, respectively) as well as a panel of eight bacterial stains expressing plasmid-encoded extended spectrum β-lactamases, including E. coli CTX-M and K. pneumoniae SHV-2 (MICs = 1 and 0.25 μg/ml, respectively). In vivo, ceftibuten reduces the number of mice killed within 6 days of a K. pneumoniae, E. coli, S. pneumoniae, or S. aureus infection by 50% when administered subcutaneously at doses of 0.125, 2, 1,024, and >512 mg/kg, respectively.{42367} Formulations containing ceftibuten have been used in the treatment of bacterial infections including bronchitis, pneumonia, and enteritis.  

     

    Brand:
    Cayman
    SKU:25334 - 25 mg

    Available on backorder

  • Ceftibuten is an orally bioavailable broad-spectrum cephalosporin antibiotic that inhibits the growth of B. catarrhalis, H. influenzae, pathogenic Neisseria, Streptococcus, penicillin-susceptible S. pneumoniae, and eleven Enterobacteriaceae strains (MICs = 0.25, ≤0.06, ≤0.06, 0.5-1, 4, and ≤0.06-0.5 μg/ml, respectively).{42366,42365} Ceftibuten is also active against E. coli expressing β-lactamase type I, III, and V and K. oxytoca expressing β-lactamase type IV (MICs = 8, 0.25, 0.5, and ≤0.06 μg/ml, respectively) as well as a panel of eight bacterial stains expressing plasmid-encoded extended spectrum β-lactamases, including E. coli CTX-M and K. pneumoniae SHV-2 (MICs = 1 and 0.25 μg/ml, respectively). In vivo, ceftibuten reduces the number of mice killed within 6 days of a K. pneumoniae, E. coli, S. pneumoniae, or S. aureus infection by 50% when administered subcutaneously at doses of 0.125, 2, 1,024, and >512 mg/kg, respectively.{42367} Formulations containing ceftibuten have been used in the treatment of bacterial infections including bronchitis, pneumonia, and enteritis.  

     

    Brand:
    Cayman
    SKU:25334 - 50 mg

    Available on backorder

  • Ceftiofur is a broad-spectrum cephalosporin antibiotic.{36441} It is active against porcine isolates of A. pleuropneumoniae, P. multocida, S. typhimurium, S. cholerae-suis, E. coli, S. suis, and β-hemolytic streptococci with MIC90 values of less than or equal to 2 μg/ml. Ceftiofur exhibits curative rates of 43, 88, and 100% in a lactating bovine model of intramammary S. uberis infection when administered via intramammary infusion at a dose of 125 mg per infected quarter for 2, 5, and 8 days, respectively.{47446} Formulations containing ceftiofur have been used in the veterinary treatment of bacterial infections.  

     

    Brand:
    Cayman
    SKU:27301 - 1 g

    Available on backorder

  • Ceftiofur is a broad-spectrum cephalosporin antibiotic.{36441} It is active against porcine isolates of A. pleuropneumoniae, P. multocida, S. typhimurium, S. cholerae-suis, E. coli, S. suis, and β-hemolytic streptococci with MIC90 values of less than or equal to 2 μg/ml. Ceftiofur exhibits curative rates of 43, 88, and 100% in a lactating bovine model of intramammary S. uberis infection when administered via intramammary infusion at a dose of 125 mg per infected quarter for 2, 5, and 8 days, respectively.{47446} Formulations containing ceftiofur have been used in the veterinary treatment of bacterial infections.  

     

    Brand:
    Cayman
    SKU:27301 - 10 g

    Available on backorder

  • Ceftiofur is a broad-spectrum cephalosporin antibiotic.{36441} It is active against porcine isolates of A. pleuropneumoniae, P. multocida, S. typhimurium, S. cholerae-suis, E. coli, S. suis, and β-hemolytic streptococci with MIC90 values of less than or equal to 2 μg/ml. Ceftiofur exhibits curative rates of 43, 88, and 100% in a lactating bovine model of intramammary S. uberis infection when administered via intramammary infusion at a dose of 125 mg per infected quarter for 2, 5, and 8 days, respectively.{47446} Formulations containing ceftiofur have been used in the veterinary treatment of bacterial infections.  

     

    Brand:
    Cayman
    SKU:27301 - 25 g

    Available on backorder

  • Ceftiofur is a broad-spectrum cephalosporin antibiotic.{36441} It is active against porcine isolates of A. pleuropneumoniae, P. multocida, S. typhimurium, S. cholerae-suis, E. coli, S. suis, and β-hemolytic streptococci with MIC90 values of less than or equal to 2 μg/ml. Ceftiofur exhibits curative rates of 43, 88, and 100% in a lactating bovine model of intramammary S. uberis infection when administered via intramammary infusion at a dose of 125 mg per infected quarter for 2, 5, and 8 days, respectively.{47446} Formulations containing ceftiofur have been used in the veterinary treatment of bacterial infections.  

     

    Brand:
    Cayman
    SKU:27301 - 5 g

    Available on backorder

  • Ceftriaxone is a third-generation, broad-spectrum cephalosporin antibiotic that disrupts the synthesis of the peptidoglycan layer of bacterial cell walls.{27903,29387,25856} It has been shown to increase excitatory amino acid transporter-2 pump expression in the central nervous system and to reduce glutamatergic toxicity in both in vitro and in vivo models.{30535}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Ceftriaxone is a third-generation, broad-spectrum cephalosporin antibiotic that disrupts the synthesis of the peptidoglycan layer of bacterial cell walls.{27903,29387,25856} It has been shown to increase excitatory amino acid transporter-2 pump expression in the central nervous system and to reduce glutamatergic toxicity in both in vitro and in vivo models.{30535}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Ceftriaxone is a third-generation, broad-spectrum cephalosporin antibiotic that disrupts the synthesis of the peptidoglycan layer of bacterial cell walls.{27903,29387,25856} It has been shown to increase excitatory amino acid transporter-2 pump expression in the central nervous system and to reduce glutamatergic toxicity in both in vitro and in vivo models.{30535}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Cefuroxime is a cephalosporin antibiotic with broad-spectrum activity against Gram-positive and Gram-negative bacteria including S. pyogenes, S. pneumoniae, S. viridans, E. coli, P. mirabilis, H. influenzae, and N. gonorrhoeae (mean MICs = 0.005-8.2 μg/ml).{40366} Like other cephalosporins, cefuroxime inhibits peptidoglycan crosslinking and bacterial cell wall synthesis.{40367} It is resistant to hydrolysis by bacterial β-lactamases, increasing its efficacy against β-lactamase producing Gram-negative bacteria.{40368} Cefuroxime is protective against Gram-positive and Gram-negative infections in vivo with mean ED50 values ranging from 2 to 35 and 1 to 55 mg/kg, in mice and rats, respectively.{40369} Formulations containing cefuroxime have been used to treat urinary tract infections.{40370}  

     

    Brand:
    Cayman
    SKU:23627 - 1 g

    Available on backorder

  • Cefuroxime is a cephalosporin antibiotic with broad-spectrum activity against Gram-positive and Gram-negative bacteria including S. pyogenes, S. pneumoniae, S. viridans, E. coli, P. mirabilis, H. influenzae, and N. gonorrhoeae (mean MICs = 0.005-8.2 μg/ml).{40366} Like other cephalosporins, cefuroxime inhibits peptidoglycan crosslinking and bacterial cell wall synthesis.{40367} It is resistant to hydrolysis by bacterial β-lactamases, increasing its efficacy against β-lactamase producing Gram-negative bacteria.{40368} Cefuroxime is protective against Gram-positive and Gram-negative infections in vivo with mean ED50 values ranging from 2 to 35 and 1 to 55 mg/kg, in mice and rats, respectively.{40369} Formulations containing cefuroxime have been used to treat urinary tract infections.{40370}  

     

    Brand:
    Cayman
    SKU:23627 - 500 mg

    Available on backorder

  • Cefuroxime-d3 is intended for use as an internal standard for the quantification of cefuroxime (Item No. 23627) by GC- or LC-MS. Cefuroxime is a cephalosporin antibiotic with broad-spectrum activity against Gram-positive and Gram-negative bacteria including S. pyogenes, S. pneumoniae, S. viridans, E. coli, P. mirabilis, H. influenzae, and N. gonorrhoeae (mean MICs = 0.005-8.2 μg/ml).{40366} Like other cephalosporins, cefuroxime inhibits peptidoglycan crosslinking and bacterial cell wall synthesis.{40367} It is resistant to hydrolysis by bacterial β-lactamases, increasing its efficacy against β-lactamase-producing Gram-negative bacteria.{40368} Cefuroxime is protective against Gram-positive and Gram-negative infections in vivo with mean ED50 values ranging from 2 to 35 and 1 to 55 mg/kg, in mice and rats, respectively.{40369} Formulations containing cefuroxime have been used to treat urinary tract infections.  

     

    Brand:
    Cayman
    SKU:31163 - 1 mg

    Available on backorder

  • Celastramycin A is a bioactive compound isolated from endophytic bacteria living in plants of the Celastraceae family.{17765} This benzoyl pyrrole inhibits the growth of bacteria and mycobacteria, with a minimal inhibitory concentration as low as 0.05 μg/ml.{17765} Celastramycin A also suppresses the production of IL-8 in human umbilical vein endothelial cells as stimulated by TNF-α (IC50 = 0.01 μg/ml).{17766}  

     

    Brand:
    Cayman
    SKU:-
  • Celastramycin A is a bioactive compound isolated from endophytic bacteria living in plants of the Celastraceae family.{17765} This benzoyl pyrrole inhibits the growth of bacteria and mycobacteria, with a minimal inhibitory concentration as low as 0.05 μg/ml.{17765} Celastramycin A also suppresses the production of IL-8 in human umbilical vein endothelial cells as stimulated by TNF-α (IC50 = 0.01 μg/ml).{17766}  

     

    Brand:
    Cayman
    SKU:-
  • Celastramycin A is a bioactive compound isolated from endophytic bacteria living in plants of the Celastraceae family.{17765} This benzoyl pyrrole inhibits the growth of bacteria and mycobacteria, with a minimal inhibitory concentration as low as 0.05 μg/ml.{17765} Celastramycin A also suppresses the production of IL-8 in human umbilical vein endothelial cells as stimulated by TNF-α (IC50 = 0.01 μg/ml).{17766}  

     

    Brand:
    Cayman
    SKU:-
  • A variety of natural products from plant sources, particularly flavonoids, have long been observed to have antioxidant activity with potential benefits for human health.{7442,6817,8914} Antioxidant triterpenes are less common. Celastrol is a triterpenoid antioxidant compound isolated from Chinese thunder god vine (T. wilfordii). In an isolated rat liver assay of lipid peroxidation, celastrol had an IC50 value of 7 µM, equivalent to about 15 times the antioxidant potency of α-tocopherol.{11647}  

     

    Brand:
    Cayman
    SKU:70950 - 10 mg

    Available on backorder

  • A variety of natural products from plant sources, particularly flavonoids, have long been observed to have antioxidant activity with potential benefits for human health.{7442,6817,8914} Antioxidant triterpenes are less common. Celastrol is a triterpenoid antioxidant compound isolated from Chinese thunder god vine (T. wilfordii). In an isolated rat liver assay of lipid peroxidation, celastrol had an IC50 value of 7 µM, equivalent to about 15 times the antioxidant potency of α-tocopherol.{11647}  

     

    Brand:
    Cayman
    SKU:70950 - 100 mg

    Available on backorder

  • A variety of natural products from plant sources, particularly flavonoids, have long been observed to have antioxidant activity with potential benefits for human health.{7442,6817,8914} Antioxidant triterpenes are less common. Celastrol is a triterpenoid antioxidant compound isolated from Chinese thunder god vine (T. wilfordii). In an isolated rat liver assay of lipid peroxidation, celastrol had an IC50 value of 7 µM, equivalent to about 15 times the antioxidant potency of α-tocopherol.{11647}  

     

    Brand:
    Cayman
    SKU:70950 - 5 mg

    Available on backorder

  • A variety of natural products from plant sources, particularly flavonoids, have long been observed to have antioxidant activity with potential benefits for human health.{7442,6817,8914} Antioxidant triterpenes are less common. Celastrol is a triterpenoid antioxidant compound isolated from Chinese thunder god vine (T. wilfordii). In an isolated rat liver assay of lipid peroxidation, celastrol had an IC50 value of 7 µM, equivalent to about 15 times the antioxidant potency of α-tocopherol.{11647}  

     

    Brand:
    Cayman
    SKU:70950 - 50 mg

    Available on backorder

  • Celecoxib is a selective inhibitor of COX-2 (IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively).{11633,8926} In vivo, celecoxib (0.3 ml of a 0.4% solution) administered intra-articularly reduces production of IL-1β, TNF-α, and MMP-3 as well as articular cartilage damage in a rabbit model of osteoarthritis.{41721} It reduces blood glucose and improves renal function and memory deficits via downregulation of COX-2 expression and increased BDNF -TrkB signaling in rats with diabetes induced by streptozotocin (Item No. 13104).{41722} Celecoxib also displays chemopreventive activity in multiple tumor types via proapoptotic effects that are independent of COX-2 inhibition.{12660,11712,13638} Formulations containing celecoxib have been used in the treatment of inflammation while circumventing the gastrointestinal toxicity associated with traditional non-steroidal anti-inflammatory drugs, however, the use of celecoxib has been tempered due to its ability to induce adverse cardiovascular events.{14766}  

     

    Brand:
    Cayman
    SKU:10008672 - 100 mg

    Available on backorder

  • Celecoxib is a selective inhibitor of COX-2 (IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively).{11633,8926} In vivo, celecoxib (0.3 ml of a 0.4% solution) administered intra-articularly reduces production of IL-1β, TNF-α, and MMP-3 as well as articular cartilage damage in a rabbit model of osteoarthritis.{41721} It reduces blood glucose and improves renal function and memory deficits via downregulation of COX-2 expression and increased BDNF -TrkB signaling in rats with diabetes induced by streptozotocin (Item No. 13104).{41722} Celecoxib also displays chemopreventive activity in multiple tumor types via proapoptotic effects that are independent of COX-2 inhibition.{12660,11712,13638} Formulations containing celecoxib have been used in the treatment of inflammation while circumventing the gastrointestinal toxicity associated with traditional non-steroidal anti-inflammatory drugs, however, the use of celecoxib has been tempered due to its ability to induce adverse cardiovascular events.{14766}  

     

    Brand:
    Cayman
    SKU:10008672 - 250 mg

    Available on backorder

  • Celecoxib is a selective inhibitor of COX-2 (IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively).{11633,8926} In vivo, celecoxib (0.3 ml of a 0.4% solution) administered intra-articularly reduces production of IL-1β, TNF-α, and MMP-3 as well as articular cartilage damage in a rabbit model of osteoarthritis.{41721} It reduces blood glucose and improves renal function and memory deficits via downregulation of COX-2 expression and increased BDNF -TrkB signaling in rats with diabetes induced by streptozotocin (Item No. 13104).{41722} Celecoxib also displays chemopreventive activity in multiple tumor types via proapoptotic effects that are independent of COX-2 inhibition.{12660,11712,13638} Formulations containing celecoxib have been used in the treatment of inflammation while circumventing the gastrointestinal toxicity associated with traditional non-steroidal anti-inflammatory drugs, however, the use of celecoxib has been tempered due to its ability to induce adverse cardiovascular events.{14766}  

     

    Brand:
    Cayman
    SKU:10008672 - 50 mg

    Available on backorder

  • Celecoxib carboxylic acid acyl-β-D-glucuronide is a phase II metabolite of celecoxib (Item No. 10008672). Celecoxib is an anti-inflammatory compound from the diaryl heterocycle class that selectively inhibits cyclooxygenase-2 (COX-2; IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively).{11633,8926} Celecoxib carboxylic acid acyl-β-D-glucuronide is a minor metabolite, accounting for 2% of the administered dose in human urine and rat bile.{37044,37045}  

     

    Brand:
    Cayman
    SKU:22457 -

    Out of stock

  • Celecoxib carboxylic acid acyl-β-D-glucuronide is a phase II metabolite of celecoxib (Item No. 10008672). Celecoxib is an anti-inflammatory compound from the diaryl heterocycle class that selectively inhibits cyclooxygenase-2 (COX-2; IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively).{11633,8926} Celecoxib carboxylic acid acyl-β-D-glucuronide is a minor metabolite, accounting for 2% of the administered dose in human urine and rat bile.{37044,37045}  

     

    Brand:
    Cayman
    SKU:22457 -

    Out of stock

  • Celecoxib-d7 is intended for use as an internal standard for the quantification of celecoxib (Item No. 10008672) by GC- or LC-MS. Celecoxib is a selective inhibitor of COX-2 (IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively).{11633,8926} It displays chemopreventive activity in multiple tumor types via proapoptotic effects that are independent of COX-2 inhibition.{12660,11712,13638} Formulations containing celecoxib have been used in the treatment of inflammation while circumventing the gastrointestinal toxicity associated with traditional non-sterodial anti-inflammatory drugs, however, the use of celecoxib has been tempered due to its ability to induce adverse cardiovascular events.{14766}  

     

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    Cayman
    SKU:-

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  • Celecoxib-d7 is intended for use as an internal standard for the quantification of celecoxib (Item No. 10008672) by GC- or LC-MS. Celecoxib is a selective inhibitor of COX-2 (IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively).{11633,8926} It displays chemopreventive activity in multiple tumor types via proapoptotic effects that are independent of COX-2 inhibition.{12660,11712,13638} Formulations containing celecoxib have been used in the treatment of inflammation while circumventing the gastrointestinal toxicity associated with traditional non-sterodial anti-inflammatory drugs, however, the use of celecoxib has been tempered due to its ability to induce adverse cardiovascular events.{14766}  

     

    Brand:
    Cayman
    SKU:-

    Available on backorder

  • Celecoxib-d7 is intended for use as an internal standard for the quantification of celecoxib (Item No. 10008672) by GC- or LC-MS. Celecoxib is a selective inhibitor of COX-2 (IC50s = 22.9 and 0.05 μM for COX-1 and COX-2, respectively).{11633,8926} It displays chemopreventive activity in multiple tumor types via proapoptotic effects that are independent of COX-2 inhibition.{12660,11712,13638} Formulations containing celecoxib have been used in the treatment of inflammation while circumventing the gastrointestinal toxicity associated with traditional non-sterodial anti-inflammatory drugs, however, the use of celecoxib has been tempered due to its ability to induce adverse cardiovascular events.{14766}  

     

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    Cayman
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  • Celiprolol is a β1 adrenergic receptor antagonist and a β2 adrenergic receptor partial agonist that has been shown to relax human arteries and veins with ED50 values of 40-50 µM in vitro.{27275} At 1-10 mg/kg/h, celiprolol can reduce myocardial infarct size and increase nitric oxide (NO) production in a rabbit model of myocardial ischemia.{27273} Furthermore, 100 mg/kg/d celiprolol has been reported to stimulate expression and activate phosphorylation of endothelial NO synthase in rat cardiac myocytes.{27274}  

     

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    Cayman
    SKU:-

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  • Celiprolol is a β1 adrenergic receptor antagonist and a β2 adrenergic receptor partial agonist that has been shown to relax human arteries and veins with ED50 values of 40-50 µM in vitro.{27275} At 1-10 mg/kg/h, celiprolol can reduce myocardial infarct size and increase nitric oxide (NO) production in a rabbit model of myocardial ischemia.{27273} Furthermore, 100 mg/kg/d celiprolol has been reported to stimulate expression and activate phosphorylation of endothelial NO synthase in rat cardiac myocytes.{27274}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Celiprolol is a β1 adrenergic receptor antagonist and a β2 adrenergic receptor partial agonist that has been shown to relax human arteries and veins with ED50 values of 40-50 µM in vitro.{27275} At 1-10 mg/kg/h, celiprolol can reduce myocardial infarct size and increase nitric oxide (NO) production in a rabbit model of myocardial ischemia.{27273} Furthermore, 100 mg/kg/d celiprolol has been reported to stimulate expression and activate phosphorylation of endothelial NO synthase in rat cardiac myocytes.{27274}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Celiprolol is a β1 adrenergic receptor antagonist and a β2 adrenergic receptor partial agonist that has been shown to relax human arteries and veins with ED50 values of 40-50 µM in vitro.{27275} At 1-10 mg/kg/h, celiprolol can reduce myocardial infarct size and increase nitric oxide (NO) production in a rabbit model of myocardial ischemia.{27273} Furthermore, 100 mg/kg/d celiprolol has been reported to stimulate expression and activate phosphorylation of endothelial NO synthase in rat cardiac myocytes.{27274}  

     

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    Cayman
    SKU:-

    Out of stock

  • Cellobiosan is an anhydro sugar formed during biofuel production from the fast pyrolysis of wood.{29234}  

     

    Brand:
    Cayman
    SKU:-

    Out of stock

  • Cellobiosan is an anhydro sugar formed during biofuel production from the fast pyrolysis of wood.{29234}  

     

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    Cayman
    SKU:-

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  • Cellocidin is an antibiotic originally isolated from S. chibaensis.{36482} It is active against various bacterial strains including M. tuberculosis and against the trypanosomes T. brucei and T. rhodesiense (IC50s = 150 and 30 ng/ml, respectively).{36482,24919} It inhibits proliferation of LCL1 and LCL2 cells transformed by Epstein-Barr virus (EBV), activates the c-Myc and NF-κB pathways in BC3 and LCL1 cells, and induces necrotic cell death in B cells infected with gammaherpes virus.{36480} Cellocidin (100-200 ppm) is protective against bacterial leaf blight in rice plants and inhibits α-ketoglutarate oxidation in X. oryzae, the bacterium that causes leaf blight, when used at a concentration of 1 ppm, suggesting that it inhibits the citric acid cycle.{36481} Formulations containing cellocidin have been used as agricultural pesticides.  

     

    Brand:
    Cayman
    SKU:23637 - 10 mg

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  • Cellocidin is an antibiotic originally isolated from S. chibaensis.{36482} It is active against various bacterial strains including M. tuberculosis and against the trypanosomes T. brucei and T. rhodesiense (IC50s = 150 and 30 ng/ml, respectively).{36482,24919} It inhibits proliferation of LCL1 and LCL2 cells transformed by Epstein-Barr virus (EBV), activates the c-Myc and NF-κB pathways in BC3 and LCL1 cells, and induces necrotic cell death in B cells infected with gammaherpes virus.{36480} Cellocidin (100-200 ppm) is protective against bacterial leaf blight in rice plants and inhibits α-ketoglutarate oxidation in X. oryzae, the bacterium that causes leaf blight, when used at a concentration of 1 ppm, suggesting that it inhibits the citric acid cycle.{36481} Formulations containing cellocidin have been used as agricultural pesticides.  

     

    Brand:
    Cayman
    SKU:23637 - 25 mg

    Available on backorder

  • Cellocidin is an antibiotic originally isolated from S. chibaensis.{36482} It is active against various bacterial strains including M. tuberculosis and against the trypanosomes T. brucei and T. rhodesiense (IC50s = 150 and 30 ng/ml, respectively).{36482,24919} It inhibits proliferation of LCL1 and LCL2 cells transformed by Epstein-Barr virus (EBV), activates the c-Myc and NF-κB pathways in BC3 and LCL1 cells, and induces necrotic cell death in B cells infected with gammaherpes virus.{36480} Cellocidin (100-200 ppm) is protective against bacterial leaf blight in rice plants and inhibits α-ketoglutarate oxidation in X. oryzae, the bacterium that causes leaf blight, when used at a concentration of 1 ppm, suggesting that it inhibits the citric acid cycle.{36481} Formulations containing cellocidin have been used as agricultural pesticides.  

     

    Brand:
    Cayman
    SKU:23637 - 5 mg

    Available on backorder

  • Cellocidin is an antibiotic originally isolated from S. chibaensis.{36482} It is active against various bacterial strains including M. tuberculosis and against the trypanosomes T. brucei and T. rhodesiense (IC50s = 150 and 30 ng/ml, respectively).{36482,24919} It inhibits proliferation of LCL1 and LCL2 cells transformed by Epstein-Barr virus (EBV), activates the c-Myc and NF-κB pathways in BC3 and LCL1 cells, and induces necrotic cell death in B cells infected with gammaherpes virus.{36480} Cellocidin (100-200 ppm) is protective against bacterial leaf blight in rice plants and inhibits α-ketoglutarate oxidation in X. oryzae, the bacterium that causes leaf blight, when used at a concentration of 1 ppm, suggesting that it inhibits the citric acid cycle.{36481} Formulations containing cellocidin have been used as agricultural pesticides.  

     

    Brand:
    Cayman
    SKU:23637 - 50 mg

    Available on backorder

  • CeMMEC1 is an N-methylisoquinolinone that inhibits the second bromodomain of TAF1 (Kd = 1.8 µM; IC50 = 0.9 µM).{31547} It does not bind to either the first or second bromodomain of BRD4.{31547} This compound synergizes with (+)-JQ1 (Item No. 11187) to inhibit the proliferation of THP-1 and H23 lung adenocarcinoma cells.{31547}  

     

    Brand:
    Cayman
    SKU:19956 -

    Available on backorder

  • CeMMEC1 is an N-methylisoquinolinone that inhibits the second bromodomain of TAF1 (Kd = 1.8 µM; IC50 = 0.9 µM).{31547} It does not bind to either the first or second bromodomain of BRD4.{31547} This compound synergizes with (+)-JQ1 (Item No. 11187) to inhibit the proliferation of THP-1 and H23 lung adenocarcinoma cells.{31547}  

     

    Brand:
    Cayman
    SKU:19956 -

    Available on backorder

  • CeMMEC1 is an N-methylisoquinolinone that inhibits the second bromodomain of TAF1 (Kd = 1.8 µM; IC50 = 0.9 µM).{31547} It does not bind to either the first or second bromodomain of BRD4.{31547} This compound synergizes with (+)-JQ1 (Item No. 11187) to inhibit the proliferation of THP-1 and H23 lung adenocarcinoma cells.{31547}  

     

    Brand:
    Cayman
    SKU:19956 -

    Available on backorder

  • CeMMEC1 is an N-methylisoquinolinone that inhibits the second bromodomain of TAF1 (Kd = 1.8 µM; IC50 = 0.9 µM).{31547} It does not bind to either the first or second bromodomain of BRD4.{31547} This compound synergizes with (+)-JQ1 (Item No. 11187) to inhibit the proliferation of THP-1 and H23 lung adenocarcinoma cells.{31547}  

     

    Brand:
    Cayman
    SKU:19956 -

    Available on backorder

  • CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF1 (IC50 = 2.1 µM).{31547} It does not bind to bromodomains of BRD4, BRD9, or CREBBP.{31547} CeMMEC13 synergizes with (+)-JQ1 (Item No. 11187) to inhibit the proliferation of THP-1 and H23 lung adenocarcinoma cells.{31547}  

     

    Brand:
    Cayman
    SKU:20224 -

    Available on backorder

  • CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF1 (IC50 = 2.1 µM).{31547} It does not bind to bromodomains of BRD4, BRD9, or CREBBP.{31547} CeMMEC13 synergizes with (+)-JQ1 (Item No. 11187) to inhibit the proliferation of THP-1 and H23 lung adenocarcinoma cells.{31547}  

     

    Brand:
    Cayman
    SKU:20224 -

    Available on backorder

  • CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF1 (IC50 = 2.1 µM).{31547} It does not bind to bromodomains of BRD4, BRD9, or CREBBP.{31547} CeMMEC13 synergizes with (+)-JQ1 (Item No. 11187) to inhibit the proliferation of THP-1 and H23 lung adenocarcinoma cells.{31547}  

     

    Brand:
    Cayman
    SKU:20224 -

    Available on backorder

  • CeMMEC13 is an isoquinolinone that selectively inhibits the second bromodomain of TAF1 (IC50 = 2.1 µM).{31547} It does not bind to bromodomains of BRD4, BRD9, or CREBBP.{31547} CeMMEC13 synergizes with (+)-JQ1 (Item No. 11187) to inhibit the proliferation of THP-1 and H23 lung adenocarcinoma cells.{31547}  

     

    Brand:
    Cayman
    SKU:20224 -

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  • Cenerimod is a sphingosine-1-phosphate receptor 1 (S1P1) modulator with an EC50 value of 1 nM in a [35S]GTPɣS binding assay.{52269} It is selective for S1P1 over S1P2, -3, -4, and -5 (EC50s = >10,000, 228, 2,137, and 36 nM, respectively). Cenerimod (5 µM) decreases TGF-β-induced increases in collagen levels in primary mouse skin fibroblasts.{52270} It inhibits CD4+ T cell, CD8+ T cell, and CD11b+ cell infiltration, reduces IL1b, Il6, and Il13 expression, as well as decreases fibrosis in the skin of a mouse model of sclerodermatous chronic graft versus host disease induced by allogenic bone marrow transplant when administered at a dose of 10 mg/kg per day. Cenerimod (6 mg/kg per day for 32 days) reduces paralysis and spinal cord demyelination in a mouse model of experimental autoimmune encephalitis (EAE).  

     

    Brand:
    Cayman
    SKU:29665 - 10 mg

    Available on backorder