Chemicals
Showing 31351–31500 of 41137 results
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Pelargonidin is an anthocyanidin that has been found in P. granatum and has diverse biological activities.{61058,61059,61060,61061} It scavenges superoxide anions in cell-free assays (IC50 = 130 µg/ml) and inhibits hydrogen peroxide-induced lipid peroxidation in rat brain homogenates (IC50 = 85 µM).{61058} Pelargonidin (3 mg/kg) reduces serum levels of alanine aminotransferase (ALT) and aspartate aminotransferase (AST), hepatocyte apoptosis, and hepatic levels of IL-1β, IL-6, TNF-α, and TGF-β in a mouse model of hepatotoxicity induced by acetaminophen (Item No. 10024).{61059} It increases survival and reduces pulmonary fibrosis and leukocyte infiltration in a mouse model of LPS-induced endotoxemia.{61060} Pelargonidin (0.04-0.4 mg/kg) reduces serum levels of nitric oxide (NO), TNF-α, and IL-6 and increases renal myeloperoxidase (MPO), superoxide dismutase (SOD), and catalase (CAT) activities, as well as increases survival, in a mouse model of cecal ligation and puncture-induced sepsis.{61061} It also decreases escape latency in the Morris water maze, reduces hippocampal malondialdehyde (MDA) levels, and increases hippocampal acetylcholinesterase (AChE) activity in a rat model of Alzheimer’s disease induced by amyloid-β 25-35 (Aβ (25-35); Item No. 24155).{61062}
Brand:CaymanSKU:19753 -Available on backorder
Pelargonidin 3-O-glucoside is an anthocyanin and the 3-O-glucoside of pelargonidin (Item No. 19753) that has been found in Fragaria and has transporter inhibitory and antioxidant properties.{54079,54080} It inhibits bilitranslocase transporter activity in isolated rat liver plasma membrane vesicles (Ki = 2.8 µM).{54079} Pelargonidin 3-O-glucoside scavenges peroxyl radicals in an oxygen radical absorbance capacity (ORAC) assay.{54080}
Brand:CaymanSKU:30224 - 1 mgAvailable on backorder
Pelitinib is a cyanoquinoline that irreversibly inhibits the EGFR receptor tyrosine kinase (IC50 = 39 nM).{21790} It inhibits HER2 with a much weaker potency (IC50 = 1.2 μM).{21790} By disrupting Akt and MAPK pathways, pelitinib can induce apoptosis and suppress the growth of tumor cell lines, displaying particularly strong efficacy against hepatocellular carcinoma cells (IC50s = ~2 μM).{25562}
Brand:CaymanSKU:- Pelitinib is a cyanoquinoline that irreversibly inhibits the EGFR receptor tyrosine kinase (IC50 = 39 nM).{21790} It inhibits HER2 with a much weaker potency (IC50 = 1.2 μM).{21790} By disrupting Akt and MAPK pathways, pelitinib can induce apoptosis and suppress the growth of tumor cell lines, displaying particularly strong efficacy against hepatocellular carcinoma cells (IC50s = ~2 μM).{25562}
Brand:CaymanSKU:- Pelitinib is a cyanoquinoline that irreversibly inhibits the EGFR receptor tyrosine kinase (IC50 = 39 nM).{21790} It inhibits HER2 with a much weaker potency (IC50 = 1.2 μM).{21790} By disrupting Akt and MAPK pathways, pelitinib can induce apoptosis and suppress the growth of tumor cell lines, displaying particularly strong efficacy against hepatocellular carcinoma cells (IC50s = ~2 μM).{25562}
Brand:CaymanSKU:- Pelitinib is a cyanoquinoline that irreversibly inhibits the EGFR receptor tyrosine kinase (IC50 = 39 nM).{21790} It inhibits HER2 with a much weaker potency (IC50 = 1.2 μM).{21790} By disrupting Akt and MAPK pathways, pelitinib can induce apoptosis and suppress the growth of tumor cell lines, displaying particularly strong efficacy against hepatocellular carcinoma cells (IC50s = ~2 μM).{25562}
Brand:CaymanSKU:-
Pellitorine is an amide alkaloid that has been found in P. nigrum and has diverse biological activities.{49685,49686,49687,49688} It induces mortality in C. pipiens pallens, A. aegypti, and A. togoi third instar larvae with LC50 values of 0.86, 0.92, and 0.71 ppm, respectively.{49686} Pellitorine is cytotoxic to HL-60 leukemia and MCF-7 breast cancer cells (IC50s = 13 and 1.8 µg/ml, respectively).{49687} It inhibits production of TNF-α, IL-1α, and IL-1β and phosphorylation of ERK1/2 induced by high mobility group protein B1 (HMGB1) in human umbilical vein endothelial cells (HUVECs) when used at concentrations of 10 and 20 µM.{49688} Pellitorine (9 µg/animal, i.v.) prolongs survival time in a mouse model of sepsis induced by HMGB1.
Brand:CaymanSKU:11662 - 1 mgAvailable on backorder
Pellitorine is an amide alkaloid that has been found in P. nigrum and has diverse biological activities.{49685,49686,49687,49688} It induces mortality in C. pipiens pallens, A. aegypti, and A. togoi third instar larvae with LC50 values of 0.86, 0.92, and 0.71 ppm, respectively.{49686} Pellitorine is cytotoxic to HL-60 leukemia and MCF-7 breast cancer cells (IC50s = 13 and 1.8 µg/ml, respectively).{49687} It inhibits production of TNF-α, IL-1α, and IL-1β and phosphorylation of ERK1/2 induced by high mobility group protein B1 (HMGB1) in human umbilical vein endothelial cells (HUVECs) when used at concentrations of 10 and 20 µM.{49688} Pellitorine (9 µg/animal, i.v.) prolongs survival time in a mouse model of sepsis induced by HMGB1.
Brand:CaymanSKU:11662 - 10 mgAvailable on backorder
Pellitorine is an amide alkaloid that has been found in P. nigrum and has diverse biological activities.{49685,49686,49687,49688} It induces mortality in C. pipiens pallens, A. aegypti, and A. togoi third instar larvae with LC50 values of 0.86, 0.92, and 0.71 ppm, respectively.{49686} Pellitorine is cytotoxic to HL-60 leukemia and MCF-7 breast cancer cells (IC50s = 13 and 1.8 µg/ml, respectively).{49687} It inhibits production of TNF-α, IL-1α, and IL-1β and phosphorylation of ERK1/2 induced by high mobility group protein B1 (HMGB1) in human umbilical vein endothelial cells (HUVECs) when used at concentrations of 10 and 20 µM.{49688} Pellitorine (9 µg/animal, i.v.) prolongs survival time in a mouse model of sepsis induced by HMGB1.
Brand:CaymanSKU:11662 - 5 mgAvailable on backorder
Pemetrexed is an antifolate with anticancer activity.{22488,22487,53309} It is an inhibitor of folate-dependent enzymes involved in purine synthesis, including thymidylate synthase and dihydrofolate reductase (Kis = 109 and 7 nM, respectively, for the human recombinant enzymes), and the potency for thymidylate kinase is increased following polyglutamination of pemetrexed (Ki = 1.3 nM for pemetrexed-glu5).{22488,22487} Pemetrexed is an inhibitor of other nucleotide metabolism enzymes in a polyglutamination-dependent manner, including glycinamide ribonucleotide formyltransferase, with Ki values of 9,300 and 65 nM for the non-glutaminated and polyglutaminated mouse recombinant enzyme, respectively, and aminoimidazole carboxamide ribonucleotide formyltransferase, with Ki values of 3,600 and 265 nM for the non-glutaminated and polyglutaminated human enzyme, respectively. It inhibits proliferation of CCRF-CEM cells but not 5,10-dideazatetrahydrofolate-resistant CR15 cells (IC50s = 0.254 and 200 µM, respectively).{22488} Pemetrexed (100 mg/kg, i.p.) reduces tumor growth in A549, H1299, and PC-9 non-small cell lung cancer cell (NSCLC) mouse xenograft models but not in models using the same cell lines overexpressing thymidylate kinase.{53309}
Brand:CaymanSKU:- Pemetrexed is an antifolate with anticancer activity.{22488,22487,53309} It is an inhibitor of folate-dependent enzymes involved in purine synthesis, including thymidylate synthase and dihydrofolate reductase (Kis = 109 and 7 nM, respectively, for the human recombinant enzymes), and the potency for thymidylate kinase is increased following polyglutamination of pemetrexed (Ki = 1.3 nM for pemetrexed-glu5).{22488,22487} Pemetrexed is an inhibitor of other nucleotide metabolism enzymes in a polyglutamination-dependent manner, including glycinamide ribonucleotide formyltransferase, with Ki values of 9,300 and 65 nM for the non-glutaminated and polyglutaminated mouse recombinant enzyme, respectively, and aminoimidazole carboxamide ribonucleotide formyltransferase, with Ki values of 3,600 and 265 nM for the non-glutaminated and polyglutaminated human enzyme, respectively. It inhibits proliferation of CCRF-CEM cells but not 5,10-dideazatetrahydrofolate-resistant CR15 cells (IC50s = 0.254 and 200 µM, respectively).{22488} Pemetrexed (100 mg/kg, i.p.) reduces tumor growth in A549, H1299, and PC-9 non-small cell lung cancer cell (NSCLC) mouse xenograft models but not in models using the same cell lines overexpressing thymidylate kinase.{53309}
Brand:CaymanSKU:- Pemetrexed is an antifolate with anticancer activity.{22488,22487,53309} It is an inhibitor of folate-dependent enzymes involved in purine synthesis, including thymidylate synthase and dihydrofolate reductase (Kis = 109 and 7 nM, respectively, for the human recombinant enzymes), and the potency for thymidylate kinase is increased following polyglutamination of pemetrexed (Ki = 1.3 nM for pemetrexed-glu5).{22488,22487} Pemetrexed is an inhibitor of other nucleotide metabolism enzymes in a polyglutamination-dependent manner, including glycinamide ribonucleotide formyltransferase, with Ki values of 9,300 and 65 nM for the non-glutaminated and polyglutaminated mouse recombinant enzyme, respectively, and aminoimidazole carboxamide ribonucleotide formyltransferase, with Ki values of 3,600 and 265 nM for the non-glutaminated and polyglutaminated human enzyme, respectively. It inhibits proliferation of CCRF-CEM cells but not 5,10-dideazatetrahydrofolate-resistant CR15 cells (IC50s = 0.254 and 200 µM, respectively).{22488} Pemetrexed (100 mg/kg, i.p.) reduces tumor growth in A549, H1299, and PC-9 non-small cell lung cancer cell (NSCLC) mouse xenograft models but not in models using the same cell lines overexpressing thymidylate kinase.{53309}
Brand:CaymanSKU:- Pemetrexed is an antifolate with anticancer activity.{22488,22487,53309} It is an inhibitor of folate-dependent enzymes involved in purine synthesis, including thymidylate synthase and dihydrofolate reductase (Kis = 109 and 7 nM, respectively, for the human recombinant enzymes), and the potency for thymidylate kinase is increased following polyglutamination of pemetrexed (Ki = 1.3 nM for pemetrexed-glu5).{22488,22487} Pemetrexed is an inhibitor of other nucleotide metabolism enzymes in a polyglutamination-dependent manner, including glycinamide ribonucleotide formyltransferase, with Ki values of 9,300 and 65 nM for the non-glutaminated and polyglutaminated mouse recombinant enzyme, respectively, and aminoimidazole carboxamide ribonucleotide formyltransferase, with Ki values of 3,600 and 265 nM for the non-glutaminated and polyglutaminated human enzyme, respectively. It inhibits proliferation of CCRF-CEM cells but not 5,10-dideazatetrahydrofolate-resistant CR15 cells (IC50s = 0.254 and 200 µM, respectively).{22488} Pemetrexed (100 mg/kg, i.p.) reduces tumor growth in A549, H1299, and PC-9 non-small cell lung cancer cell (NSCLC) mouse xenograft models but not in models using the same cell lines overexpressing thymidylate kinase.{53309}
Brand:CaymanSKU:-
Pemirolast is a histamine H1 receptor antagonist and a mast cell stabilizer that prevents the release of histamine.{29107} It also blocks the release of substance P, neurokinin A, and calcitonin gene-related peptide from sensory nerves.{29108} Pemirolast has been used for the treatment of allergic conjunctivitis.{29106}
Brand:CaymanSKU:-Available on backorder
Pemirolast is a histamine H1 receptor antagonist and a mast cell stabilizer that prevents the release of histamine.{29107} It also blocks the release of substance P, neurokinin A, and calcitonin gene-related peptide from sensory nerves.{29108} Pemirolast has been used for the treatment of allergic conjunctivitis.{29106}
Brand:CaymanSKU:-Available on backorder
Pemirolast is a histamine H1 receptor antagonist and a mast cell stabilizer that prevents the release of histamine.{29107} It also blocks the release of substance P, neurokinin A, and calcitonin gene-related peptide from sensory nerves.{29108} Pemirolast has been used for the treatment of allergic conjunctivitis.{29106}
Brand:CaymanSKU:-Available on backorder
Pemirolast is a histamine H1 receptor antagonist and a mast cell stabilizer that prevents the release of histamine.{29107} It also blocks the release of substance P, neurokinin A, and calcitonin gene-related peptide from sensory nerves.{29108} Pemirolast has been used for the treatment of allergic conjunctivitis.{29106}
Brand:CaymanSKU:-Available on backorder
Penbutolol is an antagonist of β-adrenergic receptors (β-ARs; IC50 = 2.8 nM) and the serotonin (5-HT) receptor subtype 5-HT1A (IC50 = 9.9 nM).{53262} It inhibits adenylate cyclase activity induced by the β-AR agonist isoprenaline (isoproterenol; Item No. 15592) in guinea pig myocardial membranes with a Ki value of 2.4 nM.{53263} Penbutolol reduces basal renin activity and blood pressure in spontaneously hypertonic rats.{53264} It decreases isolation-induced aggressive behavior in mice (ED50 = 56 µmol/kg) and reverses reductions in aggression induced by 8-hydroxy-DPAT (Item No. 22608) and TFMPP with ED50 values of 8.1 and 2.1 µmol/kg, respectively.{53262} Formulations containing penbutolol were previously used in the treatment of arterial hypertension.
Brand:CaymanSKU:29524 - 10 mgAvailable on backorder
Penbutolol is an antagonist of β-adrenergic receptors (β-ARs; IC50 = 2.8 nM) and the serotonin (5-HT) receptor subtype 5-HT1A (IC50 = 9.9 nM).{53262} It inhibits adenylate cyclase activity induced by the β-AR agonist isoprenaline (isoproterenol; Item No. 15592) in guinea pig myocardial membranes with a Ki value of 2.4 nM.{53263} Penbutolol reduces basal renin activity and blood pressure in spontaneously hypertonic rats.{53264} It decreases isolation-induced aggressive behavior in mice (ED50 = 56 µmol/kg) and reverses reductions in aggression induced by 8-hydroxy-DPAT (Item No. 22608) and TFMPP with ED50 values of 8.1 and 2.1 µmol/kg, respectively.{53262} Formulations containing penbutolol were previously used in the treatment of arterial hypertension.
Brand:CaymanSKU:29524 - 100 mgAvailable on backorder
Penbutolol is an antagonist of β-adrenergic receptors (β-ARs; IC50 = 2.8 nM) and the serotonin (5-HT) receptor subtype 5-HT1A (IC50 = 9.9 nM).{53262} It inhibits adenylate cyclase activity induced by the β-AR agonist isoprenaline (isoproterenol; Item No. 15592) in guinea pig myocardial membranes with a Ki value of 2.4 nM.{53263} Penbutolol reduces basal renin activity and blood pressure in spontaneously hypertonic rats.{53264} It decreases isolation-induced aggressive behavior in mice (ED50 = 56 µmol/kg) and reverses reductions in aggression induced by 8-hydroxy-DPAT (Item No. 22608) and TFMPP with ED50 values of 8.1 and 2.1 µmol/kg, respectively.{53262} Formulations containing penbutolol were previously used in the treatment of arterial hypertension.
Brand:CaymanSKU:29524 - 5 mgAvailable on backorder
Penbutolol is an antagonist of β-adrenergic receptors (β-ARs; IC50 = 2.8 nM) and the serotonin (5-HT) receptor subtype 5-HT1A (IC50 = 9.9 nM).{53262} It inhibits adenylate cyclase activity induced by the β-AR agonist isoprenaline (isoproterenol; Item No. 15592) in guinea pig myocardial membranes with a Ki value of 2.4 nM.{53263} Penbutolol reduces basal renin activity and blood pressure in spontaneously hypertonic rats.{53264} It decreases isolation-induced aggressive behavior in mice (ED50 = 56 µmol/kg) and reverses reductions in aggression induced by 8-hydroxy-DPAT (Item No. 22608) and TFMPP with ED50 values of 8.1 and 2.1 µmol/kg, respectively.{53262} Formulations containing penbutolol were previously used in the treatment of arterial hypertension.
Brand:CaymanSKU:29524 - 50 mgAvailable on backorder
Penciclovir is a guanosine analog with antiviral activity.{41028} It has activity against multiple laboratory and clinical isolate strains of herpes simplex virus 1 (HSV-1), HSV-2, and varicella zoster virus (VZV) in a plaque reduction assay (IC50s = 0.4-3.1 μg/ml). Penciclovir inhibits HSV-1 and HSV-2 replication (IC99s = 0.4 and 0.7 μg/ml, respectively) and DNA synthesis (IC50 = 0.04 μg/ml) in MRC-5 cells.{41028},{41029} In vivo, topical and systemic administration of penciclovir reduces the severity of skin lesions caused by HSV-1 in guinea pigs and mice.{41030} It also prevents development of HSV-2-induced genital lesions in guinea pigs infected intravaginally.
Brand:CaymanSKU:22918 - 1 gAvailable on backorder
Penciclovir is a guanosine analog with antiviral activity.{41028} It has activity against multiple laboratory and clinical isolate strains of herpes simplex virus 1 (HSV-1), HSV-2, and varicella zoster virus (VZV) in a plaque reduction assay (IC50s = 0.4-3.1 μg/ml). Penciclovir inhibits HSV-1 and HSV-2 replication (IC99s = 0.4 and 0.7 μg/ml, respectively) and DNA synthesis (IC50 = 0.04 μg/ml) in MRC-5 cells.{41028},{41029} In vivo, topical and systemic administration of penciclovir reduces the severity of skin lesions caused by HSV-1 in guinea pigs and mice.{41030} It also prevents development of HSV-2-induced genital lesions in guinea pigs infected intravaginally.
Brand:CaymanSKU:22918 - 100 mgAvailable on backorder
Penciclovir is a guanosine analog with antiviral activity.{41028} It has activity against multiple laboratory and clinical isolate strains of herpes simplex virus 1 (HSV-1), HSV-2, and varicella zoster virus (VZV) in a plaque reduction assay (IC50s = 0.4-3.1 μg/ml). Penciclovir inhibits HSV-1 and HSV-2 replication (IC99s = 0.4 and 0.7 μg/ml, respectively) and DNA synthesis (IC50 = 0.04 μg/ml) in MRC-5 cells.{41028},{41029} In vivo, topical and systemic administration of penciclovir reduces the severity of skin lesions caused by HSV-1 in guinea pigs and mice.{41030} It also prevents development of HSV-2-induced genital lesions in guinea pigs infected intravaginally.
Brand:CaymanSKU:22918 - 250 mgAvailable on backorder
Penciclovir is a guanosine analog with antiviral activity.{41028} It has activity against multiple laboratory and clinical isolate strains of herpes simplex virus 1 (HSV-1), HSV-2, and varicella zoster virus (VZV) in a plaque reduction assay (IC50s = 0.4-3.1 μg/ml). Penciclovir inhibits HSV-1 and HSV-2 replication (IC99s = 0.4 and 0.7 μg/ml, respectively) and DNA synthesis (IC50 = 0.04 μg/ml) in MRC-5 cells.{41028},{41029} In vivo, topical and systemic administration of penciclovir reduces the severity of skin lesions caused by HSV-1 in guinea pigs and mice.{41030} It also prevents development of HSV-2-induced genital lesions in guinea pigs infected intravaginally.
Brand:CaymanSKU:22918 - 500 mgAvailable on backorder
Penfluridol is a first generation typical antipsychotic that binds to dopamine receptors (IC50 = 5.6 nM).{42533} It binds to dopamine D4 receptors and also to serotonin (5-HT) receptors (Kis = 31 and 63.1 nM, respectively).{42534,42535} Penfluridol (1.25 and 2.5 mg/kg) inhibits stereotypic behavior induced by apomorphine (Item No. 16094) in cynomolgus monkeys.{42536} It also inhibits proliferation of triple-negative breast cancer cells (TNBCs; IC50s = 6-8 µM), as well as inhibits migration and invasion of TNBCs and decreases the expression of integrin α6 and β4.{42537} Penfluridol reduces tumor growth and metastasis in a 4T1 orthotopic mouse model when administered at a dose of 10 mg/kg per day.
Brand:CaymanSKU:26071 - 1 gAvailable on backorder
Penfluridol is a first generation typical antipsychotic that binds to dopamine receptors (IC50 = 5.6 nM).{42533} It binds to dopamine D4 receptors and also to serotonin (5-HT) receptors (Kis = 31 and 63.1 nM, respectively).{42534,42535} Penfluridol (1.25 and 2.5 mg/kg) inhibits stereotypic behavior induced by apomorphine (Item No. 16094) in cynomolgus monkeys.{42536} It also inhibits proliferation of triple-negative breast cancer cells (TNBCs; IC50s = 6-8 µM), as well as inhibits migration and invasion of TNBCs and decreases the expression of integrin α6 and β4.{42537} Penfluridol reduces tumor growth and metastasis in a 4T1 orthotopic mouse model when administered at a dose of 10 mg/kg per day.
Brand:CaymanSKU:26071 - 100 mgAvailable on backorder
Penfluridol is a first generation typical antipsychotic that binds to dopamine receptors (IC50 = 5.6 nM).{42533} It binds to dopamine D4 receptors and also to serotonin (5-HT) receptors (Kis = 31 and 63.1 nM, respectively).{42534,42535} Penfluridol (1.25 and 2.5 mg/kg) inhibits stereotypic behavior induced by apomorphine (Item No. 16094) in cynomolgus monkeys.{42536} It also inhibits proliferation of triple-negative breast cancer cells (TNBCs; IC50s = 6-8 µM), as well as inhibits migration and invasion of TNBCs and decreases the expression of integrin α6 and β4.{42537} Penfluridol reduces tumor growth and metastasis in a 4T1 orthotopic mouse model when administered at a dose of 10 mg/kg per day.
Brand:CaymanSKU:26071 - 250 mgAvailable on backorder
Penfluridol is a first generation typical antipsychotic that binds to dopamine receptors (IC50 = 5.6 nM).{42533} It binds to dopamine D4 receptors and also to serotonin (5-HT) receptors (Kis = 31 and 63.1 nM, respectively).{42534,42535} Penfluridol (1.25 and 2.5 mg/kg) inhibits stereotypic behavior induced by apomorphine (Item No. 16094) in cynomolgus monkeys.{42536} It also inhibits proliferation of triple-negative breast cancer cells (TNBCs; IC50s = 6-8 µM), as well as inhibits migration and invasion of TNBCs and decreases the expression of integrin α6 and β4.{42537} Penfluridol reduces tumor growth and metastasis in a 4T1 orthotopic mouse model when administered at a dose of 10 mg/kg per day.
Brand:CaymanSKU:26071 - 500 mgAvailable on backorder
Penicillamine is an orally bioavailable copper chelator and penicillin degradation product.{40699,40700} It increases urinary and fecal copper excretion and decreases liver copper concentration in a rat model of copper overload when administered at 0.67 mmol/kg per day, but does not affect kidney, spleen, or brain copper levels.{40701} Penicillamine (100 mg/kg per day) dissolves copper-rich granules in hepatic lysosomes of Long-Evans cinnamon (LEC) rats, which spontaneously develop hepatic injury and acute hepatitis and have a mutation homologous to that of the human Wilson disease gene.{40702} Penicillamine has anticonvulsant and proconvulsant effects in mice when administered at 0.5 and 250 mg/kg, respectively, which are blocked by the nitric oxide synthase (NOS) inhibitors L-NAME (Item No. 80210) and 7-nitroindazole (Item No. 81340).{40703} Formulations containing penicillamine have been used to treat Wilson disease, cystinuria, and active rheumatoid arthritis.
Brand:CaymanSKU:23955 - 1 gAvailable on backorder
Penicillamine is an orally bioavailable copper chelator and penicillin degradation product.{40699,40700} It increases urinary and fecal copper excretion and decreases liver copper concentration in a rat model of copper overload when administered at 0.67 mmol/kg per day, but does not affect kidney, spleen, or brain copper levels.{40701} Penicillamine (100 mg/kg per day) dissolves copper-rich granules in hepatic lysosomes of Long-Evans cinnamon (LEC) rats, which spontaneously develop hepatic injury and acute hepatitis and have a mutation homologous to that of the human Wilson disease gene.{40702} Penicillamine has anticonvulsant and proconvulsant effects in mice when administered at 0.5 and 250 mg/kg, respectively, which are blocked by the nitric oxide synthase (NOS) inhibitors L-NAME (Item No. 80210) and 7-nitroindazole (Item No. 81340).{40703} Formulations containing penicillamine have been used to treat Wilson disease, cystinuria, and active rheumatoid arthritis.
Brand:CaymanSKU:23955 - 10 gAvailable on backorder
Penicillamine is an orally bioavailable copper chelator and penicillin degradation product.{40699,40700} It increases urinary and fecal copper excretion and decreases liver copper concentration in a rat model of copper overload when administered at 0.67 mmol/kg per day, but does not affect kidney, spleen, or brain copper levels.{40701} Penicillamine (100 mg/kg per day) dissolves copper-rich granules in hepatic lysosomes of Long-Evans cinnamon (LEC) rats, which spontaneously develop hepatic injury and acute hepatitis and have a mutation homologous to that of the human Wilson disease gene.{40702} Penicillamine has anticonvulsant and proconvulsant effects in mice when administered at 0.5 and 250 mg/kg, respectively, which are blocked by the nitric oxide synthase (NOS) inhibitors L-NAME (Item No. 80210) and 7-nitroindazole (Item No. 81340).{40703} Formulations containing penicillamine have been used to treat Wilson disease, cystinuria, and active rheumatoid arthritis.
Brand:CaymanSKU:23955 - 5 gAvailable on backorder
Gram negative bacteria utilize N-acylated homoserine lactones to coordinate expression of virulence in response to the density of the surrounding bacterial population in a process termed quorum sensing. By interfering with this communication and thereby disrupting virulence expression, quorum sensing inhibitors are emerging as an alternative to the conventional ways of fighting bacterial infections. Penicillic acid is a mycotoxin produced from Penicillium species identified in molds on corn and other grains. At 80 μM, penicillic acid inhibits bacterial quorum sensing communication in P. aeruginosa by selectively repressing various virulence factor and other quorum sensing-regulated genes.{20838} It has been shown to inhibit Fas-mediated apoptosis at 100-200 μM by targeting caspase-8 activity in Burkitt’s lymphoma Raji cells.{20839}
Brand:CaymanSKU:11440 - 10 mgAvailable on backorder
Gram negative bacteria utilize N-acylated homoserine lactones to coordinate expression of virulence in response to the density of the surrounding bacterial population in a process termed quorum sensing. By interfering with this communication and thereby disrupting virulence expression, quorum sensing inhibitors are emerging as an alternative to the conventional ways of fighting bacterial infections. Penicillic acid is a mycotoxin produced from Penicillium species identified in molds on corn and other grains. At 80 μM, penicillic acid inhibits bacterial quorum sensing communication in P. aeruginosa by selectively repressing various virulence factor and other quorum sensing-regulated genes.{20838} It has been shown to inhibit Fas-mediated apoptosis at 100-200 μM by targeting caspase-8 activity in Burkitt’s lymphoma Raji cells.{20839}
Brand:CaymanSKU:11440 - 25 mgAvailable on backorder
Gram negative bacteria utilize N-acylated homoserine lactones to coordinate expression of virulence in response to the density of the surrounding bacterial population in a process termed quorum sensing. By interfering with this communication and thereby disrupting virulence expression, quorum sensing inhibitors are emerging as an alternative to the conventional ways of fighting bacterial infections. Penicillic acid is a mycotoxin produced from Penicillium species identified in molds on corn and other grains. At 80 μM, penicillic acid inhibits bacterial quorum sensing communication in P. aeruginosa by selectively repressing various virulence factor and other quorum sensing-regulated genes.{20838} It has been shown to inhibit Fas-mediated apoptosis at 100-200 μM by targeting caspase-8 activity in Burkitt’s lymphoma Raji cells.{20839}
Brand:CaymanSKU:11440 - 5 mgAvailable on backorder
Penicillide is a fungal metabolite originally isolated from Penicillium that has diverse biological activities.{42654,42655,42656,42657,42658} It is an inhibitor of calpain 2/m-calpain (IC50 = 7.1 µM) and acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 22.9 µM).{42655,42656} It is also an antagonist of oxytocin receptors (IC50 = 67 µM).{42657} Penicillide inhibits RNA synthesis in P388 murine leukemia cells.{42658}
Brand:CaymanSKU:26912 - 1 mgAvailable on backorder
Penicillide is a fungal metabolite originally isolated from Penicillium that has diverse biological activities.{42654,42655,42656,42657,42658} It is an inhibitor of calpain 2/m-calpain (IC50 = 7.1 µM) and acyl-coenzyme A:cholesterol acyltransferase (ACAT; IC50 = 22.9 µM).{42655,42656} It is also an antagonist of oxytocin receptors (IC50 = 67 µM).{42657} Penicillide inhibits RNA synthesis in P388 murine leukemia cells.{42658}
Brand:CaymanSKU:26912 - 500 µgAvailable on backorder
Penicillin G is a β-lactam antibiotic that is effective mainly for Gram-positive bacteria.{37156} It has MIC90 values of 0.03, 1, and 4 µg/ml for penicillin-susceptible, -intermediate, and -resistant strains of S. pneumoniae, respectively, and 16-128 µg/ml for various Bacteroides isolates in a broth dilution assay.{37157},{37155} Formulations containing penicillin G have been used for the treatment of bacterial infections and in livestock production.
Brand:CaymanSKU:21615 -Out of stock
Penicillin G is a β-lactam antibiotic that is effective mainly for Gram-positive bacteria.{37156} It has MIC90 values of 0.03, 1, and 4 µg/ml for penicillin-susceptible, -intermediate, and -resistant strains of S. pneumoniae, respectively, and 16-128 µg/ml for various Bacteroides isolates in a broth dilution assay.{37157},{37155} Formulations containing penicillin G have been used for the treatment of bacterial infections and in livestock production.
Brand:CaymanSKU:21615 -Out of stock
Penicillin G is a β-lactam antibiotic that is effective mainly for Gram-positive bacteria.{37156} It has MIC90 values of 0.03, 1, and 4 µg/ml for penicillin-susceptible, -intermediate, and -resistant strains of S. pneumoniae, respectively, and 16-128 µg/ml for various Bacteroides isolates in a broth dilution assay.{37157},{37155} Formulations containing penicillin G have been used for the treatment of bacterial infections and in livestock production.
Brand:CaymanSKU:21615 -Out of stock
Penicillin V is a β-lactam antibiotic that inhibits the growth of bacteria.{36398,36399,36400} In vitro, penicillin V inhibits the growth of clinical isolates of Streptococci (MICs = 0.004-0.008 mg/l) and C. difficile (MICs = 1 to >256 mg/l).{36398,36399} Penicillin V also inhibits growth of S. aureus in vitro (MIC = 0.016 mg/l) and in vivo in a thigh model of infection in mice.{36400} It inhibits the growth of S. pyogenes in mice following one or two dose therapy with curative dose (CD50) values of 0.207 and 0.031 mg, respectively.{36401} Penicillin V (100 mg/kg per day, p.o.) prevents experimental acute otitis media in rats when administered prior to infection by pneumococci.{36402} Formulations containing penicillin V have been used to treat bacterial infections of the skin, throat, ear, mouth, and respiratory tract.
Brand:CaymanSKU:23635 - 10 gAvailable on backorder
Penicillin V is a β-lactam antibiotic that inhibits the growth of bacteria.{36398,36399,36400} In vitro, penicillin V inhibits the growth of clinical isolates of Streptococci (MICs = 0.004-0.008 mg/l) and C. difficile (MICs = 1 to >256 mg/l).{36398,36399} Penicillin V also inhibits growth of S. aureus in vitro (MIC = 0.016 mg/l) and in vivo in a thigh model of infection in mice.{36400} It inhibits the growth of S. pyogenes in mice following one or two dose therapy with curative dose (CD50) values of 0.207 and 0.031 mg, respectively.{36401} Penicillin V (100 mg/kg per day, p.o.) prevents experimental acute otitis media in rats when administered prior to infection by pneumococci.{36402} Formulations containing penicillin V have been used to treat bacterial infections of the skin, throat, ear, mouth, and respiratory tract.
Brand:CaymanSKU:23635 - 100 gAvailable on backorder
Penicillin V is a β-lactam antibiotic that inhibits the growth of bacteria.{36398,36399,36400} In vitro, penicillin V inhibits the growth of clinical isolates of Streptococci (MICs = 0.004-0.008 mg/l) and C. difficile (MICs = 1 to >256 mg/l).{36398,36399} Penicillin V also inhibits growth of S. aureus in vitro (MIC = 0.016 mg/l) and in vivo in a thigh model of infection in mice.{36400} It inhibits the growth of S. pyogenes in mice following one or two dose therapy with curative dose (CD50) values of 0.207 and 0.031 mg, respectively.{36401} Penicillin V (100 mg/kg per day, p.o.) prevents experimental acute otitis media in rats when administered prior to infection by pneumococci.{36402} Formulations containing penicillin V have been used to treat bacterial infections of the skin, throat, ear, mouth, and respiratory tract.
Brand:CaymanSKU:23635 - 25 gAvailable on backorder
Penicillin V is a β-lactam antibiotic that inhibits the growth of bacteria.{36398,36399,36400} In vitro, penicillin V inhibits the growth of clinical isolates of Streptococci (MICs = 0.004-0.008 mg/l) and C. difficile (MICs = 1 to >256 mg/l).{36398,36399} Penicillin V also inhibits growth of S. aureus in vitro (MIC = 0.016 mg/l) and in vivo in a thigh model of infection in mice.{36400} It inhibits the growth of S. pyogenes in mice following one or two dose therapy with curative dose (CD50) values of 0.207 and 0.031 mg, respectively.{36401} Penicillin V (100 mg/kg per day, p.o.) prevents experimental acute otitis media in rats when administered prior to infection by pneumococci.{36402} Formulations containing penicillin V have been used to treat bacterial infections of the skin, throat, ear, mouth, and respiratory tract.
Brand:CaymanSKU:23635 - 50 gAvailable on backorder
Penicinoline is an alkaloid that has been found in Penicillium and has antimalarial, insecticidal, and anticancer activities.{53392,53393} It is active against chloroquine-sensitive and -resistant strains of P. falciparum (IC50 = 25 µM for both).{53392} Penicinoline (1,000 ppm) is also active against the aphid A. gossypii.{53393} It inhibits proliferation of 95-D and HepG2 cancer cells (IC50s = 0.57 and 6.5 µg/ml, respectively) but not HeLa, KB, KBv200, or Hep-2 cells (IC50s = >100 µg/ml).
Brand:CaymanSKU:29932 - 1 mgAvailable on backorder
Penicinoline is an alkaloid that has been found in Penicillium and has antimalarial, insecticidal, and anticancer activities.{53392,53393} It is active against chloroquine-sensitive and -resistant strains of P. falciparum (IC50 = 25 µM for both).{53392} Penicinoline (1,000 ppm) is also active against the aphid A. gossypii.{53393} It inhibits proliferation of 95-D and HepG2 cancer cells (IC50s = 0.57 and 6.5 µg/ml, respectively) but not HeLa, KB, KBv200, or Hep-2 cells (IC50s = >100 µg/ml).
Brand:CaymanSKU:29932 - 5 mgAvailable on backorder
Penicolinate A is a fungal metabolite produced by Penicillium sp. BCC16054 with diverse biological activities.{41718} It exhibits antimalarial and antituberculosis activity (MICs = 3.25 and 12.5 mg/ml for P. falciparum and M. tuberculosis H37Ra, respectively). Penicolinate A is cytotoxic to MCF-7, KB, NCI-H187, and Vero cells (IC50s = 7.49, 18.43, 4.4, and 14.08 μM, respectively).
Brand:CaymanSKU:25013 - 1 mgAvailable on backorder
Penicolinate A is a fungal metabolite produced by Penicillium sp. BCC16054 with diverse biological activities.{41718} It exhibits antimalarial and antituberculosis activity (MICs = 3.25 and 12.5 mg/ml for P. falciparum and M. tuberculosis H37Ra, respectively). Penicolinate A is cytotoxic to MCF-7, KB, NCI-H187, and Vero cells (IC50s = 7.49, 18.43, 4.4, and 14.08 μM, respectively).
Brand:CaymanSKU:25013 - 5 mgAvailable on backorder
Penigequinolone A is an alkaloid isolated from Penicillium. It is lethal to P. penetrans (LD50 = 100 mg/L) but has no effect on C. elegans at concentrations up to 1000 mg/L.{40469} Penigequinolone A also accelerates the root growth of rice seedlings in a dose-dependent manner.
Brand:CaymanSKU:23647 - 1 mgAvailable on backorder
Penigequinolone A is an alkaloid isolated from Penicillium. It is lethal to P. penetrans (LD50 = 100 mg/L) but has no effect on C. elegans at concentrations up to 1000 mg/L.{40469} Penigequinolone A also accelerates the root growth of rice seedlings in a dose-dependent manner.
Brand:CaymanSKU:23647 - 500 µgAvailable on backorder
Penitrem A is a tremorgenic fungal toxin that acts as an inhibitor of the large conductance calcium-activated potassium channel BKCa (SLO1, Maxi-K, KCa1.1), inhibiting the binding of charybdotoxin with an IC50 value of 1.7 μM.{20613} It is currently used to evaluate the role of BKCa-mediated potassium flux in various cell processes and responses.{20622,20623}
Brand:CaymanSKU:11347 - 1 mgAvailable on backorder
Penitrem A is a tremorgenic fungal toxin that acts as an inhibitor of the large conductance calcium-activated potassium channel BKCa (SLO1, Maxi-K, KCa1.1), inhibiting the binding of charybdotoxin with an IC50 value of 1.7 μM.{20613} It is currently used to evaluate the role of BKCa-mediated potassium flux in various cell processes and responses.{20622,20623}
Brand:CaymanSKU:11347 - 10 mgAvailable on backorder
Penitrem A is a tremorgenic fungal toxin that acts as an inhibitor of the large conductance calcium-activated potassium channel BKCa (SLO1, Maxi-K, KCa1.1), inhibiting the binding of charybdotoxin with an IC50 value of 1.7 μM.{20613} It is currently used to evaluate the role of BKCa-mediated potassium flux in various cell processes and responses.{20622,20623}
Brand:CaymanSKU:11347 - 5 mgAvailable on backorder
Root nodules, like those induced on the roots of leguminous plants by Rhizobium bacteria, are important sites for the conversion of atmospheric nitrogen into ammonia. The initiation and development of these growths are driven by a variety of nodulation (Nod) proteins produced by the infecting bacteria. Penta-N-acetylchitopentaose is a pentameric chito-oligosaccharide involved in nodulation. It can be produced by NodC, a chito-oligosaccharide synthase, and serve as a substrate for NodL, an O-acetyltransferase.{26339,26337,26334} This bacterial product binds plant root lectins, and this interaction may be important in the promotion of cell division in the root cortex.{26333,26336} Penta-N-acetylchitopentaose, as well as chitin and chitosan, inhibits nitric oxide production in LPS-activated RAW 264.7 macrophages.{26338}
Brand:CaymanSKU:- Root nodules, like those induced on the roots of leguminous plants by Rhizobium bacteria, are important sites for the conversion of atmospheric nitrogen into ammonia. The initiation and development of these growths are driven by a variety of nodulation (Nod) proteins produced by the infecting bacteria. Penta-N-acetylchitopentaose is a pentameric chito-oligosaccharide involved in nodulation. It can be produced by NodC, a chito-oligosaccharide synthase, and serve as a substrate for NodL, an O-acetyltransferase.{26339,26337,26334} This bacterial product binds plant root lectins, and this interaction may be important in the promotion of cell division in the root cortex.{26333,26336} Penta-N-acetylchitopentaose, as well as chitin and chitosan, inhibits nitric oxide production in LPS-activated RAW 264.7 macrophages.{26338}
Brand:CaymanSKU:- Root nodules, like those induced on the roots of leguminous plants by Rhizobium bacteria, are important sites for the conversion of atmospheric nitrogen into ammonia. The initiation and development of these growths are driven by a variety of nodulation (Nod) proteins produced by the infecting bacteria. Penta-N-acetylchitopentaose is a pentameric chito-oligosaccharide involved in nodulation. It can be produced by NodC, a chito-oligosaccharide synthase, and serve as a substrate for NodL, an O-acetyltransferase.{26339,26337,26334} This bacterial product binds plant root lectins, and this interaction may be important in the promotion of cell division in the root cortex.{26333,26336} Penta-N-acetylchitopentaose, as well as chitin and chitosan, inhibits nitric oxide production in LPS-activated RAW 264.7 macrophages.{26338}
Brand:CaymanSKU:-
Pentaacetylquercetin is a pentaacetylated derivative of the flavonoid quercetin (Item No. 10005169) that has diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties.{45115,45116,45117} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in vitro (IC50 = 3.74 μg/ml) and inhibits iron(II) chloride-induced lipid peroxidation in rat liver mitochondria (IC50 = 20.2 μg/ml).{45115} Pentaacetylquercetin inhibits LPS-induced increases in nitrite (IC50 = 8.7 μM) and PGE2 (Item No. 14010) production, as well as inducible nitric oxide synthase (iNOS) and COX-2 levels, in RAW 264.7 cells when used at concentrations of 20 and 40 μM.{45116} It also inhibits the growth of HL-60, U937, and SK-MEL-1 cells (IC50s = 38, 25, and 58 μM, respectively).{45117}
Brand:CaymanSKU:26694 - 10 mgAvailable on backorder
Pentaacetylquercetin is a pentaacetylated derivative of the flavonoid quercetin (Item No. 10005169) that has diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties.{45115,45116,45117} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in vitro (IC50 = 3.74 μg/ml) and inhibits iron(II) chloride-induced lipid peroxidation in rat liver mitochondria (IC50 = 20.2 μg/ml).{45115} Pentaacetylquercetin inhibits LPS-induced increases in nitrite (IC50 = 8.7 μM) and PGE2 (Item No. 14010) production, as well as inducible nitric oxide synthase (iNOS) and COX-2 levels, in RAW 264.7 cells when used at concentrations of 20 and 40 μM.{45116} It also inhibits the growth of HL-60, U937, and SK-MEL-1 cells (IC50s = 38, 25, and 58 μM, respectively).{45117}
Brand:CaymanSKU:26694 - 100 mgAvailable on backorder
Pentaacetylquercetin is a pentaacetylated derivative of the flavonoid quercetin (Item No. 10005169) that has diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties.{45115,45116,45117} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in vitro (IC50 = 3.74 μg/ml) and inhibits iron(II) chloride-induced lipid peroxidation in rat liver mitochondria (IC50 = 20.2 μg/ml).{45115} Pentaacetylquercetin inhibits LPS-induced increases in nitrite (IC50 = 8.7 μM) and PGE2 (Item No. 14010) production, as well as inducible nitric oxide synthase (iNOS) and COX-2 levels, in RAW 264.7 cells when used at concentrations of 20 and 40 μM.{45116} It also inhibits the growth of HL-60, U937, and SK-MEL-1 cells (IC50s = 38, 25, and 58 μM, respectively).{45117}
Brand:CaymanSKU:26694 - 50 mgAvailable on backorder
Pentaacetylquercetin is a pentaacetylated derivative of the flavonoid quercetin (Item No. 10005169) that has diverse biological activities, including antioxidant, anti-inflammatory, and anticancer properties.{45115,45116,45117} It scavenges 2,2-diphenyl-1-picrylhydrazyl (DPPH; Item No. 14805) radicals in vitro (IC50 = 3.74 μg/ml) and inhibits iron(II) chloride-induced lipid peroxidation in rat liver mitochondria (IC50 = 20.2 μg/ml).{45115} Pentaacetylquercetin inhibits LPS-induced increases in nitrite (IC50 = 8.7 μM) and PGE2 (Item No. 14010) production, as well as inducible nitric oxide synthase (iNOS) and COX-2 levels, in RAW 264.7 cells when used at concentrations of 20 and 40 μM.{45116} It also inhibits the growth of HL-60, U937, and SK-MEL-1 cells (IC50s = 38, 25, and 58 μM, respectively).{45117}
Brand:CaymanSKU:26694 - 500 mgAvailable on backorder
Brand:CaymanSKU:- Brand:CaymanSKU:- Brand:CaymanSKU:-
Long chain saturated fatty acids and their esters are common components of plant lipids. Pentacosanoic acid methyl ester is the methyl ester of the 25-carbon, fully saturated fatty acid pentacosanoic acid. This product is designed to be used as a standard in total fatty acid analysis.
Brand:CaymanSKU:10006451 - 1 gAvailable on backorder
Long chain saturated fatty acids and their esters are common components of plant lipids. Pentacosanoic acid methyl ester is the methyl ester of the 25-carbon, fully saturated fatty acid pentacosanoic acid. This product is designed to be used as a standard in total fatty acid analysis.
Brand:CaymanSKU:10006451 - 100 mgAvailable on backorder
Long chain saturated fatty acids and their esters are common components of plant lipids. Pentacosanoic acid methyl ester is the methyl ester of the 25-carbon, fully saturated fatty acid pentacosanoic acid. This product is designed to be used as a standard in total fatty acid analysis.
Brand:CaymanSKU:10006451 - 500 mgAvailable on backorder
Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants. It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:-Available on backorder
Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants. It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:-Available on backorder
Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants. It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:-Available on backorder
Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants. It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:-Available on backorder
Pentadecanoic acid methyl ester is an esterified form of pentadecanoic acid (Item No. 17399). It has been found as a minor component in biodiesels made from the transesterification of beef tallow, soybean oil, and babassu oil blends.{48265} It has also been found in latent fingerprint residue samples.{48210}
Brand:CaymanSKU:26722 - 1 gAvailable on backorder
Pentadecanoic acid methyl ester is an esterified form of pentadecanoic acid (Item No. 17399). It has been found as a minor component in biodiesels made from the transesterification of beef tallow, soybean oil, and babassu oil blends.{48265} It has also been found in latent fingerprint residue samples.{48210}
Brand:CaymanSKU:26722 - 5 gAvailable on backorder
Pentadecanoic acid methyl ester is an esterified form of pentadecanoic acid (Item No. 17399). It has been found as a minor component in biodiesels made from the transesterification of beef tallow, soybean oil, and babassu oil blends.{48265} It has also been found in latent fingerprint residue samples.{48210}
Brand:CaymanSKU:26722 - 500 mgAvailable on backorder
Pentadecanoic acid-d29 is intended for use as an internal standard for the quantification of pentadecanoic acid (Item No. 17399) by GC- or LC-MS. Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants.{29188} It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:28081 - 1 mgAvailable on backorder
Pentadecanoic acid-d29 is intended for use as an internal standard for the quantification of pentadecanoic acid (Item No. 17399) by GC- or LC-MS. Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants.{29188} It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:28081 - 10 mgAvailable on backorder
Pentadecanoic acid-d29 is intended for use as an internal standard for the quantification of pentadecanoic acid (Item No. 17399) by GC- or LC-MS. Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants.{29188} It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:28081 - 5 mgAvailable on backorder
Pentadecanoic acid-d3 is intended for use as an internal standard for the quantification of pentadecanoic acid (Item No. 17399) by GC- or LC-MS. Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants.{29188} It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:28596 - 1 mgAvailable on backorder
Pentadecanoic acid-d3 is intended for use as an internal standard for the quantification of pentadecanoic acid (Item No. 17399) by GC- or LC-MS. Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants.{29188} It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:28596 - 10 mgAvailable on backorder
Pentadecanoic acid-d3 is intended for use as an internal standard for the quantification of pentadecanoic acid (Item No. 17399) by GC- or LC-MS. Pentadecanoic acid is a 15:0 saturated fatty acid found in esterified form in the lipids of many bacterial species and in the milk fat of ruminants.{29188} It has been used as a biological marker for the intake of dairy fat in the assessment of metabolic risk factors.{29188,29189}
Brand:CaymanSKU:28596 - 5 mgAvailable on backorder
Pentadecanoyl ethanolamide is a member of the family of fatty N-acyl ethanolamines collectively called endocannabinoids.{1202,1712,13153,22439,22438} The specific role and relative importance of this ethanolamine metabolite have not been determined.
Brand:CaymanSKU:9001740 - 10 mgAvailable on backorder
Pentadecanoyl ethanolamide is a member of the family of fatty N-acyl ethanolamines collectively called endocannabinoids.{1202,1712,13153,22439,22438} The specific role and relative importance of this ethanolamine metabolite have not been determined.
Brand:CaymanSKU:9001740 - 100 mgAvailable on backorder