Cayman
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4-Hydroxymethamphetamine (hydrochloride) is an analytical reference standard categorized as an amphetamine. It is a metabolite of methamphetamine (Item Nos. 14216 | ISO60168).{47743} This product is intended for research and forensic applications.
Brand:CaymanSKU:9002128 - 1 mgAvailable on backorder
4-Hydroxymethamphetamine (hydrochloride) is an analytical reference standard categorized as an amphetamine. It is a metabolite of methamphetamine (Item Nos. 14216 | ISO60168).{47743} This product is intended for research and forensic applications.
Brand:CaymanSKU:9002128 - 5 mgAvailable on backorder
4-Hydroxyphenylacetic acid is a phenolic acid with anti-inflammatory activity.{46255} It is formed via microbial metabolism of aromatic amino acids and polyphenolic compounds, including flavonoid glycosides, by gut microbiota.{46256,46257,46258} 4-Hydroxyphenylacetic acid (100 mg/kg) inhibits seawater instillation-induced increases in TNF-α, IL-1β, and IL-6 levels in lung tissue and white blood cell numbers in bronchoalveolar lavage fluid (BALF) and prevents lung edema in a rat model of acute lung injury.{46255} Levels of 4-hydroxyphenylacetic acid are increased and decreased in serum and urine, respectively, in rats fed a high-fat diet.{46256} Serum levels of 4-hydroxyphenylacetic acid are increased in patients with stage III pancreatic cancer.{46259}
Brand:CaymanSKU:26613 - 100 gAvailable on backorder
4-Hydroxyphenylacetic acid is a phenolic acid with anti-inflammatory activity.{46255} It is formed via microbial metabolism of aromatic amino acids and polyphenolic compounds, including flavonoid glycosides, by gut microbiota.{46256,46257,46258} 4-Hydroxyphenylacetic acid (100 mg/kg) inhibits seawater instillation-induced increases in TNF-α, IL-1β, and IL-6 levels in lung tissue and white blood cell numbers in bronchoalveolar lavage fluid (BALF) and prevents lung edema in a rat model of acute lung injury.{46255} Levels of 4-hydroxyphenylacetic acid are increased and decreased in serum and urine, respectively, in rats fed a high-fat diet.{46256} Serum levels of 4-hydroxyphenylacetic acid are increased in patients with stage III pancreatic cancer.{46259}
Brand:CaymanSKU:26613 - 25 gAvailable on backorder
4-Hydroxyphenylacetic acid is a phenolic acid with anti-inflammatory activity.{46255} It is formed via microbial metabolism of aromatic amino acids and polyphenolic compounds, including flavonoid glycosides, by gut microbiota.{46256,46257,46258} 4-Hydroxyphenylacetic acid (100 mg/kg) inhibits seawater instillation-induced increases in TNF-α, IL-1β, and IL-6 levels in lung tissue and white blood cell numbers in bronchoalveolar lavage fluid (BALF) and prevents lung edema in a rat model of acute lung injury.{46255} Levels of 4-hydroxyphenylacetic acid are increased and decreased in serum and urine, respectively, in rats fed a high-fat diet.{46256} Serum levels of 4-hydroxyphenylacetic acid are increased in patients with stage III pancreatic cancer.{46259}
Brand:CaymanSKU:26613 - 250 gAvailable on backorder
4-Hydroxyphenylacetic acid is a phenolic acid with anti-inflammatory activity.{46255} It is formed via microbial metabolism of aromatic amino acids and polyphenolic compounds, including flavonoid glycosides, by gut microbiota.{46256,46257,46258} 4-Hydroxyphenylacetic acid (100 mg/kg) inhibits seawater instillation-induced increases in TNF-α, IL-1β, and IL-6 levels in lung tissue and white blood cell numbers in bronchoalveolar lavage fluid (BALF) and prevents lung edema in a rat model of acute lung injury.{46255} Levels of 4-hydroxyphenylacetic acid are increased and decreased in serum and urine, respectively, in rats fed a high-fat diet.{46256} Serum levels of 4-hydroxyphenylacetic acid are increased in patients with stage III pancreatic cancer.{46259}
Brand:CaymanSKU:26613 - 50 gAvailable on backorder
4-IBP is a sigma-1 (σ1) receptor ligand (Ki = 1.7 nM).{61020,61021} It is selective for σ1 over σ2 receptors (Ki = 25.2 nM). It inhibits the growth and migration of PC3 prostate cancer and A549 non-small cell lung cancer (NSCLC) cells, as well as the migration of C32 melanoma and U373 MG glioblastoma cells, when used at a concentration of 10 µM.{61020} 4-IBP (2 mg/kg) increases survival in a U373 MG mouse xenograft model. It also increases firing of serotonergic neurons in the rat dorsal raphe nucleus when administered at a dose of 2 mg/kg.{61021}
Brand:CaymanSKU:31518 - 10 mgAvailable on backorder
4-IBP is a sigma-1 (σ1) receptor ligand (Ki = 1.7 nM).{61020,61021} It is selective for σ1 over σ2 receptors (Ki = 25.2 nM). It inhibits the growth and migration of PC3 prostate cancer and A549 non-small cell lung cancer (NSCLC) cells, as well as the migration of C32 melanoma and U373 MG glioblastoma cells, when used at a concentration of 10 µM.{61020} 4-IBP (2 mg/kg) increases survival in a U373 MG mouse xenograft model. It also increases firing of serotonergic neurons in the rat dorsal raphe nucleus when administered at a dose of 2 mg/kg.{61021}
Brand:CaymanSKU:31518 - 25 mgAvailable on backorder
4-IBP is a sigma-1 (σ1) receptor ligand (Ki = 1.7 nM).{61020,61021} It is selective for σ1 over σ2 receptors (Ki = 25.2 nM). It inhibits the growth and migration of PC3 prostate cancer and A549 non-small cell lung cancer (NSCLC) cells, as well as the migration of C32 melanoma and U373 MG glioblastoma cells, when used at a concentration of 10 µM.{61020} 4-IBP (2 mg/kg) increases survival in a U373 MG mouse xenograft model. It also increases firing of serotonergic neurons in the rat dorsal raphe nucleus when administered at a dose of 2 mg/kg.{61021}
Brand:CaymanSKU:31518 - 5 mgAvailable on backorder
4-IBP is a sigma-1 (σ1) receptor ligand (Ki = 1.7 nM).{61020,61021} It is selective for σ1 over σ2 receptors (Ki = 25.2 nM). It inhibits the growth and migration of PC3 prostate cancer and A549 non-small cell lung cancer (NSCLC) cells, as well as the migration of C32 melanoma and U373 MG glioblastoma cells, when used at a concentration of 10 µM.{61020} 4-IBP (2 mg/kg) increases survival in a U373 MG mouse xenograft model. It also increases firing of serotonergic neurons in the rat dorsal raphe nucleus when administered at a dose of 2 mg/kg.{61021}
Brand:CaymanSKU:31518 - 50 mgAvailable on backorder
4-iodo-SAHA is a hydrophobic derivative of the class I and class II histone deacetylase (HDAC) inhibitor SAHA. At 1 μM it demonstrates >60% inhibition of HDAC1 and HDAC6 activity in a deacetylase activity assay, similar to that of SAHA. 4-iodo-SAHA inhibits proliferation of SK-BR-3 breast-derived and HT29 colon-derived cell lines with EC50 values comparable to that of SAHA (1.1 and 0.95 μM versus 2.1 and 2 μM, respectively). It is 10-fold more potent as an inhibitor of U937 leukemia cell proliferation compared to SAHA (0.12 μM versus 1.2 μM, respectively).{18112}
Brand:CaymanSKU:10495 - 100 mgAvailable on backorder
4-iodo-SAHA is a hydrophobic derivative of the class I and class II histone deacetylase (HDAC) inhibitor SAHA. At 1 μM it demonstrates >60% inhibition of HDAC1 and HDAC6 activity in a deacetylase activity assay, similar to that of SAHA. 4-iodo-SAHA inhibits proliferation of SK-BR-3 breast-derived and HT29 colon-derived cell lines with EC50 values comparable to that of SAHA (1.1 and 0.95 μM versus 2.1 and 2 μM, respectively). It is 10-fold more potent as an inhibitor of U937 leukemia cell proliferation compared to SAHA (0.12 μM versus 1.2 μM, respectively).{18112}
Brand:CaymanSKU:10495 - 250 mgAvailable on backorder
4-iodo-SAHA is a hydrophobic derivative of the class I and class II histone deacetylase (HDAC) inhibitor SAHA. At 1 μM it demonstrates >60% inhibition of HDAC1 and HDAC6 activity in a deacetylase activity assay, similar to that of SAHA. 4-iodo-SAHA inhibits proliferation of SK-BR-3 breast-derived and HT29 colon-derived cell lines with EC50 values comparable to that of SAHA (1.1 and 0.95 μM versus 2.1 and 2 μM, respectively). It is 10-fold more potent as an inhibitor of U937 leukemia cell proliferation compared to SAHA (0.12 μM versus 1.2 μM, respectively).{18112}
Brand:CaymanSKU:10495 - 50 mgAvailable on backorder
4-iodo-SAHA is a hydrophobic derivative of the class I and class II histone deacetylase (HDAC) inhibitor SAHA. At 1 μM it demonstrates >60% inhibition of HDAC1 and HDAC6 activity in a deacetylase activity assay, similar to that of SAHA. 4-iodo-SAHA inhibits proliferation of SK-BR-3 breast-derived and HT29 colon-derived cell lines with EC50 values comparable to that of SAHA (1.1 and 0.95 μM versus 2.1 and 2 μM, respectively). It is 10-fold more potent as an inhibitor of U937 leukemia cell proliferation compared to SAHA (0.12 μM versus 1.2 μM, respectively).{18112}
Brand:CaymanSKU:10495 - 500 mgAvailable on backorder
Some halogenated amphetamines deplete brain serotonin levels and display pronounced neurotoxicity.{25537} 4-Iodoamphetamine is a halogenated amphetamine featuring an iodine atom at the para position of the phenyl group. It selectively induces serotonin release and inhibits reuptake by rat brain synaptosomes while showing reduced neurotoxic properties.{20299,20234} This product is intended for forensic and research applications.
Brand:CaymanSKU:9001853 - 1 mgAvailable on backorder
Some halogenated amphetamines deplete brain serotonin levels and display pronounced neurotoxicity.{25537} 4-Iodoamphetamine is a halogenated amphetamine featuring an iodine atom at the para position of the phenyl group. It selectively induces serotonin release and inhibits reuptake by rat brain synaptosomes while showing reduced neurotoxic properties.{20299,20234} This product is intended for forensic and research applications.
Brand:CaymanSKU:9001853 - 10 mgAvailable on backorder
Some halogenated amphetamines deplete brain serotonin levels and display pronounced neurotoxicity.{25537} 4-Iodoamphetamine is a halogenated amphetamine featuring an iodine atom at the para position of the phenyl group. It selectively induces serotonin release and inhibits reuptake by rat brain synaptosomes while showing reduced neurotoxic properties.{20299,20234} This product is intended for forensic and research applications.
Brand:CaymanSKU:9001853 - 5 mgAvailable on backorder
4-IPP is an inhibitor of macrophage migration inhibitory factor (MIF).{59363} It acts as a suicide substrate for MIF, leading to covalent modification of the N-terminal proline required for activation of its catalytic activity. 4-IPP (10 and 100 µM) inhibits the migration and anchorage-independent growth of A549 non-small cell lung cancer (NSCLC) cells. It inhibits proliferation of, and induces apoptosis in, TPC-1 thyroid carcinoma cells when used at concentrations of 50 and 100 µM.{59364} 4-IPP (~50 mg/kg) also inhibits the tautomerase activity of MIF in mouse liver in vivo.{59363}
Brand:CaymanSKU:31770 - 10 mgAvailable on backorder
4-IPP is an inhibitor of macrophage migration inhibitory factor (MIF).{59363} It acts as a suicide substrate for MIF, leading to covalent modification of the N-terminal proline required for activation of its catalytic activity. 4-IPP (10 and 100 µM) inhibits the migration and anchorage-independent growth of A549 non-small cell lung cancer (NSCLC) cells. It inhibits proliferation of, and induces apoptosis in, TPC-1 thyroid carcinoma cells when used at concentrations of 50 and 100 µM.{59364} 4-IPP (~50 mg/kg) also inhibits the tautomerase activity of MIF in mouse liver in vivo.{59363}
Brand:CaymanSKU:31770 - 25 mgAvailable on backorder
4-IPP is an inhibitor of macrophage migration inhibitory factor (MIF).{59363} It acts as a suicide substrate for MIF, leading to covalent modification of the N-terminal proline required for activation of its catalytic activity. 4-IPP (10 and 100 µM) inhibits the migration and anchorage-independent growth of A549 non-small cell lung cancer (NSCLC) cells. It inhibits proliferation of, and induces apoptosis in, TPC-1 thyroid carcinoma cells when used at concentrations of 50 and 100 µM.{59364} 4-IPP (~50 mg/kg) also inhibits the tautomerase activity of MIF in mouse liver in vivo.{59363}
Brand:CaymanSKU:31770 - 5 mgAvailable on backorder
4-IPP is an inhibitor of macrophage migration inhibitory factor (MIF).{59363} It acts as a suicide substrate for MIF, leading to covalent modification of the N-terminal proline required for activation of its catalytic activity. 4-IPP (10 and 100 µM) inhibits the migration and anchorage-independent growth of A549 non-small cell lung cancer (NSCLC) cells. It inhibits proliferation of, and induces apoptosis in, TPC-1 thyroid carcinoma cells when used at concentrations of 50 and 100 µM.{59364} 4-IPP (~50 mg/kg) also inhibits the tautomerase activity of MIF in mouse liver in vivo.{59363}
Brand:CaymanSKU:31770 - 50 mgAvailable on backorder
4-isocyanato TEMPO is a spin labeling reagent used to label the 2’-position in RNA.{39230} It has been used to study HIV-1 transactivation response RNA and hammerhead ribosome dynamics by electron paramagnetic resonance (EPR) spectroscopy.{39231, 39232}
Brand:CaymanSKU:23075 - 1 mgAvailable on backorder
4-isocyanato TEMPO is a spin labeling reagent used to label the 2’-position in RNA.{39230} It has been used to study HIV-1 transactivation response RNA and hammerhead ribosome dynamics by electron paramagnetic resonance (EPR) spectroscopy.{39231, 39232}
Brand:CaymanSKU:23075 - 10 mgAvailable on backorder
4-isocyanato TEMPO is a spin labeling reagent used to label the 2’-position in RNA.{39230} It has been used to study HIV-1 transactivation response RNA and hammerhead ribosome dynamics by electron paramagnetic resonance (EPR) spectroscopy.{39231, 39232}
Brand:CaymanSKU:23075 - 5 mgAvailable on backorder
4-isocyanato TEMPO is a spin labeling reagent used to label the 2’-position in RNA.{39230} It has been used to study HIV-1 transactivation response RNA and hammerhead ribosome dynamics by electron paramagnetic resonance (EPR) spectroscopy.{39231, 39232}
Brand:CaymanSKU:23075 - 500 µgAvailable on backorder
4-methoxy PCE (Item No. 9001356) is an analytical reference standard categorized as an arylcyclohexylamine. This product is intended for research and forensic applications.
Brand:CaymanSKU:9001356 - 1 mgAvailable on backorder
4-methoxy PCE (Item No. 9001356) is an analytical reference standard categorized as an arylcyclohexylamine. This product is intended for research and forensic applications.
Brand:CaymanSKU:9001356 - 5 mgAvailable on backorder
Phencyclidine (PCP), known more commonly as angel dust, is a psychoactive drug that is regulated as a schedule I compound in the United States.{21020} 4-methoxy PCP is an analog of PCP which has recently been commercially produced as a designer drug.{22306} It preferentially binds the σ-2 receptor (Ki = 143 nM) and less weakly binds the NMDA receptor and serotonin transporter (Kis = 404 and 844 nM, respectively).{22308} The toxicological properties of this compound have not been reported. This product is intended for forensic and research purposes.
Brand:CaymanSKU:11136 - 10 mgAvailable on backorder
Phencyclidine (PCP), known more commonly as angel dust, is a psychoactive drug that is regulated as a schedule I compound in the United States.{21020} 4-methoxy PCP is an analog of PCP which has recently been commercially produced as a designer drug.{22306} It preferentially binds the σ-2 receptor (Ki = 143 nM) and less weakly binds the NMDA receptor and serotonin transporter (Kis = 404 and 844 nM, respectively).{22308} The toxicological properties of this compound have not been reported. This product is intended for forensic and research purposes.
Brand:CaymanSKU:11136 - 5 mgAvailable on backorder
Phencyclidine (PCP), known more commonly as angel dust, is a psychoactive drug that is regulated as a schedule I compound in the United States.{21020} 4-methoxy PCP is an analog of PCP which has recently been commercially produced as a designer drug.{22306} It preferentially binds the σ-2 receptor (Ki = 143 nM) and less weakly binds the NMDA receptor and serotonin transporter (Kis = 404 and 844 nM, respectively).{22308} The toxicological properties of this compound have not been reported. This product is intended for forensic and research purposes.
Brand:CaymanSKU:11136 - 50 mgAvailable on backorder
Methedrone (4-methoxymethcathinone) is a substituted cathinone with psychoactive actions. Its use as a recreational drug and its toxicity have recently been reported.{19508,20369} 4-methyl-N,N-DMC is an analog of methedrone, differing by the presence of a second aminomethyl group. Its biological and toxicological properties have not been evaluated. This product is intended for forensic and research applications.
Brand:CaymanSKU:11666 - 10 mgAvailable on backorder
Methedrone (4-methoxymethcathinone) is a substituted cathinone with psychoactive actions. Its use as a recreational drug and its toxicity have recently been reported.{19508,20369} 4-methyl-N,N-DMC is an analog of methedrone, differing by the presence of a second aminomethyl group. Its biological and toxicological properties have not been evaluated. This product is intended for forensic and research applications.
Brand:CaymanSKU:11666 - 5 mgAvailable on backorder
Methedrone (4-methoxymethcathinone) is a substituted cathinone with psychoactive actions. Its use as a recreational drug and its toxicity have recently been reported.{19508,20369} 4-methyl-N,N-DMC is an analog of methedrone, differing by the presence of a second aminomethyl group. Its biological and toxicological properties have not been evaluated. This product is intended for forensic and research applications.
Brand:CaymanSKU:11666 - 50 mgAvailable on backorder
Pyrrolidinophenones are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs. 4-methoxy-α-Pyrrolidinopentiophenone (4-MeO-α-PVP) (hydrochloride) shares structural features with the stimulant α-PVP. The mechanism of action is unknown for α-PVP, but is believed to be similar to that of the designer drug MDPV (Item No. 10624), which acts as a norepinephrine-dopamine reuptake inhibitor.{18946,18943} This product is intended to be used for forensic and research applications.
Brand:CaymanSKU:- Pyrrolidinophenones are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs. 4-methoxy-α-Pyrrolidinopentiophenone (4-MeO-α-PVP) (hydrochloride) shares structural features with the stimulant α-PVP. The mechanism of action is unknown for α-PVP, but is believed to be similar to that of the designer drug MDPV (Item No. 10624), which acts as a norepinephrine-dopamine reuptake inhibitor.{18946,18943} This product is intended to be used for forensic and research applications.
Brand:CaymanSKU:- Pyrrolidinophenones are a family of compounds that feature a pyrrolidinyl group affixed to the narcotic cathinone. Many have been identified as components of designer drugs. 4-methoxy-α-Pyrrolidinopentiophenone (4-MeO-α-PVP) (hydrochloride) shares structural features with the stimulant α-PVP. The mechanism of action is unknown for α-PVP, but is believed to be similar to that of the designer drug MDPV (Item No. 10624), which acts as a norepinephrine-dopamine reuptake inhibitor.{18946,18943} This product is intended to be used for forensic and research applications.
Brand:CaymanSKU:-
4-methoxy-α-Pyrrolidinopropiophenone (hydrochloride) (Item No. 10394), also known as MOPPP, is an analytical reference standard that is structurally categorized as a cathinone. It is a designer drug that has appeared on the illicit drug market.{19734} Its metabolism in rats has been described.{19734,19874} The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.
Brand:CaymanSKU:10394 - 1 mgAvailable on backorder
4-methoxy-α-Pyrrolidinopropiophenone (hydrochloride) (Item No. 10394), also known as MOPPP, is an analytical reference standard that is structurally categorized as a cathinone. It is a designer drug that has appeared on the illicit drug market.{19734} Its metabolism in rats has been described.{19734,19874} The physiological and toxicological properties of this compound are not known. This product is intended for research and forensic applications.
Brand:CaymanSKU:10394 - 5 mgAvailable on backorder
4-Methoxyamphetamine (4-MA), is a serotonergic drug of the amphetamine class.{19874} 4-MA exhibits both structural and pharmacological similarity to 3,4-methylenedioxymethamphetamine and may be a more potent hallucinogen, particularly through its effects on serotonergic transmission and through reversible inhibition of the enzyme MAO-A. 4-Methoxyamphetamine (4-MA), is a serotonergic drug of the amphetamine class.{19874} 4-MA exhibits both structural and pharmacological similarity to 3,4-methylenedioxymethamphetamine and may be a more potent hallucinogen, particularly through its effects on serotonergic transmission and through reversible inhibition of the enzyme MAO-A.{19874,21436,21437,21435} This product is intended for research and forensic applications.
Brand:CaymanSKU:-
4-methoxythio Benzamide is a synthetic intermediate useful for pharmaceutical synthesis. Thiobenzamides, including 4-methoxythio benzamide, are potent hepatotoxins in vivo.{18419,18420}
Brand:CaymanSKU:10552 - 1 gAvailable on backorder
4-methoxythio Benzamide is a synthetic intermediate useful for pharmaceutical synthesis. Thiobenzamides, including 4-methoxythio benzamide, are potent hepatotoxins in vivo.{18419,18420}
Brand:CaymanSKU:10552 - 5 gAvailable on backorder
4-methoxythio Benzamide is a synthetic intermediate useful for pharmaceutical synthesis. Thiobenzamides, including 4-methoxythio benzamide, are potent hepatotoxins in vivo.{18419,18420}
Brand:CaymanSKU:10552 - 500 mgAvailable on backorder
Erlotinib (Item No. 10483) is a tyrosine kinase inhibitor that acts on the epidermal growth factor receptor (EGFR), inhibiting EGFR-associated kinase activity (IC50 = 2.5 µM).{18354,18362} It binds to the EGF-activated receptor, with the phenyl group at one end sequestered in a hydrophobic pocket of the kinase domain and the ether linkages at the opposite end projecting into solvent.{24659,24660} 4-methyl Erlotinib is an analog of erlotinib characterized by the addition of a methyl group at the four position of the phenyl group. The biochemical and physiological properties of this compound are not known.
Brand:CaymanSKU:9001510 - 1 mgAvailable on backorder
Erlotinib (Item No. 10483) is a tyrosine kinase inhibitor that acts on the epidermal growth factor receptor (EGFR), inhibiting EGFR-associated kinase activity (IC50 = 2.5 µM).{18354,18362} It binds to the EGF-activated receptor, with the phenyl group at one end sequestered in a hydrophobic pocket of the kinase domain and the ether linkages at the opposite end projecting into solvent.{24659,24660} 4-methyl Erlotinib is an analog of erlotinib characterized by the addition of a methyl group at the four position of the phenyl group. The biochemical and physiological properties of this compound are not known.
Brand:CaymanSKU:9001510 - 10 mgAvailable on backorder
Erlotinib (Item No. 10483) is a tyrosine kinase inhibitor that acts on the epidermal growth factor receptor (EGFR), inhibiting EGFR-associated kinase activity (IC50 = 2.5 µM).{18354,18362} It binds to the EGF-activated receptor, with the phenyl group at one end sequestered in a hydrophobic pocket of the kinase domain and the ether linkages at the opposite end projecting into solvent.{24659,24660} 4-methyl Erlotinib is an analog of erlotinib characterized by the addition of a methyl group at the four position of the phenyl group. The biochemical and physiological properties of this compound are not known.
Brand:CaymanSKU:9001510 - 5 mgAvailable on backorder
4-methyl PCP (hydrochloride) (Item No. 31007) is an analytical reference standard categorized as an arylcyclohexylamine. This product is intended for research and forensic applications.
Brand:CaymanSKU:31007 - 1 mgAvailable on backorder
4-methyl PCP (hydrochloride) (Item No. 31007) is an analytical reference standard categorized as an arylcyclohexylamine. This product is intended for research and forensic applications.
Brand:CaymanSKU:31007 - 5 mgAvailable on backorder
4-methyl-1-Pentanol is a branched chain primary alcohol found in wine and produced during fermentation.{29972} As a volatile compound it is reported to have a nutty odor. It is also used in cosmetic compounds for its antimicrobial effects.{29971}
Brand:CaymanSKU:-Available on backorder
4-methyl-1-Pentanol is a branched chain primary alcohol found in wine and produced during fermentation.{29972} As a volatile compound it is reported to have a nutty odor. It is also used in cosmetic compounds for its antimicrobial effects.{29971}
Brand:CaymanSKU:-Available on backorder
4-methyl-1-Pentanol is a branched chain primary alcohol found in wine and produced during fermentation.{29972} As a volatile compound it is reported to have a nutty odor. It is also used in cosmetic compounds for its antimicrobial effects.{29971}
Brand:CaymanSKU:-Available on backorder
4-methyl-1-Pentanol is a branched chain primary alcohol found in wine and produced during fermentation.{29972} As a volatile compound it is reported to have a nutty odor. It is also used in cosmetic compounds for its antimicrobial effects.{29971}
Brand:CaymanSKU:-Available on backorder
4-methyl-2-Oxovalerate is an immediate precursor and metabolite of L-leucine. It is a precursor leading to the synthesis of 2-methylpropyl glucosinolate, via L-leucine, in plants. 4-methyl-2-Oxovalerate is one of several plasma metabolites found to differ significantly between type 2 diabetes and control subjects.{33223}
Brand:CaymanSKU:21052 -Out of stock
4-methyl-2-Oxovalerate is an immediate precursor and metabolite of L-leucine. It is a precursor leading to the synthesis of 2-methylpropyl glucosinolate, via L-leucine, in plants. 4-methyl-2-Oxovalerate is one of several plasma metabolites found to differ significantly between type 2 diabetes and control subjects.{33223}
Brand:CaymanSKU:21052 -Out of stock
4-methyl-2-Oxovalerate is an immediate precursor and metabolite of L-leucine. It is a precursor leading to the synthesis of 2-methylpropyl glucosinolate, via L-leucine, in plants. 4-methyl-2-Oxovalerate is one of several plasma metabolites found to differ significantly between type 2 diabetes and control subjects.{33223}
Brand:CaymanSKU:21052 -Out of stock
4-methyl-2-Oxovalerate is an immediate precursor and metabolite of L-leucine. It is a precursor leading to the synthesis of 2-methylpropyl glucosinolate, via L-leucine, in plants. 4-methyl-2-Oxovalerate is one of several plasma metabolites found to differ significantly between type 2 diabetes and control subjects.{33223}
Brand:CaymanSKU:21052 -Out of stock
4-Methyl-7-(2-nitrophenoxy)-2H-chromen-2-one is a fluorescent coumarin derivative.{51048,51047} It displays excitation/emission maxima of 323/445 nm, respectively.{51048}
Brand:CaymanSKU:28473 - 1 mgAvailable on backorder
4-Methyl-7-(2-nitrophenoxy)-2H-chromen-2-one is a fluorescent coumarin derivative.{51048,51047} It displays excitation/emission maxima of 323/445 nm, respectively.{51048}
Brand:CaymanSKU:28473 - 10 mgAvailable on backorder
4-Methyl-7-(2-nitrophenoxy)-2H-chromen-2-one is a fluorescent coumarin derivative.{51048,51047} It displays excitation/emission maxima of 323/445 nm, respectively.{51048}
Brand:CaymanSKU:28473 - 25 mgAvailable on backorder
4-Methyl-7-(2-nitrophenoxy)-2H-chromen-2-one is a fluorescent coumarin derivative.{51048,51047} It displays excitation/emission maxima of 323/445 nm, respectively.{51048}
Brand:CaymanSKU:28473 - 5 mgAvailable on backorder
4-Methyl-7-(4-nitro-2-(trifluoromethyl)phenoxy)-2H-chromen-2-one is a turn-on fluorescent probe for the detection of hydrogen sulfide (H2S).{51047} It can be excited at 348 nm in DMSO and fluorescence intensity increases in the presence of bisulfide (HS-). 4-Methyl-7-(4-nitro-2-(trifluoromethyl)phenoxy)-2H-chromen-2-one is selective for HS- over cysteine, AcO-, F-, H2PO4-, Cl-, Br-, and I- and is not cytotoxic up to a concentration of 150 µg/ml.
Brand:CaymanSKU:28471 - 1 mgAvailable on backorder
4-Methyl-7-(4-nitro-2-(trifluoromethyl)phenoxy)-2H-chromen-2-one is a turn-on fluorescent probe for the detection of hydrogen sulfide (H2S).{51047} It can be excited at 348 nm in DMSO and fluorescence intensity increases in the presence of bisulfide (HS-). 4-Methyl-7-(4-nitro-2-(trifluoromethyl)phenoxy)-2H-chromen-2-one is selective for HS- over cysteine, AcO-, F-, H2PO4-, Cl-, Br-, and I- and is not cytotoxic up to a concentration of 150 µg/ml.
Brand:CaymanSKU:28471 - 10 mgAvailable on backorder
4-Methyl-7-(4-nitro-2-(trifluoromethyl)phenoxy)-2H-chromen-2-one is a turn-on fluorescent probe for the detection of hydrogen sulfide (H2S).{51047} It can be excited at 348 nm in DMSO and fluorescence intensity increases in the presence of bisulfide (HS-). 4-Methyl-7-(4-nitro-2-(trifluoromethyl)phenoxy)-2H-chromen-2-one is selective for HS- over cysteine, AcO-, F-, H2PO4-, Cl-, Br-, and I- and is not cytotoxic up to a concentration of 150 µg/ml.
Brand:CaymanSKU:28471 - 25 mgAvailable on backorder
4-Methyl-7-(4-nitro-2-(trifluoromethyl)phenoxy)-2H-chromen-2-one is a turn-on fluorescent probe for the detection of hydrogen sulfide (H2S).{51047} It can be excited at 348 nm in DMSO and fluorescence intensity increases in the presence of bisulfide (HS-). 4-Methyl-7-(4-nitro-2-(trifluoromethyl)phenoxy)-2H-chromen-2-one is selective for HS- over cysteine, AcO-, F-, H2PO4-, Cl-, Br-, and I- and is not cytotoxic up to a concentration of 150 µg/ml.
Brand:CaymanSKU:28471 - 5 mgAvailable on backorder
4-Methyl-7-(4-nitrophenoxy)-2H-chromen-2-one is a fluorescent coumarin derivative.{51048,51047} It displays excitation/emission maxima of 323/445 nm, respectively.{51048} Unlike the hydrogen sulfide probe 7-(2,4-dinitrophenoxy)-4-methyl-2H-chromen-2-one (Item No. 28472), 4-methyl-7-(4-nitrophenoxy)-2H-chromen-2-one does not undergo an increase in fluoresence intensity in the presence of sulfur-containing molecules.{51048,51047}
Brand:CaymanSKU:28474 - 1 mgAvailable on backorder
4-Methyl-7-(4-nitrophenoxy)-2H-chromen-2-one is a fluorescent coumarin derivative.{51048,51047} It displays excitation/emission maxima of 323/445 nm, respectively.{51048} Unlike the hydrogen sulfide probe 7-(2,4-dinitrophenoxy)-4-methyl-2H-chromen-2-one (Item No. 28472), 4-methyl-7-(4-nitrophenoxy)-2H-chromen-2-one does not undergo an increase in fluoresence intensity in the presence of sulfur-containing molecules.{51048,51047}
Brand:CaymanSKU:28474 - 10 mgAvailable on backorder
4-Methyl-7-(4-nitrophenoxy)-2H-chromen-2-one is a fluorescent coumarin derivative.{51048,51047} It displays excitation/emission maxima of 323/445 nm, respectively.{51048} Unlike the hydrogen sulfide probe 7-(2,4-dinitrophenoxy)-4-methyl-2H-chromen-2-one (Item No. 28472), 4-methyl-7-(4-nitrophenoxy)-2H-chromen-2-one does not undergo an increase in fluoresence intensity in the presence of sulfur-containing molecules.{51048,51047}
Brand:CaymanSKU:28474 - 25 mgAvailable on backorder
4-Methyl-7-(4-nitrophenoxy)-2H-chromen-2-one is a fluorescent coumarin derivative.{51048,51047} It displays excitation/emission maxima of 323/445 nm, respectively.{51048} Unlike the hydrogen sulfide probe 7-(2,4-dinitrophenoxy)-4-methyl-2H-chromen-2-one (Item No. 28472), 4-methyl-7-(4-nitrophenoxy)-2H-chromen-2-one does not undergo an increase in fluoresence intensity in the presence of sulfur-containing molecules.{51048,51047}
Brand:CaymanSKU:28474 - 5 mgAvailable on backorder
4-methyl-N,N-Dimethylcathinone (hydrochloride) (Item No. 17393) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.
Brand:CaymanSKU:-Available on backorder
4-methyl-N,N-Dimethylcathinone (hydrochloride) (Item No. 17393) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.
Brand:CaymanSKU:-Available on backorder
4-methyl-N,N-Dimethylcathinone (hydrochloride) (Item No. 17393) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.
Brand:CaymanSKU:-Available on backorder
α-Ethyltryptamine (AET), like α-methyltryptamine (Item No. 11135), is a psychedelic drug with schedule 1 status in the United States. Both alter monoamine release and re-uptake in the brain.{20018,19758} 4-methyl-α-Ethyltryptamine is a homolog of AET. Its physiological and toxicological properties remain to be elucidated. This product is intended for forensic and research applications.
Brand:CaymanSKU:- α-Ethyltryptamine (AET), like α-methyltryptamine (Item No. 11135), is a psychedelic drug with schedule 1 status in the United States. Both alter monoamine release and re-uptake in the brain.{20018,19758} 4-methyl-α-Ethyltryptamine is a homolog of AET. Its physiological and toxicological properties remain to be elucidated. This product is intended for forensic and research applications.
Brand:CaymanSKU:- α-Ethyltryptamine (AET), like α-methyltryptamine (Item No. 11135), is a psychedelic drug with schedule 1 status in the United States. Both alter monoamine release and re-uptake in the brain.{20018,19758} 4-methyl-α-Ethyltryptamine is a homolog of AET. Its physiological and toxicological properties remain to be elucidated. This product is intended for forensic and research applications.
Brand:CaymanSKU:-
4-methyl-α-Isopropylaminovalerophenone (hydrochloride) (Item No. 31008) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.
Brand:CaymanSKU:31008 - 1 mgAvailable on backorder
4-methyl-α-Isopropylaminovalerophenone (hydrochloride) (Item No. 31008) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.
Brand:CaymanSKU:31008 - 5 mgAvailable on backorder
4-methyl-α-Pyrrolidinobutiophenone (4-methyl PBP) is a synthetic cathinone with psychoactive properties which has recently been identified in party pills and powders.{19193,20009} The metabolism of methyl PBP has been characterized.{19963,20462} The biological and toxicological properties of this compound are unknown. This product is intended for forensic and research applications.
Brand:CaymanSKU:9001190 - 10 mgAvailable on backorder
4-methyl-α-Pyrrolidinobutiophenone (4-methyl PBP) is a synthetic cathinone with psychoactive properties which has recently been identified in party pills and powders.{19193,20009} The metabolism of methyl PBP has been characterized.{19963,20462} The biological and toxicological properties of this compound are unknown. This product is intended for forensic and research applications.
Brand:CaymanSKU:9001190 - 5 mgAvailable on backorder
4-methyl-α-Pyrrolidinobutiophenone (4-methyl PBP) is a synthetic cathinone with psychoactive properties which has recently been identified in party pills and powders.{19193,20009} The metabolism of methyl PBP has been characterized.{19963,20462} The biological and toxicological properties of this compound are unknown. This product is intended for forensic and research applications.
Brand:CaymanSKU:9001190 - 50 mgAvailable on backorder
4-methyl-α-Pyrrolidinoisohexanophenone (hydrochloride) (Item No. 31013) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.
Brand:CaymanSKU:31013 - 1 mgAvailable on backorder
4-methyl-α-Pyrrolidinoisohexanophenone (hydrochloride) (Item No. 31013) is an analytical reference standard categorized as a cathinone. This product is intended for research and forensic applications.
Brand:CaymanSKU:31013 - 5 mgAvailable on backorder
4-Methylaminoantipyrine is a major active metabolite of the non-opioid prodrug metamizole (Item No. 15771).{25749} It is formed from metamizole by non-enzymatic hydrolysis in the gastrointestinal tract.{57230} 4-Methylaminoantipyrine (0.1 mM) inhibits production of prostaglandin E2 (PGE2; Item No. 14010) induced by the calcium ionophore A23187 (Item Nos. 11016 | 22030) in isolated mouse peritoneal macrophages.{57231} It increases the paw withdrawal threshold in a rat model of carrageenan-induced hyperalgesia when administered at a dose of 160 µg/paw.{57232} 4-Methylaminoantipyrine (60, 90, and 120 mg/kg) reduces LPS-induced pyrexia in rats.{57233} It is also a potential impurity found in commercial preparations of metamizole.{57234}
Brand:CaymanSKU:31612 - 1 mgAvailable on backorder