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Cytochrome P450

Cytochrome P450

Cytochrome p450 comprises a superfamily of heme-thiolate proteins named for the spectral absorbance peak of their carbon-monoxide-bound species at 450 nm. The p450 superfamily, which has members in every class of organisms, including Archaea, is thought to have descended from an ancestor gene that existed more than 3 billion years ago.One of the biggest multigene families has subsequently been created as a result of repeated gene duplications. These enzymes stand out for the variety of reactions they catalyze as well as the variety of chemically diverse substrates they act on. The oxidative, peroxidative, and reductive metabolism of endogenous and exogenous substrates like environmental toxins, agrochemicals, plant allelochemicals, steroids, prostaglandins, and fatty acids is supported by cytochrome p450s. Drug interactions and interindividual variability in drug metabolism are two of the most important issues in clinical pharmacology, and cytochrome p450s in humans are best known for their central role in phase I drug metabolism.

Cytochrome P450 related products

Structure Cat No. Product Name CAS No. Product Description
2-Methoxy-5-acetoxyfuranogermacr-1(10)-en-6-one V124767 2-Methoxy-5-acetoxyfuranogermacr-1(10)-en-6-one 75412-96-3 2-Methoxy-5-acetoxyfuranogermacr-1(10)-en-6-one is an aromatase (CYP19) inhibitor with an IC50 value of 0.21 μM for human targets.
2-Pentylbenzimidazole V112176 2-Pentylbenzimidazole 5851-46-7 2-Pentylbenzimidazole (compound 10f) is a benzimidazole derivative and an inhibitor of aminopyrine N-demethylase, with a pIC50 value of 4.3.
20-HETE IN-3 V124338 20-HETE IN-3 3119850-82-4 20-HETE IN-3 is an orally bioavailable 20-HETE synthesis inhibitor.
20-HETE inhibitor-1 V73948 20-HETE inhibitor-1 2472030-28-5 20-HETE inhibitor-1 (comp 83) is an inhibitor (blocker/antagonist) of 20-HETE synthesis.
3,4-Methylenedioxyphenmetrazine hydrochloride V111715 3,4-Methylenedioxyphenmetrazine hydrochloride 3,4-Methylenedioxybenzomorpholine (3,4-MDPM) hydrochloride is a psychoactive substance.
3,5,7-三羟基黄酮 V21477 Galangin 548-83-4 Galangin (Norizalpinin) is a modulator of arylhydrocarbon receptors and inhibits CYP1A1 activity.
3-Methylbenzofuran V113211 3-Methylbenzofuran 21535-97-7 3-Methylbenzofuran is a cytochrome P450 CYP2A6 inhibitor with an IC50 value of 7.35 μM.
3-Methylquinoline V112293 3-Methylquinoline 612-58-8 3-Methylquinoline is a selective cytochrome P450 (CYP1A2) inhibitor with an IC50 value of 13 μM.
3-氰基-7-乙氧基香豆素 V9500 3-CETC 117620-77-6 3-CETC (3-Cyano-7-ethoxycoumarin) is a novel and potent fluorescent CYP1A1 &1A2 substrate.
4,5-Dimethoxycanthin-6-one V73963 4,5-Dimethoxycanthin-6-one 18110-87-7 4,5-Dimethoxycanthin-6-one is a potent, noncompetitive inhibitor of CYP1A2-mediated phenacetin O-deethylation with IC50 of 1.7 μM and a Ki of 2.6 μM.
4,8-Dioxa-3H-perfluorononanoic acid V107217 4,8-Dioxa-3H-perfluorononanoic acid 919005-14-4 4,8-Dioxa-3H-perfluorononanoic acid is a per- and polyfluoroalkyl substance (PFAS) with affinity and potential agonist activity for human pregnane X receptor (hPXR).
4-Ipomeanol V114342 4-Ipomeanol 32954-58-8 4-Isosorbide is a pulmonary toxin.
4-Phenyl-1,2,3-thiadiazole V102736 4-Phenyl-1,2,3-thiadiazole 25445-77-6 4-Phenyl-1,2,3-thiadiazole is an inhibitor of CYP2B4 and CYP2E1.
4-甲基吡唑 V2677 Fomepizole 7554-65-6 Fomepizole (also known as4-methylpyrazole, Antizol, Antizol-Vet)is a competitive inhibitor of alcohol dehydrogenase, an enzyme that catalyzes the initial steps in the metabolism of ethylene glycol,ethanol and methanol to their toxic metabolites.
5,7,2',6'-Tetrahydroxyflavone V73979 5,7,2',6'-Tetrahydroxyflavone 82475-00-1 5,7,2',6'-Tetrahydroxyflavone is a naturally occurring flavonoid that can inhibit hepatic testosterone 6β-hydroxylation (CYP3A4) activity with IC50 of 7.8 μM.
5-Methylchrysene V106602 5-Methylchrysene 3697-24-3 5-Methylrefractory can be activated by several isozymes of cytochrome P450 to form mutagenic metabolites.
5α-Androst-2-en-17-one V127211 5α-Androst-2-en-17-one 963-75-7 5α-Androst-2-en-17-one is a steroidal compound and an aromatase inhibitor.
6',7'-Dihydroxybergamottin (6',7'-DHB) V73981 6',7'-Dihydroxybergamottin (6',7'-DHB) 145414-76-2 6',7'-Dihydroxybergamomottin (6',7'-DHB) is a furanocoumarin that can inhibit CYP3A4 and is present in grapefruit juice and Seville orange juice.
6-Methylchrysene V127434 6-Methylchrysene 1705-85-7 6-Methylchrysene is a weak carcinogen.
7-Benzyloxy-4-(trifluoromethyl)coumarin (7-BFC) V73957 7-Benzyloxy-4-(trifluoromethyl)coumarin (7-BFC) 220001-53-6 7-Benzyloxy-4-(trifluoromethyl)coumarin (7-BFC) is a coumarin fluorescent substrate.
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