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P450

Cytochrome P450 are a family of heme-containing monoxygenases catalyzing the metabolism of xenobiotics in the body where P450 enzymes use O2 and two electrons provided by NAD(P)H with the help of redox partner flavoproteins and iron-sulfur proteins to catalyze the monooxygenation of a variety of substrates. Based on how electrons from NAD(P)H are delivered to the catalytic site, P450 enzymes are divided into four classes, including Class I requiring both an FAD-containing reductase and an iron sulfur redoxin, Class II requiring only an FAD/FMN-containg P450 reductase, Class III requiring no electron donor and Class IV requiring electrons directly from NAD(P)H.

Products for  P450

  1. Cat.No. Product Name Information
  2. GC37632 Seviteronel racemate Seviteronel racemate (VT-464 racemate) is the racemate form of Seviteronel (VT-464), which is a potent CYP17 lyase inhibitor(h-Lyase IC50=nM)inhibition. Seviteronel racemate  Chemical Structure
  3. GC16259 SKF 525A (hydrochloride) SKF 525A (hydrochloride) is a Cytochrome P450 inhibitor (IC50 = 19μM). SKF 525A (hydrochloride)  Chemical Structure
  4. GC16951 Stiripentol An LDH inhibitor Stiripentol  Chemical Structure
  5. GC11638 Sulfaphenazole CYP2C9 inhibitor Sulfaphenazole  Chemical Structure
  6. GC17063 Talarozole Talarozole  Chemical Structure
  7. GC37727 Talarozole R enantiomer Talarozole R enantiomer is a potent and selective inhibitor of cytochrome P450 26-mediated breakdown of endogenous all-trans retinoic acid for the treatment of psoriasis and acne. Talarozole R enantiomer  Chemical Structure
  8. GC32160 Tebuconazole A triazole fungicide Tebuconazole  Chemical Structure
  9. GC33833 Tetrahydrocurcumin (HZIV 81-2) Tetrahydrocurcumin (HZIV 81-2) is a Curcuminoid found in turmeric (Curcuma longa) that is produced by the reduction of Curcumin. Tetrahydrocurcumin (HZIV 81-2)  Chemical Structure
  10. GC15244 Thienyldecyl Isothiocyanate cytochrome P450 inhibitor Thienyldecyl Isothiocyanate  Chemical Structure
  11. GC15445 TMS cytochrome P450 1B1 inhibitor TMS  Chemical Structure
  12. GC13362 TOK-001 TOK-001 (TOK-001) is a multifunctional antiandrogen and CYP17 inhibitor (IC50=47 nM) in castration resistant prostate cancer (CRPC). TOK-001  Chemical Structure
  13. GC45582 trans-ε-Viniferin ε-Viniferin, the dimer of Resveratrol and isolated from Vitis vinifera, displays a potent inhibitory for all the CYP activities, with Ki values from 0.5-20 μM. trans-ε-Viniferin  Chemical Structure
  14. GC17112 Uniconazole cytochrome P450 707As inhibitor Uniconazole  Chemical Structure
  15. GC31791 Veledimex (INXN-1001) Veledimex (INXN-1001) (INXN-1001), a synthetic analog of the insect molting hormone ecdysone, is an orally active activator ligand for a proprietary gene therapy promoter system. Veledimex (INXN-1001)  Chemical Structure
  16. GC33870 Veledimex racemate (RG-115932 racemate) Veledimex racemate (RG-115932 racemate) (INXN-1001 racemate) is the racemate of veledimex. Veledimex racemate (RG-115932 racemate)  Chemical Structure
  17. GC30705 Veledimex S enantiomer (INXN-1001 S enantiome) Veledimex S enantiomer (INXN-1001 S enantiomer) is the S enantiomer of veledimex. Veledimex is an oral activator ligand for a proprietary gene therapy promoter system, and a moderate inhibitor of and substrate for CYP3A4/5. Veledimex S enantiomer (INXN-1001 S enantiome)  Chemical Structure
  18. GC15056 β-Nicotyrine

    cytochrome P450 (CYP) isoforms, CYP2A6 and CYP2A13 inhibitor

    β-Nicotyrine  Chemical Structure

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