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P450 (e.g. CYP)

P450 (e.g. CYP)

P450 (e.g. CYP) related products

Structure Cat No. Product Name CAS No. Product Description
DMU-2105(CYP1B1 inhibitor 7k) V2226 DMU-2105(CYP1B1 inhibitor 7k) 1031063-36-1 DMU-2105(CYP1B1 inhibitor 7k), is a novel,potent and selective CYP1B1 inhibitor with IC50s of 10 nM and 742 nM for CYP1B1 and CYP1A1, respectively.
Orteronel (racemic) V4600 Orteronel (racemic) 426219-18-3 Orteronel racemate, the mixture of S-enantiomer and R-enantiomer of Orteronel (aslo known as TAK-700) which is a novel, potent and highly selective, orally bioavailable non-steroidal androgen synthesis inhibitor of human 17,20-lyase inhibitor with IC50 of 38 nM, it exhibits >1000-fold selectivity over other CYPs (e.
PF-4981517 V0816 PF-4981517 1390637-82-7 PF-4981517 (also named as PF 04981517; PF04981517,CYP-3cide,PF 4981517;PF4981517) is a specific andtime-dependent inactivator of human CYP3A4(P450) with IC50 of 0.03 μM, it exhibits >500-fold selectivity for inhibiting CYP3A4 over CYP3A5 and CYP3A7 and a time-dependent inactivation of human CYP3A4.
TAK-700/Orteronel (s-isomer) V0819 TAK-700/Orteronel (s-isomer) 566939-85-3 Orterone (aslo known as TAK-700; TAK 700;TAK700) is an orally bioavailable non-steroidal androgen synthesis inhibitor of human 17,20-lyase inhibitor with potential anticancer activity.
丹参素钠 V0822 Sodium Danshensu 67920-52-9 Sodium Danshensu (Danshensu Sodium), the sodium saltof danshensu, is a novel, potent,naturally occuring phenolic acid of caffeic acid derivatives isolated from Salvia miltiorrhiza with various biological activity (e.
乙酸阿比特龙酯 V0801 Abiraterone Acetate (Zytiga; formerly CB-7598; CB7598; CB 7598) 154229-18-2 Abiraterone Acetate (brand name Zytiga; formerly CB-7598; CB7598;CB 7598),the 3-acetylated and prodrug form of Abiraterone, is an irreversible and steroidal cytochrome CYP17 inhibitor with potential antitumor activity.
伊曲康唑 V0805 Itraconazole 84625-61-6 Itraconazole (Orungal, Oriconazole, Sporanox,R51211;R-51211), a marketedtriazole-based antifungal drug since 1984, is a potent inhibitor of CYP3A4 that has been widely used for the treatment of fungal infections.
伏立康唑 V0802 Voriconazole 137234-62-9 Voriconazole (UK-109496; UK109496; trade name Vfend) is a 2nd-generation and potent triazole-based antifungal drug used for treating a variety of fungal infections.
依珠曲米 V2872 Ezutromid (BMN-195, SMTC-1100) 945531-77-1 Ezutromid (also known as BMN-195 and SMTC-1100) is a first-in-class, orally bioavailable,small molecule modulator of the utrophins translation with EC50 of 0.4 uM.
克拉霉素 V0814 Clarithromycin 81103-11-9 Clarithromycin (A56268; Abbott 56268; A 56268; Abbott-56268; A-56268; trade name Biaxin) is an approved macrolide antibiotic medication acting as a CYP3A4 inhibitor.
加来特龙; 伽来特隆 V0811 Galeterone 851983-85-2 Galeterone (formerly known as NX 41765;TOK001;VN/124-1; NX-41765; VN-1241;TOK-001) is a novel, potent and selective, orally bioavailable CYP17 lyase inhibitor and androgen receptor (AR) antagonist with potential anticancer activity.
可比西他 V0815 Cobicistat (GS9350) 1004316-88-4 Cobicistat (trade name Tybost;Genvoya;GS-9350; GS 9350) is a novel, potent and selective inhibitor of CYP3A (cytochrome P450 3A) with IC50 of 30-285 nM.
吡格列酮盐酸盐 V0820 Pioglitazone HCl 112529-15-4 Pioglitazone HCl (also known as Actos;U-72107A;AD-4833; AD4833, U-72107E), the hydrochloride salt of Pioglitazone which is approved and thiazolidinedione-based anti-diabetic drug, is a selective PPARϒ agonist with hypoglycemic activity.
奥扎格雷 V0818 Ozagrel 82571-53-7 Ozagrel (OKY046;KCT-0809;OKY046;Cataclot;KCT0809;Xanbo),an antiplatelet agent, is a potent and selective inhibitor of thromboxane A2 (TXA2 synthetase (IC50 = 11 nM) with antiplatelet activity.
柏木脑 V13078 Cedrol 77-53-2 Cedrol is a bioactive sesquiterpene and a potent competitive inhibitor of cytochrome P-450 (CYP) enzymes.
柚皮素 V0812 Naringenin 480-41-1 Naringenin(S-Dihydrogenistein; Salipurol;NSC 11855; NSC-11855; NSC11855) is a naturally occuring flavanone extracted from plant food (e.
氟康唑 V0806 Fluconazole (UK49858) 86386-73-4 Fluconazole (Diflucan,UK-49858;UK 49858; Triflucan, Elazor, Biozolene) is a novel, potent, and orally bioavailable triazole-based antifungal drug that works by inhibiting fungal lanosterol 14 alpha-demethylase-dependent biosynthesis of ergosterol, which is an essential component of fungal cell membrane.
盐酸达唑氧苯 V26981 Dazoxiben HCl 74226-22-5 Dazoxiben is a potent orally bioactive thromboxane (TX) synthase inhibitor.
胡椒碱 V0809 Piperine 94-62-2 Piperine (1-Piperoylpiperidine;Bioperine; 1-Piperoyl piperidine),a natural alkaloid found inPiper nigrum L,is an alkaloid accounting for the pungency of black pepper and long pepper, which has been used in some forms of traditional medicine and as an insecticide.
芹菜素 V0808 Apigenin 520-36-5 Apigenin (NSC-83244, LY-080400;4,5,7-Trihydroxyflavone; Apigenol; C.
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