Home   >  
Protease/Metabolic Enzyme
  • Protease/Metabolic Enzyme
∨
  >  
Cytochrome P450

Classified by application

All Products

Signaling Pathways

Research Areas

Nature products

Antibodies

Peptides

Catalysts

Impurities

Intermediate

Raw Materials

Cytochrome P450

Chemical Structure Cat. No. Product Name CAS No.
Verapamil Chemical Structure
 BCP37129 Verapamil 52-53-9
Verapamil is a calcium channel blocker that is a class IV anti-arrhythmia agent.
PC945 Chemical Structure
 BCP36481 PC945 1931946-73-4
PC945, a potent, long-acting antifungal triazole, possesses activity against a broad range of both azole-susceptible and azole-resistant strains of Aspergillus fumigatus. PC945 is also a potent, tightly binding inhibitor of A. fumigatus sterol 14α-demethylase activity, CYP51A and CYP51B, with IC50s of 0.23 μM and 0.22 μM, respectively.
Clomethiazole Chemical Structure
 BCP36337 Clomethiazole 533-45-9
Chlormethiazole is an potent and orally active GABAA agonist. Chlormethiazole inhibits cytochrome P450 isoforms: CYP2A6 and CYP2E1 in human liver microsomes. Chlormethiazole is an anticonvulsant agent and has the potential for treating convulsive status epilepticus.
DMU2105 Chemical Structure
 BCP35214 DMU2105 1031063-36-1
DMU2105(CYP1B1 inhibitor 7k) is a potent and specific CYP1B1 inhibitor.
Doxepin-d3 Hydrochloride Chemical Structure
 BCP33258 Doxepin-d3 Hydrochloride 347840-07-7
Doxepin D3 Hydrochloride is a deuterium labeled Doxepin Hydrochloride.Doxepin is a tricyclic antidepressant (TCA) used for the treatment of major depression and anxiety.
Phillyrin Chemical Structure
 BCP26036 Phillyrin 487-41-2
Phillyrin is a natural lignan that has the potential to ameliorate the inflammatory changes and insulin resistance in obese adipose tissue.
(R)-Talarozole Chemical Structure
 BCP21218 (R)-Talarozole 870093-23-5
(R)-Talarozole 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.
20(S)-Ginsenoside C-K Chemical Structure
 BCP30926 20(S)-Ginsenoside C-K 39262-14-1
Ginsenoside C-K, a bacterial metabolite of G-Rb1, exhibits anti-inflammatory effects by reducing iNOS and COX-2. Ginsenoside C-K exhibits an inhibition against the activity of CYP2C9 and CYP2A6 in human liver microsomes with IC50s of 32.0±3.6 μM and 63.6±4.2 μM, respectively.
Abiraterone Acetate Chemical Structure
 BCP02949 Abiraterone Acetate 154229-18-2
Abiraterone acetate(CB 7630) is a novel steroidal inhibitor of human Cytochrome P450(17α-Hydroxylase-C17,20-lyase).
Naringin Chemical Structure
 BCP28297 Naringin 10236-47-2
Naringin is a major flavanone glycoside obtained from tomatoes, grapefruits, and many other citrus fruits. Naringin exhibits biological properties such as antioxidant, anti-inflammatory, and antiapoptotic activities.
123下一頁末頁共 35 條記錄 1 / 4 頁 
0086-13720134139
福建36选7奖金 凯尔特人队标图片 福建快3 360彩票 k神传说的国标麻将教程 怎么知道手机麻将有没有作弊 gpk捕鱼大富翁漏洞 老虎机软件 好运彩99937_com手机登录 黑龙江36选7技巧 大嘴棋牌官方下载 黄大仙四肖三期必中一 南粤风采26选5详情 三分彩怎么玩 白山在线 白山棋牌下载 呼和浩特麻将微信群 血流换三张宜昌版下载