cyp17

CYP17-IN-1 是一种有效的 CYP17 口服抑制剂，可抑制大鼠和人类的 CYP17，IC50 分别为 15.8 和 20.1 nM。

Seviteronel (VT-464) 是一种新型 CYP17 裂解酶抑制剂和雄激素受体拮抗剂，可用于研究乳腺癌和前列腺癌。

Galeterone (VN 124) 是CYP17抑制剂，能够多功能的抗雄激素，在去势抵抗性前列腺癌中，其IC50值为 47 nM。

(4S,5S)-(+)-Germacrone-4,5-epoxide inhibits certain subtypes of cytochrome P450 (CYP).

Actein 是从升麻的根茎中分离的一种三萜糖苷，通过促进ROS JNK 活化和钝化人膀胱癌中的AKT 途径来抑制细胞增殖，诱导自噬和凋亡。

Licopyranocoumarin could as a potent neuroprotective drug via markedly blocked MPP+-induced neuronal PC12D cell death and disappearance of mitochondrial membrane potential, which were mediated by JNK.

Zederone（蓬莪术环氧酮）是一种天然的倍半萜烯，能够调节炎症反应、放松平滑肌和内分泌来治疗痛经；能够下调mTOR和p70s6K的mRNA水平从而抑制卵巢癌细胞增殖，与降糖蛋白3L4Y和5UBA相互作用从而抗糖尿病和抗氧化。

Abiraterone (CB-7598) 是不可逆的CYP17A1抑制剂，具有抗雄激素作用，抑制细胞色素 p450 酶 CYP17 的 17α-羟化酶 (IC50:2.5 nM) 和 17,20-裂合酶 (IC50:15 nM) 活性。

Abiraterone Acetate (CB7630) 是一种具有口服活性的、不可逆的 CYP17A1选择性抑制剂，具有抗雄激素作用。它是 Abiraterone 的前药。

2,3',4,6-Tetrahydroxybenzophenone possesses significant antioxidant activity.

β-Sparteine is a class 1a antiarrhythmic agent, a sodium channel blocker. The deficient debrisoquine hydroxylation of Sparteine is due to the absence of P-450IID1 protein in the livers of poor metabolizers.

6',7'-Dihydroxybergamottin(DHB), a well-known inhibitor of CYP3A4, the inhibition of CYP3A4 activity by DHB includes the inhibition of POR activity, DHB can inhibit nifedipine oxidation in a concentration-dependent manner.

Canadine has antioxidant activity with low-toxic effect.

5,6,7-Trimethoxycoumarin shows moderate inhibitory activity against Micrococcus luteus, it also displays an intermediate cytotoxic effects against brine shrimp larvae. 5,6,7-Trimethoxycoumarin can improve gastroprotective effects, and it has low toxicity

Pisatin is an isoflavonoid phytoalexin synthesized by pea (Pisum sativum L.).

Hypaconitine 是从乌头属种分离的一种高毒性成分，可研究风湿病。

Myristicin (Myristicine) 是一种在香料和伞形植物中发现的天然产物。肉豆蔻素具有抗胆碱能、抗菌和肝保护作用，还具有抗炎作用，其通过钙途径抑制dsrna 刺激的巨噬细胞中的NO、细胞因子、趋化因子和生长因子。Myristicin 可以诱导细胞凋亡，其特征是改变线粒体膜电位、细胞色素c 释放、Caspase-3激活、parp 切割和DNA 断裂。

8alpha-Tigloyloxyhirsutinolide 13-O-acetate shows inhibitory activity toward CYP2A6 and MAO-A and MAO-B enzymes. 8alpha-Tigloyloxyhirsutinolide 13-O-acetate has anti-cancer activity, it is active against both cancer cell lines (IC50 = 3.50 microM for HT29

15-Hydroxydehydroabietic acid exhibits a promising alpha-glucosidase inhibitory activity, it also shows significant antibacterial activities.

Rutacridone has mutagenicity.

Dipterocarpol is a dammarane-type triterpenoid, as are the major bioactive compounds of ginseng. Dipterocarpol A shows moderate acetylcholinesterase inhibitory activity with the IC50 value of 8.28 uM.

8alpha-(2-Methylacryloyloxy)hirsutinolide 13-O-acetate shows inhibitory activity toward CYP2A6 and MAO-A and MAO-B enzymes.

Chalepensin 是一种从芸香科植物 Ruta chalepensis L. 分离得到的呋喃香豆素，是一种选择性 CYP2A6 抑制剂，抑制 CYP1A1、CYP1A2、CYP2A13、CYP2C9、CYP2D6、CYP2E1 和 CYP3A4。Chalepensin 具有抗原生动物活性，抑制耐甲氧西林金黄色葡萄球菌 （MRSA），MIC值在32-128 μg mL范围内。

Lecanoric acid 是一种来自 Lecanoric acid 的化合物，具有抗氧化活性，可促进益生菌的生长，