Cat. No. | Product Name | Target | Signaling Pathways |
---|---|---|---|
T2216 |
Entacapone
OR-611,恩他卡朋 |
Transferase | Metabolism |
Entacapone (OR-611) 是可逆的、具有口服活性的、外周作用的儿茶酚-O-甲基转移酶抑制剂。它对大鼠脑、红细胞和肝脏 COMT 有抑制作用。它对 COMT 的选择性优于其他儿茶酚胺代谢酶。它抑制 FTO 去甲基化活性,可用于研究代谢紊乱。它可用于研究帕金森病。 | |||
T2020 |
RGW 611
|
Others | Others |
RGW 611 是一种能够增强辐射且诱导缺氧 V79-379A 细胞死亡的吗啉衍生物。 | |||
T39082 |
AL-611
|
||
AL-611 is an HCV NS5B polymerase inhibitor ( EC 50 = 5 nM). | |||
T69349 |
HPR-611
|
||
HPR-611 is a potent inhibitor of anaphylactic chemical mediator release. | |||
T71521 |
NK-611 free acid
|
||
NK-611 free acid is a new semisynthetic analogue of etoposide, which presumably also acts through inhibition of topoisomerase II, and has been found to be more potent against several cancer cell lines in vitro than etoposide. | |||
T0696 |
Naftopidil
KT-611,萘哌地尔,BM-15275 |
Adrenergic Receptor | GPCR/G Protein; Neuroscience |
Naftopidil (KT-611) 是一种选择性的 alpha1-肾上腺素受体 (α1-adrenoceptor) 拮抗剂,对克隆的人类 α1a、α1b 和 α1d 亚型肾上腺素受体的亲和力Ki 分别为 3.7 nM、20 nM 、1.2 nM。它具有抗增殖活性,可用于研究前列腺增生。 |