中文名 | Acolbifene |
英文名 | Acolbifene |
别名 | 阿考比芬 化合物 T10239 |
英文别名 | EM652 Em-652 Em 652 Sch 57068 ACOLBIFENE Acolbifene Acolbifene (EM 652, SCH57068) (S)-3-(4-hydroxyphenyl)-4-Methyl-2-[4-[2-(1-piperidinyl)ethoxy]phenyl]-2H-1-benzopyran-7-ol 2H-1-Benzopyran-7-ol, 3-(4-hydroxyphenyl)-4-methyl-2-(4-(2-(1-piperidinyl)ethoxy)phenyl)-, (S)- ( )-(2S)-3-(4-Hydroxyphenyl)-4-methyl-2-(4-(2-(piperidin-1-yl)ethoxy)phenyl)-2H-1-benzopyran-7-ol |
CAS | 182167-02-8 |
化学式 | C29H31NO4 |
分子量 | 457.56074 |
密度 | 1.217±0.06 g/cm3(Predicted) |
沸点 | 651.5±55.0 °C(Predicted) |
酸度系数 | 9.70±0.40(Predicted) |
存储条件 | Room Temprature |
体外研究 | Acolbifene (ACOL) does not affect pathways of cholesterol synthesis, supporting the involvement of the clearance-related receptors in its hypocholesterolemic action. Acolbifene (EM-652) shows no agonistic activity on ERα and ERβ transcriptional function and blocks the estradiol (E2)-mediated activation of both ERα and ERβ. Acolbifene (EM-652) shows the most potent inhibition of estradiol-stimulated cell proliferation in human breast cancer cancer cells (ZR-75-1, MCF-7, T-47D) and is devoid of any intrinsic estrogenic activity. |
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