FUDAEUIGIJZUAY-UMIRZPQISA-N
中文名称 | FUDAEUIGIJZUAY-UMIRZPQISA-N |
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中文同义词 | 化合物 T13404 |
英文名称 | FUDAEUIGIJZUAY-UMIRZPQISA-N |
英文同义词 | FUDAEUIGIJZUAY-UMIRZPQISA-N;ZK168281;ZK-168281,ZK168281;2-Propenoic acid, 3-[1-[(1R,2E,4R)-4-[(1R,3aS,4E,7aR)-4-[(2Z)-2-[(3S,5R)-3,5-dihydroxy-2-methylenecyclohexylidene]ethylidene]octahydro-7a-methyl-1H-inden-1-yl]-1-hydroxy-2-penten-1-yl]cyclopropyl]-, ethyl ester, (2E)- |
CAS号 | 186371-96-0 |
分子式 | C32H46O5 |
分子量 | 510.7 |
EINECS号 | |
相关类别 | |
Mol文件 | 186371-96-0.mol |
结构式 |
FUDAEUIGIJZUAY-UMIRZPQISA-N 性质
沸点 | 652.9±55.0 °C(Predicted) |
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密度 | 1.15±0.1 g/cm3(Predicted) |
储存条件 | 4°C, protect from light, stored under nitrogen |
酸度系数(pKa) | 14.29±0.20(Predicted) |
Kd: 0.1 nM (VDR)
ZK168281 resembles more the mouse constitutive androstane receptor (CAR) inverse agonist Androstanol in its ability to recruit corepressor (CoR) proteins. A salt bridge between the CoR and a conserved lysine in helix 4 of the nuclear receptor (NR) is central to this interaction, but also helix 12 was stabilized by direct contacts with residues of the CoR. Fixation of helix 12 in the antagonistic/inverse agonistic conformation prevents an energetically unfavorable free floatation of the C terminus.
安全信息
更新日期 | 产品编号 | 产品名称 | CAS号 | 包装 | 价格 |
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2024/04/30 | HY-12407 | FUDAEUIGIJZUAY-UMIRZPQISA-N ZK168281 | 186371-96-0 | 1mg | 8500元 |