购物车
- 全部删除
- 您的购物车当前为空
G36是一种细胞可渗透的G 蛋白偶联雌激素受体(GPER/GPR30)的非甾体拮抗剂。G36抑制17β-雌二醇或GPER 选择性激动剂G-1的激活(IC50分别为112和165 nM)。G36对ERα或ERβ均无可检测的结合活性。G36通过GPER 阻断由雌激素触发的PI3K 的激活或钙动员,并且它通过雌激素或G-1而不是通过EGF 抑制ERK 的激活。
为众多的药物研发团队赋能,
让新药发现更简单!
G36是一种细胞可渗透的G 蛋白偶联雌激素受体(GPER/GPR30)的非甾体拮抗剂。G36抑制17β-雌二醇或GPER 选择性激动剂G-1的激活(IC50分别为112和165 nM)。G36对ERα或ERβ均无可检测的结合活性。G36通过GPER 阻断由雌激素触发的PI3K 的激活或钙动员,并且它通过雌激素或G-1而不是通过EGF 抑制ERK 的激活。
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
1 mg | ¥ 348 | 现货 | |
5 mg | ¥ 828 | 现货 | |
10 mg | ¥ 1,350 | 现货 | |
25 mg | ¥ 1,980 | 现货 | |
50 mg | ¥ 2,780 | 现货 | |
100 mg | ¥ 3,950 | 现货 | |
500 mg | ¥ 8,670 | 现货 | |
1 mL x 10 mM (in DMSO) | ¥ 913 | 现货 |
产品描述 | G36 is a cell-permeable non-steroidal antagonist of GPER. G36 inhibits activation by either 17β-estradiol or the GPER-selective agonist G-1 (IC50 = 112 and 165 nM, respectively). G36 has no detectable binding activity to either ERα or ERβ. G36 blocks the activation of PI3K or calcium mobilization triggered by estrogen through GPER and it suppresses ERK activation by estrogen or G-1 but not by EGF. G-36 can be used in combination with GPER-selective agonists, like G-1, to distinguish the roles of GPER from those of ERα and ERβ in complex biological systems. |
靶点活性 | GPER:165 nM |
别名 | G-36 |
分子量 | 412.32 |
分子式 | C22H22BrNO2 |
CAS No. | 1392487-51-2 |
Smiles | [H][C@]12CC=C[C@@]1([H])c1cc(ccc1N[C@H]2c1cc2OCOc2cc1Br)C(C)C |
密度 | 1.367 g/cm3 (Predicted) |
存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice. | |||||||||||||||||||||||||||||||||||
溶解度信息 | DMSO: 55 mg/mL (133.39 mM), Sonication and heating to 80℃ are recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
|
版权所有©2015-2024 TargetMol Chemicals Inc.保留所有权利.
评论内容