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AR antagonist 1 是 AR 拮抗剂,能够与 E3 连接酶配体结合,与 VHL 蛋白结合亲和力较弱,用于 PROTACARD-266 合成。


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AR antagonist 1 是 AR 拮抗剂,能够与 E3 连接酶配体结合,与 VHL 蛋白结合亲和力较弱,用于 PROTACARD-266 合成。
| 规格 | 价格 | 库存 | 数量 |
|---|---|---|---|
| 1 mg | ¥ 546 | In stock | |
| 5 mg | ¥ 1,220 | In stock | |
| 10 mg | ¥ 1,810 | In stock | |
| 25 mg | ¥ 2,880 | In stock | |
| 50 mg | ¥ 3,910 | In stock | |
| 100 mg | ¥ 5,250 | In stock | |
| 200 mg | ¥ 6,930 | In stock | |
| 1 mL x 10 mM (in DMSO) | ¥ 1,090 | In stock |
AR antagonist 1 相关产品
| 产品描述 | AR antagonist 1 is a potent antagonist of the androgen receptor. It binds to E3 ligase ligands with weak binding affinities to VHL protein in the synthesis of PROTAC ARD-266. |
| 靶点活性 | Androgen receptor: |
| 体外活性 | AR antagonist 1 是ARD-266靶向连接酶的配体。ARD-266是一种基于VHL E3连接酶的高效雄激素受体(AR)PROTAC降解剂。AR antagonist 1 对其E3连接酶复合物表现出微摩尔级的结合亲和力,因此它可以有效用于设计高效的PROTAC降解剂。 |
| 分子量 | 278.78 |
| 分子式 | C15H19ClN2O |
| CAS No. | 1818885-54-9 |
| Smiles | CC1(C)[C@H](N)C(C)(C)[C@H]1Oc1ccc(C#N)c(Cl)c1 |
| 密度 | 1.18 g/cm3 (Predicted) |
| 颜色 | White |
| 物理性状 | Solid |
| 存储 | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice/Shipping at ambient temperature. | |||||||||||||||||||||||||||||||||||
| 溶解度信息 | DMSO: 60 mg/mL (215.22 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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