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XL041 (BMS-852927) is an agonist of LXRβ-selective.
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XL041 (BMS-852927) is an agonist of LXRβ-selective.
规格 | 价格 | 库存 | 数量 |
---|---|---|---|
5 mg | 询价 | 8-10周 | |
25 mg | 询价 | 8-10周 | |
50 mg | 询价 | 8-10周 | |
100 mg | 询价 | 8-10周 | |
1 mL x 10 mM (in DMSO) | 询价 | 8-10周 |
产品描述 | XL041 (BMS-852927) is an agonist of LXRβ-selective. |
体外活性 | XL041 (BMS-852927) is an LXRβ-selective agonist with 20% LXRα and 88% LXRβ activity compared to a full pan agonist in transactivation assays. BMS-852927 has similar binding affinity to LXRα and LXRβ (19 and 12 nM, respectively)[1]. XL041 is potent, with an EC50=9 nM and 26% activity in an in vitro human whole-blood endogenous target gene activation assay (WBA). |
体内活性 | XL041 (BMS-852927) which has a very favorable profile at efficacious doses in cynomolgus monkeys and mice. In a separate study, XL041 inhibits the progression of atherosclerosis in a 12 week study in LDLR KO mice. XL041 pre-treatment of C57BL/6J mice for 7 days results in potent, dose-dependent stimulation of cholesterol efflux in this system; reaching a maximum in the 3 mg/kg/day dose group of 70% above vehicle in the initial efflux rate. Similar results are obtained in LDLR knockout (KO) mice. Importantly, the dose response for inhibition of atherosclerosis (0.1-3 mg/kg/day) is similar to the dose response for macrophage reverse cholesterol transport (RCT) stimulation (0.03-3 mg/kg/day), a major underlying mechanism through which LXR agonists affect the disease[1]. |
别名 | BMS-852927 |
分子量 | 609.51 |
分子式 | C29H28Cl2F2N2O4S |
CAS No. | 1256918-39-4 |
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: 100 mg/mL (164.07 mM), Sonication is recommended. | |||||||||||||||||||||||||||||||||||
溶液配制表 | ||||||||||||||||||||||||||||||||||||
DMSO
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