BMS-852927

BMS-852927 Suppliers list
Company Name: Sichuan Wei Keqi Biological Technology Co., Ltd.  
Tel: 028-81700200 18116577057
Email: 3003855609@qq.com
Company Name: Shanghai YuanYe Biotechnology Co., Ltd.  
Tel: 15026964105
Email: 2881489226@qq.com
Company Name: ShangHai Biochempartner Co.,Ltd  
Tel: 177-54423994 17754423994
Email: 2853530910@QQ.com
Company Name: Twochem Co.Ltd.  
Tel: 021-58111628 15800915896
Email: sales@twochem.com
Company Name: Tianjin Kaifu Pharmaceutical Technology Co., Ltd.  
Tel: 18081075745
Email: chemflowtech@sina.com
BMS-852927 Basic information
Product Name:BMS-852927
Synonyms:BMS-852927;2-(2-(2-(2,6-dichlorophenyl)propan-2-yl)-1-(3,3'-difluoro-4'-(hydroxymethyl)-5'-(methylsulfonyl)-[1,1'-biphenyl]-4-yl)-1H-imidazol-4-yl)propan-2-ol;BMS-852927 (BMS 852927;XL-041);1H-Imidazole-4-methanol, 2-[1-(2,6-dichlorophenyl)-1-methylethyl]-1-[3,3'-difluoro-4'-(hydroxymethyl)-5'-(methylsulfonyl)[1,1'-biphenyl]-4-yl]-α,α-dimethyl-;XL041(BMS-852927);XL041,XL-041;XL041
CAS:1256918-39-4
MF:C29H28Cl2F2N2O4S
MW:609.51
EINECS:
Product Categories:
Mol File:1256918-39-4.mol
BMS-852927 Structure
BMS-852927 Chemical Properties
Boiling point 810.6±75.0 °C(Predicted)
density 1.36±0.1 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO : ≥ 150 mg/mL (246.10 mM)
form Solid
pka11.20±0.10(Predicted)
color White to off-white
Safety Information
MSDS Information
BMS-852927 Usage And Synthesis
UsesXL041 (BMS-852927) is an LXRβ-selective agonist.
in vivo

XL041 (BMS-852927), has a very favorable profile at efficacious doses in cynomolgus monkeys and 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. In a separate study, XL041 inhibits the progression of atherosclerosis in a 12 week study in LDLR 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].

References[1] Kirchgessner TG, et al. Beneficial and Adverse Effects of an LXR Agonist on Human Lipid and Lipoprotein Metabolism and Circulating Neutrophils. Cell Metab. 2016 Aug 9;24(2):223-33. DOI:10.1016/j.cmet.2016.07.016
BMS-852927 Preparation Products And Raw materials
Tag:BMS-852927(1256918-39-4) Related Product Information
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