(4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-({2-[4-fluoro-2-methoxy-5-(propan-2-yl)phenyl]-5-(trifluoromethyl)phenyl}methyl)-4-methyl-1,3-oxazolidin-2-one

• ChemBase编号: 73301
• 分子式: C30H25F10NO3
• 平均质量: 637.508432
• 单一同位素质量: 637.16747587
• SMILES: c1c(cc(c(c1)c1cc(c(cc1OC)F)C(C)C)CN1C(=O)O[C@@H]([C@@H]1C)c1cc(cc(c1)C(F)(F)F)C(F)(F)F)C(F)(F)F
• Canonical SMILES: COc1cc(F)c(cc1c1ccc(cc1CN1C(=O)O[C@@H]([C@@H]1C)c1cc(cc(c1)C(F)(F)F)C(F)(F)F)C(F)(F)F)C(C)C
• InChI: InChI=1S/C30H25F10NO3/c1-14(2)22-11-23(25(43-4)12-24(22)31)21-6-5-18(28(32,33)34)9-17(21)13-41-15(3)26(44-27(41)42)16-7-19(29(35,36)37)10-20(8-16)30(38,39)40/h5-12,14-15,26H,13H2,1-4H3/t15-,26-/m0/s1
• InChIKey: MZZLGJHLQGUVPN-HAWMADMCSA-N

名称和登记号

名称

• IUPAC标准名: (4S,5R)-5-[3,5-bis(trifluoromethyl)phenyl]-3-({2-[4-fluoro-2-methoxy-5-(propan-2-yl)phenyl]-5-(trifluoromethyl)phenyl}methyl)-4-methyl-1,3-oxazolidin-2-one
• IUPAC传统名: anacetrapib
• 别名: MK-0859; Anacetrapib; (4S,5R)-5-[3,5-Bis(trifluoromethyl)phenyl]-3-[[4'-fluoro-2'-methoxy-5'-(1-methylethyl)-4-(trifluoromethyl)[1,1'-biphenyl]-2-yl]methyl]-4-methyl-2-oxazolidinone; (4S,5R)-5-[3,5-Bis(trifluoromethyl)phenyl]-3-[[4'-fluoro-5'-isopropyl-2'-methoxy-4-(trifluoromethyl)biphenyl-2-yl]methyl]-4-methyl-1,3-oxazolidin-2-one; MK 0859

登记号

• CAS号: 875446-37-0
• PubChem SID: 162038221
• PubChem CID: 11556427
• CHEMBL: 1800807
• Chemspider ID: 9731205
• KEGG ID: D08855
• 维基百科标题: Anacetrapib

理论计算性质

• 质子受体: 2
• 质子供体: 0
• LogD (pH = 5.5): 9.300929
• LogD (pH = 7.4): 9.300929
• Log P: 9.300929
• 摩尔折射率: 141.1558 cm^3
• 极化性: 52.43115 Å^3
• 极化表面积: 38.77 Å^2
• 可自由旋转的化学键: 9
• 里宾斯基五规则: false

分子性质

安全信息

• 保存条件: -20°C

产品相关信息

• 成盐信息: Free Base

详细说明

Selleck Chemicals - S2748

Research Area

• Description: Hyperlipidaemia, Hypercholesterolaemia , Atherosclerosis

Biological Activity

• Description: Anacetrapib (MK0859) is a potent and selective rhCETP and mutant CETP(C13S) inhibitor with IC50 of 7.9 nM and 11.8 nM, respectively
• Targets: rhCETP; Mutant CETP (C13S)
• IC50: 7.9 nM; 11.8 nM ^[1]
• In Vitro: Anacetrapib is not only able to increase HDL-cholesterol, but also further decreases LDL-cholesterol when taken in combination with a statin. Anacetrapib dose-dependently and significantly decreases the transfer of CE from HDL3 to HDL2. Anacetrapib doesn’t affect the amount of [^14C]-dalcetrapibthiol bound to rhCETP. Anacetrapib decreases pre-β-HDL formation by more than 46%. ^[1] Anacetrapib potently blocks CE and TG transfer in 95% human serum.^[2]
• In Vivo: In a dyslipidemic hamster model, 60 mg/kg/day Anacetrapib for 2 weeks results in a 94% reduction in CETP activity and 47% increase in HDL-cholesterol compared with control animals; non-HDL-cholesterol concentrations are not affected. In addition, Anacetrapib promotes reverse cholesterol transport from macrophages, and leads to a 30% increase in fecal cholesterol content. HDL from Anacetrapib-treated hamsters reveals an increase in SR-B1- and ABCG1-mediated efflux compared with controls. ^[2] After oral administration of [^14C]Anacetrapib at 10 mg/kg, ～80 and 90% of the radioactive dose is recovered over 48 hous postdose from rats and monkeys, respectively. The majority of the administered radioactive dose is excreted unchanged in feces in both species. ^[3]
• Clinical Trials: Anacetrapib is in a phase III study among people with established vascular disease.

Protocol

• Protocol: Kinase Assay ^[2]
• Radioactive assays: The ability of Anacetrapib to block CETP-mediated CE and TG transfer is measured by radioactive CETP transfer assay with 2% human serum. The procedure is similar to the 95% human serum transfer assay, except that purified human HDL (128 μg/mL) and [^3H] cholesteryl oleate or [^3H] triolein-labeled LDL are used as acceptor and donor particles, respectively. The [^3H] cholesteryl oleate or [^3H] triolein from exogenous LDL to HDL is transferred by purified recombinant CETP (30 nM) in standard CETP Buffer (50 mM Tris pH 7.4, 100 nM NaCl, and 1 mM EDTA) with 2% human serum. The transfer reaction is terminated by precipitation of LDL with one volume of ice cold human serum and 2 volumes of 20% W/V PEG 8000. The samples are centrifuged and an aliquot of the HDL-containing supernatant is counted by liquid scintillation. Counts present in the supernatant for controls (without CETP addition) are subtracted from those reactivated with CETP to correct for non-specific transfer.
• Protocol: Animal Study ^[3]
• Animal Models: Adult male Sprague-Dawley rats weighing 280 to 330 g
• Formulation: In polyethylene glycol 300-water (7:3, v/v)
• Doses: 2.5 mL/kg (2.5, 25, 50, 250 mg/mL)
• Administration: Oral gavage

References

• References: [1] Niesor EJ, et al. J Lipid Res. 2010, 51(12), 3443-3454.
• References: [2] Ranalletta M, et al. J Lipid Res. 2010, 51(9), 2739-2752.
• References: [3] Tan EY, et al. Drug Metab Dispos. 2010, 38(3), 459-473.

Toronto Research Chemicals - A637200

An orally active and potent cholesterol ester transfer protein (CETP) inhibitor for the treatment of atherosclerosis, in particular dyslipidemia.

参考文献

• Niesor EJ, et al. J Lipid Res. 2010, 51(12), 3443-3454.
• Ranalletta M, et al. J Lipid Res. 2010, 51(9), 2739-2752.
• Tan EY, et al. Drug Metab Dispos. 2010, 38(3), 459-473.
• Krishna, R. et al.: Br. J. Clin. Pharmacol., 67, 520 (2009)
• Vergeer, M. et al.: Nat. Clin. Pract. Cardiovasc. Med., 5, 302 (2009)
• Masson, D.: Curr. Opin. Invest. Drugs, 10, 980 (2009)