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S81170

DGAT-1 inhibitor

源叶(MedMol) 98%
  • 英文名:
  • DGAT-1 inhibitor
  • 别名:
  • DGAT-1 抑制剂;(1R,2R)-2-[[4'-[[(苯基氨基)羰基]氨基][1,1'-联苯]-4-基]甲酰基]环戊烷羧酸;(1R,2R)-2-[[4'-[[(Phenylamino)carbonyl]amino][1,1'-biphenyl]-4-yl]carbonyl]cyclopentanecarboxylic acid;DGAT-1 inhibitor;Diacyl glycerola
  • CAS号:
  • 959122-11-3
  • 分子式:
  • C26H24N2O4
  • 分子量:
  • 428.486
  • 核磁/质谱:
品牌货号产品规格价格(RMB) 库存(上海) 北京 武汉 南京 数量计量单位 加入购物车...
源叶(MedMol) S81170-5mg 98% ¥480.00元 4 0 0 0 EA 加入购物车
源叶(MedMol) S81170-10mg 98% ¥720.00元 4 0 0 0 EA 加入购物车
源叶(MedMol) S81170-25mg 98% ¥1440.00元 4 0 0 0 EA 加入购物车
源叶(MedMol) S81170-100mg 98% ¥4000.00元 2 0 0 0 EA 加入购物车
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  • 提示:详情请下载说明书。
  • 产品描述: A 922500 (DGAT-1 Inhibitor 4a) is a potent, selective, and orally bioavailable diacylglycerol acyltransferase 1 (DGAT-1) inhibitor with IC50s of 9 and 22 nM against human and mouse DGAT-1, respectively.
  • 靶点: IC50: 9 nM (human DGAT-1), 22 nM (mouse DGAT-1)
  • 体外研究: A 922500 (A-922500) demonstrates excellent selectivity over other acyltransferases, including DGAT-2 (IC50=53 μM) and the phylogenetic family members acyl coenzyme A cholesterol acyltransferase-1 and -2 (IC50=296 μM)
  • 体内研究: DGAT-1 inhibitor A 922500 (A-922500) reduces serum triglyceride levels from baseline at all doses tested; however, this is only statistically significant at the 3 mg/kg dose, which lowers serum triglycerides by 53%. Similarly, the 3 mg/kg dose of A 922500 significantly reduces serum FFA concentrations by 55% and total cholesterol by 25%. DGAT-1 inhibition has no significant effect on body weight at any dose tested. Although A 922500 dpes not significantly affect LDL-cholesterol or HDL-cholesterol individually, the serum LDL/HDL-cholesterol ratio is significantly improved by A 922500 at 0.3 and 3 mg/kg. Similar to the dyslipidemic hamster, treatment with 3 mg/kg A 922500 significantly reduces serum triglyceride concentrations (39%). FFA levels significantly increase over the 14-day period in vehicle-treated animals. This increase is inhibited in a dose-dependent manner by A 922500 such that FFA concentrations are 32% lower after 14 days of treatment with the DGAT-1 inhibitor at 3 mg/kg, compared with the vehicle group (p < 0.05). HDL-cholesterol is significantly increased from baseline levels by A 922500 at 0.3 and 3 mg/kg; however, this is only significantly increased compared with vehicle at the 3 mg/kg dose. Body weight significantly increases over the 2-week period in vehicle-treated rats, and this is not affected by A 922500. LDL-cholesterol is significantly reduced in the vehicle treated group. DGAT-1 inhibition does not further reduce LDL-cholesterol and has no effect on total cholesterol
  • 参考文献:
    1. King AJ, et al. Diacylglycerol acyltransferase 1 inhibition lowers serum triglycerides in the Zucker fatty rat and the hyperlipidemic hamster. J Pharmacol Exp Ther. 2009 Aug;330(2):526-31.
  • 溶解性: Soluble  in  DMSO
  • 保存条件: -20℃
  • 配置溶液浓度参考:
    1mg 5mg 10mg
    1 mM 2.334 ml 11.669 ml 23.338 ml
    5 mM 0.467 ml 2.334 ml 4.668 ml
    10 mM 0.233 ml 1.167 ml 2.334 ml
    50 mM 0.047 ml 0.233 ml 0.467 ml
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