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GW 4064

    99%

GW 4064

源葉(MedMol)
S80584
278779-30-9
C28H22Cl3NO4
542.84
3-(2,6-二氯苯基)-4-(3'-羧基-2-氯二苯乙烯-4-基)氧甲基-5-異丙基異惡唑;GW4064; GW 4064; 3-(2,6-Dichlorophenyl)-4-(3'-carboxy-2-chlorostilben-4-yl)oxymethyl-5-isopropylisoxazole;
品牌 貨號 產(chǎn)品規(guī)格 價格(RMB) 庫存(上海) 北京 武漢 南京 購買數(shù)量
源葉(MedMol) S80584-5mg 99% ¥320.00元 >10 - - -
源葉(MedMol) S80584-10mg 99% ¥544.00元 >10 - - -
源葉(MedMol) S80584-25mg 99% ¥960.00元 >10 - - -
源葉(MedMol) S80584-100mg 99% ¥2560.00元 >10 - - -
產(chǎn)品介紹 參考文獻(1篇) 質檢證書(COA) 摩爾濃度計算器 相關產(chǎn)品

產(chǎn)品介紹

GW 4064 is a potent FXR agonist with an EC50 of 65 nM.
產(chǎn)品描述: GW 4064 is a potent FXR agonist with an EC50 of 65 nM.
靶點: EC50: 65 nM (FXR);FXR;Autophagy
體內(nèi)研究: GW4064 suppresses weight gain in C57BL/6 mice fed with either a high-fat diet (HFD) or high-fat, high-cholesterol diet. GW4064 treatment of mice on HFD significantly represses diet-induced hepatic steatosis as evidenced by lower triglyceride and free fatty acid level in the liver. GW4064 markedly reduces lipid transporter CD36 expression without affecting expression of genes that are directly involved in lipogenesis. GW4064 treatment attenuates hepatic inflammation while having no effect on white adipose tissue. GW4064 (30 mg/kg) treatment results in substantial, statistically significant reductions in serum activities of ALT, AST, LDH, and ALP in the ANIT-treated rats. Serum bile acid levels are also significantly reduced by GW4064 treatment. Bilirubin levels are decreased in the GW4064-treated rats, but statistical significance is not achieved. Notably, GW4064 is much more effective in decreasing these markers of liver damage than TUDCA, which reduces only LDH levels
參考文獻: 1. Akwabi-Ameyaw A, et al.Conformationally constrained farnesoid X receptor (FXR) agonists: Naphthoic acid-based analogs of GW 4064. Bioorg Med Chem Lett, 2008, 18(15), 4339-4343. 2. Ma Y, et al. Synthetic FXR agonist GW4064 prevents diet-induced hepatic steatosis and resistance. Pharm Res. 2013 May;30(5):1447-57. 3. Liu Y, et al. Hepatoprotection by the farnesoid X receptor agonist GW4064 in rat models of intra- and extrahepatic cholestasis. J Clin Invest. 2003 Dec;112(11):1678-87.
溶解性: DMSO  :  100  mg/mL  (184.22  mM;  Need  ultrasonic)    DMF  :  100  mg/mL  (184.22  mM;  Need  ultrasonic)
保存條件: 2-8℃
配置溶液濃度參考:
1mg 5mg 10mg
1 mM 1.842 ml 9.211 ml 18.422 ml
5 mM 0.368 ml 1.842 ml 3.684 ml
10 mM 0.184 ml 0.921 ml 1.842 ml
50 mM 0.037 ml 0.184 ml 0.368 ml
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