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Fatostatin A Hydrobromide

    
99.90%

Fatostatin A Hydrobromide

源叶(MedMol)
S88092 一键复制产品信息
298197-04-3
98968-68-4
375.33
Fatostatin hydrobromide
货号 规格 价格 上海 北京 珠海 重庆 武汉 购买数量
S88092-5mg买3赠1
99.90%

¥204.00

4 - - - -
S88092-10mg买3赠1
99.90%

¥306.00

4 - - - -
S88092-25mg买3赠1
99.90%

¥640.00

4 - - - -
S88092-50mg促销
99.90%

¥930.00 ¥744.00

1 - - - -
S88092-100mg促销
≥98%

¥1390.00 ¥1110.00

货期:2-3天 - - - -
产品介绍 参考文献 质检证书(COA) 摩尔浓度计算器 相关产品
产品描述: Fatostatin ia an inhibitor of sterol regulatory element binding protein (SREBP). It impairs the activation of SREBP-1 and SREBP-2.
靶点: Fatty Acid Synthase;NPC1L1;NPC1L1; FattyAcidSynthase
体内研究: Fatostatin significantly inhibits subcutaneous C4-2B tumor growth and markedly decreases serum PSA level compared to the control group. Fatostatin blocks increases in body weight, blood glucose, and hepatic fat accumulation in obese ob/ob mice, even under uncontrolled food intake.
细胞实验: Cell lines: CHO-K1 cells. Concentrations: 20 μM. Incubation Time: 20 h. Method: On day 0,CHO-K1 cells are plated out onto a 96-well plate in medium A.On day 2,the cells are transiently cotransfected with pCMV-PLAP-BP2(513–1141),pCMV-SCAP,and pAc-β-gal,using Lipofectamine reagent.After incubation for 5 hr,the cells are washed with PBS and then incubated in medium B,in the absence or presence of fatostatin (20 μM) or sterols (10 μg/mL cholesterol and 1 μg/mL 25-hydroxycholesterol).After 20 hr of incubation,an aliquot of the medium is assayed for secreted alkaline phosphatase activity.The cells in each well are lysed and used for measurement of β-galactosidase activities.The alkaline phosphatase activity is normalized by the activity of β-galactosidase.
动物实验: Animal Models: Obese (ob/ob) mice (C57BL/6J background). Formulation: 10% DMSO in PBS. Dosages: 30 mg/kg. Administration: intraperitoneal injection
参考文献: 1. Li X, et al. Mol Cancer Ther. 2014, 13(4):855-66. 2. Zhang Z, He J, Zhao Y, et al. Asiatic acid prevents renal fibrosis in UUO rats via promoting the production of 15d-PGJ2, an endogenous ligand of PPAR-γ[J]. Acta Pharmacologica Sinica. 2020, 41(3): 373-382. 3. Kamisuki S, et al. Chem Biol. 2009, 16(8):882-92.
溶解性: Soluble  in  DMSO、Ethanol
保存条件: -20℃
配置溶液浓度参考:
1mg 5mg 10mg
1 mM 2.664 ml 13.322 ml 26.643 ml
5 mM 0.533 ml 2.664 ml 5.329 ml
10 mM 0.266 ml 1.332 ml 2.664 ml
50 mM 0.053 ml 0.266 ml 0.533 ml
注意: 部分产品我司仅能提供部分信息,我司不保证所提供信息的权威性,仅供客户参考交流研究之用。

参考文献

质检证书(COA)

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摩尔浓度计算器

质量 (mg) = 浓度 (mM) x 体积 (mL) x 分子摩尔量 (g/mol)

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