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SCD1 inhibitor-3

    级别和纯度:
  • ≥98%
  • CAS编号: 1282606-48-7
  • 分子式: C19H16FN7O2
  • 分子量: 393.37
有货

库存信息

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库存信息

关闭

库存信息

关闭

库存信息

关闭
货号 (SKU) 包装规格 是否现货 价格 数量
S649076-5mg
5mg 期货 Stock Image
S649076-10mg
10mg 期货 Stock Image
S649076-25mg
25mg 期货 Stock Image
S649076-50mg
50mg 期货 Stock Image

基本描述

别名 SCD1抑制剂-3
规格或纯度 ≥98%
英文名称 SCD1 inhibitor-3
生化机理 SCD1 抑制剂-3 是一种安全、强效且具有口服活性的 SCD1 抑制剂。SCD1 抑制剂-3 可用于研究肥胖、II 型糖尿病、血脂异常等代谢性疾病,以及皮肤病、痤疮和癌症。
储存温度 -20°C储存
运输条件 超低温冰袋运输
产品介绍


SCD1 inhibitor-3 is a safe, potent and orally active SCD1 inhibitor. SCD1 inhibitor-3 can be used for the research of metabolic diseases such as obesity, type II diabetes and dyslipidemia, as well as skin diseases, acne and cancer

In Vivo

SCD1 inhibitor-3 (compound 17a) (5 mg/kg; p.o.; 4 hours) reduces the plasma C16:1/C16:0 triglycerides desaturation index by 54 % . SCD1 inhibitor-3 (2~10 mg/kg; p.o.; 4 hours) makes a dose-responsive reduction of plasma triglycerides desaturation index . MCE has not independently confirmed the accuracy of these methods. They are for reference only. Animal Model: Lewis rats Dosage: 5 mg/kg Administration: P.o.; 4 hours Result: Reduced the plasma C16:1/C16:0 triglycerides desaturation index by 54 %. Animal Model: Lewis rats Dosage: 2~10 mg/kg Administration: P.o.; 4 hours Result: A dose-responsive reduction of plasma triglycerides desaturation index.

Form:Solid

IC50& Target:SCD1

纯度 ≥98%

名称和识别符

Smiles O=C(C1=NNC(N2C=NN(CC3=CC=C(F)C=C3)C2=O)=C1)NCC4=CC=CN=C4
分子量 393.37

化学和物理性质

溶解性 DMSO : ≥ 125 mg/mL (317.77 mM)

质检证书(CoA,COO,BSE/TSE 和分析图谱)

C of A & Other Certificates(BSE/TSE, COO):
输入批号以搜索分析图谱:

溶液计算器