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569406 Stearoyl-CoA Desaturase 1 Inhibitor, MF-438 - Calbiochem

Stearoyl-CoA Desaturase 1 Inhibitor, MF-438, CAS 921605-87-0, is a cell-permeable inhibitor of Stearoyl-CoA Desaturase 1 (SCD1; IC50 of 2.3 nM).

MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

同义词: 2-methyl-5-(6-(4-(2-(trifluoromethyl)phenoxy)piperidin-1-yl)pyridazin-3-yl)-1,3,4-thiadiazole

569406
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概述

Replacement Information

Products

产品目录编号包装 数量 / 包装
569406-10MGCN 玻璃瓶 10 mg
Description
OverviewA cell-permeable, thiadiazole-pyridazine compound that acts as an inhibitor of Stearoyl-CoA Desaturase 1 (SCD1) with an IC50 of 2.3 nM. In vivo, it exhibits an ED50 of 1-3 mg/kg, p.o., in mouse liver PD assays.
Catalogue Number569406
Brand Family Calbiochem®
Synonyms2-methyl-5-(6-(4-(2-(trifluoromethyl)phenoxy)piperidin-1-yl)pyridazin-3-yl)-1,3,4-thiadiazole
References
ReferencesLeger, S., et al. 2010. Bioorg Med Chem Lett. 2, 499.
Product Information
FormOff-white powder
Hill FormulaC₁₉H₁₈F₃N₅OS
Chemical formulaC₁₉H₁₈F₃N₅OS
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
ApplicationStearoyl-CoA Desaturase 1 Inhibitor, MF-438, CAS 921605-87-0, is a cell-permeable inhibitor of Stearoyl-CoA Desaturase 1 (SCD1; IC50 of 2.3 nM).
Biological Information
Purity≥99% by HPLC
Physicochemical Information
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Standard Handling
Storage +2°C to +8°C
Do not freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Packaging Information
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
产品目录编号 GTIN
569406-10MGCN 04055977190557

Documentation

Stearoyl-CoA Desaturase 1 Inhibitor, MF-438 - Calbiochem MSDS

职位

物料安全数据表 (MSDS) 

Stearoyl-CoA Desaturase 1 Inhibitor, MF-438 - Calbiochem 分析证书

标题批号
569406

参考

参考信息概述
Leger, S., et al. 2010. Bioorg Med Chem Lett. 2, 499.
数据表

Note that this data sheet is not lot-specific and is representative of the current specifications for this product. Please consult the vial label and the certificate of analysis for information on specific lots. Also note that shipping conditions may differ from storage conditions.

Revision10-May-2013 JSW
Synonyms2-methyl-5-(6-(4-(2-(trifluoromethyl)phenoxy)piperidin-1-yl)pyridazin-3-yl)-1,3,4-thiadiazole
DescriptionA cell-permeable, thiadiazole-pyridazine compound that acts as an inhibitor of Stearoyl-CoA Desaturase 1 (SCD1) with an IC50 of 2.3 nM. In vivo, it exhibits an ED50 of 1-3 mg/kg, p.o., in mouse liver PD assays.
FormOff-white powder
Chemical formulaC₁₉H₁₈F₃N₅OS
Structure formulaStructure formula
Purity≥99% by HPLC
SolubilityDMSO (10 mg/ml)
Storage +2°C to +8°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution, aliquot and freeze (-20°C). Stock solutions are stable for up to 3 months at -20°C.
Toxicity Standard Handling
ReferencesLeger, S., et al. 2010. Bioorg Med Chem Lett. 2, 499.