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517301 P-Glycoprotein Inhibitor, C-4 - CAS 864426-22-2 - Calbiochem

517301
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概述

Replacement Information

重要规格表

CAS #Empirical Formula
864426-22-2C₂₃H₁₈ClNO₄

Products

产品目录编号包装 数量 / 包装
517301-10MGCN 塑胶安瓿;塑胶针药瓶 10 mg
Description
OverviewA cell-permeable cinnamoyl compound that reversibly inhibits P-gp (P-glycoprotein) efflux function and reverses the MDR (multidrug resistance) phenotype with no noticeable effect on P-gp expression. Shown to significantly enhance Paclitaxel- (Cat. No. 580555) and Vincristine- (Cat. No. 677181) induced cytotoxicity as well as apoptosis in P-gp expressing KBV20C cells.
Catalogue Number517301
Brand Family Calbiochem®
Synonyms(E)-4-Chloro-N-(3-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)benzamide, C-4
References
ReferencesKim, Y.K., et al. 2007. Biochem. Biophys. Res. Commun. 355, 136.
Woo, H.B., et al. 2005. Bioorg. Med. Chem. Lett. 15, 3782.
Product Information
CAS number864426-22-2
ATP CompetitiveN
FormYellow solid
Hill FormulaC₂₃H₁₈ClNO₄
Chemical formulaC₂₃H₁₈ClNO₄
ReversibleY
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetP-Glycoprotein
Purity≥95% by HPLC
Physicochemical Information
Cell permeableY
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
Protect from Light Protect from light
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
Packaged under inert gas Packaged under inert gas
Transport Information
Supplemental Information
Specifications
Global Trade Item Number
产品目录编号 GTIN
517301-10MGCN 04055977271874

Documentation

P-Glycoprotein Inhibitor, C-4 - CAS 864426-22-2 - Calbiochem MSDS

职位

物料安全数据表 (MSDS) 

P-Glycoprotein Inhibitor, C-4 - CAS 864426-22-2 - Calbiochem 分析证书

标题批号
517301

参考

参考信息概述
Kim, Y.K., et al. 2007. Biochem. Biophys. Res. Commun. 355, 136.
Woo, H.B., et al. 2005. Bioorg. Med. Chem. Lett. 15, 3782.
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.

Revision21-January-2008 JSW
Synonyms(E)-4-Chloro-N-(3-(3-(4-hydroxy-3-methoxyphenyl)acryloyl)phenyl)benzamide, C-4
DescriptionA cell-permeable cinnamoyl compound that reversibly inhibits P-gp (P-glycoprotein) efflux function and reverses the MDR (multidrug resistance) phenotype with no noticeable effect on P-gp expression. Shown to significantly enhance Paclitaxel- (Cat. No. 580555) and Vincristine- (Cat. No. 677181) induced cytotoxicity as well as apoptosis in P-gp expressing KBV20C cells.
FormYellow solid
Intert gas (Yes/No) Packaged under inert gas
CAS number864426-22-2
Chemical formulaC₂₃H₁₈ClNO₄
Structure formulaStructure formula
Purity≥95% by HPLC
SolubilityDMSO (10 mg/ml)
Storage Protect from light
+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
ReferencesKim, Y.K., et al. 2007. Biochem. Biophys. Res. Commun. 355, 136.
Woo, H.B., et al. 2005. Bioorg. Med. Chem. Lett. 15, 3782.