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178385 Apocynin - CAS 498-02-2 - Calbiochem

A cell-permeable, anti-inflammatory phenolic compound that acts as a potent and selective inhibitor of NADPH oxidase.

Apocynin - CAS 498-02-2 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

同义词: 4-Hydroxy-3-methoxyacetophenone, Acetovanillone, NADPH Oxidase Inhibitor V, NOX Inhibitor V

Primary Target: NADPH oxidase
178385
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概述

Replacement Information

重要规格表

CAS #Empirical Formula
498-02-2C₉H₁₀O₃

Products

产品目录编号包装 数量 / 包装
178385-1GMCN 塑胶安瓿;塑胶针药瓶 1 gm
Description
OverviewA cell-permeable, anti-inflammatory phenolic compound that acts as a potent and selective inhibitor of NADPH oxidase. Shown to block peroxynitrite formation in murine macrophages. Reported to increase glutathione synthesis through activation of AP-1. Also reported to prevent phagocytosis of myelin by macrophages (10 mM).
Catalogue Number178385
Brand Family Calbiochem®
Synonyms4-Hydroxy-3-methoxyacetophenone, Acetovanillone, NADPH Oxidase Inhibitor V, NOX Inhibitor V
References
ReferencesAbid, M.R., et al. 2000. FEBS Lett. 486, 252.
Muijsers, R.B., et al. 2000. Br. J. Pharmacol. 130, 932.
Lapperre, T.S., et al. 1999. FEBS Lett. 443, 235.
Supinski, G., et al. 1999, J. Appl. Physiol. 87, 776.
van der Goes, A., et al. 1998. J. Neuroimmunol. 92, 67.
Hart, B.A., and Simmons, J.M. 1992. Biotechnol. Ther. 3, 3.
Product Information
CAS number498-02-2
ATP CompetitiveN
FormWhite to off-white powder
Hill FormulaC₉H₁₀O₃
Chemical formulaC₉H₁₀O₃
ReversibleN
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetNADPH oxidase
Purity≥98% by GC
Physicochemical Information
Cell permeableY
Dimensions
Materials Information
Toxicological Information
Safety Information according to GHS
RTECSAM8800000
Safety Information
Product Usage Statements
Storage and Shipping Information
Ship Code Ambient Temperature Only
Toxicity Irritant
Storage -20°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 6 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
178385-1GMCN 04055977222463

Documentation

Apocynin - CAS 498-02-2 - Calbiochem MSDS

职位

物料安全数据表 (MSDS) 

Apocynin - CAS 498-02-2 - Calbiochem 分析证书

标题批号
178385

参考

参考信息概述
Abid, M.R., et al. 2000. FEBS Lett. 486, 252.
Muijsers, R.B., et al. 2000. Br. J. Pharmacol. 130, 932.
Lapperre, T.S., et al. 1999. FEBS Lett. 443, 235.
Supinski, G., et al. 1999, J. Appl. Physiol. 87, 776.
van der Goes, A., et al. 1998. J. Neuroimmunol. 92, 67.
Hart, B.A., and Simmons, J.M. 1992. Biotechnol. Ther. 3, 3.

小册子

标题
Pathways and Biomarkers of Oxidative Stress
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.

Revision27-February-2018 JSW
Synonyms4-Hydroxy-3-methoxyacetophenone, Acetovanillone, NADPH Oxidase Inhibitor V, NOX Inhibitor V
DescriptionA cell-permeable, anti-inflammatory phenol that acts as a potent and selective inhibitor of NADPH oxidase. Also blocks peroxynitrite formation in murine macrophages. Reported to increase glutathione synthesis through the activation of AP-1. Shown to prevent phagocytosis of myelin by macrophages (10 mM).
FormWhite to off-white powder
Intert gas (Yes/No) Packaged under inert gas
CAS number498-02-2
RTECSAM8800000
Chemical formulaC₉H₁₀O₃
Structure formulaStructure formula
Purity≥98% by GC
SolubilityDMSO (10 mg/ml) or Ethanol (20 mg/ml)
Storage Protect from light
-20°C
Do Not Freeze Ok to freeze
Special InstructionsFollowing reconstitution aliquot and freeze (-20°C). Stock solutions are stable for up to 6 months at -20°C.
Toxicity Irritant
Merck USA index14, 741
ReferencesAbid, M.R., et al. 2000. FEBS Lett. 486, 252.
Muijsers, R.B., et al. 2000. Br. J. Pharmacol. 130, 932.
Lapperre, T.S., et al. 1999. FEBS Lett. 443, 235.
Supinski, G., et al. 1999, J. Appl. Physiol. 87, 776.
van der Goes, A., et al. 1998. J. Neuroimmunol. 92, 67.
Hart, B.A., and Simmons, J.M. 1992. Biotechnol. Ther. 3, 3.