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572660 SU11652 - CAS 326914-10-7 - Calbiochem

A cell-permeable pyrrole-indolinone compound that acts as a potent, reversible, and ATP-competitive tyrosine kinase receptor and angiogenic inhibitor.

SU11652 - CAS 326914-10-7 - Calbiochem MSDS (material safety data sheet) or SDS, CoA and CoQ, dossiers, brochures and other available documents.

同义词: 5-[(Z)-(5-Chloro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)methyl]-N-[2-(diethylamino)ethyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide, VEGFR Tyrosine Kinase Inhibitor XVII, VEGFR2 Kinase Inhibitor XIV, PDGFR Tyrosine Kinase Inhibitor VIII

Primary Target: PDGFRB
572660
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概述

Replacement Information

重要规格表

CAS #Empirical Formula
326914-10-7C₂₂H₂₇ClN₄O₂

Products

产品目录编号包装 数量 / 包装
572660-500UGCN 塑胶安瓿;塑胶针药瓶 500 μg
Description
OverviewA cell-permeable pyrrole-indolinone compound that acts as a potent, reversible, and ATP-competitive tyrosine kinase receptor and angiogenic inhibitor that exhibits greater selectivity for PDGFRβ (IC50 = 3 nM), VEGFR2 (IC50 = 27 nM), FGFR1 (IC50 = 170 nM), and Kit family members (IC50 = ~ 10-500 nM) over EGFR (IC50 >20 µM). Reported to display anti-proliferative and pro-apoptotic properties in tumor cells.
Catalogue Number572660
Brand Family Calbiochem®
Synonyms5-[(Z)-(5-Chloro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)methyl]-N-[2-(diethylamino)ethyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide, VEGFR Tyrosine Kinase Inhibitor XVII, VEGFR2 Kinase Inhibitor XIV, PDGFR Tyrosine Kinase Inhibitor VIII
References
ReferencesHeryanto, B., et al. 2003. Reproduction 125, 334.
Sun, L., et al. 2003. J. Med. Chem. 46, 1116.
Liao, A.T., et al. 2002. Blood 100, 585.
Product Information
CAS number326914-10-7
ATP CompetitiveY
FormOrange powder
Hill FormulaC₂₂H₂₇ClN₄O₂
Chemical formulaC₂₂H₂₇ClN₄O₂
ReversibleY
Structure formula ImageStructure formula Image
Quality LevelMQ100
Applications
Biological Information
Primary TargetPDGFRB
Primary Target IC<sub>50</sub>3 nM, 27 nM, 170 nM against PDGFRβ, VEGFR2, and FGFR1, respectively
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 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
572660-500UGCN 04055977266320

Documentation

SU11652 - CAS 326914-10-7 - Calbiochem MSDS

职位

物料安全数据表 (MSDS) 

SU11652 - CAS 326914-10-7 - Calbiochem 分析证书

标题批号
572660

参考

参考信息概述
Heryanto, B., et al. 2003. Reproduction 125, 334.
Sun, L., et al. 2003. J. Med. Chem. 46, 1116.
Liao, A.T., et al. 2002. Blood 100, 585.
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.

Revision24-September-2010 JSW
Synonyms5-[(Z)-(5-Chloro-2-oxo-1,2-dihydro-3H-indol-3-ylidene)methyl]-N-[2-(diethylamino)ethyl]-2,4-dimethyl-1H-pyrrole-3-carboxamide, VEGFR Tyrosine Kinase Inhibitor XVII, VEGFR2 Kinase Inhibitor XIV, PDGFR Tyrosine Kinase Inhibitor VIII
DescriptionA cell-permeable, potent, reversible, and ATP-competitive inhibitor of tyrosine kinase activity of PDGFRβ (IC50 = 3 nM), VEGFR2 (IC50 = 27 nM), FGFR1 (IC50 = 170 nM), and Kit family members (IC50 ~10-500 nM). Does not effect the activity of EGFR (IC50 >20 µM). Reported to display anti-proliferative, antiangiogenic and pro-apoptotic properties in tumor cells.
FormOrange powder
Intert gas (Yes/No) Packaged under inert gas
CAS number326914-10-7
Chemical formulaC₂₂H₂₇ClN₄O₂
Structure formulaStructure formula
Purity≥95% by HPLC
SolubilityDMSO (4 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 6 months at -20°C.
Toxicity Standard Handling
ReferencesHeryanto, B., et al. 2003. Reproduction 125, 334.
Sun, L., et al. 2003. J. Med. Chem. 46, 1116.
Liao, A.T., et al. 2002. Blood 100, 585.