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GW441756
本产品不向个人销售,仅用作科学研究,不用于任何人体实验及非科研性质的动物实验。
GW441756图片
CAS NO:504433-23-2
规格:≥98%
包装与价格:
包装价格(元)
5mg询价
10mg询价
25mg询价
50mg询价
100mg询价
250mg询价
500mg询价

理化性质和储存条件
Molecular Weight (MW)275.3
FormulaC17H13N3O
CAS No.504433-23-2
Storage-20℃ for 3 years in powder form
-80℃ for 2 years in solvent
Solubility (In vitro)DMSO: 25 mg/mL (90.8 mM)
Water: <1 mg/mL
Ethanol: <1 mg/mL
Other infoChemical Name: 1,3-dihydro-3-[(1-methyl-1H-indol-3-yl)methylene]-2H-pyrrolo[3,2-b]pyridin-2-one
InChi Key: NXNQLECPAXXYTR-LCYFTJDESA-N
InChi Code: InChI=1S/C17H13N3O/c1-20-10-11(12-5-2-3-7-15(12)20)9-13-16-14(19-17(13)21)6-4-8-18-16/h2-10H,1H3,(H,19,21)/b13-9-
SMILES Code: O=C1/C(C2=NC=CC=C2N1)=C\C3=CN(C)C4=C3C=CC=C4
SynonymsGW 441756; GW441756; GW-441756
实验参考方法
In Vitro

In vitro activity: GW441756 can specifically block TrkA-induced cell death in a dose-dependent manner. GW441756 can block TrkA-mediated γH2AX production and apoptosis in TrkA-overexpressing cells.


Kinase Assay: GW 441756 is a specific Tropomyosin-related kinase A (TrkA) inhibitor with an IC50 value of 2 nM; little activity to c-Raf1 and CDK2. IC50 Value: 2 nM.


Cell Assay: GW441756 specifically blocked TrkA-induced cell death in a dose-dependent manner, but there was no effect in uninduced cells. TrkA ability to induce γH2AX production was significantly downregulated by both K-252a and GW441756 in the absence of DNA damage inducer. In addition, it was also suppressed by K-252a during DNA damage by doxorubicin treatment, but not by GW441756

In Vivo
Animal model
Formulation & Dosage
ReferencesBioorg Med Chem Lett. 2004 Feb 23;14(4):953-7.
 
 
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