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Merck
CN

SML1991

Sigma-Aldrich

PS432

≥98% (HPLC)

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别名:
2-[5-(4-chlorophenyl)-2-furanyl]-2,5-dihydro-4-hydroxy-1-(6-methyl-2-benzothiazolyl)-5-oxo-1H-pyrrole-3-carboxylic acid ethyl ester
经验公式(希尔记法):
C25H19ClN2O5S
分子量:
494.95
UNSPSC代码:
12352200
NACRES:
NA.77

检测方案

≥98% (HPLC)

颜色

white to beige

溶解性

DMSO: 2 mg/mL, clear

运输

ambient

储存温度

2-8°C

SMILES字符串

O=C1C(O)=C(C(OCC)=O)C(C2=CC=C(C3=CC=C(Cl)C=C3)O2)N1C4=NC(C=CC(C)=C5)=C5S4

生化/生理作用

PS432 is an allosteric inhibitor of Protein Kinase C (PKC) that targets regulatory site (PIF-pocket) present in the kinase domain. PS432 potently inhibits non-small cell lung cancer cells proliferation and tumor growth without side effects in a mouse xenograft model.

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Jose M Arencibia et al.
ACS chemical biology, 12(2), 564-573 (2017-01-04)
There is a current and pressing need for improved cancer therapies. The use of small molecule kinase inhibitors and their application in combinatorial regimens represent an approach to personalized targeted cancer therapy. A number of AGC kinases, including atypical Protein

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