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Merck

SML2541

Sigma-Aldrich

JWG-071

≥98% (HPLC)

别名:

11-(sec-butyl)-2-((2-methoxy-4-(4-(4-methylpiperazin-1-yl)piperidine-1-carbonyl)phenyl)amino)-5-methyl-5,11-dihydro-6H-benzo[e]pyrimido[5,4-b][1,4]diazepin-6-one, 5,11-Dihydro-2-[[2-methoxy-4-[[4-(4-methyl-1-piperazinyl)-1-piperidinyl]carbonyl]phenyl]amino]-5-methyl-11-(1-methylpropyl)-6H-pyrimido[4,5-b][1,4]benzodiazepin-6-one

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About This Item

经验公式(希尔记法):
C34H44N8O3
分子量:
612.76
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77
价格与库存信息目前不能提供

方案

≥98% (HPLC)

表单

powder

颜色

white to beige

溶解性

DMSO: 2 mg/mL, clear

储存温度

2-8°C

SMILES字符串

N6(CCN(CC6)C)C1CCN(CC1)C(=O)c2cc(c(cc2)Nc3nc4[n](c5c([c]([n](c4cn3)C)=O)cccc5)C(CC)C)OC

InChI

1S/C34H44N8O3/c1-6-23(2)42-28-10-8-7-9-26(28)33(44)39(4)29-22-35-34(37-31(29)42)36-27-12-11-24(21-30(27)45-5)32(43)41-15-13-25(14-16-41)40-19-17-38(3)18-20-40/h7-12,21-23,25H,6,13-20H2,1-5H3,(H,35,36,37)

InChI key

ACWOMSOYIIVIRV-UHFFFAOYSA-N

生化/生理作用

JWG-071 is a selective inhibitor of ERK5 (MAPK7) and LRRK2 with an IC50 value of 88nM for ERK5 inhibition and 109 nM for LRRK2 inhibition.
Selective ERK5 (MAPK7) Inhibitor

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


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Jinhua Wang et al.
ACS chemical biology, 13(9), 2438-2448 (2018-08-14)
Bromodomains have been pursued intensively over the past several years as emerging targets for the development of anticancer and anti-inflammatory agents. It has recently been shown that some kinase inhibitors are able to potently inhibit the bromodomains of BRD4. The

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