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Merck
CN

SML2213

Sigma-Aldrich

CPI-637

≥98% (HPLC)

别名:

(4R)-1,3,4,5-Tetrahydro-4-methyl-6-[1-methyl-3-(1-methyl-1H-pyrazol-4-yl)-1H-indazol-5-yl]-2H-1,5-benzodiazepin-2-one, (4R)-4-Methyl-6-[1-methyl-3-(1-methylpyrazol-4-yl)indazol-5-yl]-1,3,4,5-tetrahydro-1,5-benzodiazepin-2-one, 2H-1,5-Benzodiazepin-2-one, 1,3,4,5-tetrahydro-4-methyl-6-[1-methyl-3-(1-methyl-1H-pyrazol-4-yl)-1H-indazol-5-yl]-, (4R)-, CPI 637

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About This Item

经验公式(希尔记法):
C22H22N6O
分子量:
386.45
MDL编号:
UNSPSC代码:
12352200
NACRES:
NA.77

方案

≥98% (HPLC)

表单

powder

旋光性

[α]/D -39 to -49°, c = 1.0 in chloroform-d

颜色

white to beige

溶解性

DMSO: 2 mg/mL, clear

储存温度

−20°C

SMILES字符串

[n]1(ncc(c1)c2n[n](c3c2cc(cc3)c4c5c(ccc4)NC(=O)C[C@H](N5)C)C)C

InChI

1S/C22H22N6O/c1-13-9-20(29)25-18-6-4-5-16(22(18)24-13)14-7-8-19-17(10-14)21(26-28(19)3)15-11-23-27(2)12-15/h4-8,10-13,24H,9H2,1-3H3,(H,25,29)/t13-/m1/s1

InChI key

BFTKDWYIRJGJCA-CYBMUJFWSA-N

生化/生理作用

CBP/p300 Bromodomain inhibitor
CPI-637 is a cell penetrant, selective and potent CBP/p300 bromodomain inhibitor.

储存分类代码

11 - Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Alexander M Taylor et al.
ACS medicinal chemistry letters, 7(5), 531-536 (2016-05-18)
CBP and EP300 are highly homologous, bromodomain-containing transcription coactivators involved in numerous cellular pathways relevant to oncology. As part of our effort to explore the potential therapeutic implications of selectively targeting bromodomains, we set out to identify a CBP/EP300 bromodomain
Terry D Crawford et al.
Journal of medicinal chemistry, 59(23), 10549-10563 (2016-09-30)
The single bromodomain of the closely related transcriptional regulators CBP/EP300 is a target of much recent interest in cancer and immune system regulation. A co-crystal structure of a ligand-efficient screening hit and the CBP bromodomain guided initial design targeting the

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