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Cdk2/9抑制剂

更新时间:2025-08-25 11:50:28

Cdk2/9抑制剂结构式
Cdk2/9抑制剂结构式
品牌特惠专场
常用名 Cdk2/9抑制剂 英文名 CK7
CAS号 507487-89-0 分子量 328.34900
密度 N/A 沸点 N/A
分子式 C14H12N6O2S 熔点 N/A
MSDS N/A 闪点 N/A

 Cdk2/9抑制剂用途


CK7是一种Cdk2/9抑制剂,可用于合成Nek1抑制剂BSc5231和BSc5367[1]。

 Cdk2/9抑制剂名称

中文名 Cdk2/9抑制剂
英文名 4-methyl-5-[2-(3-nitroanilino)pyrimidin-4-yl]-1,3-thiazol-2-amine
英文别名 更多

 Cdk2/9抑制剂物理化学性质

分子式 C14H12N6O2S
分子量 328.34900
精确质量 328.07400
PSA 151.51000
LogP 3.66880
InChIKey DYTKVFHLKPDNRW-UHFFFAOYSA-N
SMILES Cc1nc(N)sc1-c1ccnc(Nc2cccc([N+](=O)[O-])c2)n1

 Cdk2/9抑制剂合成线路

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Cdk2/9抑制剂结构式

Cdk2/9抑制剂

507487-89-0

文献:Wang, Shudong; Meades, Christopher; Wood, Gavin; Osnowski, Andrew; Anderson, Sian; Yuill, Rhoda; Thomas, Mark; Mezna, Mokdad; Jackson, Wayne; Midgley, Carol; Griffiths, Gary; Fleming, Ian; Green, Simon; McNae, Iain; Wu, Su-Ying; McInnes, Campbell; Zheleva, Daniella; Walkinshaw, Malcolm D.; Fischer, Peter M. Journal of Medicinal Chemistry, 2004 , vol. 47, # 7 p. 1662 - 1675

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Cdk2/9抑制剂结构式

Cdk2/9抑制剂

507487-89-0

文献:Wang, Shudong; Midgley, Carol A.; Scaerou, Frederic; Grabarek, Joanna B.; Griffiths, Gary; Jackson, Wayne; Kontopidis, George; McClue, Steven J.; McInnes, Campbell; Meades, Christopher; Mezna, Mokdad; Plater, Andy; Stuart, Iain; Thomas, Mark P.; Wood, Gavin; Clarke, Rosemary G.; Blake, David G.; Zheleva, Daniella I.; Lane, David P.; Jackson, Robert C.; Glover, David M.; Fischer, Peter M. Journal of Medicinal Chemistry, 2010 , vol. 53, # 11 p. 4367 - 4378

 Cdk2/9抑制剂上下游产品

Cdk2/9抑制剂上游产品  2

Cdk2/9抑制剂下游产品  0

 Cdk2/9抑制剂靶点实验

查看更多实验

实验名称:Selectivity ratio of Ki for human recombinant Aurora B to Ki for CDK9
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1119873
实验名称:Selectivity ratio of Ki for human recombinant Aurora B to Ki for CDK2
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1119872
实验名称:Selectivity ratio of Ki for human recombinant Aurora A to Ki for CDK9
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1119871
实验名称:Selectivity ratio of Ki for human recombinant Aurora A to Ki for CDK2
来源:ChEMBL
靶标:N/A
External Id:CHEMBL1119488
实验名称:CDK Kinase Inhibition Assay from Article 10.1021/jm0309957: "2-Anilino-4-(thiazol-5-y...
来源:BindingDB
靶标:N/A
External Id:BindingDB_1010_1
实验名称:Cytotoxicity against human MIAPaCa2 cells after 96 hrs by MTT assay
来源:ChEMBL
靶标:MIA PaCa-2
External Id:CHEMBL1119486
实验名称:Cytotoxicity against human A2780 cells after 96 hrs by MTT assay
来源:ChEMBL
靶标:A2780
External Id:CHEMBL1119485
实验名称:Inhibition of Cdk2/ cyclin E
来源:ChEMBL
靶标:N/A
External Id:CHEMBL936788
实验名称:Delta TM value showing the stabilisation of CAMK2G produced by compound binding
来源:ChEMBL
靶标:Calcium/calmodulin-dependent protein kinase type II subunit gamma
External Id:CHEMBL3430795
实验名称:Delta TM value showing the stabilisation of CAMK4 produced by compound binding
来源:ChEMBL
靶标:Calcium/calmodulin-dependent protein kinase type IV
External Id:CHEMBL3430796
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 Cdk2/9抑制剂英文别名

2wev
CK7
2c5p
1pxo
Cdk2/9 Inhibitor
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