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TH287

更新时间:2025-08-25 17:37:12

TH287结构式
TH287结构式
品牌特惠专场
常用名 TH287 英文名 TH287
CAS号 1609960-30-6 分子量 269.130
密度 1.4±0.1 g/cm3 沸点 512.2±60.0 °C at 760 mmHg
分子式 C11H10Cl2N4 熔点 N/A
MSDS N/A 闪点 263.5±32.9 °C

 TH287用途


TH287是MTH1 (NUDT1)高效选择性抑制剂,IC50值0.8nM,对MTH2, NUDT5, NUDT12, NUDT14等抑制力弱。

 TH287名称

中文名 TH287
英文名 th287
英文别名 更多

 TH287生物活性

描述 TH287是MTH1 (NUDT1)高效选择性抑制剂,IC50值0.8nM,对MTH2, NUDT5, NUDT12, NUDT14等抑制力弱。
相关类别
参考文献

[1]. Gad H, et al. MTH1 inhibition eradicates cancer by preventing sanitation of the dNTP pool. Nature. 2014 Apr 10;508(7495):215-21.

 TH287物理化学性质

密度 1.4±0.1 g/cm3
沸点 512.2±60.0 °C at 760 mmHg
分子式 C11H10Cl2N4
分子量 269.130
闪点 263.5±32.9 °C
精确质量 268.028259
PSA 37.81000
LogP 3.48
InChIKey URWCXPXBBITYLR-UHFFFAOYSA-N
SMILES CNc1cc(-c2cccc(Cl)c2Cl)nc(N)n1
外观性状 white solid
蒸汽压 0.0±1.3 mmHg at 25°C
折射率 1.681
储存条件 2-8℃

 TH287靶点实验

查看更多实验

实验名称:Drug screen in LFS_MB_P medulloblastoma cells to determine synergistic drug combinati...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_LFS_MB_P
实验名称:Drug screen in ICB984 medulloblastoma cells to determine synergistic drug combination...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_ICB984_MB
实验名称:Drug screen in HDN33 neuroblastoma cells to determine synergistic drug combinations t...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_HDN33
实验名称:Drug screen in HD-MB03 medulloblastoma cells to determine synergistic drug combinatio...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_HD-MB03
实验名称:Experimentally measured binding affinity data (IC50) for protein-ligand complexes der...
来源:Shanghai Institute of Organic Chemistry
靶标:N/A
External Id:PDBbind-IC50 for protein-ligand complexes
实验名称:Drug screen in CRL2098 osteosarcoma cells to determine synergistic drug combinations ...
来源:25008
靶标:N/A
External Id:DKFZ_drug_screen_chromothripsis_CRL2098
实验名称:Inhibition of MTH1 in human U2OS cell lysates assessed as hydrolysis of 8-oxodGTP to ...
来源:ChEMBL
靶标:Oxidized purine nucleoside triphosphate hydrolase
External Id:CHEMBL3783609
实验名称:Binding affinity to recombinant C-terminal 6xHis-tagged MTH1 (3 to 156 residues) (unk...
来源:ChEMBL
靶标:Oxidized purine nucleoside triphosphate hydrolase
External Id:CHEMBL4339322
实验名称:Inhibition of MTH1 in human U2OS cells assessed as hydrolysis of 8-oxodGTP to 8-oxodG...
来源:ChEMBL
靶标:Oxidized purine nucleoside triphosphate hydrolase
External Id:CHEMBL3783608
实验名称:Cytotoxicity against human U2OS cells assessed as reduction in cell viability incubat...
来源:ChEMBL
靶标:U2OS
External Id:CHEMBL4345256
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 TH287英文别名

6-(2,3-dichlorophenyl)-N4-methylpyrimidine-2,4-diamine
6-(2,3-Dichlorophenyl)-N-methyl-2,4-pyrimidinediamine
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