MEK抑制剂I结构式
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常用名 | MEK抑制剂I | 英文名 | MEK Inhibitor I |
|---|---|---|---|---|
| CAS号 | 297744-42-4 | 分子量 | 374.459 | |
| 密度 | 1.4±0.1 g/cm3 | 沸点 | 671.9±55.0 °C at 760 mmHg | |
| 分子式 | C21H18N4OS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | 360.2±31.5 °C |
MEK抑制剂I用途MEK-IN-4是MEK抑制剂。MEK-IN-4可用于炎症性疾病和癌症的研究[1]。 |
| 中文名 | MEK抑制剂I |
|---|---|
| 英文名 | MEK Inhibitor I |
| 英文别名 | 更多 |
| 描述 | MEK-IN-4是MEK抑制剂。MEK-IN-4可用于炎症性疾病和癌症的研究[1]。 |
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| 相关类别 | |
| 参考文献 |
[1]. Frank W. Hobbs, et al. Amino-thio-acrylonitriles as mek inhibitors. Patent. WO2000056706A1. |
| 密度 | 1.4±0.1 g/cm3 |
|---|---|
| 沸点 | 671.9±55.0 °C at 760 mmHg |
| 分子式 | C21H18N4OS |
| 分子量 | 374.459 |
| 闪点 | 360.2±31.5 °C |
| 精确质量 | 374.120117 |
| LogP | -0.11 |
| InChIKey | NHBMKTBZZSJUGA-FXBPSFAMSA-N |
| SMILES | N#CC(=C(N)Sc1ccccc1N)c1cccc(C(O)c2ccncc2)c1 |
| 蒸汽压 | 0.0±2.2 mmHg at 25°C |
| 折射率 | 1.727 |
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实验名称:Inhibitory concentration against AP-1 transcription in COS-7 cells
来源:ChEMBL
靶标:COS-7
External Id:CHEMBL838885
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实验名称:In vivo effective dose against TPA-induced ear edema in mouse upon intraperitoneal ad...
来源:ChEMBL
靶标:Mus musculus
External Id:CHEMBL736780
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实验名称:Discovery of Small Molecules to Inhibit Human Cytomegalovirus Nuclear Egress
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:HCMV UL50
External Id:HMS1262
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实验名称:Human mitogen-activated protein kinase kinase 1 (STE7 family)
来源:IUPHAR-DB
靶标:mitogen-activated protein kinase kinase 1 (STE7 family) [Homo sapiens]
External Id:2062_Human
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实验名称:Inhibitory potency against mitogen activated protein kinase kinase 1
来源:ChEMBL
靶标:Dual specificity mitogen-activated protein kinase kinase 1
External Id:CHEMBL729500
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| MEK Inhibitor I |
| (2Z)-3-Amino-3-[(2-aminophenyl)sulfanyl]-2-{3-[hydroxy(4-pyridinyl)methyl]phenyl}acrylonitrile |
| (2Z)-3-amino-3-[(2-aminophenyl)sulfanyl]-2-{3-[hydroxy(pyridin-4-yl)methyl]phenyl}prop-2-enenitrile |