(3S)-3-Methyl-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one

• 常用名: (3S)-3-Methyl-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one
• 英文名: (3S)-3-Methyl-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one
• CAS号: 62492-80-2
• 分子量: 250.29
• 密度: N/A
• 沸点: N/A
• 分子式: C₁₆H₁₄N₂O
• 熔点: N/A
• 闪点: N/A

名称

• 英文名: (3S)-3-Methyl-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one

物理化学性质

• 分子式: C₁₆H₁₄N₂O
• 分子量: 250.29
• InChIKey: QFCQGJLUYWNOAC-NSHDSACASA-N
• SMILES: CC1N=C(c2ccccc2)c2ccccc2NC1=O

靶点实验

查看更多实验

实验名称：Antiproliferative activity against v-Src transformed mouse NIH 3T3 fibroblast at 150 ... 来源：ChEMBL 靶标：NON-PROTEIN TARGET External Id：CHEMBL892720

实验名称：Cytotoxicity against human A2058 cells after 72 hrs by WST-1 colorimetric test 来源：ChEMBL 靶标：A2058 External Id：CHEMBL892721

实验名称：Cytotoxicity against human HeLa cells after 72 hrs by WST-1 colorimetric test 来源：ChEMBL 靶标：HeLa External Id：CHEMBL892722

实验名称：Selectivity ratio of IC50 for human KDAC6 to IC50 for human KDAC1 来源：ChEMBL 靶标：N/A External Id：CHEMBL3998883

实验名称：Selectivity ratio of IC50 for human KDAC1 to IC50 for human KDAC3 来源：ChEMBL 靶标：N/A External Id：CHEMBL3998882

实验名称：Selectivity ratio of IC50 for human KDAC1 to IC50 for human KDAC8 来源：ChEMBL 靶标：N/A External Id：CHEMBL3998885

实验名称：Selectivity ratio of IC50 for human KDAC8 to IC50 for human KDAC1 来源：ChEMBL 靶标：N/A External Id：CHEMBL3998884

实验名称：Inhibition of human KDAC3 at 30 uM using FITC-labeled p53 acetylated peptide as subst... 来源：ChEMBL 靶标：Histone deacetylase 3 External Id：CHEMBL3998879

实验名称：Inhibition of Schistosoma mansoni KDAC8 using (FAM)-labeled peptide as substrate afte... 来源：ChEMBL 靶标：Histone deacetylase 8 External Id：CHEMBL4014727

实验名称：Inhibition of human KDAC6 at 30 uM using FITC-labeled histone H4 acetylated peptide a... 来源：ChEMBL 靶标：Histone deacetylase 6 External Id：CHEMBL3998878

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