3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine结构式
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常用名 | 3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine | 英文名 | 3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine |
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| CAS号 | 2226941-29-1 | 分子量 | 480.51 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C28H24N4O4 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
用途3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine (Compound 7) 是一种蛋白激酶抑制剂,对 PKC-α、ROCK、ASK1 的 IC50 为 0.092, 0.26, 0.77 μM。3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine 对 PC-3 癌细胞具有有效的细胞毒性,IC50 值为 0.16 μM。 |
| 英文名 | 3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine |
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| 描述 | 3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine (Compound 7) 是一种蛋白激酶抑制剂,对 PKC-α、ROCK、ASK1 的 IC50 为 0.092, 0.26, 0.77 μM。3′-O-Demethyl-4′-N-demethyl-4′-N-acetyl-4′-epi-staurosporine 对 PC-3 癌细胞具有有效的细胞毒性,IC50 值为 0.16 μM。 |
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| 参考文献 |
| 分子式 | C28H24N4O4 |
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| 分子量 | 480.51 |
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实验名称:Inhibition of N-terminal His10-StrepII tagged human ROCK2 catalytic domain (1 to 553 ...
来源:ChEMBL
靶标:Rho-associated protein kinase 2
External Id:CHEMBL5387668
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来源:ChEMBL
靶标:Protein kinase C alpha type
External Id:CHEMBL4256095
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来源:ChEMBL
靶标:PC-3
External Id:CHEMBL4256094
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来源:ChEMBL
靶标:Protein kinase C theta type
External Id:CHEMBL4672563
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实验名称:Inhibition of ASK1 (unknown origin) by HTRF assay
来源:ChEMBL
靶标:Mitogen-activated protein kinase kinase kinase 5
External Id:CHEMBL4256097
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实验名称:Inhibition of ROCK2 (unknown origin) by HTRF assay
来源:ChEMBL
靶标:Rho-associated protein kinase 2
External Id:CHEMBL4256096
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实验名称:Inhibition of PKCtheta (unknown origin) at 2.5 ug/ml by HTRF assay relative to contro...
来源:ChEMBL
靶标:Protein kinase C theta type
External Id:CHEMBL4672562
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