PfGSK3/PfPK6-IN-2结构式
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常用名 | PfGSK3/PfPK6-IN-2 | 英文名 | PfGSK3/PfPK6-IN-2 |
|---|---|---|---|---|
| CAS号 | 2797225-47-7 | 分子量 | 502.46 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C24H25Cl2N5OS | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
PfGSK3/PfPK6-IN-2用途PfGSK3/PfPK6-IN-2是一种有效的双PfGSK2/PfPK6(恶性疟原虫GSK3/PK6)抑制剂(IC50:172nM和11nM)。PfGSK3/PfPK6-IN-2可用于疟疾研究[1]。 |
| 英文名 | PfGSK3/PfPK6-IN-2 |
|---|
| 描述 | PfGSK3/PfPK6-IN-2是一种有效的双PfGSK2/PfPK6(恶性疟原虫GSK3/PK6)抑制剂(IC50:172nM和11nM)。PfGSK3/PfPK6-IN-2可用于疟疾研究[1]。 |
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| 相关类别 | |
| 靶点实验 |
Plasmodium falciparum GSK3/PK6 (PfGSK3/PfPK6)[1] |
| 体外研究 | PfGSK3/PfPK6-IN-2(化合物23d)抑制红细胞中恶性疟原虫3D7负载(EC50:552nM)[1]。PfGSK3/PfPK6-IN-2(2μM)显示出对HepG2细胞的细胞毒性[1]。 |
| 分子式 | C24H25Cl2N5OS |
|---|---|
| 分子量 | 502.46 |
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实验名称:Selectivity index, ratio of CC50 for human HepG2 cells to EC50 for Plasmodium berghei
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5107055
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实验名称:Kinetic solubility of the compound in PBS buffer at pH 7.4
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5107051
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实验名称:Cytotoxicity against human HepG2 cells assessed as reduction in cell viability at 200...
来源:ChEMBL
靶标:HepG2
External Id:CHEMBL5107046
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实验名称:Cytotoxicity against human HepG2 cells assessed as reduction in cell viability at 2 u...
来源:ChEMBL
靶标:HepG2
External Id:CHEMBL5107047
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实验名称:Antiplasmodial activity against Plasmodium falciparum 3D7 infected in human erythrocy...
来源:ChEMBL
靶标:Plasmodium falciparum
External Id:CHEMBL5107048
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实验名称:Inhibition of Plasmodium falciparum GSK3 measured after 2 hrs by luciferin-based lumi...
来源:ChEMBL
靶标:Glycogen synthase kinase 3
External Id:CHEMBL5107042
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实验名称:Inhibition of Plasmodium falciparum PK6 measured after 2 hrs by luciferin-based lumin...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL5107043
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