TDP1 Inhibitor-2结构式
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常用名 | TDP1 Inhibitor-2 | 英文名 | TDP1 Inhibitor-2 |
|---|---|---|---|---|
| CAS号 | 859142-95-3 | 分子量 | 465.28 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C25H14Cl2O5 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
TDP1 Inhibitor-2用途TDP1抑制剂-2(化合物5)是TDP1(酪氨酸DNA磷酸二酯酶1)的有效抑制剂,IC50为99 nM。TDP1抑制剂-2也可以抑制SCAN1(伴有轴突神经病变的脊髓小脑共济失调综合征),IC50为3.5μM[1]。 |
| 英文名 | TDP1 Inhibitor-2 |
|---|
| 描述 | TDP1抑制剂-2(化合物5)是TDP1(酪氨酸DNA磷酸二酯酶1)的有效抑制剂,IC50为99 nM。TDP1抑制剂-2也可以抑制SCAN1(伴有轴突神经病变的脊髓小脑共济失调综合征),IC50为3.5μM[1]。 |
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| 相关类别 | |
| 靶点实验 |
IC50: 0.099 ± 0.044 μM (TDP1), 3.5 ± 2.3 μM (SCAN1)[1] |
| 体外研究 | TDP1抑制剂-2(化合物5)显示出强大的抗TDP1活性、低细胞毒性以及与Top1抗癌剂topotecan的协同作用[1]。 |
| 参考文献 |
| 分子式 | C25H14Cl2O5 |
|---|---|
| 分子量 | 465.28 |
| InChIKey | QEOYHBDGERTIQV-UHFFFAOYSA-N |
| SMILES | O=c1cc(-c2cc3ccccc3oc2=O)c2ccc(OCc3c(Cl)cccc3Cl)cc2o1 |
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实验名称:Cytotoxicity against human T98G cells at 1 uM after 72 hrs in presence of topotecan b...
来源:ChEMBL
靶标:T98G
External Id:CHEMBL4614270
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实验名称:Potentiation of topotecan-induced cytotoxicity against human A549 cells at 1 uM after...
来源:ChEMBL
靶标:A549
External Id:CHEMBL4614269
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实验名称:Potentiation of topotecan-induced cytotoxicity against human A549 cells assessed as c...
来源:ChEMBL
靶标:A549
External Id:CHEMBL4614272
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实验名称:Cytotoxicity against human WI38 cells at 1 uM after 72 hrs in presence of topotecan b...
来源:ChEMBL
靶标:WI-38
External Id:CHEMBL4614271
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实验名称:Inhibition of TDP1 (unknown origin) using 5'-(5,6 FAM-AAC GTC AGG GTC TTC C- BHQ1)-3'...
来源:ChEMBL
靶标:Tyrosyl-DNA phosphodiesterase 1
External Id:CHEMBL4614262
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实验名称:Inhibition of TDP1 SCAN1 mutant (unknown origin) using 5'-(5,6 FAM-AAC GTC AGG GTC TT...
来源:ChEMBL
靶标:N/A
External Id:CHEMBL4614263
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实验名称:Cytotoxicity against human A549 cells assessed as reduction in cell viability after 7...
来源:ChEMBL
靶标:A549
External Id:CHEMBL4614268
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