3-Pyridinecarbonitrile, 1,2-dihydro-6-hydroxy-4-methyl-2-oxo结构式
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常用名 | 3-Pyridinecarbonitrile, 1,2-dihydro-6-hydroxy-4-methyl-2-oxo | 英文名 | 3-Pyridinecarbonitrile, 1,2-dihydro-6-hydroxy-4-methyl-2-oxo |
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| CAS号 | 40401-47-6 | 分子量 | 150.13 | |
| 密度 | N/A | 沸点 | N/A | |
| 分子式 | C7H6N2O2 | 熔点 | N/A | |
| MSDS | N/A | 闪点 | N/A |
| 英文名 | 3-Pyridinecarbonitrile, 1,2-dihydro-6-hydroxy-4-methyl-2-oxo |
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| 分子式 | C7H6N2O2 |
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| 分子量 | 150.13 |
| InChIKey | YRGYYQCOWUULNF-UHFFFAOYSA-N |
| SMILES | CC1=CC(=O)NC(=C1C#N)O |
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实验名称:Inhibition of human recombinant UP1 expressed in Escherichia coli Rosetta (DE3) using...
来源:ChEMBL
靶标:Uridine phosphorylase 1
External Id:CHEMBL3090767
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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:Screen for inhibitors of RMI FANCM (MM2) intereaction
来源:11908
靶标:N/A
External Id:RMI-FANCM-MM2
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实验名称:A screen for compounds that inhibit the activity of LtaS in Staphylococcus aureus
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
External Id:HMS979
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实验名称:Potentiation of 5-FU-induced cytotoxicity against human SW620 cells assessed as reduc...
来源:ChEMBL
靶标:SW-620
External Id:CHEMBL3090517
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实验名称:Stabilization of p53 in human papillomavirus-positive cells
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Cellular tumor antigen p53
External Id:HMS1485
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实验名称:Potentiation of 5-FU-induced cytotoxicity against human HT-29 cells assessed as reduc...
来源:ChEMBL
靶标:HT-29
External Id:CHEMBL3090749
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实验名称:A screen for compounds that inhibit viral RNA polymerase binding and polymerization a...
来源:ICCB-Longwood/NSRB Screening Facility, Harvard Medical School
靶标:Chain A, Poliovirus Polymerase With Gtp
External Id:HMS750
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实验名称:Discovering small molecule activators of G protein-gated inwardly-rectifying potassiu...
来源:15621
靶标:G protein-activated inward rectifier potassium channel 2
External Id:VANDERBILT_HTS_GIRK2_HPP
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实验名称:Effect on 5-FU-induced cytotoxicity against human HaCaT cells at 30 uM after 72 hrs b...
来源:ChEMBL
靶标:HaCaT
External Id:CHEMBL3090750
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