Inhibitors | Comment | Organism | Structure |
---|---|---|---|
(2S,3R)-5-hydroxy-2-(4-hydroxy-3-methoxyphenyl)-3-(hydroxymethyl)-8-phenyl-2,3,8,9-tetrahydro-10H-[1,4]dioxino[2,3-f]chromen-10-one | - |
Homo sapiens | |
1-(alpha-L-idopyranosyl)-N-(2-methylbenzoyl)-5-(methylsulfanyl)-1H-1,2,4-triazol-3-amine | - |
Homo sapiens | |
1-[2-(dimethylamino)ethyl]-3-[(4-methylphenyl)sulfonyl]-1H-pyrrolo[2,3-b]quinoxalin-2-amine | - |
Homo sapiens | |
3-amino-4-chloro-9,10-dioxo-9,10-dihydroanthracene-2-sulfonic acid | - |
Homo sapiens | |
4-(2-hydroxyethyl)-6-([2-[(2-hydroxyethyl)amino]ethyl]amino)-1,2,3,4-tetrahydronaphtho[2,3-f]quinoxaline-7,12-dione | - |
Homo sapiens | |
4-chloro-N-[5-imino-1-(quinoxalin-2-yl)-2,5-dihydro-1H-1,2,4-triazol-3-yl]-5-methyl-2-sulfanylbenzenesulfonamide | - |
Homo sapiens | |
4-[[(6-amino-3-methylpyrido[2,3-b]pyrazin-8-yl)amino]methyl]benzenesulfonamide | - |
Homo sapiens | |
6-[(2-chlorobenzyl)sulfanyl]-9-(beta-L-ribofuranosyl)-9H-purin-2-amine | - |
Homo sapiens | |
8-bromo-9-cyano-7-(alpha-L-xylofuranosyl)-3,7-dihydroimidazo[1,2-c]pyrrolo[3,2-e]pyrimidin-4-ium | - |
Homo sapiens | |
camptothecin | - |
Homo sapiens | |
irinotecan | - |
Homo sapiens | |
methyl [[5-carbamoyl-6-(methylsulfanyl)-4-oxo-3-phenyl-4,7-dihydro-3H-pyrrolo[2,3-d]pyrimidin-2-yl]sulfanyl]acetate | - |
Homo sapiens | |
additional information | inhibitor design and evaluation, DNA cleavage inhibition and cytotoxic activities, docking study, overview | Homo sapiens | |
N-[9-acetyl-6-(benzylsulfanyl)-9H-purin-2-yl]acetamide | - |
Homo sapiens | |
topotecan | - |
Homo sapiens |
Organism | UniProt | Comment | Textmining |
---|---|---|---|
Homo sapiens | - |
- |
- |
Synonyms | Comment | Organism |
---|---|---|
DNA topoisomerase I | - |
Homo sapiens |
Top1 | - |
Homo sapiens |