Reaction Details |
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Target | Putative nitroreductase |
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Ligand | BDBM50520024 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1878864 (CHEMBL4380258) |
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Ki | 283±n/a nM |
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Citation | Tokay, E; Güngör, T; Hac?o?lu, N; Önder, FC; Gülhan, ÜG; Tok, TT; Çelik, A; Ay, M; Köçkar, F Prodrugs for nitroreductase-based cancer therapy-3: Antitumor activity of the novel dinitroaniline prodrugs/Ssap-NtrB enzyme suicide gene system: Synthesis, in vitro and in silico evaluation in prostate cancer. Eur J Med Chem187:0 (2020) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Putative nitroreductase |
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Name: | Putative nitroreductase |
Synonyms: | Putative nitroreductase |
Type: | PROTEIN |
Mol. Mass.: | 23400.09 |
Organism: | Staphylococcus saprophyticus subsp. saprophyticus (strain ATCC 15305 / DSM20229 / NCIMB 8711 / NCTC 7292 / S-41) |
Description: | ChEMBL_119673 |
Residue: | 208 |
Sequence: | MINNNFEEILMNRKSVKVFDEQVKIPKAEMDEMIKKATTAPSSVNMQPWRFLVVESDEGK
DTLRPLIRFNTRQNDSSAAMVVIFGDMKSQTNAEEIYGNAVKHDLMPEEVKQEMLKKVIP
LYDNAPKEQMNDIVKIDSSLAAMQFMLVAKAHGYDTNPIGGFESDQIADAFGIDSERYVP
VLIVAIGKAKNPAHGSYRLPTETVTKYV
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BDBM50520024 |
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n/a |
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Name | BDBM50520024 |
Synonyms: | CHEMBL4564160 |
Type | Small organic molecule |
Emp. Form. | C14H12N6O8 |
Mol. Mass. | 392.2805 |
SMILES | [O-][N+](=O)c1ccc(NCCNc2ccc(cc2[N+]([O-])=O)[N+]([O-])=O)c(c1)[N+]([O-])=O |
Structure |
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