Reaction Details |
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Target | Thiosulfate sulfurtransferase |
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Ligand | BDBM50571158 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_2114020 (CHEMBL4822870) |
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IC50 | >100000±n/a nM |
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Citation | Ray, AM; Salim, N; Stevens, M; Chitre, S; Abdeen, S; Washburn, A; Sivinski, J; O'Hagan, HM; Chapman, E; Johnson, SM Exploiting the HSP60/10 chaperonin system as a chemotherapeutic target for colorectal cancer. Bioorg Med Chem40:0 (2021) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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Thiosulfate sulfurtransferase |
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Name: | Thiosulfate sulfurtransferase |
Synonyms: | 2.8.1.1 | Rhodanese | THTR_HUMAN | TST | Thiosulfate sulfurtransferase |
Type: | PROTEIN |
Mol. Mass.: | 33432.06 |
Organism: | Homo sapiens |
Description: | ChEMBL_118080 |
Residue: | 297 |
Sequence: | MVHQVLYRALVSTKWLAESIRTGKLGPGLRVLDASWYSPGTREARKEYLERHVPGASFFD
IEECRDTASPYEMMLPSEAGFAEYVGRLGISNHTHVVVYDGEHLGSFYAPRVWWMFRVFG
HRTVSVLNGGFRNWLKEGHPVTSEPSRPEPAVFKATLDRSLLKTYEQVLENLESKRFQLV
DSRSQGRFLGTEPEPDAVGLDSGHIRGAVNMPFMDFLTEDGFEKGPEELRALFQTKKVDL
SQPLIATCRKGVTACHVALAAYLCGKPDVAVYDGSWSEWFRRAPPESRVSQGKSEKA
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BDBM50571158 |
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n/a |
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Name | BDBM50571158 |
Synonyms: | CHEMBL4855678 |
Type | Small organic molecule |
Emp. Form. | C28H22N4O7S |
Mol. Mass. | 558.562 |
SMILES | COc1ccc(cc1)S(=O)(=O)Nc1ccc2oc(nc2c1)-c1ccc(NC(=O)c2cccc(C)c2[N+]([O-])=O)cc1 |
Structure |
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