Reaction Details |
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Target | 17-beta-hydroxysteroid dehydrogenase type 3 |
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Ligand | BDBM50111763 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1510493 (CHEMBL3607519) |
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IC50 | 28±n/a nM |
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Citation | Djigoué, GB; Kenmogne, LC; Roy, J; Maltais, R; Poirier, D Design, chemical synthesis and biological evaluation of 3-spiromorpholinone/3-spirocarbamate androsterone derivatives as inhibitors of 17ß-hydroxysteroid dehydrogenase type 3. Bioorg Med Chem23:5433-51 (2015) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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17-beta-hydroxysteroid dehydrogenase type 3 |
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Name: | 17-beta-hydroxysteroid dehydrogenase type 3 |
Synonyms: | DHB3_RAT | Edh17b3 | Hsd17b3 | Testosterone 17-beta-dehydrogenase 3 |
Type: | PROTEIN |
Mol. Mass.: | 34235.73 |
Organism: | Rattus norvegicus |
Description: | ChEMBL_1510493 |
Residue: | 306 |
Sequence: | MEQFLLSVGLLVCLVCLVKCVRFSRYLFLSFCKALPGSFLRSMGQWAVITGAGDGIGKAY
SFELARHGLNVVLISRTLEKLQVISEEIERTTGSRVKVVQADFTREDIYDHIEEQLKGLE
IGVLVNNVGMLPNLLPSHFLSTSGESQSVIHCNITSVVKMTQLVLKHMESRRRGLILNIS
SGVGVRPWPLYSLYSASKAFVCTFSKALNVEYRDKGIIIQVLTPYSVSTPMTKYLNTSRV
TKTADEFVKESLKYVTIGAETCGCLAHEILAIILNLIPSRIFYSSTTQRFLLKQFSDYLK
SNISNR
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BDBM50111763 |
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n/a |
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Name | BDBM50111763 |
Synonyms: | CHEMBL3605211 |
Type | Small organic molecule |
Emp. Form. | C29H36F3NO5S |
Mol. Mass. | 567.66 |
SMILES | [H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@]3(CC[C@]12C)CN(CC(=O)O3)S(=O)(=O)c1ccc(cc1)C(F)(F)F |r| |
Structure |
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