Reaction Details |
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Target | 17-beta-hydroxysteroid dehydrogenase type 3 |
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Ligand | BDBM17639 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_1510493 (CHEMBL3607519) |
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IC50 | 90±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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BDBM17639 |
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n/a |
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Name | BDBM17639 |
Synonyms: | (1S,2S,5R,7S,10R,11S,15S)-5-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadecan-14-one | Androsterone | CHEMBL87285 |
Type | Steroid |
Emp. Form. | C19H30O2 |
Mol. Mass. | 290.4403 |
SMILES | [H][C@@]12CCC(=O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CC[C@@]2([H])C[C@H](O)CC[C@]12C |
Structure |
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