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Target3-oxo-5-alpha-steroid 4-dehydrogenase 1/2
LigandBDBM8885
Substrate/Competitorn/a
Meas. Tech.ChEMBL_204598 (CHEMBL813360)
IC50 1900±n/a nM
Citation Rasmusson, GHReynolds, GFSteinberg, NGWalton, EPatel, GFLiang, TCascieri, MACheung, AHBrooks, JRBerman, C Azasteroids: structure-activity relationships for inhibition of 5 alpha-reductase and of androgen receptor binding. J Med Chem29:2298-315 (1986) [PubMed]
More Info.:Get all data from this article,  Assay Method
 
3-oxo-5-alpha-steroid 4-dehydrogenase 1/2
Name:3-oxo-5-alpha-steroid 4-dehydrogenase 1/2
Synonyms:Steroid 5-alpha-reductase
Type:n/a
Mol. Mass.:n/a
Description:ASSAY_ID of ChEMBL is 204723
Components:This complex has 2 components.
Component 1
Name:3-oxo-5-alpha-steroid 4-dehydrogenase 1
Synonyms:S5A1_RAT | Srd5a1 | Steroid 5-alpha-reductase | Steroid 5-alpha-reductase 1
Type:PROTEIN
Mol. Mass.:29788.29
Organism:Rattus norvegicus
Description:ChEMBL_1441437
Residue:259
Sequence:
MVPLMELDELCLLDMLVYLEGFMAFVSIVGLRSVGSPYGRYSPQWPGIRVPARPAWFIQE
LPSMAWPLYEYIRPAAARLGNLPNRVLLAMFLIHYVQRTLVFPVLIRGGKPTLLVTFVLA
FLFCTFNGYVQSRYLSQFAVYAEDWVTHPCFLTGFALWLVGMVINIHSDHILRNLRKPGE
TGYKIPRGGLFEYVSAANYFGELVEWCGFALASWSLQGVVFALFTLSTLLTRAKQHHQWY
HEKFEDYPKSRKILIPFVL
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Component 2
Name:3-oxo-5-alpha-steroid 4-dehydrogenase 2
Synonyms:S5A2_RAT | Srd5a2 | Steroid 5-alpha-reductase | Steroid 5-alpha-reductase 2
Type:PROTEIN
Mol. Mass.:28784.15
Organism:Rattus norvegicus
Description:ChEMBL_205054
Residue:254
Sequence:
MQIVCHQVPVLAGSATLATMGTLILCLGKPASYGKHTESVSSGVPFLPARIAWFLQELPS
FVVSVGMLAWQPRSLFGPPGNVLLALFSAHYFHRTFIYSLLTRGRPFPAVLFLRATAFCI
GNGLLQAYYLVYCAEYPEEWYTDVRFSFGVFLFILGMGINIHSDYTLRQLRKPGEVIYRI
PRGGLFTYVSGANFLGEIIEWIGYALATWSVPAFAFAFFTLCFLGMQAFYHHRFYLKMFK
DYPKSRKALIPFIF
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BDBM8885
n/a
NameBDBM8885
Synonyms:(1S,2R,10R,11S,14S,15S)-14-hydroxy-2,15-dimethyltetracyclo[8.7.0.0^{2,7}.0^{11,15}]heptadec-6-en-5-one | 17beta-Hydroxyandrost-4-en-3-one | Testosterone | Testosterone, 1 | US9682960, Testosterone
TypeSteroid
Emp. Form.C19H28O2
Mol. Mass.288.4244
SMILES[H][C@@]12CC[C@H](O)[C@@]1(C)CC[C@@]1([H])[C@@]2([H])CCC2=CC(=O)CC[C@]12C |r,t:18|
Structure
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