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SMILES: C[C@]12CC[C@H]3[C@@H](CC[C@H]4C[C@]5(CC[C@]34C)CN[C@@H](Cc3ccccc3)C(=O)O5)[C@@H]1CCC2=O

InChI Key: InChIKey=OVBVPGFTBBLZOR-ZRXWQUTISA-N

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 1 hit for monomerid = 50443291   
Target/Host
(Institution)		LigandTarget/Host
Links		Ligand
Links		Trg + Lig
Links		Ki
nM		ΔG°
kcal/mole		IC50
nM		Kd
nM		EC50/IC50
nM		koff
s-1		kon
M-1s-1		pHTemp
°C
17-beta-hydroxysteroid dehydrogenase type 3


(Rattus norvegicus)		BDBM50443291
PNG
(CHEMBL3088087)
Show SMILES C[C@]12CC[C@H]3[C@@H](CC[C@H]4C[C@]5(CC[C@]34C)CN[C@@H](Cc3ccccc3)C(=O)O5)[C@@H]1CCC2=O |r|
Show InChI InChI=1S/C29H39NO3/c1-27-14-15-29(18-30-24(26(32)33-29)16-19-6-4-3-5-7-19)17-20(27)8-9-21-22-10-11-25(31)28(22,2)13-12-23(21)27/h3-7,20-24,30H,8-18H2,1-2H3/t20-,21-,22-,23-,24-,27-,28-,29+/m0/s1
KEGG

UniProtKB/SwissProt

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PC cid
PC sid
UniChem

Similars
Article
PubMed
n/an/a 22n/an/an/an/an/an/a



Laval University

Curated by ChEMBL


Assay Description
Inhibition of 17beta-HSD3 in rat testes microsomal fraction using [14C]-4-androstene-3,17-dione as substrate assessed as testosterone formation after...

Bioorg Med Chem Lett 23: 6360-2 (2013)


Article DOI: 10.1016/j.bmcl.2013.09.072
BindingDB Entry DOI: 10.7270/Q2KP83M4
More data for this
Ligand-Target Pair