BDBM50350421 CHEMBL1813731
SMILES C[C@@H]1CN([C@@H](C)CN1C[C@@]1(O)CC[C@@]2(C)[C@@H](CC[C@H]3[C@@H]4CCC(=O)[C@@]4(C)CC[C@H]23)C1)S(=O)(=O)c1ccccc1C(F)(F)F
InChI Key InChIKey=IYHGEKFCMCXIEF-AIQQMPNKSA-N
Data 5 IC50
Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB
Found 5 hits for monomerid = 50350421
Target17-beta-hydroxysteroid dehydrogenase type 3(Rattus norvegicus)
Chu De Qu£Bec-Research Center (Chul)
Curated by ChEMBL
Chu De Qu£Bec-Research Center (Chul)
Curated by ChEMBL
Affinity DataIC50: 13nMAssay Description:Inhibition of 17beta-HSD3 in rat testes microsomes using [14C]-4-androstene-3,17-dione as substrate after 2 hrsMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chuq (Chul)-Research Center
Curated by ChEMBL
Chuq (Chul)-Research Center
Curated by ChEMBL
Affinity DataIC50: 6nMAssay Description:Inhibition of 17Beta-HSD3 expressed in intact HEK293 cells assessed as transformation of [14C]-4-androstene-3,17-dione into [14C]-testosterone in pre...More data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chuq (Chul)-Research Center
Curated by ChEMBL
Chuq (Chul)-Research Center
Curated by ChEMBL
Affinity DataIC50: 85nMAssay Description:Inhibition of 17betaHSD3 (unknown origin) transfected in human LNCAP cells assessed as conversion of [14C]-4-androstene-3,17-dione into [14C]-testost...More data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chuq (Chul)-Research Center
Curated by ChEMBL
Chuq (Chul)-Research Center
Curated by ChEMBL
Affinity DataIC50: 6nMAssay Description:Inhibition of 17betaHSD3 (unknown origin) transfected in HEK293 cellsMore data for this Ligand-Target Pair
Target17-beta-hydroxysteroid dehydrogenase type 3(Homo sapiens (Human))
Chuq (Chul)-Research Center
Curated by ChEMBL
Chuq (Chul)-Research Center
Curated by ChEMBL
Affinity DataIC50: 110nMAssay Description:Inhibition of 17-beta-HSD3 (unknown origin) expressed in human LNCaP cells using [14C]-4-androstene-3,17-dione as substrate assessed as reduction of ...More data for this Ligand-Target Pair