BindingDB logo
myBDB logout

8 similar compounds to monomer 50043604

Compile data set for download or QSAR
Wt: 399.5
BDBM50031890
Wt: 427.6
BDBM50057448
Wt: 441.6
BDBM50057469
Wt: 329.4
BDBM50334789
Wt: 441.6
BDBM50406346
Wt: 413.5
BDBM50406355
Wt: 425.6
BDBM50406356
Wt: 413.5
BDBM50406358

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 16 hits for monomerid = 50031890,50057448,50057469,50334789,50406346,50406355,50406356,50406358   
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
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50057448
PNG
((10R,13S,17S)-17-Diisopropylcarbamoyl-10,13-dimeth...)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C27H41NO3/c1-16(2)28(17(3)4)24(29)23-10-9-21-20-8-7-19-15-18(25(30)31)11-13-26(19,5)22(20)12-14-27(21,23)6/h7,15-17,20-23H,8-14H2,1-6H3,(H,30,31)/t20?,21?,22?,23-,26+,27+/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
7n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Steroid 5-alpha-reductase was determined in human prostatic tissue expressed as apparent inhibition constant; Ra...


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50406356
PNG
(CHEMBL426217)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C=C(CC[C@]4(C)C3C=C[C@]12C)C(O)=O
Show InChI InChI=1S/C27H39NO3/c1-16(2)28(17(3)4)24(29)23-10-9-21-20-8-7-19-15-18(25(30)31)11-13-26(19,5)22(20)12-14-27(21,23)6/h7,12,14-17,20-23H,8-11,13H2,1-6H3,(H,30,31)/t20?,21?,22?,23-,26+,27+/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
7n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in human prostatic tissue.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50057448
PNG
((10R,13S,17S)-17-Diisopropylcarbamoyl-10,13-dimeth...)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C27H41NO3/c1-16(2)28(17(3)4)24(29)23-10-9-21-20-8-7-19-15-18(25(30)31)11-13-26(19,5)22(20)12-14-27(21,23)6/h7,15-17,20-23H,8-14H2,1-6H3,(H,30,31)/t20?,21?,22?,23-,26+,27+/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
7n/an/an/an/an/an/an/an/a



TBA

Curated by ChEMBL


Assay Description
Compound was tested for inhibitory activity against human prostatic Steroid 5-alpha-reductase


Bioorg Med Chem Lett 1: 27-32 (1991)


Article DOI: 10.1016/S0960-894X(01)81084-2
BindingDB Entry DOI: 10.7270/Q29P31J1
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Rattus norvegicus)
BDBM50057448
PNG
((10R,13S,17S)-17-Diisopropylcarbamoyl-10,13-dimeth...)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C27H41NO3/c1-16(2)28(17(3)4)24(29)23-10-9-21-20-8-7-19-15-18(25(30)31)11-13-26(19,5)22(20)12-14-27(21,23)6/h7,15-17,20-23H,8-14H2,1-6H3,(H,30,31)/t20?,21?,22?,23-,26+,27+/m1/s1
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
35n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibitory activity against Steroid 5-alpha-reductase was determined in rat ventral prostates expressed as apparent inhibition constant; Ran...


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50057469
PNG
((10R,13S,17S)-17-Diisopropylcarbamoyl-4,10,13-trim...)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C(C)=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C28H43NO3/c1-16(2)29(17(3)4)25(30)24-11-10-22-20-8-9-21-18(5)19(26(31)32)12-14-27(21,6)23(20)13-15-28(22,24)7/h9,16-17,20,22-24H,8,10-15H2,1-7H3,(H,31,32)/t20?,22?,23?,24-,27+,28+/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
35n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in human prostatic tissue.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Rattus norvegicus)
BDBM50406356
PNG
(CHEMBL426217)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C=C(CC[C@]4(C)C3C=C[C@]12C)C(O)=O
Show InChI InChI=1S/C27H39NO3/c1-16(2)28(17(3)4)24(29)23-10-9-21-20-8-7-19-15-18(25(30)31)11-13-26(19,5)22(20)12-14-27(21,23)6/h7,12,14-17,20-23H,8-11,13H2,1-6H3,(H,30,31)/t20?,21?,22?,23-,26+,27+/m1/s1
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
47n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in rat ventral prostates.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50406358
PNG
(CHEMBL366660)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C=C(CC[C@@H]4C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C26H39NO3/c1-15(2)27(16(3)4)24(28)23-11-10-22-21-9-6-17-14-18(25(29)30)7-8-19(17)20(21)12-13-26(22,23)5/h6,14-16,19-23H,7-13H2,1-5H3,(H,29,30)/t19-,20?,21?,22?,23+,26-/m0/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
50n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in human prostatic tissue.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Rattus norvegicus)
BDBM50057469
PNG
((10R,13S,17S)-17-Diisopropylcarbamoyl-4,10,13-trim...)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C(C)=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C28H43NO3/c1-16(2)29(17(3)4)25(30)24-11-10-22-20-8-9-21-18(5)19(26(31)32)12-14-27(21,6)23(20)13-15-28(22,24)7/h9,16-17,20,22-24H,8,10-15H2,1-7H3,(H,31,32)/t20?,22?,23?,24-,27+,28+/m1/s1
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
70n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in rat ventral prostates.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50406355
PNG
(CHEMBL353340)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CCC4=C(CCC(=C4)C(O)=O)C3CC[C@]12C
Show InChI InChI=1S/C26H39NO3/c1-15(2)27(16(3)4)24(28)23-11-10-22-21-9-6-17-14-18(25(29)30)7-8-19(17)20(21)12-13-26(22,23)5/h14-16,20-23H,6-13H2,1-5H3,(H,29,30)/t20?,21?,22?,23-,26+/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
110n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in human prostatic tissue.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Rattus norvegicus)
BDBM50406358
PNG
(CHEMBL366660)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC=C4C=C(CC[C@@H]4C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C26H39NO3/c1-15(2)27(16(3)4)24(28)23-11-10-22-21-9-6-17-14-18(25(29)30)7-8-19(17)20(21)12-13-26(22,23)5/h6,14-16,19-23H,7-13H2,1-5H3,(H,29,30)/t19-,20?,21?,22?,23+,26-/m0/s1
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
140n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in rat ventral prostates.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50406346
PNG
(CHEMBL367878)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC(C)=C4C=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C28H43NO3/c1-16(2)29(17(3)4)25(30)23-9-8-21-20-14-18(5)24-15-19(26(31)32)10-12-28(24,7)22(20)11-13-27(21,23)6/h15-17,20-23H,8-14H2,1-7H3,(H,31,32)/t20?,21?,22?,23-,27+,28-/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
170n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in human prostatic tissue.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Rattus norvegicus)
BDBM50406346
PNG
(CHEMBL367878)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CC(C)=C4C=C(CC[C@]4(C)C3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C28H43NO3/c1-16(2)29(17(3)4)25(30)23-9-8-21-20-14-18(5)24-15-19(26(31)32)10-12-28(24,7)22(20)11-13-27(21,23)6/h15-17,20-23H,8-14H2,1-7H3,(H,31,32)/t20?,21?,22?,23-,27+,28-/m1/s1
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
200n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in rat ventral prostates.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Rattus norvegicus)
BDBM50406355
PNG
(CHEMBL353340)
Show SMILES CC(C)N(C(C)C)C(=O)[C@H]1CCC2C3CCC4=C(CCC(=C4)C(O)=O)C3CC[C@]12C
Show InChI InChI=1S/C26H39NO3/c1-15(2)27(16(3)4)24(28)23-11-10-22-21-9-6-17-14-18(25(29)30)7-8-19(17)20(21)12-13-26(22,23)5/h14-16,20-23H,6-13H2,1-5H3,(H,29,30)/t20?,21?,22?,23-,26+/m1/s1
MMDB

UniProtKB/SwissProt

B.MOAD
DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
290n/an/an/an/an/an/an/an/a



Smith Kline & French Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of Steroid 5-alpha-reductase in rat ventral prostates.


J Med Chem 33: 943-50 (1990)


Article DOI: 10.1021/jm00165a010
BindingDB Entry DOI: 10.7270/Q25D8QSB
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50031890
PNG
((10R,13S)-17-tert-Butylcarbamoyl-10,13-dimethyl-2,...)
Show SMILES CC(C)(C)NC(=O)[C@H]1CC[C@H]2[C@@H]3CC=C4C=C(CC[C@]4(C)[C@H]3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C25H37NO3/c1-23(2,3)26-21(27)20-9-8-18-17-7-6-16-14-15(22(28)29)10-12-24(16,4)19(17)11-13-25(18,20)5/h6,14,17-20H,7-13H2,1-5H3,(H,26,27)(H,28,29)/t17-,18-,19-,20+,24-,25-/m0/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 8n/an/an/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
Compound was tested for inhibition of Type II 5-alpha-reductase in Human Prostate Homogenates (HPH)


J Med Chem 36: 421-3 (1993)


Article DOI: 10.1021/jm00055a014
BindingDB Entry DOI: 10.7270/Q2T43TQX
More data for this
Ligand-Target Pair
Steroid 5-alpha-reductase


(Homo sapiens (Human))
BDBM50334789
PNG
((4aS,4bR,10aR,10bS,12aS)-10a,12a-dimethyl-2-oxo-1,...)
Show SMILES C[C@]12CC[C@H]3[C@@H](CC=C4C=C(CC[C@]34C)C(O)=O)[C@@H]1CCC(=O)N2
Show InChI InChI=1S/C20H27NO3/c1-19-9-7-12(18(23)24)11-13(19)3-4-14-15(19)8-10-20(2)16(14)5-6-17(22)21-20/h3,11,14-16H,4-10H2,1-2H3,(H,21,22)(H,23,24)/t14-,15+,16+,19+,20+/m1/s1
Reactome pathway
KEGG

UniProtKB/SwissProt

DrugBank
GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 71n/an/an/an/an/an/a



College of Chemical and Environmental Engineering

Curated by ChEMBL


Assay Description
Inhibition of human prostate 5alpha-reductase type 2 assessed as formation dihydrotestosterone from [4-14C] testosterone


Bioorg Med Chem Lett 21: 475-8 (2010)


Article DOI: 10.1016/j.bmcl.2010.10.112
BindingDB Entry DOI: 10.7270/Q22B8Z9B
More data for this
Ligand-Target Pair
5α-Reductase 1 (5α-R1)


(Homo sapiens (Human))
BDBM50031890
PNG
((10R,13S)-17-tert-Butylcarbamoyl-10,13-dimethyl-2,...)
Show SMILES CC(C)(C)NC(=O)[C@H]1CC[C@H]2[C@@H]3CC=C4C=C(CC[C@]4(C)[C@H]3CC[C@]12C)C(O)=O
Show InChI InChI=1S/C25H37NO3/c1-23(2,3)26-21(27)20-9-8-18-17-7-6-16-14-15(22(28)29)10-12-24(16,4)19(17)11-13-25(18,20)5/h6,14,17-20H,7-13H2,1-5H3,(H,26,27)(H,28,29)/t17-,18-,19-,20+,24-,25-/m0/s1
UniProtKB/SwissProt

GoogleScholar
CHEMBL
PC cid
PC sid
UniChem

Patents


Similars

Article
PubMed
n/an/a 7.50E+3n/an/an/an/an/an/a



Lilly Research Laboratories

Curated by ChEMBL


Assay Description
In vitro inhibition of DHT production in Hs 68 (human genital fibroblast) cells.


J Med Chem 36: 421-3 (1993)


Article DOI: 10.1021/jm00055a014
BindingDB Entry DOI: 10.7270/Q2T43TQX
More data for this
Ligand-Target Pair