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BDBM50426583 CHEMBL2324370

SMILES: COc1cccc(c1)N(C)C(=O)c1ccc(s1)-c1ccc(OC)cc1OC

InChI Key: InChIKey=QMPAVJPWVCZIMK-UHFFFAOYSA-N

Data: 2 IC50

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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50426583   
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
Estradiol 17-beta-dehydrogenase 2


(Homo sapiens (Human))
BDBM50426583
PNG
(CHEMBL2324370)
Show SMILES COc1cccc(c1)N(C)C(=O)c1ccc(s1)-c1ccc(OC)cc1OC
Show InChI InChI=1S/C21H21NO4S/c1-22(14-6-5-7-15(12-14)24-2)21(23)20-11-10-19(27-20)17-9-8-16(25-3)13-18(17)26-4/h5-13H,1-4H3
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 313n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of 17beta-HSD2 in human placental microsomal fraction using [3H]E2 as substrate assessed as formation of E1 by HPLC analysis


J Med Chem 56: 167-81 (2013)


Article DOI: 10.1021/jm3014053
BindingDB Entry DOI: 10.7270/Q2ZK5J0P
More data for this
Ligand-Target Pair
Estradiol 17-beta-dehydrogenase 1 (17beta-HSD1)


(Homo sapiens (Human))
BDBM50426583
PNG
(CHEMBL2324370)
Show SMILES COc1cccc(c1)N(C)C(=O)c1ccc(s1)-c1ccc(OC)cc1OC
Show InChI InChI=1S/C21H21NO4S/c1-22(14-6-5-7-15(12-14)24-2)21(23)20-11-10-19(27-20)17-9-8-16(25-3)13-18(17)26-4/h5-13H,1-4H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 1.93E+3n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of 17beta-HSD1 in human placental cytosolic fraction using [3H]E1 as substrate assessed as formation of E2 by HPLC analysis


J Med Chem 56: 167-81 (2013)


Article DOI: 10.1021/jm3014053
BindingDB Entry DOI: 10.7270/Q2ZK5J0P
More data for this
Ligand-Target Pair