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BDBM50385878 CHEMBL2040856

SMILES: Oc1cccc(c1)-c1ccc2c(c(O)ccc2c1)-c1cccc2n(ccc12)S(=O)(=O)c1ccccc1

InChI Key: InChIKey=OIWSTPKQQPZLRW-UHFFFAOYSA-N

Data: 3 IC50

Find this compound or compounds like it in BindingDB or PDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 3 hits for monomerid = 50385878   
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 1 (17beta-HSD1)


(Homo sapiens (Human))
BDBM50385878
PNG
(CHEMBL2040856)
Show SMILES Oc1cccc(c1)-c1ccc2c(c(O)ccc2c1)-c1cccc2n(ccc12)S(=O)(=O)c1ccccc1 |(4.01,8.19,;4.01,6.65,;5.34,5.88,;5.34,4.34,;4,3.57,;2.67,4.34,;2.67,5.88,;1.33,3.57,;1.33,2.03,;-0,1.27,;-1.34,2.04,;-2.67,1.27,;-4,2.04,;-5.34,1.27,;-4,3.58,;-2.67,4.35,;-1.33,3.58,;0,4.35,;-2.67,-.27,;-4.01,-1.04,;-4.01,-2.58,;-2.68,-3.35,;-1.34,-2.58,;.12,-3.06,;1.03,-1.82,;.13,-.57,;-1.34,-1.04,;.6,-4.53,;1.93,-3.76,;1.93,-5.3,;-.49,-5.61,;-1.98,-5.22,;-3.07,-6.3,;-2.67,-7.79,;-1.18,-8.19,;-.09,-7.1,)|
Show InChI InChI=1S/C30H21NO4S/c32-23-7-4-6-20(19-23)21-12-14-25-22(18-21)13-15-29(33)30(25)27-10-5-11-28-26(27)16-17-31(28)36(34,35)24-8-2-1-3-9-24/h1-19,32-33H
PDB
MMDB

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Article
PubMed
n/an/a 1.10E+3n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of 17betaHSD1 in human T47D cells using [3H]E1 as substrate incubated for 30 mins prior to substrate addition measured after 30 mins by ra...


J Med Chem 55: 3307-18 (2012)


Article DOI: 10.1021/jm201735j
BindingDB Entry DOI: 10.7270/Q23J3F0K
More data for this
Ligand-Target Pair
Estradiol 17-beta-dehydrogenase 1 (17beta-HSD1)


(Homo sapiens (Human))
BDBM50385878
PNG
(CHEMBL2040856)
Show SMILES Oc1cccc(c1)-c1ccc2c(c(O)ccc2c1)-c1cccc2n(ccc12)S(=O)(=O)c1ccccc1 |(4.01,8.19,;4.01,6.65,;5.34,5.88,;5.34,4.34,;4,3.57,;2.67,4.34,;2.67,5.88,;1.33,3.57,;1.33,2.03,;-0,1.27,;-1.34,2.04,;-2.67,1.27,;-4,2.04,;-5.34,1.27,;-4,3.58,;-2.67,4.35,;-1.33,3.58,;0,4.35,;-2.67,-.27,;-4.01,-1.04,;-4.01,-2.58,;-2.68,-3.35,;-1.34,-2.58,;.12,-3.06,;1.03,-1.82,;.13,-.57,;-1.34,-1.04,;.6,-4.53,;1.93,-3.76,;1.93,-5.3,;-.49,-5.61,;-1.98,-5.22,;-3.07,-6.3,;-2.67,-7.79,;-1.18,-8.19,;-.09,-7.1,)|
Show InChI InChI=1S/C30H21NO4S/c32-23-7-4-6-20(19-23)21-12-14-25-22(18-21)13-15-29(33)30(25)27-10-5-11-28-26(27)16-17-31(28)36(34,35)24-8-2-1-3-9-24/h1-19,32-33H
PDB
MMDB

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Article
PubMed
n/an/a 32n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human placenta cytosolic 17betaHSD1 using [3H]E1 as substrate after 10 mins by radioflow detection assay


J Med Chem 55: 3307-18 (2012)


Article DOI: 10.1021/jm201735j
BindingDB Entry DOI: 10.7270/Q23J3F0K
More data for this
Ligand-Target Pair
Estradiol 17-beta-dehydrogenase 2


(Homo sapiens (Human))
BDBM50385878
PNG
(CHEMBL2040856)
Show SMILES Oc1cccc(c1)-c1ccc2c(c(O)ccc2c1)-c1cccc2n(ccc12)S(=O)(=O)c1ccccc1 |(4.01,8.19,;4.01,6.65,;5.34,5.88,;5.34,4.34,;4,3.57,;2.67,4.34,;2.67,5.88,;1.33,3.57,;1.33,2.03,;-0,1.27,;-1.34,2.04,;-2.67,1.27,;-4,2.04,;-5.34,1.27,;-4,3.58,;-2.67,4.35,;-1.33,3.58,;0,4.35,;-2.67,-.27,;-4.01,-1.04,;-4.01,-2.58,;-2.68,-3.35,;-1.34,-2.58,;.12,-3.06,;1.03,-1.82,;.13,-.57,;-1.34,-1.04,;.6,-4.53,;1.93,-3.76,;1.93,-5.3,;-.49,-5.61,;-1.98,-5.22,;-3.07,-6.3,;-2.67,-7.79,;-1.18,-8.19,;-.09,-7.1,)|
Show InChI InChI=1S/C30H21NO4S/c32-23-7-4-6-20(19-23)21-12-14-25-22(18-21)13-15-29(33)30(25)27-10-5-11-28-26(27)16-17-31(28)36(34,35)24-8-2-1-3-9-24/h1-19,32-33H
KEGG

UniProtKB/SwissProt

DrugBank
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 391n/an/an/an/an/an/a



Saarland University

Curated by ChEMBL


Assay Description
Inhibition of human placenta microsomal 17betaHSD2 using [3H]E2 as substrate after 20 mins by radioflow detection assay


J Med Chem 55: 3307-18 (2012)


Article DOI: 10.1021/jm201735j
BindingDB Entry DOI: 10.7270/Q23J3F0K
More data for this
Ligand-Target Pair