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BDBM50340666 6-(3-chloro-1H-indol-7-yl)-5,7-difluoro-3-hydroxy-2,2-dimethyl-2,3-dihydroquinolin-4(1H)-one O-methyl oxime::CHEMBL1762211

SMILES: CO\N=C1/C(O)C(C)(C)Nc2cc(F)c(c(F)c12)-c1cccc2c(Cl)c[nH]c12

InChI Key: InChIKey=HIEURQCNSGIVBQ-ITYLOYPMSA-N

Data: 1 KI  2 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 = 50340666   
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
Glucocorticoid receptor


(Homo sapiens (Human))
BDBM50340666
PNG
(6-(3-chloro-1H-indol-7-yl)-5,7-difluoro-3-hydroxy-...)
Show SMILES CO\N=C1/C(O)C(C)(C)Nc2cc(F)c(c(F)c12)-c1cccc2c(Cl)c[nH]c12 |(33.75,6.57,;33.74,5.03,;32.41,4.27,;32.4,2.73,;33.73,1.95,;35.07,2.7,;33.72,.41,;35.04,1.19,;35.04,-.36,;32.38,-.35,;31.05,.43,;29.72,-.33,;28.4,.44,;27.07,-.32,;28.41,1.98,;29.74,2.75,;29.74,4.28,;31.06,1.97,;27.08,2.76,;27.08,4.3,;25.75,5.08,;24.42,4.3,;24.41,2.76,;23.26,1.73,;21.92,2.5,;23.89,.32,;25.42,.48,;25.75,1.99,)|
Show InChI InChI=1S/C20H18ClF2N3O2/c1-20(2)19(27)18(26-28-3)15-13(25-20)7-12(22)14(16(15)23)10-6-4-5-9-11(21)8-24-17(9)10/h4-8,19,24-25,27H,1-3H3/b26-18-
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

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

Similars

Article
PubMed
0.700n/an/an/an/an/an/an/an/a



Ligand Pharmaceuticals

Curated by ChEMBL


Assay Description
Displacement of radiolabeled dexamethasone from glucocorticoid receptor expressed in baculovirus


Bioorg Med Chem Lett 21: 1654-7 (2011)


Article DOI: 10.1016/j.bmcl.2011.01.104
BindingDB Entry DOI: 10.7270/Q21V5F8D
More data for this
Ligand-Target Pair
Glucocorticoid receptor


(Homo sapiens (Human))
BDBM50340666
PNG
(6-(3-chloro-1H-indol-7-yl)-5,7-difluoro-3-hydroxy-...)
Show SMILES CO\N=C1/C(O)C(C)(C)Nc2cc(F)c(c(F)c12)-c1cccc2c(Cl)c[nH]c12 |(33.75,6.57,;33.74,5.03,;32.41,4.27,;32.4,2.73,;33.73,1.95,;35.07,2.7,;33.72,.41,;35.04,1.19,;35.04,-.36,;32.38,-.35,;31.05,.43,;29.72,-.33,;28.4,.44,;27.07,-.32,;28.41,1.98,;29.74,2.75,;29.74,4.28,;31.06,1.97,;27.08,2.76,;27.08,4.3,;25.75,5.08,;24.42,4.3,;24.41,2.76,;23.26,1.73,;21.92,2.5,;23.89,.32,;25.42,.48,;25.75,1.99,)|
Show InChI InChI=1S/C20H18ClF2N3O2/c1-20(2)19(27)18(26-28-3)15-13(25-20)7-12(22)14(16(15)23)10-6-4-5-9-11(21)8-24-17(9)10/h4-8,19,24-25,27H,1-3H3/b26-18-
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

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

Similars

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



Ligand Pharmaceuticals

Curated by ChEMBL


Assay Description
Transrepression activity at glucocorticoid receptor in human NHDF cells assessed as inhibition of IL-1beta-stimulated AP1 dependent IL-6 repression b...


Bioorg Med Chem Lett 21: 1654-7 (2011)


Article DOI: 10.1016/j.bmcl.2011.01.104
BindingDB Entry DOI: 10.7270/Q21V5F8D
More data for this
Ligand-Target Pair
Glucocorticoid receptor


(Homo sapiens (Human))
BDBM50340666
PNG
(6-(3-chloro-1H-indol-7-yl)-5,7-difluoro-3-hydroxy-...)
Show SMILES CO\N=C1/C(O)C(C)(C)Nc2cc(F)c(c(F)c12)-c1cccc2c(Cl)c[nH]c12 |(33.75,6.57,;33.74,5.03,;32.41,4.27,;32.4,2.73,;33.73,1.95,;35.07,2.7,;33.72,.41,;35.04,1.19,;35.04,-.36,;32.38,-.35,;31.05,.43,;29.72,-.33,;28.4,.44,;27.07,-.32,;28.41,1.98,;29.74,2.75,;29.74,4.28,;31.06,1.97,;27.08,2.76,;27.08,4.3,;25.75,5.08,;24.42,4.3,;24.41,2.76,;23.26,1.73,;21.92,2.5,;23.89,.32,;25.42,.48,;25.75,1.99,)|
Show InChI InChI=1S/C20H18ClF2N3O2/c1-20(2)19(27)18(26-28-3)15-13(25-20)7-12(22)14(16(15)23)10-6-4-5-9-11(21)8-24-17(9)10/h4-8,19,24-25,27H,1-3H3/b26-18-
PDB

KEGG

UniProtKB/SwissProt
UniProtKB/TrEMBL

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

Similars

Article
PubMed
n/an/a 14n/an/an/an/an/an/a



Ligand Pharmaceuticals

Curated by ChEMBL


Assay Description
Transrepression activity at glucocorticoid receptor in human HepG2 cells assessed as inhibition of TNFalpha/IL1beta-stimulated NFkappaB-dependent E-s...


Bioorg Med Chem Lett 21: 1654-7 (2011)


Article DOI: 10.1016/j.bmcl.2011.01.104
BindingDB Entry DOI: 10.7270/Q21V5F8D
More data for this
Ligand-Target Pair