BindingDB logo
myBDB logout

Patent code US8865750

Compile Data Set for Download or QSAR
Found 10 hits of Enzyme Inhibition Constant Data   
Target/Host
(Institution)
LigandTarget/Host
Links
Ligand
Links
Trg + Lig
Links
Ki
nM
ΔG°
kJ/mole
IC50
nM
Kd
nM
EC50/IC50
nM
koff
s-1
kon
M-1s-1
pHTemp
°C
Regulator of G-protein signaling 4


(Homo sapiens (Human))
BDBM50384774
PNG
(CHEMBL1917204 | US20230414581, Compound 6)
Show SMILES Cc1ccc(cc1)-n1sc(=O)n(Cc2ccc(F)cc2)c1=O
Show InChI InChI=1S/C16H13FN2O2S/c1-11-2-8-14(9-3-11)19-15(20)18(16(21)22-19)10-12-4-6-13(17)7-5-12/h2-9H,10H2,1H3
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 30n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 19


(Homo sapiens (Human))
BDBM50384774
PNG
(CHEMBL1917204 | US20230414581, Compound 6)
Show SMILES Cc1ccc(cc1)-n1sc(=O)n(Cc2ccc(F)cc2)c1=O
Show InChI InChI=1S/C16H13FN2O2S/c1-11-2-8-14(9-3-11)19-15(20)18(16(21)22-19)10-12-4-6-13(17)7-5-12/h2-9H,10H2,1H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 120n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 16


(Homo sapiens (Human))
BDBM50384774
PNG
(CHEMBL1917204 | US20230414581, Compound 6)
Show SMILES Cc1ccc(cc1)-n1sc(=O)n(Cc2ccc(F)cc2)c1=O
Show InChI InChI=1S/C16H13FN2O2S/c1-11-2-8-14(9-3-11)19-15(20)18(16(21)22-19)10-12-4-6-13(17)7-5-12/h2-9H,10H2,1H3
PDB
MMDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 3.50E+3n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 8


(Homo sapiens (Human))
BDBM50384774
PNG
(CHEMBL1917204 | US20230414581, Compound 6)
Show SMILES Cc1ccc(cc1)-n1sc(=O)n(Cc2ccc(F)cc2)c1=O
Show InChI InChI=1S/C16H13FN2O2S/c1-11-2-8-14(9-3-11)19-15(20)18(16(21)22-19)10-12-4-6-13(17)7-5-12/h2-9H,10H2,1H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

CHEMBL
MCE
PC cid
PC sid
UniChem

Similars

US Patent
n/an/a 1.10E+4n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 4


(Homo sapiens (Human))
BDBM136369
PNG
(US8865750, CCG- 203780)
Show SMILES BrC1=CC(=O)N(Cc2ccccc2)C1=O |t:1|
Show InChI InChI=1S/C11H8BrNO2/c12-9-6-10(14)13(11(9)15)7-8-4-2-1-3-5-8/h1-6H,7H2
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
UniChem
US Patent
n/an/a 3.20E+4n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 4


(Homo sapiens (Human))
BDBM50384773
PNG
(CHEMBL2037371)
Show SMILES Cc1ccc(cc1)C1=CC(=O)N(Cc2ccccc2)C1=O |t:8|
Show InChI InChI=1S/C18H15NO2/c1-13-7-9-15(10-8-13)16-11-17(20)19(18(16)21)12-14-5-3-2-4-6-14/h2-11H,12H2,1H3
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
US Patent
n/an/a 9.30E+4n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 8


(Homo sapiens (Human))
BDBM136368
PNG
(US8865750, CCG- 203778)
Show SMILES Cc1ccc(CN2C(=O)CN(C2=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C18H18N2O2/c1-13-3-7-15(8-4-13)11-20-17(21)12-19(18(20)22)16-9-5-14(2)6-10-16/h3-10H,11-12H2,1-2H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a>1.00E+5n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 8


(Homo sapiens (Human))
BDBM50384773
PNG
(CHEMBL2037371)
Show SMILES Cc1ccc(cc1)C1=CC(=O)N(Cc2ccccc2)C1=O |t:8|
Show InChI InChI=1S/C18H15NO2/c1-13-7-9-15(10-8-13)16-11-17(20)19(18(16)21)12-14-5-3-2-4-6-14/h2-11H,12H2,1H3
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
CHEMBL
PC cid
PC sid
UniChem
US Patent
n/an/a>1.00E+5n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 4


(Homo sapiens (Human))
BDBM136368
PNG
(US8865750, CCG- 203778)
Show SMILES Cc1ccc(CN2C(=O)CN(C2=O)c2ccc(C)cc2)cc1
Show InChI InChI=1S/C18H18N2O2/c1-13-3-7-15(8-4-13)11-20-17(21)12-19(18(20)22)16-9-5-14(2)6-10-16/h3-10H,11-12H2,1-2H3
PDB

KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem
US Patent
n/an/a>1.00E+5n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
Regulator of G-protein signaling 8


(Homo sapiens (Human))
BDBM136369
PNG
(US8865750, CCG- 203780)
Show SMILES BrC1=CC(=O)N(Cc2ccccc2)C1=O |t:1|
Show InChI InChI=1S/C11H8BrNO2/c12-9-6-10(14)13(11(9)15)7-8-4-2-1-3-5-8/h1-6H,7H2
PDB
MMDB

Reactome pathway
KEGG

UniProtKB/SwissProt

B.MOAD
antibodypedia
GoogleScholar
AffyNet 
Purchase

MCE
PC cid
PC sid
UniChem
US Patent
n/an/a>1.00E+5n/an/an/an/an/an/a



The Regents of The University of Michigan; The University of Bath

US Patent


Assay Description
FCPIA Characterization of RGS Inhibitory Activity: CCG-50014 (FIG. 1) was originally identified as a potential inhibitor of RGS8 and RGS16 in a polyp...


US Patent US8865750 (2014)


BindingDB Entry DOI: 10.7270/Q20000TC
More data for this
Ligand-Target Pair
* indicates data uncertainty>20%