BindingDB logo
myBDB logout
Compile Data Set for Download or QSAR

Found 11 hits of ic50 for UniProtKB: P23219   
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
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM17638
PNG
(2-{1-[(4-chlorophenyl)carbonyl]-5-methoxy-2-methyl...)
Show SMILES COc1ccc2n(C(=O)c3ccc(Cl)cc3)c(C)c(CC(O)=O)c2c1
Show InChI InChI=1S/C19H16ClNO4/c1-11-15(10-18(22)23)16-9-14(25-2)7-8-17(16)21(11)19(24)12-3-5-13(20)6-4-12/h3-9H,10H2,1-2H3,(H,22,23)
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents


Similars

Article
PubMed
n/an/a 260n/an/an/an/an/an/a



University of Alexandria



Assay Description
The compounds that exhibited potent anti-inflammatory profiles were futher tested for their ability to inhibit human COX-1 and COX-2 enzymes in-vitro...


J Enzyme Inhib Med Chem 24: 296-309 (2009)


Article DOI: 10.1080/14756360802188404
BindingDB Entry DOI: 10.7270/Q2S1813W
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM11639
PNG
(4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyraz...)
Show SMILES Cc1ccc(cc1)-c1cc(nn1-c1ccc(cc1)S(N)(=O)=O)C(F)(F)F
Show InChI InChI=1S/C17H14F3N3O2S/c1-11-2-4-12(5-3-11)15-10-16(17(18,19)20)22-23(15)13-6-8-14(9-7-13)26(21,24)25/h2-10H,1H3,(H2,21,24,25)
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents


Similars

n/an/a 2.43E+4n/an/an/an/an/an/a



Shahid Beheshti University



Assay Description
The ability of the test compounds to inhibit ovine COX-1 and COX-2 was determined using chemiluminescent enzyme assays kit according to our previousl...


Med Chem Res 19: 782-793 (2009)


BindingDB Entry DOI: 10.7270/Q2T72G2X
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM93106
PNG
(COX inhibitor, 9)
Show SMILES CC1SC(N(Cc2ccccc2)C1=O)c1ccccc1
Show InChI InChI=1S/C17H17NOS/c1-13-16(19)18(12-14-8-4-2-5-9-14)17(20-13)15-10-6-3-7-11-15/h2-11,13,17H,12H2,1H3
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Similars

n/an/a 7.56E+4n/an/an/an/an/an/a



Shahid Beheshti University



Assay Description
The ability of the test compounds to inhibit ovine COX-1 and COX-2 was determined using chemiluminescent enzyme assays kit according to our previousl...


Med Chem Res 19: 782-793 (2009)


BindingDB Entry DOI: 10.7270/Q2T72G2X
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM91679
PNG
(Pyrazolyl benzenesulfonamide derivative, 7b)
Show SMILES Cc1ccc(cc1)-c1nn(cc1C(N)=O)-c1ccc(cc1)S(N)(=O)=O
Show InChI InChI=1S/C17H16N4O3S/c1-11-2-4-12(5-3-11)16-15(17(18)22)10-21(20-16)13-6-8-14(9-7-13)25(19,23)24/h2-10H,1H3,(H2,18,22)(H2,19,23,24)
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 7.64E+4n/an/an/an/an/an/a



University of Alexandria



Assay Description
The compounds that exhibited potent anti-inflammatory profiles were futher tested for their ability to inhibit human COX-1 and COX-2 enzymes in-vitro...


J Enzyme Inhib Med Chem 24: 296-309 (2009)


Article DOI: 10.1080/14756360802188404
BindingDB Entry DOI: 10.7270/Q2S1813W
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM91678
PNG
(Pyrazolyl benzenesulfonamide derivative, 7a)
Show SMILES NC(=O)c1cn(nc1-c1ccccc1)-c1ccc(cc1)S(N)(=O)=O
Show InChI InChI=1S/C16H14N4O3S/c17-16(21)14-10-20(19-15(14)11-4-2-1-3-5-11)12-6-8-13(9-7-12)24(18,22)23/h1-10H,(H2,17,21)(H2,18,22,23)
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 8.36E+4n/an/an/an/an/an/a



University of Alexandria



Assay Description
The compounds that exhibited potent anti-inflammatory profiles were futher tested for their ability to inhibit human COX-1 and COX-2 enzymes in-vitro...


J Enzyme Inhib Med Chem 24: 296-309 (2009)


Article DOI: 10.1080/14756360802188404
BindingDB Entry DOI: 10.7270/Q2S1813W
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM93105
PNG
(COX inhibitor, 8)
Show SMILES CC1OC(N(Cc2ccccc2)C1=O)c1ccccc1
Show InChI InChI=1S/C17H17NO2/c1-13-16(19)18(12-14-8-4-2-5-9-14)17(20-13)15-10-6-3-7-11-15/h2-11,13,17H,12H2,1H3
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

n/an/a 8.59E+4n/an/an/an/an/an/a



Shahid Beheshti University



Assay Description
The ability of the test compounds to inhibit ovine COX-1 and COX-2 was determined using chemiluminescent enzyme assays kit according to our previousl...


Med Chem Res 19: 782-793 (2009)


BindingDB Entry DOI: 10.7270/Q2T72G2X
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM91685
PNG
(Pyrazolyl benzenesulfonamide derivative, 9b)
Show SMILES Cc1ccc(cc1)-c1nn(cc1C#N)-c1ccc(cc1)S(N)(=O)=O
Show InChI InChI=1S/C17H14N4O2S/c1-12-2-4-13(5-3-12)17-14(10-18)11-21(20-17)15-6-8-16(9-7-15)24(19,22)23/h2-9,11H,1H3,(H2,19,22,23)
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a 9.42E+4n/an/an/an/an/an/a



University of Alexandria



Assay Description
The compounds that exhibited potent anti-inflammatory profiles were futher tested for their ability to inhibit human COX-1 and COX-2 enzymes in-vitro...


J Enzyme Inhib Med Chem 24: 296-309 (2009)


Article DOI: 10.1080/14756360802188404
BindingDB Entry DOI: 10.7270/Q2S1813W
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM93103
PNG
(COX inhibitor, 5a)
Show SMILES O=C1COC(N1Cc1ccccc1)c1ccccc1
Show InChI InChI=1S/C16H15NO2/c18-15-12-19-16(14-9-5-2-6-10-14)17(15)11-13-7-3-1-4-8-13/h1-10,16H,11-12H2
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

n/an/a>1.00E+5n/an/an/an/an/an/a



Shahid Beheshti University



Assay Description
The ability of the test compounds to inhibit ovine COX-1 and COX-2 was determined using chemiluminescent enzyme assays kit according to our previousl...


Med Chem Res 19: 782-793 (2009)


BindingDB Entry DOI: 10.7270/Q2T72G2X
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM93104
PNG
(COX inhibitor, 5b)
Show SMILES O=C1CSC(N1Cc1ccccc1)c1ccccc1
Show InChI InChI=1S/C16H15NOS/c18-15-12-19-16(14-9-5-2-6-10-14)17(15)11-13-7-3-1-4-8-13/h1-10,16H,11-12H2
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

PC cid
PC sid
UniChem

Similars

n/an/a>1.00E+5n/an/an/an/an/an/a



Shahid Beheshti University



Assay Description
The ability of the test compounds to inhibit ovine COX-1 and COX-2 was determined using chemiluminescent enzyme assays kit according to our previousl...


Med Chem Res 19: 782-793 (2009)


BindingDB Entry DOI: 10.7270/Q2T72G2X
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM91684
PNG
(Pyrazolyl benzenesulfonamide derivative, 9a)
Show SMILES NS(=O)(=O)c1ccc(cc1)-n1cc(C#N)c(n1)-c1ccccc1
Show InChI InChI=1S/C16H12N4O2S/c17-10-13-11-20(19-16(13)12-4-2-1-3-5-12)14-6-8-15(9-7-14)23(18,21)22/h1-9,11H,(H2,18,21,22)
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
PC cid
PC sid
UniChem

Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



University of Alexandria



Assay Description
The compounds that exhibited potent anti-inflammatory profiles were futher tested for their ability to inhibit human COX-1 and COX-2 enzymes in-vitro...


J Enzyme Inhib Med Chem 24: 296-309 (2009)


Article DOI: 10.1080/14756360802188404
BindingDB Entry DOI: 10.7270/Q2S1813W
More data for this
Ligand-Target Pair
Prostaglandin G/H synthase 1 [582-599]


(Homo sapiens (Human))
BDBM11639
PNG
(4-[5-(4-methylphenyl)-3-(trifluoromethyl)-1H-pyraz...)
Show SMILES Cc1ccc(cc1)-c1cc(nn1-c1ccc(cc1)S(N)(=O)=O)C(F)(F)F
Show InChI InChI=1S/C17H14F3N3O2S/c1-11-2-4-12(5-3-11)15-10-16(17(18,19)20)22-23(15)13-6-8-14(9-7-13)26(21,24)25/h2-10H,1H3,(H2,21,24,25)
MMDB

Reactome pathway

UniProtKB/SwissProt

B.MOAD
GoogleScholar
AffyNet 
Purchase

CHEMBL
DrugBank
MCE
KEGG
MMDB
PC cid
PC sid
PDB
UniChem

Patents


Similars

Article
PubMed
n/an/a>1.00E+5n/an/an/an/an/an/a



University of Alexandria



Assay Description
The compounds that exhibited potent anti-inflammatory profiles were futher tested for their ability to inhibit human COX-1 and COX-2 enzymes in-vitro...


J Enzyme Inhib Med Chem 24: 296-309 (2009)


Article DOI: 10.1080/14756360802188404
BindingDB Entry DOI: 10.7270/Q2S1813W
More data for this
Ligand-Target Pair