Found 104 hits with Last Name = 'sanpablo' and Initial = 'f' Target/Host (Institution) | Ligand | Target/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 | pH | Temp °C |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15774
((2R)-1-({4-[3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]py...)Show SMILES C[C@@H](O)CNc1cc(ccn1)-c1[nH]c2cccnc2c1-c1ccc(F)cc1 |r| Show InChI InChI=1S/C21H19FN4O/c1-13(27)12-25-18-11-15(8-10-23-18)20-19(14-4-6-16(22)7-5-14)21-17(26-20)3-2-9-24-21/h2-11,13,26-27H,12H2,1H3,(H,23,25)/t13-/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15773
((2S)-1-({4-[3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]py...)Show SMILES C[C@H](O)CNc1cc(ccn1)-c1[nH]c2cccnc2c1-c1ccc(F)cc1 |r| Show InChI InChI=1S/C21H19FN4O/c1-13(27)12-25-18-11-15(8-10-23-18)20-19(14-4-6-16(22)7-5-14)21-17(26-20)3-2-9-24-21/h2-11,13,26-27H,12H2,1H3,(H,23,25)/t13-/m0/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 1 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15776
(2-({4-[3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridin...)Show SMILES CC(CO)Nc1cc(ccn1)-c1[nH]c2cccnc2c1-c1ccc(F)cc1 Show InChI InChI=1S/C21H19FN4O/c1-13(12-27)25-18-11-15(8-10-23-18)20-19(14-4-6-16(22)7-5-14)21-17(26-20)3-2-9-24-21/h2-11,13,26-27H,12H2,1H3,(H,23,25) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15775
(1-({4-[3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridin...)Show SMILES CCC(O)CNc1cc(ccn1)-c1[nH]c2cccnc2c1-c1ccc(F)cc1 Show InChI InChI=1S/C22H21FN4O/c1-2-17(28)13-26-19-12-15(9-11-24-19)21-20(14-5-7-16(23)8-6-14)22-18(27-21)4-3-10-25-22/h3-12,17,27-28H,2,13H2,1H3,(H,24,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15772
(4-({4-[3-(4-fluorophenyl)-1H-pyrrolo[3,2-b]pyridin...)Show SMILES OCCCCNc1cc(ccn1)-c1[nH]c2cccnc2c1-c1ccc(F)cc1 Show InChI InChI=1S/C22H21FN4O/c23-17-7-5-15(6-8-17)20-21(27-18-4-3-11-26-22(18)20)16-9-12-25-19(14-16)24-10-1-2-13-28/h3-9,11-12,14,27-28H,1-2,10,13H2,(H,24,25) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15756
(3-(4-Fluorophenyl)-2-(pyridin-4-yl)-1H-pyrrolo[3,2...)Show InChI InChI=1S/C18H12FN3/c19-14-5-3-12(4-6-14)16-17(13-7-10-20-11-8-13)22-15-2-1-9-21-18(15)16/h1-11,22H | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 6.5 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151775
(3-(4-Fluoro-phenylsulfanyl)-6-methanesulfonyl-2-me...)Show InChI InChI=1S/C16H14FNO2S2/c1-10-16(21-12-5-3-11(17)4-6-12)14-8-7-13(22(2,19)20)9-15(14)18-10/h3-9,18H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 20 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15764
(3-(4-Fluorophenyl)-1-methoxy-ethyl-2-pyridin-4-yl-...)Show SMILES COC(C)n1c(c(-c2ccc(F)cc2)c2ncccc12)-c1ccncc1 Show InChI InChI=1S/C21H18FN3O/c1-14(26-2)25-18-4-3-11-24-20(18)19(15-5-7-17(22)8-6-15)21(25)16-9-12-23-13-10-16/h3-14H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 21 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15765
(3-(4-Fluorophenyl)-1-ethyl-2-pyridin-4-yl-1H-pyrro...)Show InChI InChI=1S/C20H16FN3/c1-2-24-17-4-3-11-23-19(17)18(14-5-7-16(21)8-6-14)20(24)15-9-12-22-13-10-15/h3-13H,2H2,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 24 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151760
(3-(4-Fluoro-phenoxy)-6-methanesulfonyl-2-methyl-1H...)Show InChI InChI=1S/C16H14FNO3S/c1-10-16(21-12-5-3-11(17)4-6-12)14-8-7-13(22(2,19)20)9-15(14)18-10/h3-9,18H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15759
(4,7 Diazaindole 22 | 4-[7-(4-fluorophenyl)-5H-pyrr...)Show InChI InChI=1S/C17H11FN4/c18-13-3-1-11(2-4-13)14-15(12-5-7-19-8-6-12)22-17-16(14)20-9-10-21-17/h1-10H,(H,21,22) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 53 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15763
(3-(4-Fluoro-phenyl)-1-methoxy-2-pyridin-4-yl-1H-py...)Show InChI InChI=1S/C19H14FN3O/c1-24-23-16-3-2-10-22-18(16)17(13-4-6-15(20)7-5-13)19(23)14-8-11-21-12-9-14/h2-12H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 68 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151758
(3-(2-Chloro-benzyl)-6-methanesulfonyl-2-methyl-1H-...)Show InChI InChI=1S/C17H16ClNO2S/c1-11-15(9-12-5-3-4-6-16(12)18)14-8-7-13(22(2,20)21)10-17(14)19-11/h3-8,10,19H,9H2,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 70 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151763
(3-(4-Fluoro-benzyl)-6-methanesulfonyl-2-methyl-1H-...)Show InChI InChI=1S/C17H16FNO2S/c1-11-16(9-12-3-5-13(18)6-4-12)15-8-7-14(22(2,20)21)10-17(15)19-11/h3-8,10,19H,9H2,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 80 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15762
(3-(4-Fluorophenyl-2-(pyridin-4yl)furo[3,2-b]pyridi...)Show InChI InChI=1S/C18H11FN2O/c19-14-5-3-12(4-6-14)16-17-15(2-1-9-21-17)22-18(16)13-7-10-20-11-8-13/h1-11H | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Patents
| Article PubMed
| n/a | n/a | 86 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15766
(3-(4-Fluorophenyl)-1-methyl-2-pyridin-4-yl-1H-pyrr...)Show InChI InChI=1S/C19H14FN3/c1-23-16-3-2-10-22-18(16)17(13-4-6-15(20)7-5-13)19(23)14-8-11-21-12-9-14/h2-12H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 98 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151765
(3-(2,4-Difluoro-phenoxy)-6-methanesulfonyl-2-methy...)Show InChI InChI=1S/C16H13F2NO3S/c1-9-16(22-15-6-3-10(17)7-13(15)18)12-5-4-11(23(2,20)21)8-14(12)19-9/h3-8,19H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151762
(3-(2,4-Dichloro-phenoxy)-6-methanesulfonyl-2-methy...)Show SMILES Cc1[nH]c2cc(ccc2c1Oc1ccc(Cl)cc1Cl)S(C)(=O)=O Show InChI InChI=1S/C16H13Cl2NO3S/c1-9-16(22-15-6-3-10(17)7-13(15)18)12-5-4-11(23(2,20)21)8-14(12)19-9/h3-8,19H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 110 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151768
(3-(2-Chloro-phenylsulfanyl)-6-methanesulfonyl-1H-i...)Show SMILES CS(=O)(=O)c1ccc2c(Sc3ccccc3Cl)c([nH]c2c1)C#N Show InChI InChI=1S/C16H11ClN2O2S2/c1-23(20,21)10-6-7-11-13(8-10)19-14(9-18)16(11)22-15-5-3-2-4-12(15)17/h2-8,19H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15767
(1-[3-(4-fluorophenyl)-2-(pyridin-4-yl)-1H-pyrrolo[...)Show SMILES CC(O)n1c(c(-c2ccc(F)cc2)c2ncccc12)-c1ccncc1 Show InChI InChI=1S/C20H16FN3O/c1-13(25)24-17-3-2-10-23-19(17)18(14-4-6-16(21)7-5-14)20(24)15-8-11-22-12-9-15/h2-13,25H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 172 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15768
(3-(4-Fluorophenyl)-1-morpholinoethyl-2-pyridin-4-y...)Show SMILES CC(N1CCOCC1)n1c(c(-c2ccc(F)cc2)c2ncccc12)-c1ccncc1 Show InChI InChI=1S/C24H23FN4O/c1-17(28-13-15-30-16-14-28)29-21-3-2-10-27-23(21)22(18-4-6-20(25)7-5-18)24(29)19-8-11-26-12-9-19/h2-12,17H,13-16H2,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 185 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151759
(6-Methanesulfonyl-3-(4-methoxy-phenoxy)-2-methyl-1...)Show SMILES COc1ccc(Oc2c(C)[nH]c3cc(ccc23)S(C)(=O)=O)cc1 Show InChI InChI=1S/C17H17NO4S/c1-11-17(22-13-6-4-12(21-2)5-7-13)15-9-8-14(23(3,19)20)10-16(15)18-11/h4-10,18H,1-3H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151773
(4-Methanesulfonyl-3-(4-methoxy-phenoxy)-2-methyl-1...)Show SMILES COc1ccc(Oc2c(C)[nH]c3cccc(c23)S(C)(=O)=O)cc1 Show InChI InChI=1S/C17H17NO4S/c1-11-17(22-13-9-7-12(21-2)8-10-13)16-14(18-11)5-4-6-15(16)23(3,19)20/h4-10,18H,1-3H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15769
(3-(4-Fluorophenyl)-1-pyrrolidinoethyl-2-pyridin-4-...)Show SMILES CC(N1CCCC1)n1c(c(-c2ccc(F)cc2)c2ncccc12)-c1ccncc1 Show InChI InChI=1S/C24H23FN4/c1-17(28-15-2-3-16-28)29-21-5-4-12-27-23(21)22(18-6-8-20(25)9-7-18)24(29)19-10-13-26-14-11-19/h4-14,17H,2-3,15-16H2,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 217 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151766
(3-(4-Chloro-benzyl)-6-methanesulfonyl-2-methyl-1H-...)Show InChI InChI=1S/C17H16ClNO2S/c1-11-16(9-12-3-5-13(18)6-4-12)15-8-7-14(22(2,20)21)10-17(15)19-11/h3-8,10,19H,9H2,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 260 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151782
(3-(2,4-Difluoro-benzyl)-6-methanesulfonyl-2-methyl...)Show InChI InChI=1S/C17H15F2NO2S/c1-10-15(7-11-3-4-12(18)8-16(11)19)14-6-5-13(23(2,21)22)9-17(14)20-10/h3-6,8-9,20H,7H2,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 260 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151783
(6-Methanesulfonyl-3-(4-methoxy-benzyl)-2-methyl-1H...)Show SMILES COc1ccc(Cc2c(C)[nH]c3cc(ccc23)S(C)(=O)=O)cc1 Show InChI InChI=1S/C18H19NO3S/c1-12-17(10-13-4-6-14(22-2)7-5-13)16-9-8-15(23(3,20)21)11-18(16)19-12/h4-9,11,19H,10H2,1-3H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 270 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151767
(3-(4-Chloro-phenoxy)-6-methanesulfonyl-2-methyl-1H...)Show InChI InChI=1S/C16H14ClNO3S/c1-10-16(21-12-5-3-11(17)4-6-12)14-8-7-13(22(2,19)20)9-15(14)18-10/h3-9,18H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 300 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151770
(3-(2-Chloro-4-methoxy-phenylsulfanyl)-6-methanesul...)Show SMILES COc1ccc(Sc2c([nH]c3cc(ccc23)S(C)(=O)=O)C#N)c(Cl)c1 Show InChI InChI=1S/C17H13ClN2O3S2/c1-23-10-3-6-16(13(18)7-10)24-17-12-5-4-11(25(2,21)22)8-14(12)20-15(17)9-19/h3-8,20H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 330 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151776
(3-(2,4-Difluoro-phenylsulfanyl)-6-methanesulfonyl-...)Show SMILES COC(=O)c1[nH]c2cc(ccc2c1Sc1ccc(F)cc1F)S(C)(=O)=O Show InChI InChI=1S/C17H13F2NO4S2/c1-24-17(21)15-16(25-14-6-3-9(18)7-12(14)19)11-5-4-10(26(2,22)23)8-13(11)20-15/h3-8,20H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 380 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151776
(3-(2,4-Difluoro-phenylsulfanyl)-6-methanesulfonyl-...)Show SMILES COC(=O)c1[nH]c2cc(ccc2c1Sc1ccc(F)cc1F)S(C)(=O)=O Show InChI InChI=1S/C17H13F2NO4S2/c1-24-17(21)15-16(25-14-6-3-9(18)7-12(14)19)11-5-4-10(26(2,22)23)8-13(11)20-15/h3-8,20H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 380 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151784
(CHEMBL184022 | [3-(4-Fluoro-phenylsulfanyl)-6-meth...)Show SMILES CS(=O)(=O)c1ccc2c(Sc3ccc(F)cc3)c(CO)[nH]c2c1 Show InChI InChI=1S/C16H14FNO3S2/c1-23(20,21)12-6-7-13-14(8-12)18-15(9-19)16(13)22-11-4-2-10(17)3-5-11/h2-8,18-19H,9H2,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 420 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151774
(6-Methanesulfonyl-3-(4-methoxy-phenylsulfanyl)-2-m...)Show SMILES COc1ccc(Sc2c(C)[nH]c3cc(ccc23)S(C)(=O)=O)cc1 Show InChI InChI=1S/C17H17NO3S2/c1-11-17(22-13-6-4-12(21-2)5-7-13)15-9-8-14(23(3,19)20)10-16(15)18-11/h4-10,18H,1-3H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 470 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151768
(3-(2-Chloro-phenylsulfanyl)-6-methanesulfonyl-1H-i...)Show SMILES CS(=O)(=O)c1ccc2c(Sc3ccccc3Cl)c([nH]c2c1)C#N Show InChI InChI=1S/C16H11ClN2O2S2/c1-23(20,21)10-6-7-11-13(8-10)19-14(9-18)16(11)22-15-5-3-2-4-12(15)17/h2-8,19H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 570 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151779
((4-Fluoro-phenyl)-(6-methanesulfonyl-2-methyl-1H-i...)Show SMILES Cc1[nH]c2cc(ccc2c1C(=O)c1ccc(F)cc1)S(C)(=O)=O Show InChI InChI=1S/C17H14FNO3S/c1-10-16(17(20)11-3-5-12(18)6-4-11)14-8-7-13(23(2,21)22)9-15(14)19-10/h3-9,19H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 660 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151772
(3-(2,4-Difluoro-phenylsulfanyl)-6-methanesulfonyl-...)Show InChI InChI=1S/C16H13F2NO2S2/c1-9-16(22-15-6-3-10(17)7-13(15)18)12-5-4-11(23(2,20)21)8-14(12)19-9/h3-8,19H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 770 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151777
(3-(4-Fluoro-phenylsulfanyl)-6-methanesulfonyl-1H-i...)Show SMILES COC(=O)c1[nH]c2cc(ccc2c1Sc1ccc(F)cc1)S(C)(=O)=O Show InChI InChI=1S/C17H14FNO4S2/c1-23-17(20)15-16(24-11-5-3-10(18)4-6-11)13-8-7-12(25(2,21)22)9-14(13)19-15/h3-9,19H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 800 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15760
(4,6 Diazaindole 24 | 4-[7-(4-fluorophenyl)-5H-pyrr...)Show InChI InChI=1S/C17H11FN4/c18-13-3-1-11(2-4-13)15-16(12-5-7-19-8-6-12)22-14-9-20-10-21-17(14)15/h1-10,22H | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 895 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151764
(3-(2,4-Difluoro-phenylsulfanyl)-6-methanesulfonyl-...)Show SMILES CS(=O)(=O)c1ccc2c(Sc3ccc(F)cc3F)c([nH]c2c1)C#N Show InChI InChI=1S/C16H10F2N2O2S2/c1-24(21,22)10-3-4-11-13(7-10)20-14(8-19)16(11)23-15-5-2-9(17)6-12(15)18/h2-7,20H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 940 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151771
(3-(4-Fluoro-phenylsulfanyl)-6-methanesulfonyl-1H-i...)Show SMILES CS(=O)(=O)c1ccc2c(Sc3ccc(F)cc3)c([nH]c2c1)C#N Show InChI InChI=1S/C16H11FN2O2S2/c1-23(20,21)12-6-7-13-14(8-12)19-15(9-18)16(13)22-11-4-2-10(17)3-5-11/h2-8,19H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.01E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151770
(3-(2-Chloro-4-methoxy-phenylsulfanyl)-6-methanesul...)Show SMILES COc1ccc(Sc2c([nH]c3cc(ccc23)S(C)(=O)=O)C#N)c(Cl)c1 Show InChI InChI=1S/C17H13ClN2O3S2/c1-23-10-3-6-16(13(18)7-10)24-17-12-5-4-11(25(2,21)22)8-14(12)20-15(17)9-19/h3-8,20H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.09E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151778
((6-Methanesulfonyl-2-methyl-1H-indol-3-yl)-(4-meth...)Show SMILES COc1ccc(cc1)C(=O)c1c(C)[nH]c2cc(ccc12)S(C)(=O)=O Show InChI InChI=1S/C18H17NO4S/c1-11-17(18(20)12-4-6-13(23-2)7-5-12)15-9-8-14(24(3,21)22)10-16(15)19-11/h4-10,19H,1-3H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.09E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151777
(3-(4-Fluoro-phenylsulfanyl)-6-methanesulfonyl-1H-i...)Show SMILES COC(=O)c1[nH]c2cc(ccc2c1Sc1ccc(F)cc1)S(C)(=O)=O Show InChI InChI=1S/C17H14FNO4S2/c1-23-17(20)15-16(24-11-5-3-10(18)4-6-11)13-8-7-12(25(2,21)22)9-14(13)19-15/h3-9,19H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151780
(3-(4-Fluoro-phenylsulfanyl)-6-methanesulfonyl-1H-i...)Show SMILES CS(=O)(=O)c1ccc2c(Sc3ccc(F)cc3)c([nH]c2c1)C(N)=O Show InChI InChI=1S/C16H13FN2O3S2/c1-24(21,22)11-6-7-12-13(8-11)19-14(16(18)20)15(12)23-10-4-2-9(17)3-5-10/h2-8,19H,1H3,(H2,18,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.21E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151764
(3-(2,4-Difluoro-phenylsulfanyl)-6-methanesulfonyl-...)Show SMILES CS(=O)(=O)c1ccc2c(Sc3ccc(F)cc3F)c([nH]c2c1)C#N Show InChI InChI=1S/C16H10F2N2O2S2/c1-24(21,22)10-3-4-11-13(7-10)20-14(8-19)16(11)23-15-5-2-9(17)6-12(15)18/h2-7,20H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 1.27E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151759
(6-Methanesulfonyl-3-(4-methoxy-phenoxy)-2-methyl-1...)Show SMILES COc1ccc(Oc2c(C)[nH]c3cc(ccc23)S(C)(=O)=O)cc1 Show InChI InChI=1S/C17H17NO4S/c1-11-17(22-13-6-4-12(21-2)5-7-13)15-9-8-14(23(3,19)20)10-16(15)18-11/h4-10,18H,1-3H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151773
(4-Methanesulfonyl-3-(4-methoxy-phenoxy)-2-methyl-1...)Show SMILES COc1ccc(Oc2c(C)[nH]c3cccc(c23)S(C)(=O)=O)cc1 Show InChI InChI=1S/C17H17NO4S/c1-11-17(22-13-9-7-12(21-2)8-10-13)16-14(18-11)5-4-6-15(16)23(3,19)20/h4-10,18H,1-3H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151779
((4-Fluoro-phenyl)-(6-methanesulfonyl-2-methyl-1H-i...)Show SMILES Cc1[nH]c2cc(ccc2c1C(=O)c1ccc(F)cc1)S(C)(=O)=O Show InChI InChI=1S/C17H14FNO3S/c1-10-16(17(20)11-3-5-12(18)6-4-11)14-8-7-13(23(2,21)22)9-15(14)19-10/h3-9,19H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.72E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description Inhibitory concentration against human whole blood Prostaglandin G/H synthase 2 enzyme activity was determined |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Prostaglandin G/H synthase 2
(Homo sapiens (Human)) | BDBM50151769
(6-Methanesulfonyl-2-methyl-3-(pyridin-2-ylsulfanyl...)Show InChI InChI=1S/C15H14N2O2S2/c1-10-15(20-14-5-3-4-8-16-14)12-7-6-11(21(2,18)19)9-13(12)17-10/h3-9,17H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.78E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Roche Palo Alto
Curated by ChEMBL
| Assay Description In vitro inhibitory concentration against Prostaglandin G/H synthase 2 enzyme activity |
Bioorg Med Chem Lett 14: 4741-5 (2004)
Article DOI: 10.1016/j.bmcl.2004.06.075 BindingDB Entry DOI: 10.7270/Q228072S |
More data for this Ligand-Target Pair | |
Mitogen-activated protein kinase 14
(Homo sapiens (Human)) | BDBM15758
(3-(4-Fluorophenyl)-2-pyridin-4-yl-1H-indole | 3-(4...)Show InChI InChI=1S/C19H13FN2/c20-15-7-5-13(6-8-15)18-16-3-1-2-4-17(16)22-19(18)14-9-11-21-12-10-14/h1-12,22H | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a | 7.4 | 30 |
Roche Palo Alto LLC
| Assay Description Inhibition of human recombinant active p38alpha MAP kinase was tested by measuring the incorporation of 33P from gamma-[33P] ATP into myelin basic pr... |
J Med Chem 46: 4702-13 (2003)
Article DOI: 10.1021/jm0301787 BindingDB Entry DOI: 10.7270/Q2ZG6QHT |
More data for this Ligand-Target Pair | |