Found 51 hits of Enzyme Inhibition Constant Data 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 |
|---|
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50139601
(1-(4-bromo-3-(trifluoromethyl)phenyl)-3-(4-(2-(met...)Show SMILES CNC(=O)c1cc(Oc2ccc(NC(=O)Nc3ccc(Br)c(c3)C(F)(F)F)cc2)ccn1 Show InChI InChI=1S/C21H16BrF3N4O3/c1-26-19(30)18-11-15(8-9-27-18)32-14-5-2-12(3-6-14)28-20(31)29-13-4-7-17(22)16(10-13)21(23,24)25/h2-11H,1H3,(H,26,30)(H2,28,29,31) | 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 | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM16673
(4-[4-({[4-chloro-3-(trifluoromethyl)phenyl]carbamo...)Show SMILES CNC(=O)c1cc(Oc2ccc(NC(=O)Nc3ccc(Cl)c(c3)C(F)(F)F)cc2)ccn1 Show InChI InChI=1S/C21H16ClF3N4O3/c1-26-19(30)18-11-15(8-9-27-18)32-14-5-2-12(3-6-14)28-20(31)29-13-4-7-17(22)16(10-13)21(23,24)25/h2-11H,1H3,(H,26,30)(H2,28,29,31) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
DrugBank
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| DrugBank
Article
PubMed
| n/a | n/a | 12 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50139614
(4-(4-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido...)Show SMILES CCNC(=O)c1cc(Oc2ccc(NC(=O)Nc3ccc(Cl)c(c3)C(F)(F)F)cc2)ccn1 Show InChI InChI=1S/C22H18ClF3N4O3/c1-2-27-20(31)19-12-16(9-10-28-19)33-15-6-3-13(4-7-15)29-21(32)30-14-5-8-18(23)17(11-14)22(24,25)26/h3-12H,2H2,1H3,(H,27,31)(H2,29,30,32) | 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 | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249245
(4-(4-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido...)Show SMILES FC(F)(F)c1cc(NC(=O)Nc2ccc(Oc3ccnc(c3)C(=O)Nc3cccnc3)cc2)ccc1Cl Show InChI InChI=1S/C25H17ClF3N5O3/c26-21-8-5-16(12-20(21)25(27,28)29)34-24(36)33-15-3-6-18(7-4-15)37-19-9-11-31-22(13-19)23(35)32-17-2-1-10-30-14-17/h1-14H,(H,32,35)(H2,33,34,36) | 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 | 44 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50139597
(4-(4-(3-(2-methoxy-5-(trifluoromethyl)phenyl)ureid...)Show SMILES CNC(=O)c1cc(Oc2ccc(NC(=O)Nc3cc(ccc3OC)C(F)(F)F)cc2)ccn1 Show InChI InChI=1S/C22H19F3N4O4/c1-26-20(30)18-12-16(9-10-27-18)33-15-6-4-14(5-7-15)28-21(31)29-17-11-13(22(23,24)25)3-8-19(17)32-2/h3-12H,1-2H3,(H,26,30)(H2,28,29,31) | 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 | 53 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50139596
(4-(4-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido...)Show SMILES FC(F)(F)c1cc(NC(=O)Nc2ccc(Oc3ccnc(c3)C(=O)NCCN3CCOCC3)cc2)ccc1Cl Show InChI InChI=1S/C26H25ClF3N5O4/c27-22-6-3-18(15-21(22)26(28,29)30)34-25(37)33-17-1-4-19(5-2-17)39-20-7-8-31-23(16-20)24(36)32-9-10-35-11-13-38-14-12-35/h1-8,15-16H,9-14H2,(H,32,36)(H2,33,34,37) | 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 | 73 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249276
(4-(4-(3-(4-chloro-2-methoxy-5-(trifluoromethyl)phe...)Show SMILES CCNC(=O)c1cc(Oc2ccc(NC(=O)Nc3cc(c(Cl)cc3OC)C(F)(F)F)cc2)ccn1 Show InChI InChI=1S/C23H20ClF3N4O4/c1-3-28-21(32)19-10-15(8-9-29-19)35-14-6-4-13(5-7-14)30-22(33)31-18-11-16(23(25,26)27)17(24)12-20(18)34-2/h4-12H,3H2,1-2H3,(H,28,32)(H2,30,31,33) | 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 | 88 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249376
(1-(3-tert-butylisoxazol-5-yl)-3-(4-(pyridin-4-ylox...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(Oc3ccncc3)cc2)on1 Show InChI InChI=1S/C19H20N4O3/c1-19(2,3)16-12-17(26-23-16)22-18(24)21-13-4-6-14(7-5-13)25-15-8-10-20-11-9-15/h4-12H,1-3H3,(H2,21,22,24) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50139609
(3-(4-(3-(5-tert-butylisoxazol-3-yl)ureido)phenoxy)...)Show SMILES CNC(=O)c1cccc(Oc2ccc(NC(=O)Nc3cc(on3)C(C)(C)C)cc2)c1 Show InChI InChI=1S/C22H24N4O4/c1-22(2,3)18-13-19(26-30-18)25-21(28)24-15-8-10-16(11-9-15)29-17-7-5-6-14(12-17)20(27)23-4/h5-13H,1-4H3,(H,23,27)(H2,24,25,26,28) | 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 | 120 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249277
(4-(4-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido...)Show SMILES FC(F)(F)c1cc(NC(=O)Nc2ccc(Oc3ccnc(c3)C(=O)Nc3ccc(cc3)N3CCOCC3)cc2)ccc1Cl Show InChI InChI=1S/C30H25ClF3N5O4/c31-26-10-5-21(17-25(26)30(32,33)34)38-29(41)37-20-3-8-23(9-4-20)43-24-11-12-35-27(18-24)28(40)36-19-1-6-22(7-2-19)39-13-15-42-16-14-39/h1-12,17-18H,13-16H2,(H,36,40)(H2,37,38,41) | 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 | 160 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249278
(4-(4-(3-(4-chloro-3-(trifluoromethyl)phenyl)ureido...)Show SMILES CN(C)c1ccc(NC(=O)c2cc(Oc3ccc(NC(=O)Nc4ccc(Cl)c(c4)C(F)(F)F)cc3)ccn2)cc1 Show InChI InChI=1S/C28H23ClF3N5O3/c1-37(2)20-8-3-17(4-9-20)34-26(38)25-16-22(13-14-33-25)40-21-10-5-18(6-11-21)35-27(39)36-19-7-12-24(29)23(15-19)28(30,31)32/h3-16H,1-2H3,(H,34,38)(H2,35,36,39) | 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 | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50139604
(1-(5-tert-Butyl-isoxazol-3-yl)-3-[4-(pyridin-4-ylo...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(Oc3ccncc3)cc2)no1 Show InChI InChI=1S/C19H20N4O3/c1-19(2,3)16-12-17(23-26-16)22-18(24)21-13-4-6-14(7-5-13)25-15-8-10-20-11-9-15/h4-12H,1-3H3,(H2,21,22,23,24) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249279
(1-(3-methoxyphenyl)-3-(4-(pyridin-4-yloxy)phenyl)u...)Show InChI InChI=1S/C19H17N3O3/c1-24-18-4-2-3-15(13-18)22-19(23)21-14-5-7-16(8-6-14)25-17-9-11-20-12-10-17/h2-13H,1H3,(H2,21,22,23) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
PC cid
PC sid
UniChem
| Article
PubMed
| n/a | n/a | 440 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249313
(1-(5-tert-butylisoxazol-3-yl)-3-(4-(4-methoxypheno...)Show SMILES COc1ccc(Oc2ccc(NC(=O)Nc3cc(on3)C(C)(C)C)cc2)cc1 Show InChI InChI=1S/C21H23N3O4/c1-21(2,3)18-13-19(24-28-18)23-20(25)22-14-5-7-16(8-6-14)27-17-11-9-15(26-4)10-12-17/h5-13H,1-4H3,(H2,22,23,24,25) | 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 | 500 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249409
(1-(5-tert-butylisoxazol-3-yl)-3-(4-(pyridin-4-ylme...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(Cc3ccncc3)cc2)no1 Show InChI InChI=1S/C20H22N4O2/c1-20(2,3)17-13-18(24-26-17)23-19(25)22-16-6-4-14(5-7-16)12-15-8-10-21-11-9-15/h4-11,13H,12H2,1-3H3,(H2,22,23,24,25) | 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 | 590 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249377
(1-(5-tert-butylisoxazol-3-yl)-3-(2,3-dimethyl-4-ph...)Show SMILES Cc1c(NC(=O)Nc2cc(on2)C(C)(C)C)ccc(Oc2ccccc2)c1C Show InChI InChI=1S/C22H25N3O3/c1-14-15(2)18(27-16-9-7-6-8-10-16)12-11-17(14)23-21(26)24-20-13-19(28-25-20)22(3,4)5/h6-13H,1-5H3,(H2,23,24,25,26) | 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 | 650 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249346
(1-(5-tert-butylisoxazol-3-yl)-3-(4-(3-methoxypheno...)Show SMILES COc1cccc(Oc2ccc(NC(=O)Nc3cc(on3)C(C)(C)C)cc2)c1 Show InChI InChI=1S/C21H23N3O4/c1-21(2,3)18-13-19(24-28-18)23-20(25)22-14-8-10-15(11-9-14)27-17-7-5-6-16(12-17)26-4/h5-13H,1-4H3,(H2,22,23,24,25) | 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 | 700 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249406
(1-(3-tert-butyl-1-methyl-1H-pyrazol-5-yl)-3-(4-(py...)Show SMILES Cn1nc(cc1NC(=O)Nc1ccc(Oc2ccncc2)cc1)C(C)(C)C Show InChI InChI=1S/C20H23N5O2/c1-20(2,3)17-13-18(25(4)24-17)23-19(26)22-14-5-7-15(8-6-14)27-16-9-11-21-12-10-16/h5-13H,1-4H3,(H2,22,23,26) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
MCE
MMDB
PC cid
PC sid
PDB
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 800 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249347
(1-(4-(3-acetylphenoxy)phenyl)-3-(5-tert-butylisoxa...)Show SMILES CC(=O)c1cccc(Oc2ccc(NC(=O)Nc3cc(on3)C(C)(C)C)cc2)c1 Show InChI InChI=1S/C22H23N3O4/c1-14(26)15-6-5-7-18(12-15)28-17-10-8-16(9-11-17)23-21(27)24-20-13-19(29-25-20)22(2,3)4/h5-13H,1-4H3,(H2,23,24,25,27) | 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 | 820 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249310
(1-(3-tert-butylphenyl)-3-(4-(pyridin-4-yloxy)pheny...)Show SMILES CC(C)(C)c1cccc(NC(=O)Nc2ccc(Oc3ccncc3)cc2)c1 Show InChI InChI=1S/C22H23N3O2/c1-22(2,3)16-5-4-6-18(15-16)25-21(26)24-17-7-9-19(10-8-17)27-20-11-13-23-14-12-20/h4-15H,1-3H3,(H2,24,25,26) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 870 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249348
(1-(5-tert-butylisoxazol-3-yl)-3-(4-(m-tolyloxy)phe...)Show SMILES Cc1cccc(Oc2ccc(NC(=O)Nc3cc(on3)C(C)(C)C)cc2)c1 Show InChI InChI=1S/C21H23N3O3/c1-14-6-5-7-17(12-14)26-16-10-8-15(9-11-16)22-20(25)23-19-13-18(27-24-19)21(2,3)4/h5-13H,1-4H3,(H2,22,23,24,25) | 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 | 1.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105619
(1-(5-tert-Butyl-isoxazol-3-yl)-3-(4-phenoxy-phenyl...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(Oc3ccccc3)cc2)no1 Show InChI InChI=1S/C20H21N3O3/c1-20(2,3)17-13-18(23-26-17)22-19(24)21-14-9-11-16(12-10-14)25-15-7-5-4-6-8-15/h4-13H,1-3H3,(H2,21,22,23,24) | 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 | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249349
(4-(4-(3-(5-tert-butylisoxazol-3-yl)ureido)phenoxy)...)Show SMILES CNC(=O)c1ccc(Oc2ccc(NC(=O)Nc3cc(on3)C(C)(C)C)cc2)cc1 Show InChI InChI=1S/C22H24N4O4/c1-22(2,3)18-13-19(26-30-18)25-21(28)24-15-7-11-17(12-8-15)29-16-9-5-14(6-10-16)20(27)23-4/h5-13H,1-4H3,(H,23,27)(H2,24,25,26,28) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
MCE
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249408
(1-(5-tert-butylisoxazol-3-yl)-3-(2-methyl-4-phenox...)Show SMILES Cc1cc(Oc2ccccc2)ccc1NC(=O)Nc1cc(on1)C(C)(C)C Show InChI InChI=1S/C21H23N3O3/c1-14-12-16(26-15-8-6-5-7-9-15)10-11-17(14)22-20(25)23-19-13-18(27-24-19)21(2,3)4/h5-13H,1-4H3,(H2,22,23,24,25) | 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 | 1.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249444
(1-(5-tert-butylisoxazol-3-yl)-3-(4-(hydroxy(pyridi...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(cc2)C(O)c2ccncc2)no1 Show InChI InChI=1S/C20H22N4O3/c1-20(2,3)16-12-17(24-27-16)23-19(26)22-15-6-4-13(5-7-15)18(25)14-8-10-21-11-9-14/h4-12,18,25H,1-3H3,(H2,22,23,24,26) | 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 | 1.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50095399
(5-tert-Butyl-3-(3-p-tolyl-ureido)-thiophene-2-carb...)Show InChI InChI=1S/C18H22N2O3S/c1-11-6-8-12(9-7-11)19-17(22)20-13-10-14(18(2,3)4)24-15(13)16(21)23-5/h6-10H,1-5H3,(H2,19,20,22) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| Purchase
CHEMBL
PC cid
PC sid
UniChem
Patents
Similars
| Article
PubMed
| n/a | n/a | 1.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105597
(5-tert-Butyl-3-[3-(5-ethyl-[1,3,4]thiadiazol-2-yl)...)Show InChI InChI=1S/C15H20N4O3S2/c1-6-10-18-19-14(24-10)17-13(21)16-8-7-9(15(2,3)4)23-11(8)12(20)22-5/h7H,6H2,1-5H3,(H2,16,17,19,21) | 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 | 2.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249311
(1-(3-chloro-2-methoxyphenyl)-3-(4-(pyridin-4-yloxy...)Show InChI InChI=1S/C19H16ClN3O3/c1-25-18-16(20)3-2-4-17(18)23-19(24)22-13-5-7-14(8-6-13)26-15-9-11-21-12-10-15/h2-12H,1H3,(H2,22,23,24) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 2.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50095428
(5-tert-Butyl-3-(3-p-tolyl-ureido)-1H-pyrrole-2-car...)Show SMILES COC(=O)c1[nH]c(cc1NC(=O)Nc1ccc(C)cc1)C(C)(C)C Show InChI InChI=1S/C18H23N3O3/c1-11-6-8-12(9-7-11)19-17(23)20-13-10-14(18(2,3)4)21-15(13)16(22)24-5/h6-10,21H,1-5H3,(H2,19,20,23) | 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 | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105612
(5-Isopropyl-3-(3-p-tolyl-ureido)-thiophene-2-carbo...)Show InChI InChI=1S/C17H20N2O3S/c1-10(2)14-9-13(15(23-14)16(20)22-4)19-17(21)18-12-7-5-11(3)6-8-12/h5-10H,1-4H3,(H2,18,19,21) | 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 | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50237709
(4-(4-(3-(5-tert-butylisoxazol-3-yl)ureido)phenoxy)...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(Oc3ccc(cc3)C(O)=O)cc2)no1 Show InChI InChI=1S/C21H21N3O5/c1-21(2,3)17-12-18(24-29-17)23-20(27)22-14-6-10-16(11-7-14)28-15-8-4-13(5-9-15)19(25)26/h4-12H,1-3H3,(H,25,26)(H2,22,23,24,27) | 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 | 4.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249312
(1-(2-methoxy-4-nitrophenyl)-3-(4-(pyridin-4-yloxy)...)Show SMILES COc1cc(ccc1NC(=O)Nc1ccc(Oc2ccncc2)cc1)[N+]([O-])=O Show InChI InChI=1S/C19H16N4O5/c1-27-18-12-14(23(25)26)4-7-17(18)22-19(24)21-13-2-5-15(6-3-13)28-16-8-10-20-11-9-16/h2-12H,1H3,(H2,21,22,24) | 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 | 4.40E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50095430
(5-tert-Butyl-1-methyl-3-(3-p-tolyl-ureido)-1H-pyrr...)Show SMILES COC(=O)c1c(NC(=O)Nc2ccc(C)cc2)cc(n1C)C(C)(C)C Show InChI InChI=1S/C19H25N3O3/c1-12-7-9-13(10-8-12)20-18(24)21-14-11-15(19(2,3)4)22(5)16(14)17(23)25-6/h7-11H,1-6H3,(H2,20,21,24) | 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 | 5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105599
(5-Bromomethyl-3-(3-p-tolyl-ureido)-thiophene-2-car...)Show InChI InChI=1S/C15H15BrN2O3S/c1-9-3-5-10(6-4-9)17-15(20)18-12-7-11(8-16)22-13(12)14(19)21-2/h3-7H,8H2,1-2H3,(H2,17,18,20) | 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 | 6.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105613
(5-tert-Butyl-3-[3-(1-methyl-1H-pyrazol-3-yl)-ureid...)Show InChI InChI=1S/C15H20N4O3S/c1-15(2,3)10-8-9(12(23-10)13(20)22-5)16-14(21)17-11-6-7-19(4)18-11/h6-8H,1-5H3,(H2,16,17,18,21) | 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 | 6.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249374
(3-(4-(3-(5-tert-butylisoxazol-3-yl)ureido)phenoxy)...)Show SMILES CNS(=O)(=O)c1cccc(Oc2ccc(NC(=O)Nc3cc(on3)C(C)(C)C)cc2)c1 Show InChI InChI=1S/C21H24N4O5S/c1-21(2,3)18-13-19(25-30-18)24-20(26)23-14-8-10-15(11-9-14)29-16-6-5-7-17(12-16)31(27,28)22-4/h5-13,22H,1-4H3,(H2,23,24,25,26) | 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 | 7.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105598
(5-tert-Butyl-3-[3-(1-ethyl-1H-pyrrol-3-yl)-ureido]...)Show InChI InChI=1S/C17H23N3O3S/c1-6-20-8-7-11(10-20)18-16(22)19-12-9-13(17(2,3)4)24-14(12)15(21)23-5/h7-10H,6H2,1-5H3,(H2,18,19,22) | 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 | 7.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105596
(5-tert-Butyl-3-[3-(1-ethyl-1H-pyrazol-3-yl)-ureido...)Show InChI InChI=1S/C16H22N4O3S/c1-6-20-8-7-12(19-20)18-15(22)17-10-9-11(16(2,3)4)24-13(10)14(21)23-5/h7-9H,6H2,1-5H3,(H2,17,18,19,22) | 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 | 8.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105614
(5-tert-Butyl-3-[3-(1-isopropyl-1H-pyrrol-3-yl)-ure...)Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1ccn(c1)C(C)C)C(C)(C)C Show InChI InChI=1S/C18H25N3O3S/c1-11(2)21-8-7-12(10-21)19-17(23)20-13-9-14(18(3,4)5)25-15(13)16(22)24-6/h7-11H,1-6H3,(H2,19,20,23) | 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 | 8.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249407
(1-(5-tert-butylisoxazol-3-yl)-3-(4-phenoxy-3-(trif...)Show SMILES CC(C)(C)c1cc(NC(=O)Nc2ccc(Oc3ccccc3)c(c2)C(F)(F)F)no1 Show InChI InChI=1S/C21H20F3N3O3/c1-20(2,3)17-12-18(27-30-17)26-19(28)25-13-9-10-16(15(11-13)21(22,23)24)29-14-7-5-4-6-8-14/h4-12H,1-3H3,(H2,25,26,27,28) | 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 | 9.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50249375
(CHEMBL470529 | N-(3-(4-(3-(5-tert-butylisoxazol-3-...)Show SMILES CC(=O)Nc1cccc(Oc2ccc(NC(=O)Nc3cc(on3)C(C)(C)C)cc2C(F)(F)F)c1 Show InChI InChI=1S/C23H23F3N4O4/c1-13(31)27-14-6-5-7-16(10-14)33-18-9-8-15(11-17(18)23(24,25)26)28-21(32)29-20-12-19(34-30-20)22(2,3)4/h5-12H,1-4H3,(H,27,31)(H2,28,29,30,32) | 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 | 1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105604
(5-tert-Butyl-3-[3-(5-tert-butyl-[1,3,4]thiadiazol-...)Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1nnc(s1)C(C)(C)C)C(C)(C)C Show InChI InChI=1S/C17H24N4O3S2/c1-16(2,3)10-8-9(11(25-10)12(22)24-7)18-14(23)19-15-21-20-13(26-15)17(4,5)6/h8H,1-7H3,(H2,18,19,21,23) | 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 | 1.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105607
(5-tert-Butyl-3-[3-(3,4-dichloro-phenyl)-ureido]-1H...)Show SMILES COC(=O)c1[nH]c(cc1NC(=O)Nc1ccc(Cl)c(Cl)c1)C(C)(C)C Show InChI InChI=1S/C17H19Cl2N3O3/c1-17(2,3)13-8-12(14(22-13)15(23)25-4)21-16(24)20-9-5-6-10(18)11(19)7-9/h5-8,22H,1-4H3,(H2,20,21,24) | 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 | 1.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105611
(1-(2-(aminomethyl)-5-tert-butylthiophen-3-yl)-3-p-...)Show InChI InChI=1S/C17H23N3OS/c1-11-5-7-12(8-6-11)19-16(21)20-13-9-15(17(2,3)4)22-14(13)10-18/h5-9H,10,18H2,1-4H3,(H2,19,20,21) | PDB
MMDB
NCI pathway
Reactome pathway
KEGG
UniProtKB/SwissProt
B.MOAD
DrugBank
antibodypedia
GoogleScholar
AffyNet
| CHEMBL
PC cid
PC sid
UniChem
Patents
| Article
PubMed
| n/a | n/a | 1.30E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105618
(1-(5-tert-butyl-2-(dimethylcarbamoyl)thiophen-3-yl...)Show SMILES CN(C)C(=O)c1sc(cc1NC(=O)Nc1ccc(C)cc1)C(C)(C)C Show InChI InChI=1S/C19H25N3O2S/c1-12-7-9-13(10-8-12)20-18(24)21-14-11-15(19(2,3)4)25-16(14)17(23)22(5)6/h7-11H,1-6H3,(H2,20,21,24) | 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 | 1.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105608
(5-tert-Butyl-3-[3-(1-isopropyl-1H-pyrazol-3-yl)-ur...)Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1ccn(n1)C(C)C)C(C)(C)C Show InChI InChI=1S/C17H24N4O3S/c1-10(2)21-8-7-13(20-21)19-16(23)18-11-9-12(17(3,4)5)25-14(11)15(22)24-6/h7-10H,1-6H3,(H2,18,19,20,23) | 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+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50095423
(5-tert-Butyl-3-(3-phenyl-ureido)-thiophene-2-carbo...)Show InChI InChI=1S/C17H20N2O3S/c1-17(2,3)13-10-12(14(23-13)15(20)22-4)19-16(21)18-11-8-6-5-7-9-11/h5-10H,1-4H3,(H2,18,19,21) | 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 | 1.70E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50095411
(5-tert-Butyl-3-[3-(4-hydroxy-phenyl)-ureido]-thiop...)Show InChI InChI=1S/C17H20N2O4S/c1-17(2,3)13-9-12(14(24-13)15(21)23-4)19-16(22)18-10-5-7-11(20)8-6-10/h5-9,20H,1-4H3,(H2,18,19,22) | 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 | 1.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105603
(5-tert-Butyl-3-[3-(3,4-dichloro-phenyl)-ureido]-th...)Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1ccc(Cl)c(Cl)c1)C(C)(C)C Show InChI InChI=1S/C17H18Cl2N2O3S/c1-17(2,3)13-8-12(14(25-13)15(22)24-4)21-16(23)20-9-5-6-10(18)11(19)7-9/h5-8H,1-4H3,(H2,20,21,23) | 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 | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105616
(5-tert-Butyl-3-(3-m-tolyl-ureido)-thiophene-2-carb...)Show InChI InChI=1S/C18H22N2O3S/c1-11-7-6-8-12(9-11)19-17(22)20-13-10-14(18(2,3)4)24-15(13)16(21)23-5/h6-10H,1-5H3,(H2,19,20,22) | 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 | 2.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
RAF proto-oncogene serine/threonine-protein kinase
(Homo sapiens (Human)) | BDBM50105609
(5-tert-Butyl-3-[3-(3-chloro-phenyl)-ureido]-thioph...)Show SMILES COC(=O)c1sc(cc1NC(=O)Nc1cccc(Cl)c1)C(C)(C)C Show InChI InChI=1S/C17H19ClN2O3S/c1-17(2,3)13-9-12(14(24-13)15(21)23-4)20-16(22)19-11-7-5-6-10(18)8-11/h5-9H,1-4H3,(H2,19,20,22) | 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 | 2.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
China Pharmaceutical University
Curated by ChEMBL
| Assay Description
Inhibition of B-Raf1 (unknown origin) |
Eur J Med Chem 44: 1240-9 (2009)
Article DOI: 10.1016/j.ejmech.2008.09.016
BindingDB Entry DOI: 10.7270/Q28G8KJ5 |
More data for this
Ligand-Target Pair | |
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