Found 30 hits with Last Name = 'kesuma' and Initial = 'd' 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 |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM7533
((2R)-2-[[6-(benzylamino)-9-isopropyl-purin-2-yl]am...)Show SMILES CC[C@H](CO)Nc1nc(NCc2ccccc2)c2ncn(C(C)C)c2n1 |r| Show InChI InChI=1S/C19H26N6O/c1-4-15(11-26)22-19-23-17(20-10-14-8-6-5-7-9-14)16-18(24-19)25(12-21-16)13(2)3/h5-9,12-13,15,26H,4,10-11H2,1-3H3,(H2,20,22,23,24)/t15-/m1/s1 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| MMDB PDB PubMed
| n/a | n/a | 800 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cell division cycle 2 (CDK1)-cyclin B |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50111434
(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)Show InChI InChI=1S/C15H12N4/c1-9-13(18-8-17-9)15-14-11(6-7-16-15)10-4-2-3-5-12(10)19-14/h2-8,16H,1H3,(H,17,18) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 5.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 5-p35nck5a |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50111434
(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)Show InChI InChI=1S/C15H12N4/c1-9-13(18-8-17-9)15-14-11(6-7-16-15)10-4-2-3-5-12(10)19-14/h2-8,16H,1H3,(H,17,18) | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 6.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 2-cyclin A |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM5718
(2,6,9-Trisubstituted purine deriv. 26 | 2-{[6-(ben...)Show InChI InChI=1S/C15H18N6O/c1-21-10-18-12-13(17-9-11-5-3-2-4-6-11)19-15(16-7-8-22)20-14(12)21/h2-6,10,22H,7-9H2,1H3,(H2,16,17,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL DrugBank MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| DrugBank PubMed
| n/a | n/a | 7.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 5-p35nck5a |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 1/G2/mitotic-specific cyclin-B1/G2/mitotic-specific cyclin-B2/G2/mitotic-specific cyclin-B3
(Homo sapiens (Human)) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB
UniProtKB/SwissProt
antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| Purchase
DrugBank MCE KEGG PC cid PC sid PDB UniChem
Similars
| PubMed
| n/a | n/a | 1.80E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cell division cycle 2 (CDK1)-cyclin B |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| Purchase
DrugBank MCE KEGG PC cid PC sid PDB UniChem
Similars
| PubMed
| n/a | n/a | 2.10E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 5-p35nck5a |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50111433
(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)Show SMILES [O-][N+](=O)c1ccc(Cl)c(c1)-c1nccc2c1[nH]c1ccccc21 Show InChI InChI=1S/C17H10ClN3O2/c18-14-6-5-10(21(22)23)9-13(14)16-17-12(7-8-19-16)11-3-1-2-4-15(11)20-17/h1-9,20H | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 2.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 2-cyclin A |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50111435
(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)Show InChI InChI=1S/C12H9FN2/c1-7-12-10(4-5-14-7)9-3-2-8(13)6-11(9)15-12/h2-6,15H,1H3 | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 2.40E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 5-p35nck5a |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 1/G2/mitotic-specific cyclin-B1/G2/mitotic-specific cyclin-B2/G2/mitotic-specific cyclin-B3
(Homo sapiens (Human)) | BDBM50111434
(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)Show InChI InChI=1S/C15H12N4/c1-9-13(18-8-17-9)15-14-11(6-7-16-15)10-4-2-3-5-12(10)19-14/h2-8,16H,1H3,(H,17,18) | PDB
UniProtKB/SwissProt
antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 2.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 5-p35nck5a |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM50111435
(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)Show InChI InChI=1S/C12H9FN2/c1-7-12-10(4-5-14-7)9-3-2-8(13)6-11(9)15-12/h2-6,15H,1H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 3.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 2-cyclin A |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-A1/Cyclin-A2/Cyclin-dependent kinase 2
(Homo sapiens (Human)) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| Purchase
DrugBank MCE KEGG PC cid PC sid PDB UniChem
Similars
| PubMed
| n/a | n/a | 3.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 2-cyclin A |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 1/G2/mitotic-specific cyclin-B1/G2/mitotic-specific cyclin-B2/G2/mitotic-specific cyclin-B3
(Homo sapiens (Human)) | BDBM50111435
(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)Show InChI InChI=1S/C12H9FN2/c1-7-12-10(4-5-14-7)9-3-2-8(13)6-11(9)15-12/h2-6,15H,1H3 | PDB
UniProtKB/SwissProt
antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 4.20E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cell division cycle 2 (CDK1)-cyclin B |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 1/G2/mitotic-specific cyclin-B1/G2/mitotic-specific cyclin-B2/G2/mitotic-specific cyclin-B3
(Homo sapiens (Human)) | BDBM50111433
(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)Show SMILES [O-][N+](=O)c1ccc(Cl)c(c1)-c1nccc2c1[nH]c1ccccc21 Show InChI InChI=1S/C17H10ClN3O2/c18-14-6-5-10(21(22)23)9-13(14)16-17-12(7-8-19-16)11-3-1-2-4-15(11)20-17/h1-9,20H | PDB
UniProtKB/SwissProt
antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | 4.50E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cell division cycle 2 (CDK1)-cyclin B |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM50111434
(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)Show InChI InChI=1S/C15H12N4/c1-9-13(18-8-17-9)15-14-11(6-7-16-15)10-4-2-3-5-12(10)19-14/h2-8,16H,1H3,(H,17,18) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Lyn tyrosine kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
O94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139
(Homo sapiens (Human)) | BDBM50111434
(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)Show InChI InChI=1S/C15H12N4/c1-9-13(18-8-17-9)15-14-11(6-7-16-15)10-4-2-3-5-12(10)19-14/h2-8,16H,1H3,(H,17,18) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of protein kinase C |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
O94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139
(Homo sapiens (Human)) | BDBM50111435
(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)Show InChI InChI=1S/C12H9FN2/c1-7-12-10(4-5-14-7)9-3-2-8(13)6-11(9)15-12/h2-6,15H,1H3 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of protein kinase C |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
O94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139
(Homo sapiens (Human)) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| Purchase
DrugBank MCE KEGG PC cid PC sid PDB UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of protein kinase C |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
O94806/P05129/P05771/P17252/P24723/P41743/Q02156/Q04759/Q05513/Q05655/Q15139
(Homo sapiens (Human)) | BDBM50111433
(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)Show SMILES [O-][N+](=O)c1ccc(Cl)c(c1)-c1nccc2c1[nH]c1ccccc21 Show InChI InChI=1S/C17H10ClN3O2/c18-14-6-5-10(21(22)23)9-13(14)16-17-12(7-8-19-16)11-3-1-2-4-15(11)20-17/h1-9,20H | PDB
KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of protein kinase C |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50111434
(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)Show InChI InChI=1S/C15H12N4/c1-9-13(18-8-17-9)15-14-11(6-7-16-15)10-4-2-3-5-12(10)19-14/h2-8,16H,1H3,(H,17,18) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Fyn kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50111434
(1-(5-Methyl-1H-imidazol-4-yl)-9H-beta-carboline | ...)Show InChI InChI=1S/C15H12N4/c1-9-13(18-8-17-9)15-14-11(6-7-16-15)10-4-2-3-5-12(10)19-14/h2-8,16H,1H3,(H,17,18) | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50111435
(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)Show InChI InChI=1S/C12H9FN2/c1-7-12-10(4-5-14-7)9-3-2-8(13)6-11(9)15-12/h2-6,15H,1H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
DrugBank MCE KEGG PC cid PC sid PDB UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50111433
(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)Show SMILES [O-][N+](=O)c1ccc(Cl)c(c1)-c1nccc2c1[nH]c1ccccc21 Show InChI InChI=1S/C17H10ClN3O2/c18-14-6-5-10(21(22)23)9-13(14)16-17-12(7-8-19-16)11-3-1-2-4-15(11)20-17/h1-9,20H | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Fyn kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM50111435
(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)Show InChI InChI=1S/C12H9FN2/c1-7-12-10(4-5-14-7)9-3-2-8(13)6-11(9)15-12/h2-6,15H,1H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Lyn tyrosine kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM50111433
(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)Show SMILES [O-][N+](=O)c1ccc(Cl)c(c1)-c1nccc2c1[nH]c1ccccc21 Show InChI InChI=1S/C17H10ClN3O2/c18-14-6-5-10(21(22)23)9-13(14)16-17-12(7-8-19-16)11-3-1-2-4-15(11)20-17/h1-9,20H | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Lyn tyrosine kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
DrugBank MCE KEGG PC cid PC sid PDB UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Fyn kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lyn
(Homo sapiens (Human)) | BDBM100152
(7-methoxy-1-methyl-9H-beta-carboline;hydrochloride...)Show InChI InChI=1S/C13H12N2O/c1-8-13-11(5-6-14-8)10-4-3-9(16-2)7-12(10)15-13/h3-7,15H,1-2H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| Purchase
DrugBank MCE KEGG PC cid PC sid PDB UniChem
Similars
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Lyn tyrosine kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Lck
(Homo sapiens (Human)) | BDBM50111433
(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)Show SMILES [O-][N+](=O)c1ccc(Cl)c(c1)-c1nccc2c1[nH]c1ccccc21 Show InChI InChI=1S/C17H10ClN3O2/c18-14-6-5-10(21(22)23)9-13(14)16-17-12(7-8-19-16)11-3-1-2-4-15(11)20-17/h1-9,20H | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of p56 Lck tyrosine kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase Fyn
(Homo sapiens (Human)) | BDBM50111435
(7-Fluoro-1-methyl-9H-beta-carboline | CHEMBL14445)Show InChI InChI=1S/C12H9FN2/c1-7-12-10(4-5-14-7)9-3-2-8(13)6-11(9)15-12/h2-6,15H,1H3 | PDB
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >2.50E+5 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Fyn kinase |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50111433
(1-(2-Chloro-5-nitro-phenyl)-9H-beta-carboline | CH...)Show SMILES [O-][N+](=O)c1ccc(Cl)c(c1)-c1nccc2c1[nH]c1ccccc21 Show InChI InChI=1S/C17H10ClN3O2/c18-14-6-5-10(21(22)23)9-13(14)16-17-12(7-8-19-16)11-3-1-2-4-15(11)20-17/h1-9,20H | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| PubMed
| n/a | n/a | >1.20E+6 | n/a | n/a | n/a | n/a | n/a | n/a |
Institute of Molecular and Cell Biology
Curated by ChEMBL
| Assay Description Inhibition of Cyclin-dependent kinase 5-p35nck5a |
Bioorg Med Chem Lett 12: 1129-32 (2002)
BindingDB Entry DOI: 10.7270/Q2CC1006 |
More data for this Ligand-Target Pair | |