Found 52 hits Enz. Inhib. hit(s) with all data for entry = 50047347 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)) | BDBM50161356
(CHEMBL3786536)Show InChI InChI=1S/C16H12BrN3O/c1-8-2-3-9-7-11-14(10(9)6-8)19-16(18)20-15(11)12-4-5-13(17)21-12/h2-6H,7H2,1H3,(H2,18,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 23 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161347
(CHEMBL3786624)Show SMILES O=Cc1cccc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)n1 Show InChI InChI=1S/C16H13N3O/c1-9-4-5-10-8-12-14(11(10)7-9)18-16(17)19-15(12)13-3-2-6-20-13/h2-7H,8H2,1H3,(H2,17,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 25 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161348
(CHEMBL3785408)Show InChI InChI=1S/C17H14N4/c1-10-2-3-12-9-14-15(11-4-6-19-7-5-11)20-17(18)21-16(14)13(12)8-10/h2-8H,9H2,1H3,(H2,18,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 35 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161338
(CHEMBL3787480)Show InChI InChI=1S/C17H15N3O2/c1-9-2-3-10-7-13-15(12(10)6-9)19-17(18)20-16(13)14-5-4-11(8-21)22-14/h2-6,21H,7-8H2,1H3,(H2,18,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 40 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161339
(CHEMBL3787512)Show InChI InChI=1S/C15H9BrClN3O/c16-12-4-3-11(21-12)14-10-5-7-1-2-8(17)6-9(7)13(10)19-15(18)20-14/h1-4,6H,5H2,(H2,18,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 41 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161398
(CHEMBL3787292)Show InChI InChI=1S/C19H19FN4O2/c20-11-12-7-8-21-16(10-12)23-19(26)22-14-5-3-4-13-17(14)15-6-1-2-9-24(15)18(13)25/h3-5,7-8,10,15H,1-2,6,9,11H2,(H2,21,22,23,26) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 43 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161345
(CHEMBL3785575)Show InChI InChI=1S/C16H12BrN3O2/c1-21-9-3-2-8-6-11-14(10(8)7-9)19-16(18)20-15(11)12-4-5-13(17)22-12/h2-5,7H,6H2,1H3,(H2,18,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia 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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161344
(CHEMBL3786276)Show SMILES O=C(Nc1cc(CN2CCOCC2)ccn1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C18H15N3/c19-18-20-16(13-7-2-1-3-8-13)15-11-10-12-6-4-5-9-14(12)17(15)21-18/h1-9H,10-11H2,(H2,19,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 67 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50399301
(CHEMBL2180862)Show InChI InChI=1S/C18H18N4O2/c23-17-12-6-5-7-13(16(12)14-8-2-4-11-22(14)17)20-18(24)21-15-9-1-3-10-19-15/h1,3,5-7,9-10,14H,2,4,8,11H2,(H2,19,20,21,24) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia 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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50399326
(CHEMBL2180863)Show InChI InChI=1S/C17H17N5O2/c23-16-11-4-3-5-12(15(11)13-6-1-2-9-22(13)16)20-17(24)21-14-10-18-7-8-19-14/h3-5,7-8,10,13H,1-2,6,9H2,(H2,19,20,21,24) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia 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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161335
(CHEMBL3785571)Show InChI InChI=1S/C19H20N4O2/c1-12-6-5-10-20-17(12)22-19(25)21-14-8-4-7-13-16(14)15-9-2-3-11-23(15)18(13)24/h4-8,10,15H,2-3,9,11H2,1H3,(H2,20,21,22,25) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 96 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161346
(CHEMBL3786430)Show SMILES O=C(Nc1cc(CN2CCCCC2)ccn1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C21H14BrN3O/c22-18-9-8-17(26-18)20-16-11-14-7-6-13(12-4-2-1-3-5-12)10-15(14)19(16)24-21(23)25-20/h1-10H,11H2,(H2,23,24,25) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia 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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161343
(CHEMBL3787557)Show SMILES CN1CCN(Cc2ccnc(NC(=O)Nc3cccc4C(=O)N5CCCCC5c34)c2)CC1 Show InChI InChI=1S/C16H16BrN3O/c1-8-2-3-9-7-11-14(10(9)6-8)19-16(18)20-15(11)12-4-5-13(17)21-12/h2-3,6,12-13H,4-5,7H2,1H3,(H2,18,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 130 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161396
(CHEMBL3785795)Show SMILES COc1cc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)nc2ccccc12 Show InChI InChI=1S/C23H22N4O3/c1-30-19-13-20(24-16-9-3-2-7-14(16)19)26-23(29)25-17-10-6-8-15-21(17)18-11-4-5-12-27(18)22(15)28/h2-3,6-10,13,18H,4-5,11-12H2,1H3,(H2,24,25,26,29) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161360
(CHEMBL3785771)Show InChI InChI=1S/C18H19N5O2/c1-11-16(20-9-8-19-11)22-18(25)21-13-6-4-5-12-15(13)14-7-2-3-10-23(14)17(12)24/h4-6,8-9,14H,2-3,7,10H2,1H3,(H2,20,21,22,25) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia 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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161349
(CHEMBL3786332)Show InChI InChI=1S/C17H14BrN3O/c1-2-9-3-4-10-8-12-15(11(10)7-9)20-17(19)21-16(12)13-5-6-14(18)22-13/h3-7H,2,8H2,1H3,(H2,19,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia 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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161350
(CHEMBL3787093)Show SMILES COC(=O)c1cccc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)n1 Show InChI InChI=1S/C18H15N3/c1-11-7-8-13-10-15-16(12-5-3-2-4-6-12)20-18(19)21-17(15)14(13)9-11/h2-9H,10H2,1H3,(H2,19,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 320 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161397
(CHEMBL3787135)Show SMILES O=C(Nc1ccc2ccccc2n1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C22H20N4O2/c27-21-15-7-5-9-17(20(15)18-10-3-4-13-26(18)21)24-22(28)25-19-12-11-14-6-1-2-8-16(14)23-19/h1-2,5-9,11-12,18H,3-4,10,13H2,(H2,23,24,25,28) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 400 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161340
(CHEMBL3787081)Show SMILES COCc1ccnc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)c1 Show InChI InChI=1S/C17H14N4/c1-10-5-6-11-9-13-15(12(11)8-10)20-17(18)21-16(13)14-4-2-3-7-19-14/h2-8H,9H2,1H3,(H2,18,20,21) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 410 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161355
(CHEMBL3786745)Show SMILES O=C(Nc1cccc(CN2CCCCC2)n1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C19H17BrN4O/c20-16-6-5-15(25-16)18-14-9-11-3-4-12(24-7-1-2-8-24)10-13(11)17(14)22-19(21)23-18/h3-6,10H,1-2,7-9H2,(H2,21,22,23) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 760 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161358
(CHEMBL3787033)Show InChI InChI=1S/C19H18BrN3O/c1-19(2,3)11-5-4-10-8-13-16(12(10)9-11)22-18(21)23-17(13)14-6-7-15(20)24-14/h4-7,9H,8H2,1-3H3,(H2,21,22,23) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 810 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161352
(CHEMBL3785804)Show SMILES COCc1cccc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)n1 Show InChI InChI=1S/C17H13N3O/c18-17-19-14(10-6-2-1-3-7-10)13-15(20-17)11-8-4-5-9-12(11)16(13)21/h1-9,16,21H,(H2,18,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 1.20E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161351
(CHEMBL3785573)Show SMILES O=C(Nc1cccc(CN2CCOCC2)n1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C16H12N4/c17-16-19-13(10-6-2-1-3-7-10)15-14(20-16)11-8-4-5-9-12(11)18-15/h1-9,18H,(H2,17,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 1.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161348
(CHEMBL3785408)Show InChI InChI=1S/C17H14N4/c1-10-2-3-12-9-14-15(11-4-6-19-7-5-11)20-17(18)21-16(14)13(12)8-10/h2-8H,9H2,1H3,(H2,18,20,21) | PDB MMDB
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+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161347
(CHEMBL3786624)Show SMILES O=Cc1cccc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)n1 Show InChI InChI=1S/C16H13N3O/c1-9-4-5-10-8-12-14(11(10)7-9)18-16(17)19-15(12)13-3-2-6-20-13/h2-7H,8H2,1H3,(H2,17,18,19) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 2.80E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161343
(CHEMBL3787557)Show SMILES CN1CCN(Cc2ccnc(NC(=O)Nc3cccc4C(=O)N5CCCCC5c34)c2)CC1 Show InChI InChI=1S/C16H16BrN3O/c1-8-2-3-9-7-11-14(10(9)6-8)19-16(18)20-15(11)12-4-5-13(17)21-12/h2-3,6,12-13H,4-5,7H2,1H3,(H2,18,19,20) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 3.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161357
(CHEMBL3787584)Show SMILES CCN(CC)Cc1cccc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)n1 Show InChI InChI=1S/C16H11N3O/c17-16-18-13(10-6-2-1-3-7-10)15-14(19-16)11-8-4-5-9-12(11)20-15/h1-9H,(H2,17,18,19) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 3.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161346
(CHEMBL3786430)Show SMILES O=C(Nc1cc(CN2CCCCC2)ccn1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C21H14BrN3O/c22-18-9-8-17(26-18)20-16-11-14-7-6-13(12-4-2-1-3-5-12)10-15(14)19(16)24-21(23)25-20/h1-10H,11H2,(H2,23,24,25) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 3.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161335
(CHEMBL3785571)Show InChI InChI=1S/C19H20N4O2/c1-12-6-5-10-20-17(12)22-19(25)21-14-8-4-7-13-16(14)15-9-2-3-11-23(15)18(13)24/h4-8,10,15H,2-3,9,11H2,1H3,(H2,20,21,22,25) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161360
(CHEMBL3785771)Show InChI InChI=1S/C18H19N5O2/c1-11-16(20-9-8-19-11)22-18(25)21-13-6-4-5-12-15(13)14-7-2-3-10-23(14)17(12)24/h4-6,8-9,14H,2-3,7,10H2,1H3,(H2,20,21,22,25) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161339
(CHEMBL3787512)Show InChI InChI=1S/C15H9BrClN3O/c16-12-4-3-11(21-12)14-10-5-7-1-2-8(17)6-9(7)13(10)19-15(18)20-14/h1-4,6H,5H2,(H2,18,19,20) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.60E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161340
(CHEMBL3787081)Show SMILES COCc1ccnc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)c1 Show InChI InChI=1S/C17H14N4/c1-10-5-6-11-9-13-15(12(11)8-10)20-17(18)21-16(13)14-4-2-3-7-19-14/h2-8H,9H2,1H3,(H2,18,20,21) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 4.70E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161354
(CHEMBL3787061)Show SMILES O=C(Nc1cccc(CN2CCCC2)n1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C17H13N3/c18-17-19-15(11-6-2-1-3-7-11)14-10-12-8-4-5-9-13(12)16(14)20-17/h1-9H,10H2,(H2,18,19,20) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 5.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161350
(CHEMBL3787093)Show SMILES COC(=O)c1cccc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)n1 Show InChI InChI=1S/C18H15N3/c1-11-7-8-13-10-15-16(12-5-3-2-4-6-12)20-18(19)21-17(15)14(13)9-11/h2-9H,10H2,1H3,(H2,19,20,21) | PDB MMDB
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 | 5.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161344
(CHEMBL3786276)Show SMILES O=C(Nc1cc(CN2CCOCC2)ccn1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C18H15N3/c19-18-20-16(13-7-2-1-3-8-13)15-11-10-12-6-4-5-9-14(12)17(15)21-18/h1-9H,10-11H2,(H2,19,20,21) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
Similars
| Article PubMed
| n/a | n/a | 7.10E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161397
(CHEMBL3787135)Show SMILES O=C(Nc1ccc2ccccc2n1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C22H20N4O2/c27-21-15-7-5-9-17(20(15)18-10-3-4-13-26(18)21)24-22(28)25-19-12-11-14-6-1-2-8-16(14)23-19/h1-2,5-9,11-12,18H,3-4,10,13H2,(H2,23,24,25,28) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 9.00E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161336
(CHEMBL3786657)Show SMILES COC(=O)c1cccnc1NC(=O)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C20H20N4O4/c1-28-19(26)13-7-5-10-21-17(13)23-20(27)22-14-8-4-6-12-16(14)15-9-2-3-11-24(15)18(12)25/h4-8,10,15H,2-3,9,11H2,1H3,(H2,21,22,23,27) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161345
(CHEMBL3785575)Show InChI InChI=1S/C16H12BrN3O2/c1-21-9-3-2-8-6-11-14(10(8)7-9)19-16(18)20-15(11)12-4-5-13(17)22-12/h2-5,7H,6H2,1H3,(H2,18,19,20) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161355
(CHEMBL3786745)Show SMILES O=C(Nc1cccc(CN2CCCCC2)n1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C19H17BrN4O/c20-16-6-5-15(25-16)18-14-9-11-3-4-12(24-7-1-2-8-24)10-13(11)17(14)22-19(21)23-18/h3-6,10H,1-2,7-9H2,(H2,21,22,23) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161354
(CHEMBL3787061)Show SMILES O=C(Nc1cccc(CN2CCCC2)n1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C17H13N3/c18-17-19-15(11-6-2-1-3-7-11)14-10-12-8-4-5-9-13(12)16(14)20-17/h1-9H,10H2,(H2,18,19,20) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161357
(CHEMBL3787584)Show SMILES CCN(CC)Cc1cccc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)n1 Show InChI InChI=1S/C16H11N3O/c17-16-18-13(10-6-2-1-3-7-10)15-14(19-16)11-8-4-5-9-12(11)20-15/h1-9H,(H2,17,18,19) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161349
(CHEMBL3786332)Show InChI InChI=1S/C17H14BrN3O/c1-2-9-3-4-10-8-12-15(11(10)7-9)20-17(19)21-16(12)13-5-6-14(18)22-13/h3-7H,2,8H2,1H3,(H2,19,20,21) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161338
(CHEMBL3787480)Show InChI InChI=1S/C17H15N3O2/c1-9-2-3-10-7-13-15(12(10)6-9)19-17(18)20-16(13)14-5-4-11(8-21)22-14/h2-6,21H,7-8H2,1H3,(H2,18,19,20) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161356
(CHEMBL3786536)Show InChI InChI=1S/C16H12BrN3O/c1-8-2-3-9-7-11-14(10(9)6-8)19-16(18)20-15(11)12-4-5-13(17)21-12/h2-6H,7H2,1H3,(H2,18,19,20) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161353
(CHEMBL3785596)Show SMILES CN1CCN(Cc2cccc(NC(=O)Nc3cccc4C(=O)N5CCCCC5c34)n2)CC1 Show InChI InChI=1S/C17H15N3O/c1-9-3-5-11-8-13-15(12(11)7-9)19-17(18)20-16(13)14-6-4-10(2)21-14/h3-7H,8H2,1-2H3,(H2,18,19,20) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161398
(CHEMBL3787292)Show InChI InChI=1S/C19H19FN4O2/c20-11-12-7-8-21-16(10-12)23-19(26)22-14-5-3-4-13-17(14)15-6-1-2-9-24(15)18(13)25/h3-5,7-8,10,15H,1-2,6,9,11H2,(H2,21,22,23,26) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Cyclin-dependent kinase 5 activator 1
(Homo sapiens (Human)) | BDBM50161336
(CHEMBL3786657)Show SMILES COC(=O)c1cccnc1NC(=O)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C20H20N4O4/c1-28-19(26)13-7-5-10-21-17(13)23-20(27)22-14-8-4-6-12-16(14)15-9-2-3-11-24(15)18(12)25/h4-8,10,15H,2-3,9,11H2,1H3,(H2,21,22,23,27) | PDB MMDB
NCI pathway Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia 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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of human recombinant CDK5/p25 using histone H1 as substrate |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161352
(CHEMBL3785804)Show SMILES COCc1cccc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)n1 Show InChI InChI=1S/C17H13N3O/c18-17-19-14(10-6-2-1-3-7-10)13-15(20-17)11-8-4-5-9-12(11)16(13)21/h1-9,16,21H,(H2,18,19,20) | PDB MMDB
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 |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161351
(CHEMBL3785573)Show SMILES O=C(Nc1cccc(CN2CCOCC2)n1)Nc1cccc2C(=O)N3CCCCC3c12 Show InChI InChI=1S/C16H12N4/c17-16-19-13(10-6-2-1-3-7-10)15-14(20-16)11-8-4-5-9-12(11)18-15/h1-9,18H,(H2,17,19,20) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |
Dual specificity tyrosine-phosphorylation-regulated kinase 1A
(Homo sapiens (Human)) | BDBM50161396
(CHEMBL3785795)Show SMILES COc1cc(NC(=O)Nc2cccc3C(=O)N4CCCCC4c23)nc2ccccc12 Show InChI InChI=1S/C23H22N4O3/c1-30-19-13-20(24-16-9-3-2-7-14(16)19)26-23(29)25-17-10-6-8-15-21(17)18-11-4-5-12-27(18)22(15)28/h2-3,6-10,13,18H,4-5,11-12H2,1H3,(H2,24,25,26,29) | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | >1.00E+4 | n/a | n/a | n/a | n/a | n/a | n/a |
Universit£ d'Orl£ans
Curated by ChEMBL
| Assay Description Inhibition of GST fused human recombinant DYRK1A expressed in Escherichia coli using woodtide as substrate after 30 mins by scintillation counting in... |
Eur J Med Chem 115: 311-25 (2016)
Article DOI: 10.1016/j.ejmech.2016.02.072 BindingDB Entry DOI: 10.7270/Q2JM2CHT |
More data for this Ligand-Target Pair | |