Found 88 hits Enz. Inhib. hit(s) with all data for assayid = 2 entry = 50009846 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 |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532781
(CHEMBL4571241)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5cc(OC)c(OC)cc45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C30H27FN4O5/c1-6-17-7-9-23-20(11-17)28(36)27(16(2)35(23)3)29(37)34-18-8-10-24(21(31)12-18)40-30-19-13-25(38-4)26(39-5)14-22(19)32-15-33-30/h7-15H,6H2,1-5H3,(H,34,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532781
(CHEMBL4571241)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5cc(OC)c(OC)cc45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C30H27FN4O5/c1-6-17-7-9-23-20(11-17)28(36)27(16(2)35(23)3)29(37)34-18-8-10-24(21(31)12-18)40-30-19-13-25(38-4)26(39-5)14-22(19)32-15-33-30/h7-15H,6H2,1-5H3,(H,34,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 4 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50172079
(CHEMBL3809489)Show SMILES Nc1nc(Nc2ccc3CC[C@@H](CCc3c2)N2CCCC2)nn1-c1cc2CCCc3ccccc3-c2nn1 |r| Show InChI InChI=1S/C30H34N8/c31-29-33-30(32-24-13-10-20-11-14-25(15-12-22(20)18-24)37-16-3-4-17-37)36-38(29)27-19-23-8-5-7-21-6-1-2-9-26(21)28(23)35-34-27/h1-2,6,9-10,13,18-19,25H,3-5,7-8,11-12,14-17H2,(H3,31,32,33,36)/t25-/m0/s1 | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid PDB UniChem
Similars
| Article PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50172079
(CHEMBL3809489)Show SMILES Nc1nc(Nc2ccc3CC[C@@H](CCc3c2)N2CCCC2)nn1-c1cc2CCCc3ccccc3-c2nn1 |r| Show InChI InChI=1S/C30H34N8/c31-29-33-30(32-24-13-10-20-11-14-25(15-12-22(20)18-24)37-16-3-4-17-37)36-38(29)27-19-23-8-5-7-21-6-1-2-9-26(21)28(23)35-34-27/h1-2,6,9-10,13,18-19,25H,3-5,7-8,11-12,14-17H2,(H3,31,32,33,36)/t25-/m0/s1 | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid PDB UniChem
Similars
| Article PubMed
| n/a | n/a | 5 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532786
(CHEMBL4513513)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C32H26FN5O3/c1-4-19-10-12-25-22(14-19)29(39)27(18(2)38(25)3)31(40)37-21-11-13-26(24(33)15-21)41-32-28-23(20-8-6-5-7-9-20)16-34-30(28)35-17-36-32/h5-17H,4H2,1-3H3,(H,37,40)(H,34,35,36) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532786
(CHEMBL4513513)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C32H26FN5O3/c1-4-19-10-12-25-22(14-19)29(39)27(18(2)38(25)3)31(40)37-21-11-13-26(24(33)15-21)41-32-28-23(20-8-6-5-7-9-20)16-34-30(28)35-17-36-32/h5-17H,4H2,1-3H3,(H,37,40)(H,34,35,36) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM28031
(BMS-777607 | N-{4-[(2-amino-3-chloropyridin-4-yl)o...)Show SMILES CCOc1ccn(-c2ccc(F)cc2)c(=O)c1C(=O)Nc1ccc(Oc2ccnc(N)c2Cl)c(F)c1 Show InChI InChI=1S/C25H19ClF2N4O4/c1-2-35-19-10-12-32(16-6-3-14(27)4-7-16)25(34)21(19)24(33)31-15-5-8-18(17(28)13-15)36-20-9-11-30-23(29)22(20)26/h3-13H,2H2,1H3,(H2,29,30)(H,31,33) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM28031
(BMS-777607 | N-{4-[(2-amino-3-chloropyridin-4-yl)o...)Show SMILES CCOc1ccn(-c2ccc(F)cc2)c(=O)c1C(=O)Nc1ccc(Oc2ccnc(N)c2Cl)c(F)c1 Show InChI InChI=1S/C25H19ClF2N4O4/c1-2-35-19-10-12-32(16-6-3-14(27)4-7-16)25(34)21(19)24(33)31-15-5-8-18(17(28)13-15)36-20-9-11-30-23(29)22(20)26/h3-13H,2H2,1H3,(H2,29,30)(H,31,33) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| Purchase
MCE MMDB PC cid PC sid PDB UniChem
Patents
Similars
| Article PubMed
| n/a | n/a | 6 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532784
(CHEMBL4449888)Show SMILES CC(C)c1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C33H28FN5O3/c1-18(2)21-10-12-26-23(14-21)30(40)28(19(3)39(26)4)32(41)38-22-11-13-27(25(34)15-22)42-33-29-24(20-8-6-5-7-9-20)16-35-31(29)36-17-37-33/h5-18H,1-4H3,(H,38,41)(H,35,36,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532784
(CHEMBL4449888)Show SMILES CC(C)c1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C33H28FN5O3/c1-18(2)21-10-12-26-23(14-21)30(40)28(19(3)39(26)4)32(41)38-22-11-13-27(25(34)15-22)42-33-29-24(20-8-6-5-7-9-20)16-35-31(29)36-17-37-33/h5-18H,1-4H3,(H,38,41)(H,35,36,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 26 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532799
(CHEMBL4449055)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ccnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C33H27FN4O3/c1-4-20-10-12-26-23(16-20)31(39)29(19(2)38(26)3)33(40)37-22-11-13-27(25(34)17-22)41-28-14-15-35-32-30(28)24(18-36-32)21-8-6-5-7-9-21/h5-18H,4H2,1-3H3,(H,35,36)(H,37,40) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532802
(CHEMBL4550377)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)cc3F)c(=O)c2c1 Show InChI InChI=1S/C32H26FN5O3/c1-4-19-10-13-26-22(14-19)29(39)27(18(2)38(26)3)31(40)37-25-12-11-21(15-24(25)33)41-32-28-23(20-8-6-5-7-9-20)16-34-30(28)35-17-36-32/h5-17H,4H2,1-3H3,(H,37,40)(H,34,35,36) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532802
(CHEMBL4550377)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)cc3F)c(=O)c2c1 Show InChI InChI=1S/C32H26FN5O3/c1-4-19-10-13-26-22(14-19)29(39)27(18(2)38(26)3)31(40)37-25-12-11-21(15-24(25)33)41-32-28-23(20-8-6-5-7-9-20)16-34-30(28)35-17-36-32/h5-17H,4H2,1-3H3,(H,37,40)(H,34,35,36) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532799
(CHEMBL4449055)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ccnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C33H27FN4O3/c1-4-20-10-12-26-23(16-20)31(39)29(19(2)38(26)3)33(40)37-22-11-13-27(25(34)17-22)41-28-14-15-35-32-30(28)24(18-36-32)21-8-6-5-7-9-21/h5-18H,4H2,1-3H3,(H,35,36)(H,37,40) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 30 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532800
(CHEMBL4468711)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6cnn(C)c6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C30H26FN7O3/c1-5-17-6-8-23-20(10-17)27(39)25(16(2)38(23)4)29(40)36-19-7-9-24(22(31)11-19)41-30-26-21(18-12-35-37(3)14-18)13-32-28(26)33-15-34-30/h6-15H,5H2,1-4H3,(H,36,40)(H,32,33,34) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 34 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532800
(CHEMBL4468711)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6cnn(C)c6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C30H26FN7O3/c1-5-17-6-8-23-20(10-17)27(39)25(16(2)38(23)4)29(40)36-19-7-9-24(22(31)11-19)41-30-26-21(18-12-35-37(3)14-18)13-32-28(26)33-15-34-30/h6-15H,5H2,1-4H3,(H,36,40)(H,32,33,34) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 34 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532787
(CHEMBL4473545)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(ccc2n1C)C(C)(C)C Show InChI InChI=1S/C34H30FN5O3/c1-19-28(30(41)23-15-21(34(2,3)4)11-13-26(23)40(19)5)32(42)39-22-12-14-27(25(35)16-22)43-33-29-24(20-9-7-6-8-10-20)17-36-31(29)37-18-38-33/h6-18H,1-5H3,(H,39,42)(H,36,37,38) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 42 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532787
(CHEMBL4473545)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(ccc2n1C)C(C)(C)C Show InChI InChI=1S/C34H30FN5O3/c1-19-28(30(41)23-15-21(34(2,3)4)11-13-26(23)40(19)5)32(42)39-22-12-14-27(25(35)16-22)43-33-29-24(20-9-7-6-8-10-20)17-36-31(29)37-18-38-33/h6-18H,1-5H3,(H,39,42)(H,36,37,38) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 42 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532817
(CHEMBL4517938)Show SMILES CCCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C33H28FN5O3/c1-4-8-20-11-13-26-23(15-20)30(40)28(19(2)39(26)3)32(41)38-22-12-14-27(25(34)16-22)42-33-29-24(21-9-6-5-7-10-21)17-35-31(29)36-18-37-33/h5-7,9-18H,4,8H2,1-3H3,(H,38,41)(H,35,36,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 61 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532817
(CHEMBL4517938)Show SMILES CCCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C33H28FN5O3/c1-4-8-20-11-13-26-23(15-20)30(40)28(19(2)39(26)3)32(41)38-22-12-14-27(25(34)16-22)42-33-29-24(21-9-6-5-7-10-21)17-35-31(29)36-18-37-33/h5-7,9-18H,4,8H2,1-3H3,(H,38,41)(H,35,36,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 61 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532797
(CHEMBL4456472)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ccnc(N)c4Cl)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C25H22ClFN4O3/c1-4-14-5-7-18-16(11-14)23(32)21(13(2)31(18)3)25(33)30-15-6-8-19(17(27)12-15)34-20-9-10-29-24(28)22(20)26/h5-12H,4H2,1-3H3,(H2,28,29)(H,30,33) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 72 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532797
(CHEMBL4456472)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ccnc(N)c4Cl)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C25H22ClFN4O3/c1-4-14-5-7-18-16(11-14)23(32)21(13(2)31(18)3)25(33)30-15-6-8-19(17(27)12-15)34-20-9-10-29-24(28)22(20)26/h5-12H,4H2,1-3H3,(H2,28,29)(H,30,33) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 72 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532807
(CHEMBL4549099)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(OC(F)(F)F)ccc2n1C Show InChI InChI=1S/C31H21F4N5O4/c1-16-25(27(41)20-13-19(44-31(33,34)35)9-10-23(20)40(16)2)29(42)39-18-8-11-24(22(32)12-18)43-30-26-21(17-6-4-3-5-7-17)14-36-28(26)37-15-38-30/h3-15H,1-2H3,(H,39,42)(H,36,37,38) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 74 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532807
(CHEMBL4549099)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(OC(F)(F)F)ccc2n1C Show InChI InChI=1S/C31H21F4N5O4/c1-16-25(27(41)20-13-19(44-31(33,34)35)9-10-23(20)40(16)2)29(42)39-18-8-11-24(22(32)12-18)43-30-26-21(17-6-4-3-5-7-17)14-36-28(26)37-15-38-30/h3-15H,1-2H3,(H,39,42)(H,36,37,38) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 74 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532803
(CHEMBL4588522)Show SMILES Cc1ccc2n(C)c(-c3ccccc3)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C36H26FN5O3/c1-21-13-15-28-25(17-21)33(43)31(32(42(28)2)23-11-7-4-8-12-23)35(44)41-24-14-16-29(27(37)18-24)45-36-30-26(22-9-5-3-6-10-22)19-38-34(30)39-20-40-36/h3-20H,1-2H3,(H,41,44)(H,38,39,40) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 78 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532803
(CHEMBL4588522)Show SMILES Cc1ccc2n(C)c(-c3ccccc3)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C36H26FN5O3/c1-21-13-15-28-25(17-21)33(43)31(32(42(28)2)23-11-7-4-8-12-23)35(44)41-24-14-16-29(27(37)18-24)45-36-30-26(22-9-5-3-6-10-22)19-38-34(30)39-20-40-36/h3-20H,1-2H3,(H,41,44)(H,38,39,40) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 78 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532819
(CHEMBL4445218)Show SMILES CCc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(C)ccc2n1C Show InChI InChI=1S/C32H26FN5O3/c1-4-24-28(29(39)21-14-18(2)10-12-25(21)38(24)3)31(40)37-20-11-13-26(23(33)15-20)41-32-27-22(19-8-6-5-7-9-19)16-34-30(27)35-17-36-32/h5-17H,4H2,1-3H3,(H,37,40)(H,34,35,36) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 78 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532819
(CHEMBL4445218)Show SMILES CCc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(C)ccc2n1C Show InChI InChI=1S/C32H26FN5O3/c1-4-24-28(29(39)21-14-18(2)10-12-25(21)38(24)3)31(40)37-20-11-13-26(23(33)15-20)41-32-27-22(19-8-6-5-7-9-19)16-34-30(27)35-17-36-32/h5-17H,4H2,1-3H3,(H,37,40)(H,34,35,36) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 78 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532808
(CHEMBL4593206)Show SMILES COc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C31H24FN5O4/c1-17-26(28(38)21-14-20(40-3)10-11-24(21)37(17)2)30(39)36-19-9-12-25(23(32)13-19)41-31-27-22(18-7-5-4-6-8-18)15-33-29(27)34-16-35-31/h4-16H,1-3H3,(H,36,39)(H,33,34,35) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 99 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532808
(CHEMBL4593206)Show SMILES COc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C31H24FN5O4/c1-17-26(28(38)21-14-20(40-3)10-11-24(21)37(17)2)30(39)36-19-9-12-25(23(32)13-19)41-31-27-22(18-7-5-4-6-8-18)15-33-29(27)34-16-35-31/h4-16H,1-3H3,(H,36,39)(H,33,34,35) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 99 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532792
(CHEMBL4469879)Show SMILES Cc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C31H24FN5O3/c1-17-9-11-24-21(13-17)28(38)26(18(2)37(24)3)30(39)36-20-10-12-25(23(32)14-20)40-31-27-22(19-7-5-4-6-8-19)15-33-29(27)34-16-35-31/h4-16H,1-3H3,(H,36,39)(H,33,34,35) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532792
(CHEMBL4469879)Show SMILES Cc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C31H24FN5O3/c1-17-9-11-24-21(13-17)28(38)26(18(2)37(24)3)30(39)36-20-10-12-25(23(32)14-20)40-31-27-22(19-7-5-4-6-8-19)15-33-29(27)34-16-35-31/h4-16H,1-3H3,(H,36,39)(H,33,34,35) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 100 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532801
(CHEMBL4541303)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)cc3)c(=O)c2c1 Show InChI InChI=1S/C32H27N5O3/c1-4-20-10-15-26-24(16-20)29(38)27(19(2)37(26)3)31(39)36-22-11-13-23(14-12-22)40-32-28-25(21-8-6-5-7-9-21)17-33-30(28)34-18-35-32/h5-18H,4H2,1-3H3,(H,36,39)(H,33,34,35) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 105 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532801
(CHEMBL4541303)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)cc3)c(=O)c2c1 Show InChI InChI=1S/C32H27N5O3/c1-4-20-10-15-26-24(16-20)29(38)27(19(2)37(26)3)31(39)36-22-11-13-23(14-12-22)40-32-28-25(21-8-6-5-7-9-21)17-33-30(28)34-18-35-32/h5-18H,4H2,1-3H3,(H,36,39)(H,33,34,35) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 105 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532822
(CHEMBL4565473)Show SMILES Cc1ccc2n(C)cc(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C30H22FN5O3/c1-17-8-10-24-20(12-17)27(37)22(15-36(24)2)29(38)35-19-9-11-25(23(31)13-19)39-30-26-21(18-6-4-3-5-7-18)14-32-28(26)33-16-34-30/h3-16H,1-2H3,(H,35,38)(H,32,33,34) | PDB
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UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532783
(CHEMBL4516966)Show SMILES CCn1c(C)c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(C)ccc12 Show InChI InChI=1S/C32H26FN5O3/c1-4-38-19(3)27(29(39)22-14-18(2)10-12-25(22)38)31(40)37-21-11-13-26(24(33)15-21)41-32-28-23(20-8-6-5-7-9-20)16-34-30(28)35-17-36-32/h5-17H,4H2,1-3H3,(H,37,40)(H,34,35,36) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532783
(CHEMBL4516966)Show SMILES CCn1c(C)c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(C)ccc12 Show InChI InChI=1S/C32H26FN5O3/c1-4-38-19(3)27(29(39)22-14-18(2)10-12-25(22)38)31(40)37-21-11-13-26(24(33)15-21)41-32-28-23(20-8-6-5-7-9-20)16-34-30(28)35-17-36-32/h5-17H,4H2,1-3H3,(H,37,40)(H,34,35,36) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532811
(CHEMBL4471186)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(ccc2n1C)C(F)(F)F Show InChI InChI=1S/C31H21F4N5O3/c1-16-25(27(41)20-12-18(31(33,34)35)8-10-23(20)40(16)2)29(42)39-19-9-11-24(22(32)13-19)43-30-26-21(17-6-4-3-5-7-17)14-36-28(26)37-15-38-30/h3-15H,1-2H3,(H,39,42)(H,36,37,38) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532822
(CHEMBL4565473)Show SMILES Cc1ccc2n(C)cc(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C30H22FN5O3/c1-17-8-10-24-20(12-17)27(37)22(15-36(24)2)29(38)35-19-9-11-25(23(31)13-19)39-30-26-21(18-6-4-3-5-7-18)14-32-28(26)33-16-34-30/h3-16H,1-2H3,(H,35,38)(H,32,33,34) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532811
(CHEMBL4471186)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(ccc2n1C)C(F)(F)F Show InChI InChI=1S/C31H21F4N5O3/c1-16-25(27(41)20-12-18(31(33,34)35)8-10-23(20)40(16)2)29(42)39-19-9-11-24(22(32)13-19)43-30-26-21(17-6-4-3-5-7-17)14-36-28(26)37-15-38-30/h3-15H,1-2H3,(H,39,42)(H,36,37,38) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 150 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532782
(CHEMBL4583626)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]ccc45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C26H22FN5O3/c1-4-15-5-7-20-18(11-15)23(33)22(14(2)32(20)3)25(34)31-16-6-8-21(19(27)12-16)35-26-17-9-10-28-24(17)29-13-30-26/h5-13H,4H2,1-3H3,(H,31,34)(H,28,29,30) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 157 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532782
(CHEMBL4583626)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]ccc45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C26H22FN5O3/c1-4-15-5-7-20-18(11-15)23(33)22(14(2)32(20)3)25(34)31-16-6-8-21(19(27)12-16)35-26-17-9-10-28-24(17)29-13-30-26/h5-13H,4H2,1-3H3,(H,31,34)(H,28,29,30) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 157 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532788
(CHEMBL4515742)Show SMILES CC(=C)c1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C33H26FN5O3/c1-18(2)21-10-12-26-23(14-21)30(40)28(19(3)39(26)4)32(41)38-22-11-13-27(25(34)15-22)42-33-29-24(20-8-6-5-7-9-20)16-35-31(29)36-17-37-33/h5-17H,1H2,2-4H3,(H,38,41)(H,35,36,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532788
(CHEMBL4515742)Show SMILES CC(=C)c1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4ncnc5[nH]cc(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C33H26FN5O3/c1-18(2)21-10-12-26-23(14-21)30(40)28(19(3)39(26)4)32(41)38-22-11-13-27(25(34)15-22)42-33-29-24(20-8-6-5-7-9-20)16-35-31(29)36-17-37-33/h5-17H,1H2,2-4H3,(H,38,41)(H,35,36,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 170 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532789
(CHEMBL4464266)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4cccc5occ(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C34H27FN2O4/c1-4-21-13-15-27-24(17-21)33(38)31(20(2)37(27)3)34(39)36-23-14-16-28(26(35)18-23)41-30-12-8-11-29-32(30)25(19-40-29)22-9-6-5-7-10-22/h5-19H,4H2,1-3H3,(H,36,39) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 192 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532789
(CHEMBL4464266)Show SMILES CCc1ccc2n(C)c(C)c(C(=O)Nc3ccc(Oc4cccc5occ(-c6ccccc6)c45)c(F)c3)c(=O)c2c1 Show InChI InChI=1S/C34H27FN2O4/c1-4-21-13-15-27-24(17-21)33(38)31(20(2)37(27)3)34(39)36-23-14-16-28(26(35)18-23)41-30-12-8-11-29-32(30)25(19-40-29)22-9-6-5-7-10-22/h5-19H,4H2,1-3H3,(H,36,39) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 192 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532809
(CHEMBL4566072)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(ccc2n1C)C1CCCC1 Show InChI InChI=1S/C35H30FN5O3/c1-20-30(32(42)25-16-23(21-8-6-7-9-21)12-14-28(25)41(20)2)34(43)40-24-13-15-29(27(36)17-24)44-35-31-26(22-10-4-3-5-11-22)18-37-33(31)38-19-39-35/h3-5,10-19,21H,6-9H2,1-2H3,(H,40,43)(H,37,38,39) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532809
(CHEMBL4566072)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(ccc2n1C)C1CCCC1 Show InChI InChI=1S/C35H30FN5O3/c1-20-30(32(42)25-16-23(21-8-6-7-9-21)12-14-28(25)41(20)2)34(43)40-24-13-15-29(27(36)17-24)44-35-31-26(22-10-4-3-5-11-22)18-37-33(31)38-19-39-35/h3-5,10-19,21H,6-9H2,1-2H3,(H,40,43)(H,37,38,39) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 200 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532810
(CHEMBL4470280)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(ccc2n1C)C1CC1 Show InChI InChI=1S/C33H26FN5O3/c1-18-28(30(40)23-14-21(19-8-9-19)10-12-26(23)39(18)2)32(41)38-22-11-13-27(25(34)15-22)42-33-29-24(20-6-4-3-5-7-20)16-35-31(29)36-17-37-33/h3-7,10-17,19H,8-9H2,1-2H3,(H,38,41)(H,35,36,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |
Tyrosine-protein kinase receptor UFO
(Homo sapiens (Human)) | BDBM50532810
(CHEMBL4470280)Show SMILES Cc1c(C(=O)Nc2ccc(Oc3ncnc4[nH]cc(-c5ccccc5)c34)c(F)c2)c(=O)c2cc(ccc2n1C)C1CC1 Show InChI InChI=1S/C33H26FN5O3/c1-18-28(30(40)23-14-21(19-8-9-19)10-12-26(23)39(18)2)32(41)38-22-11-13-27(25(34)15-22)42-33-29-24(20-6-4-3-5-7-20)16-35-31(29)36-17-37-33/h3-7,10-17,19H,8-9H2,1-2H3,(H,38,41)(H,35,36,37) | PDB
KEGG
UniProtKB/SwissProt
B.MOAD antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 230 | n/a | n/a | n/a | n/a | n/a | n/a |
Chinese Academy of Sciences
Curated by ChEMBL
| Assay Description Inhibition of human recombinant AXL incubated for 1 to 1.5 hrs by FRET based Z'-Lyte kinase assay |
J Med Chem 59: 6807-25 (2016)
Article DOI: 10.1021/acs.jmedchem.6b00608 BindingDB Entry DOI: 10.7270/Q2N301FS |
More data for this Ligand-Target Pair | |