Found 6 hits with Last Name = 'maxwell' and Initial = 'ds' 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 |
Breakpoint cluster region protein/Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM13530
(4-[(4-methylpiperazin-1-yl)methyl]-N-[4-methyl-3-[...)Show SMILES CN1CCN(Cc2ccc(cc2)C(=O)Nc2ccc(C)c(Nc3nccc(n3)-c3cccnc3)c2)CC1 Show InChI InChI=1S/C29H31N7O/c1-21-5-10-25(18-27(21)34-29-31-13-11-26(33-29)24-4-3-12-30-19-24)32-28(37)23-8-6-22(7-9-23)20-36-16-14-35(2)15-17-36/h3-13,18-19H,14-17,20H2,1-2H3,(H,32,37)(H,31,33,34) | 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
| PDB Article PubMed
| n/a | n/a | 116 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Texas M.D. Anderson Cancer Center
Curated by ChEMBL
| Assay Description Inhibition of Bcr-Abl (unknown origin) phosphorylation by spectrophotometric assay |
Bioorg Med Chem 22: 623-32 (2013)
Article DOI: 10.1016/j.bmc.2013.10.040 BindingDB Entry DOI: 10.7270/Q27S7Q76 |
More data for this Ligand-Target Pair | 3D Structure (crystal) |
Breakpoint cluster region protein/Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50444656
(CHEMBL3098614)Show SMILES Cc1ccc(NC(=O)c2ccc(CN3CCN(Cc4ccc(I)cc4)CC3)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C35H34IN7O/c1-25-4-13-31(21-33(25)41-35-38-16-14-32(40-35)29-3-2-15-37-22-29)39-34(44)28-9-5-26(6-10-28)23-42-17-19-43(20-18-42)24-27-7-11-30(36)12-8-27/h2-16,21-22H,17-20,23-24H2,1H3,(H,39,44)(H,38,40,41) | 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 | 740 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Texas M.D. Anderson Cancer Center
Curated by ChEMBL
| Assay Description Inhibition of Bcr-Abl (unknown origin) phosphorylation by spectrophotometric assay |
Bioorg Med Chem 22: 623-32 (2013)
Article DOI: 10.1016/j.bmc.2013.10.040 BindingDB Entry DOI: 10.7270/Q27S7Q76 |
More data for this Ligand-Target Pair | |
Breakpoint cluster region protein/Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50444658
(CHEMBL3098616)Show SMILES Cc1ccc(NC(=O)c2ccc(CN3CCN(CCF)CC3)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C30H32FN7O/c1-22-4-9-26(19-28(22)36-30-33-13-10-27(35-30)25-3-2-12-32-20-25)34-29(39)24-7-5-23(6-8-24)21-38-17-15-37(14-11-31)16-18-38/h2-10,12-13,19-20H,11,14-18,21H2,1H3,(H,34,39)(H,33,35,36) | 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 | 1.38E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Texas M.D. Anderson Cancer Center
Curated by ChEMBL
| Assay Description Inhibition of Bcr-Abl (unknown origin) phosphorylation by spectrophotometric assay |
Bioorg Med Chem 22: 623-32 (2013)
Article DOI: 10.1016/j.bmc.2013.10.040 BindingDB Entry DOI: 10.7270/Q27S7Q76 |
More data for this Ligand-Target Pair | |
Probable ubiquitin carboxyl-terminal hydrolase FAF-X
(Homo sapiens (Human)) | BDBM50447833
(CHEMBL3114085)Show SMILES Brc1cccc(\C=C(\C#N)C(=O)NCc2cccc(CNC(=O)C(=C/c3cccc(Br)n3)\C#N)c2)n1 Show InChI InChI=1S/C26H18Br2N6O2/c27-23-8-2-6-21(33-23)11-19(13-29)25(35)31-15-17-4-1-5-18(10-17)16-32-26(36)20(14-30)12-22-7-3-9-24(28)34-22/h1-12H,15-16H2,(H,31,35)(H,32,36)/b19-11-,20-12- | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| CHEMBL PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 2.50E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Texas M.D. Anderson Cancer Center
Curated by ChEMBL
| Assay Description Inhibition of human recombinant N-terminal His6-Smt3-fusion-tagged Usp9x catalytic domain expressed in Escherichia coli using Ub-AMC as substrate inc... |
Bioorg Med Chem 22: 1450-8 (2014)
Article DOI: 10.1016/j.bmc.2013.12.048 BindingDB Entry DOI: 10.7270/Q2BP0499 |
More data for this Ligand-Target Pair | |
Probable ubiquitin carboxyl-terminal hydrolase FAF-X
(Homo sapiens (Human)) | BDBM50437695
(CHEMBL1923233)Show SMILES CCC[C@H](NC(=O)C(=C\c1cccc(Br)n1)\C#N)c1ccccc1 |r| Show InChI InChI=1S/C19H18BrN3O/c1-2-7-17(14-8-4-3-5-9-14)23-19(24)15(13-21)12-16-10-6-11-18(20)22-16/h3-6,8-12,17H,2,7H2,1H3,(H,23,24)/b15-12+/t17-/m0/s1 | PDB
Reactome pathway KEGG
UniProtKB/SwissProt
antibodypedia GoogleScholar AffyNet
| Purchase
CHEMBL MCE PC cid PC sid UniChem
| Article PubMed
| n/a | n/a | 5.90E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Texas M.D. Anderson Cancer Center
Curated by ChEMBL
| Assay Description Inhibition of human recombinant N-terminal His6-Smt3-fusion-tagged Usp9x catalytic domain expressed in Escherichia coli using Ub-AMC as substrate inc... |
Bioorg Med Chem 22: 1450-8 (2014)
Article DOI: 10.1016/j.bmc.2013.12.048 BindingDB Entry DOI: 10.7270/Q2BP0499 |
More data for this Ligand-Target Pair | |
Breakpoint cluster region protein/Tyrosine-protein kinase ABL1
(Homo sapiens (Human)) | BDBM50444657
(CHEMBL3098615)Show SMILES Cc1ccc(NC(=O)c2ccc(CN3CCN(CCO)CC3)cc2)cc1Nc1nccc(n1)-c1cccnc1 Show InChI InChI=1S/C30H33N7O2/c1-22-4-9-26(19-28(22)35-30-32-12-10-27(34-30)25-3-2-11-31-20-25)33-29(39)24-7-5-23(6-8-24)21-37-15-13-36(14-16-37)17-18-38/h2-12,19-20,38H,13-18,21H2,1H3,(H,33,39)(H,32,34,35) | 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 | 7.08E+3 | n/a | n/a | n/a | n/a | n/a | n/a |
The University of Texas M.D. Anderson Cancer Center
Curated by ChEMBL
| Assay Description Inhibition of Bcr-Abl (unknown origin) phosphorylation by spectrophotometric assay |
Bioorg Med Chem 22: 623-32 (2013)
Article DOI: 10.1016/j.bmc.2013.10.040 BindingDB Entry DOI: 10.7270/Q27S7Q76 |
More data for this Ligand-Target Pair | |