Found 2 hits in this display 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 |
Leukotriene A-4 hydrolase
(Homo sapiens (Human)) | BDBM327106
(N-{l-[4-(2,3-dihydro-1,4- benzodioxin-2- yl)benz...)Show SMILES CS(=O)(=O)NC1CCN(Cc2ccc(cc2)C2COc3ccccc3O2)CC1 Show InChI InChI=1S/C21H26N2O4S/c1-28(24,25)22-18-10-12-23(13-11-18)14-16-6-8-17(9-7-16)21-15-26-19-4-2-3-5-20(19)27-21/h2-9,18,21-22H,10-15H2,1H3 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 0.160 | n/a | n/a | n/a | n/a | n/a | n/a |
Boehringer Ingelheim International GmbH
US Patent
| Assay Description The compounds of the invention are assessed for the ability to interact with human LTA4 hydrolase in an enzymatic assay that measures the ability of ... |
US Patent US9662339 (2017)
BindingDB Entry DOI: 10.7270/Q2GT5Q8D |
More data for this Ligand-Target Pair | |
Leukotriene A-4 hydrolase
(Homo sapiens (Human)) | BDBM327140
(N-(1-{4-[(2S)-2,3-dihydro-1,4- benzodioxin-2- yl...)Show SMILES CS(=O)(=O)NC1CCN(Cc2ccc(cc2)[C@H]2COc3ccccc3O2)CC1 |r| Show InChI InChI=1S/C21H26N2O4S/c1-28(24,25)22-18-10-12-23(13-11-18)14-16-6-8-17(9-7-16)21-15-26-19-4-2-3-5-20(19)27-21/h2-9,18,21-22H,10-15H2,1H3/t21-/m1/s1 | PDB MMDB
Reactome pathway KEGG
UniProtKB/SwissProt
B.MOAD DrugBank antibodypedia GoogleScholar AffyNet
| PC cid PC sid UniChem
| US Patent
| n/a | n/a | 0.240 | n/a | n/a | n/a | n/a | n/a | n/a |
Boehringer Ingelheim International GmbH
US Patent
| Assay Description The compounds of the invention are assessed for the ability to interact with human LTA4 hydrolase in an enzymatic assay that measures the ability of ... |
US Patent US9662339 (2017)
BindingDB Entry DOI: 10.7270/Q2GT5Q8D |
More data for this Ligand-Target Pair | |