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TargetLeukotriene A-4 hydrolase
LigandBDBM50082665
Substrate/Competitorn/a
Meas. Tech.ChEMBL_1659686 (CHEMBL4009298)
IC50 790±n/a nM
Citation Lu, WYao, XOuyang, PDong, NWu, DJiang, XWu, ZZhang, CXu, ZTang, YZou, SLiu, MLi, JZeng, MLin, PCheng, FHuang, J Drug Repurposing of Histone Deacetylase Inhibitors That Alleviate Neutrophilic Inflammation in Acute Lung Injury and Idiopathic Pulmonary Fibrosis via Inhibiting Leukotriene A4 Hydrolase and Blocking LTB4 Biosynthesis. J Med Chem60:1817-1828 (2017) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Leukotriene A-4 hydrolase
Name:Leukotriene A-4 hydrolase
Synonyms:LKHA4_MOUSE | Leukotriene A4 hydrolase | Lta4h
Type:PROTEIN
Mol. Mass.:69048.58
Organism:Mus musculus
Description:ChEMBL_936852
Residue:611
Sequence:
MPEVADTCSLASPASVCRTQHLHLRCSVDFARRTLTGTAALTVQSQEENLRSLTLDTKDL
TIEKVVINGQEVKYTLGESQGYKGSPMEISLPIALSKNQEIVIEISFETSPKSSALQWLT
PEQTSGKQHPYLFSQCQAIHCRAILPCQDTPSVKLTYTAEVSVPKELVALMSAIRDGEAP
DPEDPSRKIYRFNQRVPIPCYLIALVVGALESRQIGPRTLVWSEKEQVEKSANEFSETES
MLKIAEDLGGPYVWGQYDLLVLPPSFPYGGMENPCLTFVTPTLLAGDKSLSNVIAHEISH
SWTGNLVTNKTWDHFWLNEGHTVYLERHICGRLFGEKFRHFHALGGWGELQNTIKTFGES
HPFTKLVVDLKDVDPDVAYSSIPYEKGFALLFYLEQLLGGPEVFLGFLKAYVKKFSYQSV
TTDDWKSFLYSHFKDKVDLLNQVDWNTWLYAPGLPPVKPNYDVTLTNACIALSQRWVTAK
EEDLSSFSIADLKDLSSHQLNEFLAQVLQKAPLPLGHIKRMQEVYNFNAINNSEIRFRWL
RLCIQSKWEEAIPLALKMATEQGRMKFTRPLFKDLAAFDKSHDQAVHTYQEHKASMHPVT
AMLVGRDLKVD
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50082665
n/a
NameBDBM50082665
Synonyms:4-(dimethylamino)-N-(7-(hydroxyamino)-7-oxoheptyl)benzamide | 4-Dimethylamino-N-(6-hydroxycarbamoyl-hexyl)-benzamide | CHEMBL140000 | US10188756, Compound CN52
TypeSmall organic molecule
Emp. Form.C16H25N3O3
Mol. Mass.307.388
SMILESCN(C)c1ccc(cc1)C(=O)NCCCCCCC(=O)NO
Structure
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