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TargetLeukotriene A-4 hydrolase
LigandBDBM50266280
Substrate/Competitorn/a
Meas. Tech.ChEMBL_544515 (CHEMBL1013487)
IC50 79±n/a nM
Citation Enomoto, HMorikawa, YMiyake, YTsuji, FMizuchi, MSuhara, HFujimura, KHoriuchi, MBan, M Synthesis and biological evaluation of N-mercaptoacylcysteine derivatives as leukotriene A4 hydrolase inhibitors. Bioorg Med Chem Lett19:442-6 (2008) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Leukotriene A-4 hydrolase
Name:Leukotriene A-4 hydrolase
Synonyms:LKHA4_CAVPO | LTA4H
Type:PROTEIN
Mol. Mass.:68972.78
Organism:Cavia porcellus
Description:ChEMBL_544515
Residue:611
Sequence:
MPEVVDTCSLASPATVCRTKHLHLRCSVDFTRRALTGVAALTIQSQEDNLRSLILDTKDL
TIEKVVINGQEVKYALGEKQSYKGSPMEISLPIALSKNQEVVIEISFETSPKSSALQWLT
PEQTSGKEHPYLFSQCQAIHCRAFLPCQDTPSVKLTYTAEVSVPKELVALMSAIRDGEAP
DPADPSRKIYKFSQKVPIPCYLIALVVGALESRKIGPRTLVWSEKEQVDKSAYEFSETES
MLKIAEDLGGPYVWGQYDRLVLPPSFSYGGMENPCLTFVTPTLLAGDKSLSNVIAHEISH
TWTGNLVTNKTWDHFWLNEGHTVYLERHICGRLFGEKFRHFHALGGWGELQNTVKTLGET
QAFTKLVVDLTDTDPDVAYSSVPYEKGFALLFHLEQLLGGPEVFLGFLKAYVEKFSYKSI
TTDDWKNFLFSHFKDKVDILNQVDWDAWLYSPGLPPIKPNYDMTLTNACIALSQRWITAK
EKDLNTFSATDLKDLSSHQVNEFLAQVLQRAPLPLGHVKRMQEVYNCNAINNSEIRFRWL
RLCIQSKWEEAIPLALKMATEQGRMKFTRPLFKDLAAFDKSHDQAIQTYHAHKASMHPVT
AMLVGKDLKVE
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50266280
n/a
NameBDBM50266280
Synonyms:(R)-3-(2-(4-isopropylphenyl)propan-2-ylthio)-2-((S)-3-mercapto-2-methylpropanamido)propanoic acid | CHEMBL456723
TypeSmall organic molecule
Emp. Form.C19H29NO3S2
Mol. Mass.383.568
SMILESCC(C)c1ccc(cc1)C(C)(C)SC[C@H](NC(=O)[C@H](C)CS)C(O)=O |r|
Structure
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