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TargetLysophosphatidylserine lipase ABHD12
LigandBDBM50240877
Substrate/Competitorn/a
Meas. Tech.ChEMBL_557684 (CHEMBL962979)
IC50>100000±n/a nM
Citation Hoover, HSBlankman, JLNiessen, SCravatt, BF Selectivity of inhibitors of endocannabinoid biosynthesis evaluated by activity-based protein profiling. Bioorg Med Chem Lett18:5838-41 (2008) [PubMed]  Article
More Info.:Get all data from this article,  Assay Method
 
Lysophosphatidylserine lipase ABHD12
Name:Lysophosphatidylserine lipase ABHD12
Synonyms:ABD12_HUMAN | ABHD12 | C20orf22 | Monoacylglycerol lipase ABHD12
Type:PROTEIN
Mol. Mass.:45111.32
Organism:Homo sapiens (Human)
Description:ChEMBL_1514755
Residue:398
Sequence:
MRKRTEPVALEHERCAAAGSSSSGSAAAALDADCRLKQNLRLTGPAAAEPRCAADAGMKR
ALGRRKGVWLRLRKILFCVLGLYIAIPFLIKLCPGIQAKLIFLNFVRVPYFIDLKKPQDQ
GLNHTCNYYLQPEEDVTIGVWHTVPAVWWKNAQGKDQMWYEDALASSHPIILYLHGNAGT
RGGDHRVELYKVLSSLGYHVVTFDYRGWGDSVGTPSERGMTYDALHVFDWIKARSGDNPV
YIWGHSLGTGVATNLVRRLCERETPPDALILESPFTNIREEAKSHPFSVIYRYFPGFDWF
FLDPITSSGIKFANDENVKHISCPLLILHAEDDPVVPFQLGRKLYSIAAPARSFRDFKVQ
FVPFHSDLGYRHKYIYKSPELPRILREFLGKSEPEHQH
Blast this sequence in BindingDB or PDB
  Blast E-value cutoff:
BDBM50240877
n/a
NameBDBM50240877
Synonyms:CHEMBL158897 | Quinolyl derivatives | cyclohexanone O-6-((cyclohexylideneaminooxy)carbonylamino)hexylcarbamoyl oxime
TypeSmall organic molecule
Emp. Form.C20H34N4O4
Mol. Mass.394.5084
SMILESO=[#6](-[#7]-[#6]-[#6]-[#6]-[#6]-[#6]-[#6]-[#7]-[#6](=O)-[#8]\[#7]=[#6]-1\[#6]-[#6]-[#6]-[#6]-[#6]-1)-[#8]\[#7]=[#6]-1\[#6]-[#6]-[#6]-[#6]-[#6]-1
Structure
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