BDBM50194623 (1S,5S,6R,E)-5-(hydroxymethyl)-1-methoxy-6-(6-methylhepta-2,5-dien-2-yl)bicyclo[3.1.0]hexan-2-one::CHEMBL213526::Fumarranol Analog, 8

SMILES [#6]-[#8][C@@]12[#6](\[#6](-[#6])=[#6]\[#6]\[#6]=[#6](\[#6])-[#6])[C@]1([#6]-[#8])[#6]-[#6]-[#6]2=O

InChI Key InChIKey=URUFBIPEEVURAI-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
Find this compound or compounds like it in BindingDB:
   Substructure
Similarity at least:  must be >=0.5
Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50194623   

TargetMethionine aminopeptidase 2(malaria parasite P. falciparum)
Johns Hopkins School of Medicine

LigandPNGBDBM50194623(Fumarranol Analog, 8 | CHEMBL213526 | (1S,5S,6R,E)...)
Affinity DataIC50: 5.00E+5nMAssay Description:Enzyme affinity assay using Fumarranol analogs with plasmodium falciparum methionine aminopeptidases (PfMetAPs).More data for this Ligand-Target Pair
In Depth
Date in BDB:
8/25/2011
Entry Details Article
PubMed
TargetMethionine aminopeptidase 2(Human)
The Johns Hopkins University School of Medicine

Curated by ChEMBL
LigandPNGBDBM50194623(Fumarranol Analog, 8 | CHEMBL213526 | (1S,5S,6R,E)...)
Affinity DataIC50: 3.38E+4nMAssay Description:Inhibition of human MetAP2More data for this Ligand-Target Pair
In Depth
Date in BDB:
11/10/2009
Entry Details Article
PubMed