BDBM50530670 3-ANHYDRO-6-EPI-OPHIOBOLIN A

SMILES [H][C@]12[#6][C@@]3([#6])[#6]-[#6][C@@]4([#8]-[#6@H](-[#6]-[#6@@H]4-[#6])\[#6]=[#6](\[#6])-[#6])[C@]3([H])[#6]\[#6]=[#6](-[#6]=O)/[C@]1([H])[#6](=O)-[#6]=[#6]2-[#6]

InChI Key InChIKey=HJVZKYVURJEXEK-UHFFFAOYSA-N

Data  2 IC50

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50530670   

Target3-hydroxy-3-methylglutaryl-coenzyme A reductase(Human)
Huazhong University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50530670(3-ANHYDRO-6-EPI-OPHIOBOLIN A)
Affinity DataIC50: 8.40E+3nMAssay Description:Inhibition of human HMGR using HMGCoA as substrate measured after 15 mins in presence of NADPH by UV microplate reader analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/26/2021
Entry Details Article
PubMed
Target3-hydroxy-3-methylglutaryl-coenzyme A reductase(Human)
Huazhong University of Science and Technology

Curated by ChEMBL
LigandPNGBDBM50530670(3-ANHYDRO-6-EPI-OPHIOBOLIN A)
Affinity DataIC50: 8.40E+3nMAssay Description:Inhibition of human HMGR using HMGCoA as substrate measured after 15 mins in presence of NADPH by UV microplate reader analysisMore data for this Ligand-Target Pair
In Depth
Date in BDB:
2/26/2021
Entry Details Article
PubMed