BDBM50068035 (S)-5-Hydroxy-4-{(S)-1-hydroxy-2-[(1S,2S,5R,8aR)-1,2,5-trimethyl-5-(4-methyl-pent-4-enyl)-1,2,3,5,6,7,8,8a-octahydro-naphthalen-1-yl]-ethyl}-5H-furan-2-one::5-Hydroxy-4-{1-hydroxy-2-[1,2,5-trimethyl-5-(4-methyl-pent-4-enyl)-1,2,3,5,6,7,8,8a-octahydro-naphthalen-1-yl]-ethyl}-5H-furan-2-one(dysidiolide)::CHEMBL356927

SMILES C[C@H]1CC=C2[C@H](CCC[C@]2(C)CCCC(C)=C)[C@@]1(C)C[C@H](O)C1=CC(=O)O[C@@H]1O

InChI Key InChIKey=JOYRNJIWPUZFBJ-LAXAASGQSA-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 = 50068035   

TargetM-phase inducer phosphatase 1(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50068035((S)-5-Hydroxy-4-{(S)-1-hydroxy-2-[(1S,2S,5R,8aR)-1...)
Affinity DataIC50:  1.50E+4nMAssay Description:The compound was tested for its inhibitory activity against Cell division cycle 25AMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetM-phase inducer phosphatase 2(Homo sapiens (Human))
The University Of Tokyo

Curated by ChEMBL
LigandPNGBDBM50068035((S)-5-Hydroxy-4-{(S)-1-hydroxy-2-[(1S,2S,5R,8aR)-1...)
Affinity DataIC50:  1.90E+4nMAssay Description:The compound was tested for its inhibitory activity against Cell division cycle 25BMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed