null

SMILES C[C@@H](OC(C)=O)[C@]12COCC=CC1[C@]1(C)CCC3[C@](O)(CC(=C)c4ccccc4)C(C)=C[C@@H](OC(C)=O)[C@]3(C)C1[C@H](OC(C)=O)[C@@H]2OC(C)=O

InChI Key InChIKey=KTLGTZSYLYAMTB-OJCSKBNASA-N

  Tab Delimited (TSV)   2D SDfile   Computed 3D by Vconf -m prep SDfile
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Exact match

Activity Spreadsheet -- Enzyme Inhibition Constant Data from BindingDB

Found 2 hits for monomerid = 50158227   

TargetPotassium voltage-gated channel subfamily A member 3(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50158227(Aceticacid1-[4,5,6-triacetoxy-1-hydroxy-2,4a,11b-t...)copy SMILEScopy InChI
Affinity DataIC50: 19nMAssay Description:Inhibition of voltage-gated potassium channel subunit Kv1.3 in chinese hamster ovary cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BP0281PubMed
TargetPotassium voltage-gated channel subfamily A member 3(Homo sapiens (Human))
Merck Research Laboratories

Curated by ChEMBL
LigandPNGBDBM50158227(Aceticacid1-[4,5,6-triacetoxy-1-hydroxy-2,4a,11b-t...)copy SMILEScopy InChI
Affinity DataIC50: 131nMAssay Description:Inhibitory activity against voltage-gated potassium channel subunit Kv1.3 of human T cellsMore data for this Ligand-Target Pair
In DepthDetails Article
BindingDB Entry DOI: 10.7270/Q2BP0281PubMed