BDBM50052128 CHEMBL92687::Cyclohexylmethyl-carbamic acid (3R,4aR,5S,6S,6aS,10S,10aR,10bS)-6,10,10b-trihydroxy-3,4a,7,7,10a-pentamethyl-1-oxo-3-vinyl-dodecahydro-benzo[f]chromen-5-yl ester

SMILES CC1(C)CC[C@H](O)[C@@]2(C)[C@H]1[C@H](O)[C@H](OC(=O)NCC1CCCCC1)[C@@]1(C)O[C@](C)(CC(=O)[C@]21O)C=C

InChI Key InChIKey=DJOLPWJHZINFGR-FCTGTBMNSA-N

Data  2 IC50  2 EC50

  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 4 hits for monomerid = 50052128   

TargetAdenylate cyclase type 1(Homo sapiens (Human))
Food and Drug Administration

Curated by ChEMBL
LigandPNGBDBM50052128(CHEMBL92687 | Cyclohexylmethyl-carbamic acid (3R,4...)
Affinity DataIC50: >150nMAssay Description:Inhibition of [125 I]-6-IHPP-forskolin binding to adenylate cyclase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenylate cyclase type 1(Homo sapiens (Human))
Food and Drug Administration

Curated by ChEMBL
LigandPNGBDBM50052128(CHEMBL92687 | Cyclohexylmethyl-carbamic acid (3R,4...)
Affinity DataIC50:  1.60E+3nMAssay Description:Inhibition of [125 I]-6-IHPP-forskolin binding to adenylate cyclase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenylate cyclase type 1(Homo sapiens (Human))
Food and Drug Administration

Curated by ChEMBL
LigandPNGBDBM50052128(CHEMBL92687 | Cyclohexylmethyl-carbamic acid (3R,4...)
Affinity DataEC50:  6.40E+3nMAssay Description:Conversion of [32P] ATP to [32P]-cyclic AMP mediated by adenylate cyclase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetAdenylate cyclase type 1(Homo sapiens (Human))
Food and Drug Administration

Curated by ChEMBL
LigandPNGBDBM50052128(CHEMBL92687 | Cyclohexylmethyl-carbamic acid (3R,4...)
Affinity DataEC50: >2.00E+3nMAssay Description:Ability to activate the conversion of [32P] ATP to [32P]-cyclic AMP mediated by adenylate cyclase 1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed