BDBM50071370 (3R,8S)-falcarindiol::(3R,8S,)-heptadeca-1,9-dien-4,6-diyne-3,8-diol::(3S,8S)-falcarindiol::(Z)-(3R,8S)-Heptadeca-1,9-diene-4,6-diyne-3,8-diol::(Z)-(3S,8S)-Heptadeca-1,9-diene-4,6-diyne-3,8-diol::CHEMBL69018::Falcarindiol::Heptadeca-1,9(Z)-diene-4,6-diyne-3,8-diol::Heptadeca-1,9-diene-4,6-diyne-3,8-diol

SMILES CCCCCCC\C=C/[C@H](O)C#CC#C[C@H](O)C=C

InChI Key InChIKey=QWCNQXNAFCBLLV-YWALDVPYSA-N

Data  4 KI  3 IC50  1 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 8 hits for monomerid = 50071370   

TargetD(1A) dopamine receptor(RAT)
Harvard Medical School

Curated by ChEMBL
LigandPNGBDBM50071370((3R,8S)-falcarindiol | (3R,8S,)-heptadeca-1,9-dien...)
Affinity DataKi:  192nMAssay Description:Displacement of [3H]SCH-23390 from rat HA-tagged D1 dopamine receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDelta-type opioid receptor(MOUSE)
Harvard Medical School

Curated by ChEMBL
LigandPNGBDBM50071370((3R,8S)-falcarindiol | (3R,8S,)-heptadeca-1,9-dien...)
Affinity DataKi:  1.10E+3nMAssay Description:Displacement of [3H]diprenorphine from mouse delta opioid receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetMu-type opioid receptor(Rattus norvegicus (rat))
Harvard Medical School

Curated by ChEMBL
LigandPNGBDBM50071370((3R,8S)-falcarindiol | (3R,8S,)-heptadeca-1,9-dien...)
Affinity DataKi:  1.13E+3nMAssay Description:Displacement of [3H]diprenorphine from rat mu opioid receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetKappa-type opioid receptor(Homo sapiens (Human))
Harvard Medical School

Curated by ChEMBL
LigandPNGBDBM50071370((3R,8S)-falcarindiol | (3R,8S,)-heptadeca-1,9-dien...)
Affinity DataKi:  2.52E+3nMAssay Description:Displacement of [3H]diprenorphine from human kappa opioid receptor expressed in CHO cellsMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
University Of Vienna

Curated by ChEMBL
LigandPNGBDBM50071370((3R,8S)-falcarindiol | (3R,8S,)-heptadeca-1,9-dien...)
Affinity DataEC50:  3.20E+3nMAssay Description:Activation of human PPARgamma expressed in HEK293 cells incubated for 18 hrs by luciferase reporter assay relative to controlMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
Target5-hydroxytryptamine receptor 7(Homo sapiens (Human))
University Of Illinois At Chicago

Curated by ChEMBL
LigandPNGBDBM50071370((3R,8S)-falcarindiol | (3R,8S,)-heptadeca-1,9-dien...)
Affinity DataIC50:  1.18E+5nMAssay Description:Displacement of [3H]LSD from human recombinant 5HT7 receptor expressed in CHO cells by liquid scintillation countingMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTyrosine-protein phosphatase non-receptor type 1(Homo sapiens (Human))
Chinese Academy Of Sciences

Curated by ChEMBL
LigandPNGBDBM50071370((3R,8S)-falcarindiol | (3R,8S,)-heptadeca-1,9-dien...)
Affinity DataIC50:  3.15E+4nMAssay Description:Inhibition of PTP1B (unknown origin) using pNPP substrate measured after 3 mins by colorimetric assayMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetProstaglandin G/H synthase 1(Homo sapiens (Human))
Uppsala University

Curated by ChEMBL
LigandPNGBDBM50071370((3R,8S)-falcarindiol | (3R,8S,)-heptadeca-1,9-dien...)
Affinity DataIC50:  6.60E+4nMAssay Description:Inhibition of COX1More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed