BDBM50318486 2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chromen-5-ol(cannabichromene)::CANNABICHROMENE::CHEMBL422704

SMILES [#6]-[#6]-[#6]-[#6]-[#6]-c1cc(-[#8])c2-[#6]=[#6]C([#6])([#6]-[#6]\[#6]=[#6](\[#6])-[#6])[#8]-c2c1

InChI Key InChIKey=UVOLYTDXHDXWJU-UHFFFAOYSA-N

Data  3 KI  9 IC50  7 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 19 hits for monomerid = 50318486   

TargetCannabinoid receptor 2(Homo sapiens (Human))
Concordia University Wisconsin

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataKi:  257nMAssay Description:Displacement of [3H]-CP55940 from recombinant human CB2 receptor expressed in Sf9 cell membranes co-expressing Galphai3beta1gamma2 measured after 90 ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetCannabinoid receptor 1(Homo sapiens (Human))
Concordia University Wisconsin

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataKi:  714nMAssay Description:Displacement of [3H]-CP55940 from recombinant human CB1 receptor expressed in Sf9 cell membranes co-expressing Galphai3beta1gamma2 measured after 90 ...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetL-lactate dehydrogenase A chain(Homo sapiens (Human))
The University Of Sydney

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataKi:  8.50E+3nMAssay Description:Non-competitive inhibition of human LDHA assessed as reduction in lactate production using pyruvate as substrate in presence of NADH by Lineweaver-Bu...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetDiacylglycerol lipase-alpha(Homo sapiens (Human))
Concordia University Wisconsin

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human DAGLalpha expressed in COS7 cells using [14C]-oleoyl-2-arachidonoyl-glycerol as substrate measured after 20 mins by b...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetN-acylethanolamine-hydrolyzing acid amidase(Homo sapiens (Human))
Concordia University Wisconsin

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of recombinant human NAAA expressed in HEK293 cells using [14C]-N-palmitoylethanolamine as substrate measured after 30 mins by beta-counti...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetPeroxisome proliferator-activated receptor gamma(Homo sapiens (Human))
Universit£

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataEC50: >2.50E+4nMAssay Description:Agonist activity at GAL4-tagged PPARgamma (unknown origin) transiently expressed in HEK293T cells co-transfected with GAL4-tagged luc incubated for 6...More data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataEC50:  2.42E+4nMAssay Description:Agonist activity at ionomycin-stimulated TRPV1 (unknown origin) activationMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily V member 1(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50: >5.00E+4nMAssay Description:Agonist activity at ionomycin-stimulated TRPV1 (unknown origin) channel desensitization in presence of capsaicinMore data for this Ligand-Target Pair
In DepthDetails PubMed
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50:  6.50E+3nMAssay Description:Agonist activity at ionomycin-stimulated TRPV2 (unknown origin) channel desensitization in presence of lysophosphatidylcholineMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily V member 3(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataEC50:  1.90E+3nMAssay Description:Agonist activity at ionomycin-stimulated TRPV3 (unknown origin) activationMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily V member 3(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50:  2.01E+5nMAssay Description:Agonist activity at ionomycin-stimulated TRPV3 (unknown origin) channel desensitization in presence of carvacrolMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataEC50:  600nMAssay Description:Agonist activity at ionomycin-stimulated TRPV4 (unknown origin) activationMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily V member 4(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50:  9.90E+3nMAssay Description:Agonist activity at ionomycin-stimulated TRPV4 (unknown origin) channel desensitization in presence of 4alphaPDDMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataEC50:  90nMAssay Description:Agonist activity at TRPA1 (unknown origin) activationMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily A member 1(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50:  370nMAssay Description:Agonist activity at TRPA1 (unknown origin) channel desensitization in presence of isothiocyanateMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetFatty-acid amide hydrolase 1 [30-579](Rattus norvegicus (rat))
Concordia University Wisconsin

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50: >1.00E+5nMAssay Description:Inhibition of FAAH in rat brain membranes using [14C]-AEA as substrate measured after 30 mins by scintillation counting methodMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily M member 8(Homo sapiens (Human))
Scientus Pharma

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataIC50:  4.07E+4nMAssay Description:Antagonist activity at TRPM8 (unknown origin) ion channelMore data for this Ligand-Target Pair
In DepthDetails PubMed
TargetTransient receptor potential cation channel subfamily A member 1(Rattus norvegicus)
Ferrara University

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataEC50:  60nMAssay Description:Agonist activity at rat TRPA1 channel expressed in HEK293 cells assessed as increase in intracellular calcium influxMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed
TargetTransient receptor potential cation channel subfamily A member 1(Rattus norvegicus)
Ferrara University

Curated by ChEMBL
LigandPNGBDBM50318486(2-Methyl-2-(4-methyl-pent-3-enyl)-7-pentyl-2H-chro...)
Affinity DataEC50:  3.43E+4nMAssay Description:Agonist activity at TRPA1 channel in rat DRG neurons assessed as increase in intracellular calcium influxMore data for this Ligand-Target Pair
In DepthDetails ArticlePubMed