(-)-7R-cannabicoumarononic acid A

Details

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Internal ID 8d22c146-d8db-46a7-9dbd-7603ab72fd38
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans
IUPAC Name (5R)-6,6-dimethyl-5-(3-oxobutyl)-10-pentyl-2,7-dioxatricyclo[6.3.1.04,12]dodeca-1(11),3,8(12),9-tetraene-11-carboxylic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C22H28O5/c1-5-6-7-8-14-11-17-19-15(12-26-20(19)18(14)21(24)25)16(10-9-13(2)23)22(3,4)27-17/h11-12,16H,5-10H2,1-4H3,(H,24,25)/t16-/m1/s1
InChI Key WEYZBZCYDDIMCS-MRXNPFEDSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C22H28O5
Molecular Weight 372.50 g/mol
Exact Mass 372.19367399 g/mol
Topological Polar Surface Area (TPSA) 76.70 Ų
XlogP 4.70
Atomic LogP (AlogP) 5.49
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (-)-7R-cannabicoumarononic acid A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9663 96.63%
Caco-2 + 0.6125 61.25%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability - 0.6714 67.14%
Subcellular localzation Mitochondria 0.8209 82.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8329 83.29%
OATP1B3 inhibitior + 0.9031 90.31%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior + 0.6841 68.41%
P-glycoprotein inhibitior - 0.5249 52.49%
P-glycoprotein substrate - 0.5610 56.10%
CYP3A4 substrate + 0.6073 60.73%
CYP2C9 substrate + 0.8178 81.78%
CYP2D6 substrate - 0.8602 86.02%
CYP3A4 inhibition - 0.7850 78.50%
CYP2C9 inhibition - 0.6356 63.56%
CYP2C19 inhibition - 0.7922 79.22%
CYP2D6 inhibition - 0.9298 92.98%
CYP1A2 inhibition - 0.6944 69.44%
CYP2C8 inhibition + 0.7605 76.05%
CYP inhibitory promiscuity - 0.7488 74.88%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8600 86.00%
Carcinogenicity (trinary) Non-required 0.6037 60.37%
Eye corrosion - 0.9910 99.10%
Eye irritation - 0.8262 82.62%
Skin irritation - 0.7486 74.86%
Skin corrosion - 0.9012 90.12%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7263 72.63%
Micronuclear - 0.7700 77.00%
Hepatotoxicity - 0.5000 50.00%
skin sensitisation - 0.8560 85.60%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity + 0.7375 73.75%
Nephrotoxicity + 0.5387 53.87%
Acute Oral Toxicity (c) III 0.4729 47.29%
Estrogen receptor binding + 0.7201 72.01%
Androgen receptor binding + 0.7491 74.91%
Thyroid receptor binding + 0.5631 56.31%
Glucocorticoid receptor binding + 0.8135 81.35%
Aromatase binding + 0.6263 62.63%
PPAR gamma + 0.7864 78.64%
Honey bee toxicity - 0.8798 87.98%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.5265 52.65%
Fish aquatic toxicity + 0.9968 99.68%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL2581 P07339 Cathepsin D 98.36% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.03% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 95.61% 97.25%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 92.98% 95.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 92.52% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 91.87% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.41% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.28% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 88.35% 99.17%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 87.55% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 87.37% 89.00%
CHEMBL4040 P28482 MAP kinase ERK2 85.23% 83.82%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 85.10% 92.08%
CHEMBL230 P35354 Cyclooxygenase-2 81.77% 89.63%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.11% 99.23%
CHEMBL5805 Q9NR97 Toll-like receptor 8 81.08% 96.25%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.97% 96.95%
CHEMBL3864 Q06124 Protein-tyrosine phosphatase 2C 80.93% 94.42%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.02% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Cannabis sativa

Cross-Links

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PubChem 44139614
LOTUS LTS0268120
wikiData Q105303698