Cannabinol

Details

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Internal ID 14aca9cd-aad2-4ddb-b2b2-85a0309ad0e4
Taxonomy Organoheterocyclic compounds > Benzopyrans > 1-benzopyrans > Dibenzopyrans
IUPAC Name 6,6,9-trimethyl-3-pentylbenzo[c]chromen-1-ol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H26O2/c1-5-6-7-8-15-12-18(22)20-16-11-14(2)9-10-17(16)21(3,4)23-19(20)13-15/h9-13,22H,5-8H2,1-4H3
InChI Key VBGLYOIFKLUMQG-UHFFFAOYSA-N
Popularity 1,724 references in papers

Physical and Chemical Properties

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Molecular Formula C21H26O2
Molecular Weight 310.40 g/mol
Exact Mass 310.193280068 g/mol
Topological Polar Surface Area (TPSA) 29.50 Ų
XlogP 6.10
Atomic LogP (AlogP) 5.73
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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521-35-7
Cannabinolo
Cannabinolum
6,6,9-Trimethyl-3-pentyl-6H-dibenzo(b,d)pyran-1-ol
DTXSID3048996
3-Amyl-1-hydroxy-6,6,9-trimethyl-6H-dibenzo(b,d)pyran
6H-Dibenzo(b,d)pyran-1-ol, 6,6,9-trimethyl-3-pentyl-
7UYP6MC9GH
6,6,9-trimethyl-3-pentylbenzo[c]chromen-1-ol
NSC-134455
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Cannabinol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9906 99.06%
Caco-2 + 0.9144 91.44%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.5330 53.30%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.7889 78.89%
OATP1B3 inhibitior + 0.9534 95.34%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8074 80.74%
P-glycoprotein inhibitior - 0.4479 44.79%
P-glycoprotein substrate - 0.6219 62.19%
CYP3A4 substrate + 0.6052 60.52%
CYP2C9 substrate - 0.6092 60.92%
CYP2D6 substrate + 0.5444 54.44%
CYP3A4 inhibition - 0.8832 88.32%
CYP2C9 inhibition - 0.6012 60.12%
CYP2C19 inhibition - 0.5079 50.79%
CYP2D6 inhibition - 0.8499 84.99%
CYP1A2 inhibition + 0.5273 52.73%
CYP2C8 inhibition + 0.7588 75.88%
CYP inhibitory promiscuity - 0.5139 51.39%
UGT catelyzed + 0.6000 60.00%
Carcinogenicity (binary) - 0.9100 91.00%
Carcinogenicity (trinary) Non-required 0.7169 71.69%
Eye corrosion - 0.9805 98.05%
Eye irritation - 0.5000 50.00%
Skin irritation - 0.8019 80.19%
Skin corrosion - 0.9184 91.84%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7675 76.75%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.6385 63.85%
skin sensitisation - 0.7201 72.01%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7000 70.00%
Mitochondrial toxicity + 0.6875 68.75%
Nephrotoxicity + 0.5925 59.25%
Acute Oral Toxicity (c) III 0.7936 79.36%
Estrogen receptor binding + 0.8906 89.06%
Androgen receptor binding + 0.7969 79.69%
Thyroid receptor binding + 0.7750 77.50%
Glucocorticoid receptor binding + 0.8402 84.02%
Aromatase binding + 0.8713 87.13%
PPAR gamma + 0.9150 91.50%
Honey bee toxicity - 0.9582 95.82%
Biodegradation - 0.9750 97.50%
Crustacea aquatic toxicity + 0.7647 76.47%
Fish aquatic toxicity + 0.9809 98.09%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL218 P21554 Cannabinoid CB1 receptor 308 nM
13 nM
Ki
Ki
PMID: 11020293
via Super-PRED
CHEMBL253 P34972 Cannabinoid CB2 receptor 96 nM
16 nM
126.4 nM
Ki
Ki
Ki
PMID: 11020293
via Super-PRED
PMID: 9379442
CHEMBL4878 Q16678 Cytochrome P450 1B1 148 nM
Ki
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL240 Q12809 HERG 99.62% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 98.24% 91.11%
CHEMBL2581 P07339 Cathepsin D 98.23% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.61% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 91.20% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.07% 92.08%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 90.69% 96.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.60% 86.33%
CHEMBL2996 Q05655 Protein kinase C delta 87.79% 97.79%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.40% 99.17%
CHEMBL1966 Q02127 Dihydroorotate dehydrogenase 86.56% 96.09%
CHEMBL4208 P20618 Proteasome component C5 86.39% 90.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 86.31% 95.17%
CHEMBL5979 P05186 Alkaline phosphatase, tissue-nonspecific isozyme 86.22% 85.40%
CHEMBL5805 Q9NR97 Toll-like receptor 8 86.14% 96.25%
CHEMBL1951 P21397 Monoamine oxidase A 86.03% 91.49%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 86.02% 91.71%
CHEMBL3004 P33527 Multidrug resistance-associated protein 1 85.30% 96.37%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.14% 94.80%
CHEMBL4581 P52732 Kinesin-like protein 1 83.83% 93.18%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.77% 95.56%
CHEMBL1806 P11388 DNA topoisomerase II alpha 81.62% 89.00%
CHEMBL3492 P49721 Proteasome Macropain subunit 81.34% 90.24%

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 2543
NPASS NPC16577
ChEMBL CHEMBL74415
LOTUS LTS0043385
wikiData Q265831