Cannagunine

Details

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Internal ID 90e3c3b9-bb0b-40be-b42b-c8efa9697c0c
Taxonomy Organoheterocyclic compounds > Indoles and derivatives > Pyridoindoles > Beta carbolines
IUPAC Name (1R,15S,21S)-3-methyl-17-oxa-3,13-diazapentacyclo[11.9.0.02,10.04,9.015,21]docosa-2(10),4,6,8,19-pentaen-18-one
SMILES (Canonical) CN1C2=CC=CC=C2C3=C1C4CC5C=CC(=O)OCC5CN4CC3
SMILES (Isomeric) CN1C2=CC=CC=C2C3=C1[C@H]4C[C@H]5C=CC(=O)OC[C@@H]5CN4CC3
InChI InChI=1S/C20H22N2O2/c1-21-17-5-3-2-4-15(17)16-8-9-22-11-14-12-24-19(23)7-6-13(14)10-18(22)20(16)21/h2-7,13-14,18H,8-12H2,1H3/t13-,14+,18-/m1/s1
InChI Key KSLYJCMRRQHOJW-QWQRMKEZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C20H22N2O2
Molecular Weight 322.40 g/mol
Exact Mass 322.168127949 g/mol
Topological Polar Surface Area (TPSA) 34.50 Ų
XlogP 2.60
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 4
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Cannagunine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9901 99.01%
Caco-2 + 0.7788 77.88%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4986 49.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9270 92.70%
OATP1B3 inhibitior + 0.9438 94.38%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior + 0.5250 52.50%
BSEP inhibitior + 0.7765 77.65%
P-glycoprotein inhibitior - 0.5169 51.69%
P-glycoprotein substrate + 0.6006 60.06%
CYP3A4 substrate + 0.6903 69.03%
CYP2C9 substrate - 0.8127 81.27%
CYP2D6 substrate - 0.7804 78.04%
CYP3A4 inhibition - 0.6698 66.98%
CYP2C9 inhibition - 0.8623 86.23%
CYP2C19 inhibition - 0.8053 80.53%
CYP2D6 inhibition - 0.6309 63.09%
CYP1A2 inhibition + 0.5642 56.42%
CYP2C8 inhibition - 0.8526 85.26%
CYP inhibitory promiscuity - 0.6030 60.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6802 68.02%
Eye corrosion - 0.9867 98.67%
Eye irritation - 0.9973 99.73%
Skin irritation - 0.7828 78.28%
Skin corrosion - 0.9424 94.24%
Ames mutagenesis + 0.5700 57.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9202 92.02%
Micronuclear + 0.5200 52.00%
Hepatotoxicity + 0.7181 71.81%
skin sensitisation - 0.8574 85.74%
Respiratory toxicity + 0.8889 88.89%
Reproductive toxicity + 0.8333 83.33%
Mitochondrial toxicity + 0.9500 95.00%
Nephrotoxicity + 0.5000 50.00%
Acute Oral Toxicity (c) III 0.5358 53.58%
Estrogen receptor binding + 0.7561 75.61%
Androgen receptor binding + 0.6432 64.32%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.6779 67.79%
Aromatase binding + 0.7411 74.11%
PPAR gamma - 0.6090 60.90%
Honey bee toxicity - 0.8539 85.39%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7300 73.00%
Fish aquatic toxicity + 0.8317 83.17%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 98.38% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 96.96% 85.14%
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.26% 97.25%
CHEMBL1899 P46098 Serotonin 3a (5-HT3a) receptor 93.68% 100.00%
CHEMBL2581 P07339 Cathepsin D 91.42% 98.95%
CHEMBL1806 P11388 DNA topoisomerase II alpha 90.30% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.04% 99.23%
CHEMBL1914 P06276 Butyrylcholinesterase 88.40% 95.00%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 88.30% 93.40%
CHEMBL3192 Q9BY41 Histone deacetylase 8 87.83% 93.99%
CHEMBL255 P29275 Adenosine A2b receptor 87.80% 98.59%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.70% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.56% 96.09%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 82.22% 94.00%
CHEMBL264 Q9Y5N1 Histamine H3 receptor 81.50% 91.43%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.40% 93.65%
CHEMBL5805 Q9NR97 Toll-like receptor 8 80.98% 96.25%

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.
Vaccinium oxycoccos

Cross-Links

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PubChem 101307894
LOTUS LTS0037791
wikiData Q105145490