Cananodine

Details

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Internal ID c1855589-458a-44c1-b8f1-3eb56ff06468
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Methylpyridines
IUPAC Name 2-[(5R,8R)-2,5-dimethyl-6,7,8,9-tetrahydro-5H-cyclohepta[b]pyridin-8-yl]propan-2-ol
SMILES (Canonical) CC1CCC(CC2=C1C=CC(=N2)C)C(C)(C)O
SMILES (Isomeric) C[C@@H]1CC[C@H](CC2=C1C=CC(=N2)C)C(C)(C)O
InChI InChI=1S/C15H23NO/c1-10-5-7-12(15(3,4)17)9-14-13(10)8-6-11(2)16-14/h6,8,10,12,17H,5,7,9H2,1-4H3/t10-,12-/m1/s1
InChI Key LWYMRLDOLMZJGZ-ZYHUDNBSSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C15H23NO
Molecular Weight 233.35 g/mol
Exact Mass 233.177964357 g/mol
Topological Polar Surface Area (TPSA) 33.10 Ų
XlogP 3.00
Atomic LogP (AlogP) 3.22
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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CHEMBL476684
NSC812529
NSC-812529

2D Structure

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2D Structure of Cananodine

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.6944 69.44%
Blood Brain Barrier + 0.8629 86.29%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.4276 42.76%
OATP2B1 inhibitior - 0.8547 85.47%
OATP1B1 inhibitior + 0.9310 93.10%
OATP1B3 inhibitior + 0.9414 94.14%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.6162 61.62%
P-glycoprotein inhibitior - 0.9699 96.99%
P-glycoprotein substrate - 0.6270 62.70%
CYP3A4 substrate + 0.5295 52.95%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.6892 68.92%
CYP3A4 inhibition - 0.8852 88.52%
CYP2C9 inhibition - 0.8309 83.09%
CYP2C19 inhibition - 0.7462 74.62%
CYP2D6 inhibition - 0.8597 85.97%
CYP1A2 inhibition - 0.6467 64.67%
CYP2C8 inhibition + 0.5627 56.27%
CYP inhibitory promiscuity - 0.9218 92.18%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8500 85.00%
Carcinogenicity (trinary) Non-required 0.7426 74.26%
Eye corrosion - 0.9633 96.33%
Eye irritation - 0.8378 83.78%
Skin irritation - 0.6270 62.70%
Skin corrosion - 0.8590 85.90%
Ames mutagenesis - 0.6200 62.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6445 64.45%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5392 53.92%
skin sensitisation - 0.6650 66.50%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.7617 76.17%
Acute Oral Toxicity (c) III 0.6527 65.27%
Estrogen receptor binding - 0.8423 84.23%
Androgen receptor binding - 0.8686 86.86%
Thyroid receptor binding + 0.5930 59.30%
Glucocorticoid receptor binding - 0.5545 55.45%
Aromatase binding - 0.8197 81.97%
PPAR gamma - 0.6818 68.18%
Honey bee toxicity - 0.9495 94.95%
Biodegradation - 0.9250 92.50%
Crustacea aquatic toxicity + 0.7200 72.00%
Fish aquatic toxicity + 0.7393 73.93%

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
CHEMBL1951 P21397 Monoamine oxidase A 95.70% 91.49%
CHEMBL2039 P27338 Monoamine oxidase B 94.12% 92.51%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 91.45% 93.65%
CHEMBL2243 O00519 Anandamide amidohydrolase 91.17% 97.53%
CHEMBL2581 P07339 Cathepsin D 90.80% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 89.94% 97.25%
CHEMBL3401 O75469 Pregnane X receptor 84.47% 94.73%
CHEMBL3137262 O60341 LSD1/CoREST complex 84.16% 97.09%
CHEMBL2335 P42785 Lysosomal Pro-X carboxypeptidase 84.11% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.42% 99.23%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.34% 86.33%

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.
Cananga odorata

Cross-Links

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PubChem 10059898
LOTUS LTS0155832
wikiData Q105158666