Canusesnol C

Details

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Internal ID 9e80d7f6-b01e-4c94-ab0d-cab88c43881c
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids > Eudesmane, isoeudesmane or cycloeudesmane sesquiterpenoids
IUPAC Name (1R,4aR,6R,8aS)-1,4a-dihydroxy-6-(2-hydroxypropan-2-yl)-4,8a-dimethyl-5,6,7,8-tetrahydro-1H-naphthalen-2-one
SMILES (Canonical) CC1=CC(=O)C(C2(C1(CC(CC2)C(C)(C)O)O)C)O
SMILES (Isomeric) CC1=CC(=O)[C@@H]([C@]2([C@]1(C[C@@H](CC2)C(C)(C)O)O)C)O
InChI InChI=1S/C15H24O4/c1-9-7-11(16)12(17)14(4)6-5-10(13(2,3)18)8-15(9,14)19/h7,10,12,17-19H,5-6,8H2,1-4H3/t10-,12+,14+,15-/m1/s1
InChI Key NYNFUJAJEKSDTJ-UEEZHKSASA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O4
Molecular Weight 268.35 g/mol
Exact Mass 268.16745924 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 0.30
Atomic LogP (AlogP) 1.18
H-Bond Acceptor 4
H-Bond Donor 3
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Canusesnol C

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9902 99.02%
Caco-2 - 0.5377 53.77%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.7305 73.05%
OATP2B1 inhibitior - 0.8512 85.12%
OATP1B1 inhibitior + 0.9172 91.72%
OATP1B3 inhibitior + 0.8065 80.65%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.5385 53.85%
BSEP inhibitior - 0.6098 60.98%
P-glycoprotein inhibitior - 0.9521 95.21%
P-glycoprotein substrate - 0.8486 84.86%
CYP3A4 substrate + 0.6079 60.79%
CYP2C9 substrate - 0.8086 80.86%
CYP2D6 substrate - 0.8871 88.71%
CYP3A4 inhibition - 0.7541 75.41%
CYP2C9 inhibition - 0.8116 81.16%
CYP2C19 inhibition - 0.7821 78.21%
CYP2D6 inhibition - 0.9435 94.35%
CYP1A2 inhibition - 0.8430 84.30%
CYP2C8 inhibition - 0.8596 85.96%
CYP inhibitory promiscuity - 0.9049 90.49%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6323 63.23%
Eye corrosion - 0.9932 99.32%
Eye irritation - 0.9376 93.76%
Skin irritation + 0.6024 60.24%
Skin corrosion - 0.9476 94.76%
Ames mutagenesis - 0.8170 81.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7414 74.14%
Micronuclear - 0.9500 95.00%
Hepatotoxicity + 0.5673 56.73%
skin sensitisation - 0.6124 61.24%
Respiratory toxicity + 0.6778 67.78%
Reproductive toxicity + 0.9111 91.11%
Mitochondrial toxicity + 0.8250 82.50%
Nephrotoxicity - 0.6362 63.62%
Acute Oral Toxicity (c) I 0.5654 56.54%
Estrogen receptor binding + 0.5628 56.28%
Androgen receptor binding + 0.5208 52.08%
Thyroid receptor binding + 0.5544 55.44%
Glucocorticoid receptor binding + 0.6721 67.21%
Aromatase binding - 0.5164 51.64%
PPAR gamma - 0.7136 71.36%
Honey bee toxicity - 0.9190 91.90%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9863 98.63%

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
CHEMBL253 P34972 Cannabinoid CB2 receptor 96.40% 97.25%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.63% 91.11%
CHEMBL1871 P10275 Androgen Receptor 91.76% 96.43%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.48% 95.56%
CHEMBL2581 P07339 Cathepsin D 90.65% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 88.57% 100.00%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 86.45% 93.04%
CHEMBL3137262 O60341 LSD1/CoREST complex 86.08% 97.09%
CHEMBL3192 Q9BY41 Histone deacetylase 8 83.84% 93.99%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.64% 89.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 83.41% 85.14%
CHEMBL216 P11229 Muscarinic acetylcholine receptor M1 82.33% 94.23%
CHEMBL1937 Q92769 Histone deacetylase 2 82.32% 94.75%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 81.89% 99.23%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.37% 96.09%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.44% 95.89%

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.
Capsicum annuum

Cross-Links

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PubChem 11380163
NPASS NPC58392
LOTUS LTS0082338
wikiData Q105187584