Vulgarone A

Details

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Internal ID f464b699-57ec-4a3c-87e7-0c58e70f0d56
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Bicyclic monoterpenoids
IUPAC Name 2,6,6,9-tetramethyltricyclo[5.4.0.02,10]undec-8-en-11-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H22O/c1-9-8-10-12-13(16)11(9)15(12,4)7-5-6-14(10,2)3/h8,10-12H,5-7H2,1-4H3
InChI Key KKQDNHZABGRCAS-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22O
Molecular Weight 218.33 g/mol
Exact Mass 218.167065321 g/mol
Topological Polar Surface Area (TPSA) 17.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.59
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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CHEBI:167999
DTXSID401318151
2,6,6,9-tetramethyltricyclo[5.4.0.02,10]undec-8-en-11-one
62065-10-5

2D Structure

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2D Structure of Vulgarone A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9969 99.69%
Caco-2 + 0.8566 85.66%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.4596 45.96%
OATP2B1 inhibitior - 0.8464 84.64%
OATP1B1 inhibitior + 0.8642 86.42%
OATP1B3 inhibitior + 0.9476 94.76%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9384 93.84%
P-glycoprotein inhibitior - 0.8644 86.44%
P-glycoprotein substrate - 0.9411 94.11%
CYP3A4 substrate + 0.5405 54.05%
CYP2C9 substrate - 0.7886 78.86%
CYP2D6 substrate - 0.7886 78.86%
CYP3A4 inhibition - 0.8587 85.87%
CYP2C9 inhibition - 0.7124 71.24%
CYP2C19 inhibition - 0.5273 52.73%
CYP2D6 inhibition - 0.8748 87.48%
CYP1A2 inhibition - 0.6658 66.58%
CYP2C8 inhibition - 0.9368 93.68%
CYP inhibitory promiscuity - 0.7016 70.16%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8900 89.00%
Carcinogenicity (trinary) Non-required 0.4382 43.82%
Eye corrosion - 0.9667 96.67%
Eye irritation - 0.5528 55.28%
Skin irritation + 0.6182 61.82%
Skin corrosion - 0.9321 93.21%
Ames mutagenesis - 0.7023 70.23%
Human Ether-a-go-go-Related Gene inhibition - 0.5296 52.96%
Micronuclear - 0.9400 94.00%
Hepatotoxicity + 0.5541 55.41%
skin sensitisation + 0.7849 78.49%
Respiratory toxicity - 0.5000 50.00%
Reproductive toxicity + 0.5556 55.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.6260 62.60%
Acute Oral Toxicity (c) III 0.7735 77.35%
Estrogen receptor binding - 0.5834 58.34%
Androgen receptor binding - 0.5534 55.34%
Thyroid receptor binding - 0.5319 53.19%
Glucocorticoid receptor binding - 0.6969 69.69%
Aromatase binding - 0.6884 68.84%
PPAR gamma - 0.7553 75.53%
Honey bee toxicity - 0.8485 84.85%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity + 0.5800 58.00%
Fish aquatic toxicity + 0.9654 96.54%

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 92.97% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.76% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.22% 91.11%
CHEMBL1937 Q92769 Histone deacetylase 2 88.56% 94.75%
CHEMBL2581 P07339 Cathepsin D 88.55% 98.95%
CHEMBL1994 P08235 Mineralocorticoid receptor 84.02% 100.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.45% 99.23%
CHEMBL3351 Q13085 Acetyl-CoA carboxylase 1 82.77% 93.04%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.97% 86.33%
CHEMBL4803 P29474 Nitric-oxide synthase, endothelial 81.70% 86.00%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.49% 94.45%
CHEMBL1871 P10275 Androgen Receptor 80.90% 96.43%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.42% 96.09%

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.
Artemisia douglasiana
Tanacetum vulgare subsp. vulgare

Cross-Links

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PubChem 73809947
LOTUS LTS0260076
wikiData Q105142312