3-(4-Methyl-8-oxonon-4-enylidene)-5-(2-methylprop-1-enyl)oxolan-2-one

Details

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Internal ID 34b5da5e-d9cf-4885-9f26-2c8e41e8e2d8
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Terpene lactones > Diterpene lactones
IUPAC Name 3-(4-methyl-8-oxonon-4-enylidene)-5-(2-methylprop-1-enyl)oxolan-2-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H26O3/c1-13(2)11-17-12-16(18(20)21-17)10-6-8-14(3)7-5-9-15(4)19/h7,10-11,17H,5-6,8-9,12H2,1-4H3
InChI Key FWVXVXHMEPTOAS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O3
Molecular Weight 290.40 g/mol
Exact Mass 290.18819469 g/mol
Topological Polar Surface Area (TPSA) 43.40 Ų
XlogP 3.90
Atomic LogP (AlogP) 4.29
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-(4-Methyl-8-oxonon-4-enylidene)-5-(2-methylprop-1-enyl)oxolan-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.5464 54.64%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.7636 76.36%
OATP2B1 inhibitior - 0.8545 85.45%
OATP1B1 inhibitior + 0.9216 92.16%
OATP1B3 inhibitior + 0.9110 91.10%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior + 0.5500 55.00%
BSEP inhibitior + 0.7342 73.42%
P-glycoprotein inhibitior - 0.6473 64.73%
P-glycoprotein substrate - 0.8580 85.80%
CYP3A4 substrate + 0.5276 52.76%
CYP2C9 substrate - 0.8108 81.08%
CYP2D6 substrate - 0.9004 90.04%
CYP3A4 inhibition - 0.7998 79.98%
CYP2C9 inhibition - 0.8560 85.60%
CYP2C19 inhibition - 0.7154 71.54%
CYP2D6 inhibition - 0.9242 92.42%
CYP1A2 inhibition - 0.6121 61.21%
CYP2C8 inhibition - 0.9216 92.16%
CYP inhibitory promiscuity - 0.8396 83.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.6585 65.85%
Eye corrosion - 0.9422 94.22%
Eye irritation - 0.7158 71.58%
Skin irritation + 0.5477 54.77%
Skin corrosion - 0.9396 93.96%
Ames mutagenesis - 0.5800 58.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5189 51.89%
Micronuclear - 0.9000 90.00%
Hepatotoxicity + 0.5200 52.00%
skin sensitisation - 0.5838 58.38%
Respiratory toxicity - 0.5111 51.11%
Reproductive toxicity - 0.7333 73.33%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.5398 53.98%
Acute Oral Toxicity (c) III 0.6676 66.76%
Estrogen receptor binding - 0.7711 77.11%
Androgen receptor binding - 0.7356 73.56%
Thyroid receptor binding - 0.5196 51.96%
Glucocorticoid receptor binding - 0.4799 47.99%
Aromatase binding - 0.5479 54.79%
PPAR gamma + 0.5696 56.96%
Honey bee toxicity - 0.7790 77.90%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity + 0.9882 98.82%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.80% 91.11%
CHEMBL2581 P07339 Cathepsin D 87.99% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.15% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.16% 96.09%
CHEMBL1806 P11388 DNA topoisomerase II alpha 85.03% 89.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 83.71% 99.23%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 83.17% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 82.28% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.49% 92.08%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85145679
LOTUS LTS0021853
wikiData Q105003636