3-Dodec-11-enylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one

Details

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Internal ID 3f84a012-32e1-4a45-874a-a0f301c9a11f
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Acetals > Ketals
IUPAC Name 3-dodec-11-enylidene-4-hydroxy-5-methoxy-5-methyloxolan-2-one
SMILES (Canonical) CC1(C(C(=CCCCCCCCCCC=C)C(=O)O1)O)OC
SMILES (Isomeric) CC1(C(C(=CCCCCCCCCCC=C)C(=O)O1)O)OC
InChI InChI=1S/C18H30O4/c1-4-5-6-7-8-9-10-11-12-13-14-15-16(19)18(2,21-3)22-17(15)20/h4,14,16,19H,1,5-13H2,2-3H3
InChI Key WBGZYWAQSKEEGP-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30O4
Molecular Weight 310.40 g/mol
Exact Mass 310.21440943 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 4.90
Atomic LogP (AlogP) 3.89
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3-Dodec-11-enylidene-4-hydroxy-5-methoxy-5-methyloxolan-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 + 0.8328 83.28%
Caco-2 + 0.6145 61.45%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.7849 78.49%
OATP2B1 inhibitior - 0.8537 85.37%
OATP1B1 inhibitior + 0.8936 89.36%
OATP1B3 inhibitior + 0.9326 93.26%
MATE1 inhibitior - 0.8400 84.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior + 0.5557 55.57%
P-glycoprotein inhibitior - 0.7170 71.70%
P-glycoprotein substrate - 0.8680 86.80%
CYP3A4 substrate + 0.6235 62.35%
CYP2C9 substrate - 0.6100 61.00%
CYP2D6 substrate - 0.8701 87.01%
CYP3A4 inhibition - 0.7930 79.30%
CYP2C9 inhibition - 0.8380 83.80%
CYP2C19 inhibition - 0.6501 65.01%
CYP2D6 inhibition - 0.9147 91.47%
CYP1A2 inhibition - 0.6817 68.17%
CYP2C8 inhibition - 0.6112 61.12%
CYP inhibitory promiscuity - 0.7309 73.09%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Non-required 0.6415 64.15%
Eye corrosion - 0.9231 92.31%
Eye irritation - 0.6888 68.88%
Skin irritation - 0.6908 69.08%
Skin corrosion - 0.9539 95.39%
Ames mutagenesis - 0.7100 71.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3985 39.85%
Micronuclear - 0.8100 81.00%
Hepatotoxicity + 0.5294 52.94%
skin sensitisation - 0.7707 77.07%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity + 0.5667 56.67%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.7017 70.17%
Acute Oral Toxicity (c) III 0.4785 47.85%
Estrogen receptor binding + 0.6592 65.92%
Androgen receptor binding - 0.6910 69.10%
Thyroid receptor binding + 0.6454 64.54%
Glucocorticoid receptor binding + 0.7498 74.98%
Aromatase binding + 0.5238 52.38%
PPAR gamma + 0.7165 71.65%
Honey bee toxicity - 0.8024 80.24%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity + 0.6300 63.00%
Fish aquatic toxicity + 0.9336 93.36%

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 96.79% 91.11%
CHEMBL2581 P07339 Cathepsin D 93.77% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 89.83% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.62% 96.09%
CHEMBL1937 Q92769 Histone deacetylase 2 89.05% 94.75%
CHEMBL1293249 Q13887 Kruppel-like factor 5 86.28% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 85.87% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.25% 99.17%
CHEMBL1902 P62942 FK506-binding protein 1A 82.87% 97.05%
CHEMBL2007 P16234 Platelet-derived growth factor receptor alpha 82.74% 91.07%
CHEMBL241 Q14432 Phosphodiesterase 3A 80.70% 92.94%
CHEMBL1829 O15379 Histone deacetylase 3 80.53% 95.00%
CHEMBL3524 P56524 Histone deacetylase 4 80.35% 92.97%

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.
Lindera obtusiloba
Litsea hypophaea

Cross-Links

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PubChem 75214750
LOTUS LTS0021249
wikiData Q105300740