6,10,14-Trimethylpentadeca-5,9-diene-2,13-dione

Details

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Internal ID 4abb4e55-db49-4f61-883a-15be13101e95
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 6,10,14-trimethylpentadeca-5,9-diene-2,13-dione
SMILES (Canonical) CC(C)C(=O)CCC(=CCCC(=CCCC(=O)C)C)C
SMILES (Isomeric) CC(C)C(=O)CCC(=CCCC(=CCCC(=O)C)C)C
InChI InChI=1S/C18H30O2/c1-14(2)18(20)13-12-16(4)9-6-8-15(3)10-7-11-17(5)19/h9-10,14H,6-8,11-13H2,1-5H3
InChI Key PSKPVVULUXBPSS-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30O2
Molecular Weight 278.40 g/mol
Exact Mass 278.224580195 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 4.30
Atomic LogP (AlogP) 5.03
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 10

Synonyms

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66067-36-5
DTXSID10792828
RefChem:103688
DTXCID50743571

2D Structure

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2D Structure of 6,10,14-Trimethylpentadeca-5,9-diene-2,13-dione

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9917 99.17%
Caco-2 + 0.8863 88.63%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Mitochondria 0.4959 49.59%
OATP2B1 inhibitior - 0.8524 85.24%
OATP1B1 inhibitior + 0.9391 93.91%
OATP1B3 inhibitior + 0.9304 93.04%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.8252 82.52%
P-glycoprotein inhibitior - 0.7931 79.31%
P-glycoprotein substrate - 0.9466 94.66%
CYP3A4 substrate - 0.6250 62.50%
CYP2C9 substrate - 0.8012 80.12%
CYP2D6 substrate - 0.7855 78.55%
CYP3A4 inhibition - 0.9231 92.31%
CYP2C9 inhibition - 0.8512 85.12%
CYP2C19 inhibition - 0.8480 84.80%
CYP2D6 inhibition - 0.9497 94.97%
CYP1A2 inhibition - 0.5781 57.81%
CYP2C8 inhibition - 0.9800 98.00%
CYP inhibitory promiscuity - 0.7889 78.89%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Non-required 0.6458 64.58%
Eye corrosion + 0.5943 59.43%
Eye irritation - 0.4802 48.02%
Skin irritation + 0.7220 72.20%
Skin corrosion - 0.9633 96.33%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6609 66.09%
Micronuclear - 0.9900 99.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.8573 85.73%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6383 63.83%
Acute Oral Toxicity (c) III 0.8338 83.38%
Estrogen receptor binding - 0.9267 92.67%
Androgen receptor binding - 0.8433 84.33%
Thyroid receptor binding - 0.5298 52.98%
Glucocorticoid receptor binding - 0.7986 79.86%
Aromatase binding - 0.7258 72.58%
PPAR gamma - 0.5270 52.70%
Honey bee toxicity - 0.8364 83.64%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity + 0.9390 93.90%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.35% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.28% 99.17%
CHEMBL2581 P07339 Cathepsin D 84.88% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 84.82% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.64% 91.11%
CHEMBL253 P34972 Cannabinoid CB2 receptor 83.41% 97.25%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.97% 96.47%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.46% 89.34%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.40% 100.00%

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 71369821
LOTUS LTS0087056
wikiData Q82761861