6,10,14-Trimethylpentadeca-5,9,13-triene-2,12-dione

Details

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Internal ID 855a2b22-0081-4a49-9afb-2f3ba584ccd6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name 6,10,14-trimethylpentadeca-5,9,13-triene-2,12-dione
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H28O2/c1-14(2)12-18(20)13-16(4)10-6-8-15(3)9-7-11-17(5)19/h9-10,12H,6-8,11,13H2,1-5H3
InChI Key WOSWLPBJUVEXMK-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C18H28O2
Molecular Weight 276.40 g/mol
Exact Mass 276.208930132 g/mol
Topological Polar Surface Area (TPSA) 34.10 Ų
XlogP 4.40
Atomic LogP (AlogP) 4.95
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 9

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6,10,14-Trimethylpentadeca-5,9,13-triene-2,12-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 + 0.8351 83.51%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.4959 49.59%
OATP2B1 inhibitior - 0.8561 85.61%
OATP1B1 inhibitior + 0.9427 94.27%
OATP1B3 inhibitior + 0.9304 93.04%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior + 0.5931 59.31%
P-glycoprotein inhibitior - 0.7691 76.91%
P-glycoprotein substrate - 0.8861 88.61%
CYP3A4 substrate - 0.5742 57.42%
CYP2C9 substrate - 0.8058 80.58%
CYP2D6 substrate - 0.8550 85.50%
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 - 0.9597 95.97%
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 + 0.6358 63.58%
Skin irritation + 0.7220 72.20%
Skin corrosion - 0.9633 96.33%
Ames mutagenesis - 0.6700 67.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6677 66.77%
Micronuclear - 0.9900 99.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.8573 85.73%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity + 0.6439 64.39%
Acute Oral Toxicity (c) III 0.8338 83.38%
Estrogen receptor binding - 0.7457 74.57%
Androgen receptor binding - 0.8035 80.35%
Thyroid receptor binding - 0.5906 59.06%
Glucocorticoid receptor binding - 0.6015 60.15%
Aromatase binding - 0.6230 62.30%
PPAR gamma + 0.6527 65.27%
Honey bee toxicity - 0.8985 89.85%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.5700 57.00%
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 91.61% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.65% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.10% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 85.39% 94.73%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 84.69% 94.33%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 82.67% 85.14%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.29% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 80.92% 95.50%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.57% 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 74051997
LOTUS LTS0141891
wikiData Q105309668