3,7,11-Trimethyl-1,6,10-dodecatriene

Details

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Internal ID 49f765d0-ee59-40a1-83f6-9983b3914df3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,7,11-trimethyldodeca-1,6,10-triene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H26/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,9,12,14H,1,7-8,10-11H2,2-5H3
InChI Key YSNRTFFURISHOU-UHFFFAOYSA-N
Popularity 1,026 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26
Molecular Weight 206.37 g/mol
Exact Mass 206.203450829 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 6.00
Atomic LogP (AlogP) 5.28
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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SCHEMBL4623731
SCHEMBL8059072
3,7,11-Trimethyl-1,6,10-dodecatriene

2D Structure

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2D Structure of 3,7,11-Trimethyl-1,6,10-dodecatriene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.8473 84.73%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 0.8520 85.20%
OATP1B1 inhibitior + 0.9356 93.56%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.6894 68.94%
P-glycoprotein inhibitior - 0.9567 95.67%
P-glycoprotein substrate - 0.9335 93.35%
CYP3A4 substrate - 0.5909 59.09%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9627 96.27%
CYP2C9 inhibition - 0.8903 89.03%
CYP2C19 inhibition - 0.8891 88.91%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition - 0.7161 71.61%
CYP2C8 inhibition - 0.9827 98.27%
CYP inhibitory promiscuity - 0.7252 72.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Warning 0.4862 48.62%
Eye corrosion + 0.7167 71.67%
Eye irritation + 0.9194 91.94%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4005 40.05%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5137 51.37%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.6139 61.39%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding - 0.9563 95.63%
Androgen receptor binding - 0.8667 86.67%
Thyroid receptor binding - 0.8432 84.32%
Glucocorticoid receptor binding - 0.6178 61.78%
Aromatase binding - 0.7229 72.29%
PPAR gamma + 0.5175 51.75%
Honey bee toxicity - 0.8242 82.42%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity + 0.9962 99.62%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 91.93% 92.08%
CHEMBL2581 P07339 Cathepsin D 91.01% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.25% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.28% 94.45%
CHEMBL3401 O75469 Pregnane X receptor 82.48% 94.73%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 82.44% 93.10%
CHEMBL2885 P07451 Carbonic anhydrase III 81.97% 87.45%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.24% 99.17%

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.
Helichrysum drakensbergense
Inula cappa

Cross-Links

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PubChem 53749880
LOTUS LTS0141908
wikiData Q105360169