(6E,10Z)-2,6,10-trimethyldodeca-2,6,10-triene

Details

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Internal ID 88558381-f7e3-49d2-a1c9-14000b116b99
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (6E,10Z)-2,6,10-trimethyldodeca-2,6,10-triene
SMILES (Canonical) CC=C(C)CCC=C(C)CCC=C(C)C
SMILES (Isomeric) C/C=C(/C)\CC/C=C(\C)/CCC=C(C)C
InChI InChI=1S/C15H26/c1-6-14(4)10-8-12-15(5)11-7-9-13(2)3/h6,9,12H,7-8,10-11H2,1-5H3/b14-6-,15-12+
InChI Key JXBSHSBNOVLGHF-IBAFYIADSA-N
Popularity 1 reference 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) 5.43
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 6

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (6E,10Z)-2,6,10-trimethyldodeca-2,6,10-triene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9884 98.84%
Caco-2 + 0.9633 96.33%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Nucleus 0.6684 66.84%
OATP2B1 inhibitior - 0.8541 85.41%
OATP1B1 inhibitior + 0.9286 92.86%
OATP1B3 inhibitior + 0.9380 93.80%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.6130 61.30%
P-glycoprotein inhibitior - 0.9596 95.96%
P-glycoprotein substrate - 0.9726 97.26%
CYP3A4 substrate - 0.6692 66.92%
CYP2C9 substrate - 0.8315 83.15%
CYP2D6 substrate - 0.7358 73.58%
CYP3A4 inhibition - 0.9716 97.16%
CYP2C9 inhibition - 0.9099 90.99%
CYP2C19 inhibition - 0.9168 91.68%
CYP2D6 inhibition - 0.9491 94.91%
CYP1A2 inhibition - 0.7354 73.54%
CYP2C8 inhibition - 0.9814 98.14%
CYP inhibitory promiscuity - 0.6923 69.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5700 57.00%
Carcinogenicity (trinary) Warning 0.4712 47.12%
Eye corrosion + 0.7181 71.81%
Eye irritation + 0.9243 92.43%
Skin irritation + 0.8835 88.35%
Skin corrosion - 0.9656 96.56%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3879 38.79%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7125 71.25%
skin sensitisation + 0.9505 95.05%
Respiratory toxicity - 0.9111 91.11%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity + 0.6477 64.77%
Acute Oral Toxicity (c) III 0.8971 89.71%
Estrogen receptor binding - 0.8905 89.05%
Androgen receptor binding - 0.8655 86.55%
Thyroid receptor binding - 0.7490 74.90%
Glucocorticoid receptor binding - 0.7252 72.52%
Aromatase binding - 0.7771 77.71%
PPAR gamma + 0.5181 51.81%
Honey bee toxicity - 0.9194 91.94%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.9916 99.16%

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 97.29% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.24% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 82.58% 94.73%
CHEMBL2581 P07339 Cathepsin D 82.13% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.66% 91.11%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 80.27% 93.10%

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.
Santalum spicatum

Cross-Links

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PubChem 21734683
LOTUS LTS0205464
wikiData Q105136505