2,6-Octadiene, 1-methoxy-3,7-dimethyl-

Details

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Internal ID d1748392-4dd3-4e20-90fe-7e40c675c580
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (2E)-1-methoxy-3,7-dimethylocta-2,6-diene
SMILES (Canonical) CC(=CCCC(=CCOC)C)C
SMILES (Isomeric) CC(=CCC/C(=C/COC)/C)C
InChI InChI=1S/C11H20O/c1-10(2)6-5-7-11(3)8-9-12-4/h6,8H,5,7,9H2,1-4H3/b11-8+
InChI Key AVJMJMPVWWWELJ-DHZHZOJOSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C11H20O
Molecular Weight 168.28 g/mol
Exact Mass 168.151415257 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.33
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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2,6-Octadiene, 1-methoxy-3,7-dimethyl-
2565-82-4
72152-72-8
1-Methoxy-3,7-dimethyl-2,6-octadiene
(2E)-1-methoxy-3,7-dimethylocta-2,6-diene
2,6-Octadiene, 1-methoxy-3,7-dimethyl-, (2E)-
(E)-1-Methoxy-3,7-dimethylocta-2,6-diene
2,6-Octadiene, 1-methoxy-3,7-dimethyl-, (E)-
EINECS 219-896-1
SCHEMBL114886
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,6-Octadiene, 1-methoxy-3,7-dimethyl-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9904 99.04%
Caco-2 + 0.9369 93.69%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Lysosomes 0.4234 42.34%
OATP2B1 inhibitior - 0.8527 85.27%
OATP1B1 inhibitior + 0.9428 94.28%
OATP1B3 inhibitior + 0.9340 93.40%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8692 86.92%
P-glycoprotein inhibitior - 0.9794 97.94%
P-glycoprotein substrate - 0.9696 96.96%
CYP3A4 substrate - 0.6033 60.33%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7191 71.91%
CYP3A4 inhibition - 0.9789 97.89%
CYP2C9 inhibition - 0.9353 93.53%
CYP2C19 inhibition - 0.8966 89.66%
CYP2D6 inhibition - 0.9435 94.35%
CYP1A2 inhibition - 0.8440 84.40%
CYP2C8 inhibition - 0.9413 94.13%
CYP inhibitory promiscuity - 0.8623 86.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.5476 54.76%
Eye corrosion - 0.5541 55.41%
Eye irritation + 0.9715 97.15%
Skin irritation + 0.6660 66.60%
Skin corrosion - 0.9653 96.53%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4805 48.05%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.8233 82.33%
Respiratory toxicity - 0.9778 97.78%
Reproductive toxicity - 0.9590 95.90%
Mitochondrial toxicity - 0.9125 91.25%
Nephrotoxicity + 0.6403 64.03%
Acute Oral Toxicity (c) III 0.8777 87.77%
Estrogen receptor binding - 0.9623 96.23%
Androgen receptor binding - 0.8796 87.96%
Thyroid receptor binding - 0.9002 90.02%
Glucocorticoid receptor binding - 0.9219 92.19%
Aromatase binding - 0.8870 88.70%
PPAR gamma - 0.9148 91.48%
Honey bee toxicity - 0.8354 83.54%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9385 93.85%

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 91.15% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.61% 92.08%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.47% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.56% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.21% 94.45%
CHEMBL2581 P07339 Cathepsin D 81.05% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 81.01% 94.73%

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.
Homalomena occulta

Cross-Links

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PubChem 5365849
LOTUS LTS0247247
wikiData Q82862657