Ethyl 3,7-dimethyl-3,6-octadienoate

Details

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Internal ID 49e33b11-35da-4be5-bd77-cbc8a3d38486
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name ethyl (3E)-3,7-dimethylocta-3,6-dienoate
SMILES (Canonical) CCOC(=O)CC(=CCC=C(C)C)C
SMILES (Isomeric) CCOC(=O)C/C(=C/CC=C(C)C)/C
InChI InChI=1S/C12H20O2/c1-5-14-12(13)9-11(4)8-6-7-10(2)3/h7-8H,5-6,9H2,1-4H3/b11-8+
InChI Key FNHXGYITEDATDS-DHZHZOJOSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C12H20O2
Molecular Weight 196.29 g/mol
Exact Mass 196.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.24
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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ethyl 3,7-dimethyl-3,6-octadienoate

2D Structure

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2D Structure of Ethyl 3,7-dimethyl-3,6-octadienoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9970 99.70%
Caco-2 + 0.9099 90.99%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.5429 54.29%
Subcellular localzation Mitochondria 0.6198 61.98%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9480 94.80%
OATP1B3 inhibitior + 0.9314 93.14%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.7753 77.53%
P-glycoprotein inhibitior - 0.9705 97.05%
P-glycoprotein substrate - 0.9764 97.64%
CYP3A4 substrate - 0.6087 60.87%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.9209 92.09%
CYP2C9 inhibition - 0.9077 90.77%
CYP2C19 inhibition - 0.8688 86.88%
CYP2D6 inhibition - 0.9270 92.70%
CYP1A2 inhibition - 0.7379 73.79%
CYP2C8 inhibition - 0.9607 96.07%
CYP inhibitory promiscuity - 0.6660 66.60%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Warning 0.4715 47.15%
Eye corrosion + 0.7295 72.95%
Eye irritation + 0.9772 97.72%
Skin irritation + 0.6402 64.02%
Skin corrosion - 0.9730 97.30%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5105 51.05%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5973 59.73%
skin sensitisation + 0.6003 60.03%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.5760 57.60%
Acute Oral Toxicity (c) III 0.6508 65.08%
Estrogen receptor binding - 0.9261 92.61%
Androgen receptor binding - 0.9556 95.56%
Thyroid receptor binding - 0.8969 89.69%
Glucocorticoid receptor binding - 0.8483 84.83%
Aromatase binding - 0.9106 91.06%
PPAR gamma - 0.8482 84.82%
Honey bee toxicity - 0.9012 90.12%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.6300 63.00%
Fish aquatic toxicity + 0.9817 98.17%

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
CHEMBL3401 O75469 Pregnane X receptor 91.63% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.87% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 88.73% 83.82%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.23% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 86.14% 90.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.33% 96.95%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 83.87% 87.67%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 83.46% 94.33%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.98% 97.21%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.84% 99.17%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 82.73% 89.34%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.45% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.05% 96.00%

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.
Achillea ligustica

Cross-Links

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PubChem 12485235
LOTUS LTS0111461
wikiData Q104998303