(2E)-2,3,7-trimethylocta-2,6-dienoate

Details

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Internal ID b3ee8949-6cdc-483b-81de-63ad155a164d
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (2E)-2,3,7-trimethylocta-2,6-dienoate
SMILES (Canonical) CC(=CCCC(=C(C)C(=O)[O-])C)C
SMILES (Isomeric) CC(=CCC/C(=C(\C)/C(=O)[O-])/C)C
InChI InChI=1S/C11H18O2/c1-8(2)6-5-7-9(3)10(4)11(12)13/h6H,5,7H2,1-4H3,(H,12,13)/p-1/b10-9+
InChI Key AZFOXTNJXWNTME-MDZDMXLPSA-M
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H17O2-
Molecular Weight 181.25 g/mol
Exact Mass 181.122854781 g/mol
Topological Polar Surface Area (TPSA) 40.10 Ų
XlogP 4.10
Atomic LogP (AlogP) 1.82
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E)-2,3,7-trimethylocta-2,6-dienoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9789 97.89%
Caco-2 + 0.9442 94.42%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Nucleus 0.4271 42.71%
OATP2B1 inhibitior - 0.8529 85.29%
OATP1B1 inhibitior + 0.9107 91.07%
OATP1B3 inhibitior + 0.8657 86.57%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.8486 84.86%
P-glycoprotein inhibitior - 0.9861 98.61%
P-glycoprotein substrate - 0.9747 97.47%
CYP3A4 substrate - 0.6330 63.30%
CYP2C9 substrate - 0.5781 57.81%
CYP2D6 substrate - 0.8928 89.28%
CYP3A4 inhibition - 0.9799 97.99%
CYP2C9 inhibition - 0.9036 90.36%
CYP2C19 inhibition - 0.9051 90.51%
CYP2D6 inhibition - 0.9372 93.72%
CYP1A2 inhibition - 0.8081 80.81%
CYP2C8 inhibition - 0.9772 97.72%
CYP inhibitory promiscuity - 0.8631 86.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6097 60.97%
Eye corrosion + 0.7305 73.05%
Eye irritation + 0.9760 97.60%
Skin irritation + 0.8874 88.74%
Skin corrosion - 0.7208 72.08%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5468 54.68%
Micronuclear - 0.9600 96.00%
Hepatotoxicity + 0.6500 65.00%
skin sensitisation + 0.5778 57.78%
Respiratory toxicity - 0.9000 90.00%
Reproductive toxicity - 0.9014 90.14%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.7001 70.01%
Acute Oral Toxicity (c) III 0.7682 76.82%
Estrogen receptor binding - 0.9685 96.85%
Androgen receptor binding - 0.7959 79.59%
Thyroid receptor binding - 0.8325 83.25%
Glucocorticoid receptor binding - 0.8900 89.00%
Aromatase binding - 0.8961 89.61%
PPAR gamma - 0.6431 64.31%
Honey bee toxicity - 0.8585 85.85%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity + 0.9475 94.75%

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 89.80% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.01% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 85.78% 99.17%
CHEMBL4040 P28482 MAP kinase ERK2 82.65% 83.82%
CHEMBL3401 O75469 Pregnane X receptor 80.86% 94.73%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.06% 94.33%

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.
Citrus medica
Humulus lupulus
Perilla frutescens

Cross-Links

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PubChem 22565016
NPASS NPC237921