(2E,5E)-7-hydroxy-7-methyl-3-(4-methylpent-3-enyl)octa-2,5-dienoic acid

Details

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Internal ID 50900031-9d65-482e-852a-0bc0b6b7ad98
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name (2E,5E)-7-hydroxy-7-methyl-3-(4-methylpent-3-enyl)octa-2,5-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O3/c1-12(2)7-5-8-13(11-14(16)17)9-6-10-15(3,4)18/h6-7,10-11,18H,5,8-9H2,1-4H3,(H,16,17)/b10-6+,13-11+
InChI Key MBAYQDGJQWDBHV-DKBLQGDZSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H24O3
Molecular Weight 252.35 g/mol
Exact Mass 252.17254462 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 3.40
Atomic LogP (AlogP) 3.46
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 7

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (2E,5E)-7-hydroxy-7-methyl-3-(4-methylpent-3-enyl)octa-2,5-dienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9695 96.95%
Caco-2 + 0.7703 77.03%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.7085 70.85%
OATP2B1 inhibitior - 0.8569 85.69%
OATP1B1 inhibitior + 0.8482 84.82%
OATP1B3 inhibitior + 0.9211 92.11%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7250 72.50%
BSEP inhibitior - 0.7094 70.94%
P-glycoprotein inhibitior - 0.9403 94.03%
P-glycoprotein substrate - 0.9337 93.37%
CYP3A4 substrate - 0.5228 52.28%
CYP2C9 substrate - 0.7842 78.42%
CYP2D6 substrate - 0.9073 90.73%
CYP3A4 inhibition - 0.9167 91.67%
CYP2C9 inhibition - 0.7388 73.88%
CYP2C19 inhibition - 0.8484 84.84%
CYP2D6 inhibition - 0.9170 91.70%
CYP1A2 inhibition - 0.8080 80.80%
CYP2C8 inhibition - 0.9199 91.99%
CYP inhibitory promiscuity - 0.7043 70.43%
UGT catelyzed - 0.7000 70.00%
Carcinogenicity (binary) - 0.6538 65.38%
Carcinogenicity (trinary) Non-required 0.6458 64.58%
Eye corrosion - 0.7433 74.33%
Eye irritation + 0.7309 73.09%
Skin irritation + 0.7481 74.81%
Skin corrosion - 0.9474 94.74%
Ames mutagenesis - 0.6800 68.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5223 52.23%
Micronuclear - 0.9200 92.00%
Hepatotoxicity - 0.5250 52.50%
skin sensitisation + 0.7540 75.40%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.7667 76.67%
Mitochondrial toxicity - 0.6250 62.50%
Nephrotoxicity + 0.5100 51.00%
Acute Oral Toxicity (c) III 0.7063 70.63%
Estrogen receptor binding - 0.7483 74.83%
Androgen receptor binding - 0.8434 84.34%
Thyroid receptor binding - 0.5182 51.82%
Glucocorticoid receptor binding - 0.5000 50.00%
Aromatase binding - 0.7893 78.93%
PPAR gamma + 0.5722 57.22%
Honey bee toxicity - 0.8570 85.70%
Biodegradation - 0.8250 82.50%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9371 93.71%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 88.36% 99.17%
CHEMBL2581 P07339 Cathepsin D 85.14% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.14% 91.11%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 84.38% 89.34%
CHEMBL3401 O75469 Pregnane X receptor 84.12% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 81.17% 96.09%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.31% 96.95%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 101600694
LOTUS LTS0013433
wikiData Q105160627