(2E,6E,9R)-9-hydroxy-3,7,11-trimethyldodeca-2,6,10-trienoic acid

Details

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Internal ID f3290247-bffd-4ed5-8893-35c86ab5076b
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,6E,9R)-9-hydroxy-3,7,11-trimethyldodeca-2,6,10-trienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C15H24O3/c1-11(2)8-14(16)9-12(3)6-5-7-13(4)10-15(17)18/h6,8,10,14,16H,5,7,9H2,1-4H3,(H,17,18)/b12-6+,13-10+/t14-/m0/s1
InChI Key ALIUDYHBVWJOHI-SCGYNDOXSA-N
Popularity 2 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 3.80
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,6E,9R)-9-hydroxy-3,7,11-trimethyldodeca-2,6,10-trienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9797 97.97%
Caco-2 + 0.8015 80.15%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6736 67.36%
OATP2B1 inhibitior - 0.8522 85.22%
OATP1B1 inhibitior + 0.9179 91.79%
OATP1B3 inhibitior + 0.9347 93.47%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7500 75.00%
BSEP inhibitior - 0.5874 58.74%
P-glycoprotein inhibitior - 0.9488 94.88%
P-glycoprotein substrate - 0.9103 91.03%
CYP3A4 substrate - 0.5559 55.59%
CYP2C9 substrate - 0.5754 57.54%
CYP2D6 substrate - 0.8995 89.95%
CYP3A4 inhibition - 0.8670 86.70%
CYP2C9 inhibition - 0.8661 86.61%
CYP2C19 inhibition - 0.8961 89.61%
CYP2D6 inhibition - 0.9346 93.46%
CYP1A2 inhibition - 0.7150 71.50%
CYP2C8 inhibition - 0.9388 93.88%
CYP inhibitory promiscuity - 0.8516 85.16%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6815 68.15%
Carcinogenicity (trinary) Non-required 0.7294 72.94%
Eye corrosion - 0.7734 77.34%
Eye irritation + 0.5236 52.36%
Skin irritation + 0.5000 50.00%
Skin corrosion - 0.9784 97.84%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5602 56.02%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6225 62.25%
skin sensitisation + 0.6455 64.55%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.7575 75.75%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.5743 57.43%
Acute Oral Toxicity (c) III 0.7000 70.00%
Estrogen receptor binding - 0.7802 78.02%
Androgen receptor binding - 0.5967 59.67%
Thyroid receptor binding - 0.7240 72.40%
Glucocorticoid receptor binding - 0.6522 65.22%
Aromatase binding - 0.6227 62.27%
PPAR gamma + 0.5581 55.81%
Honey bee toxicity - 0.8429 84.29%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity + 0.9566 95.66%

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
CHEMBL2581 P07339 Cathepsin D 92.44% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.24% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 91.46% 99.17%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 90.09% 85.14%
CHEMBL340 P08684 Cytochrome P450 3A4 86.16% 91.19%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 83.86% 92.08%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 82.75% 97.21%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 82.68% 96.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.48% 91.11%

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.
Artemisia gilvescens
Datura stramonium
Oenanthe fistulosa

Cross-Links

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PubChem 121491205
NPASS NPC249660
LOTUS LTS0049677
wikiData Q104914156