9-Hydroxyoctadeca-9,12-dienoic acid

Details

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Internal ID f318695a-21e5-4dec-b5b9-3be9d8cbb26f
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Lineolic acids and derivatives
IUPAC Name 9-hydroxyoctadeca-9,12-dienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H32O3/c1-2-3-4-5-6-8-11-14-17(19)15-12-9-7-10-13-16-18(20)21/h6,8,14,19H,2-5,7,9-13,15-16H2,1H3,(H,20,21)
InChI Key JDOLBVXUTAGQDQ-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C18H32O3
Molecular Weight 296.40 g/mol
Exact Mass 296.23514488 g/mol
Topological Polar Surface Area (TPSA) 57.50 Ų
XlogP 5.80
Atomic LogP (AlogP) 5.77
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 9-Hydroxyoctadeca-9,12-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 + 0.9885 98.85%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.6286 62.86%
Subcellular localzation Mitochondria 0.6821 68.21%
OATP2B1 inhibitior - 0.8503 85.03%
OATP1B1 inhibitior - 0.4778 47.78%
OATP1B3 inhibitior + 0.8673 86.73%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5608 56.08%
P-glycoprotein inhibitior - 0.8524 85.24%
P-glycoprotein substrate - 0.9161 91.61%
CYP3A4 substrate - 0.6166 61.66%
CYP2C9 substrate + 0.6230 62.30%
CYP2D6 substrate - 0.8746 87.46%
CYP3A4 inhibition - 0.9127 91.27%
CYP2C9 inhibition - 0.9112 91.12%
CYP2C19 inhibition - 0.9209 92.09%
CYP2D6 inhibition - 0.9299 92.99%
CYP1A2 inhibition + 0.6094 60.94%
CYP2C8 inhibition - 0.8323 83.23%
CYP inhibitory promiscuity - 0.8559 85.59%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.7535 75.35%
Carcinogenicity (trinary) Non-required 0.6837 68.37%
Eye corrosion - 0.6248 62.48%
Eye irritation + 0.8619 86.19%
Skin irritation - 0.5248 52.48%
Skin corrosion - 0.7733 77.33%
Ames mutagenesis - 0.9700 97.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3841 38.41%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.5125 51.25%
skin sensitisation + 0.5562 55.62%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity - 0.7956 79.56%
Mitochondrial toxicity + 0.5250 52.50%
Nephrotoxicity - 0.7829 78.29%
Acute Oral Toxicity (c) IV 0.6817 68.17%
Estrogen receptor binding + 0.6482 64.82%
Androgen receptor binding - 0.7383 73.83%
Thyroid receptor binding + 0.5412 54.12%
Glucocorticoid receptor binding - 0.6511 65.11%
Aromatase binding - 0.5903 59.03%
PPAR gamma + 0.8972 89.72%
Honey bee toxicity - 0.9917 99.17%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity + 0.8400 84.00%
Fish aquatic toxicity + 0.9662 96.62%

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 98.13% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.97% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 95.31% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.93% 92.08%
CHEMBL221 P23219 Cyclooxygenase-1 93.45% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.64% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 91.15% 97.00%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 84.47% 85.94%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.39% 96.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.12% 93.56%
CHEMBL3401 O75469 Pregnane X receptor 80.35% 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.
Begonia nantoensis

Cross-Links

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PubChem 73226949
LOTUS LTS0269355
wikiData Q105125637