10-Oxooctadec-11-ynoic acid

Details

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Internal ID c6064966-f460-4d20-a4a2-f7d31a2a3041
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name 10-oxooctadec-11-ynoic acid
SMILES (Canonical) CCCCCCC#CC(=O)CCCCCCCCC(=O)O
SMILES (Isomeric) CCCCCCC#CC(=O)CCCCCCCCC(=O)O
InChI InChI=1S/C18H30O3/c1-2-3-4-5-8-11-14-17(19)15-12-9-6-7-10-13-16-18(20)21/h2-10,12-13,15-16H2,1H3,(H,20,21)
InChI Key LSUMEQDCJHSTCL-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H30O3
Molecular Weight 294.40 g/mol
Exact Mass 294.21949481 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.73
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 10-Oxooctadec-11-ynoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9782 97.82%
Caco-2 + 0.6480 64.80%
Blood Brain Barrier - 0.5000 50.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.8213 82.13%
OATP2B1 inhibitior - 0.8487 84.87%
OATP1B1 inhibitior + 0.8305 83.05%
OATP1B3 inhibitior + 0.9047 90.47%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7823 78.23%
P-glycoprotein inhibitior - 0.8645 86.45%
P-glycoprotein substrate - 0.9067 90.67%
CYP3A4 substrate - 0.6124 61.24%
CYP2C9 substrate - 0.5905 59.05%
CYP2D6 substrate - 0.8746 87.46%
CYP3A4 inhibition - 0.8513 85.13%
CYP2C9 inhibition - 0.8521 85.21%
CYP2C19 inhibition - 0.9138 91.38%
CYP2D6 inhibition - 0.9410 94.10%
CYP1A2 inhibition + 0.5649 56.49%
CYP2C8 inhibition - 0.8430 84.30%
CYP inhibitory promiscuity - 0.9531 95.31%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7535 75.35%
Carcinogenicity (trinary) Non-required 0.7293 72.93%
Eye corrosion + 0.7192 71.92%
Eye irritation + 0.9273 92.73%
Skin irritation + 0.5230 52.30%
Skin corrosion + 0.5631 56.31%
Ames mutagenesis - 0.9900 99.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4162 41.62%
Micronuclear - 0.9300 93.00%
Hepatotoxicity + 0.7125 71.25%
skin sensitisation + 0.4910 49.10%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.8161 81.61%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity + 0.5151 51.51%
Acute Oral Toxicity (c) III 0.6012 60.12%
Estrogen receptor binding - 0.6652 66.52%
Androgen receptor binding - 0.7728 77.28%
Thyroid receptor binding + 0.5491 54.91%
Glucocorticoid receptor binding - 0.6782 67.82%
Aromatase binding - 0.8140 81.40%
PPAR gamma + 0.6385 63.85%
Honey bee toxicity - 0.9804 98.04%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity + 0.7610 76.10%
Fish aquatic toxicity + 0.9516 95.16%

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 95.22% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.03% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 94.41% 90.17%
CHEMBL230 P35354 Cyclooxygenase-2 93.79% 89.63%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.79% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.67% 96.09%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 87.32% 85.94%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 85.75% 92.26%
CHEMBL1781 P11387 DNA topoisomerase I 85.36% 97.00%
CHEMBL2001 Q9H244 Purinergic receptor P2Y12 81.79% 96.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 80.40% 91.81%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.04% 93.56%

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.
Hibiscus rosa-sinensis

Cross-Links

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PubChem 163192296
LOTUS LTS0219338
wikiData Q105156766