(10Z,14E,16E)-10,14,16-Octadecatrien-12-ynoic acid

Details

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Internal ID 009a1409-d11f-4fc8-ad47-2ac97fe9e8c5
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (10Z,14E,16E)-octadeca-10,14,16-trien-12-ynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2-5,8-9H,10-17H2,1H3,(H,19,20)/b3-2+,5-4+,9-8-
InChI Key KDVOULUCGQGVQH-IUDSIRJBSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C18H26O2
Molecular Weight 274.40 g/mol
Exact Mass 274.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.80
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 10

Synonyms

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CHEMBL2269542
CHEBI:191493
(10Z,14E,16E)-octadeca-10,14,16-trien-12-ynoic Acid
LMFA01030919

2D Structure

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2D Structure of (10Z,14E,16E)-10,14,16-Octadecatrien-12-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 + 0.9856 98.56%
Caco-2 - 0.5241 52.41%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability - 0.7143 71.43%
Subcellular localzation Mitochondria 0.4722 47.22%
OATP2B1 inhibitior - 0.8565 85.65%
OATP1B1 inhibitior + 0.7718 77.18%
OATP1B3 inhibitior + 0.8385 83.85%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5269 52.69%
P-glycoprotein inhibitior - 0.8531 85.31%
P-glycoprotein substrate - 0.9268 92.68%
CYP3A4 substrate - 0.5531 55.31%
CYP2C9 substrate + 0.6009 60.09%
CYP2D6 substrate - 0.8767 87.67%
CYP3A4 inhibition - 0.9262 92.62%
CYP2C9 inhibition - 0.7290 72.90%
CYP2C19 inhibition - 0.9452 94.52%
CYP2D6 inhibition - 0.9657 96.57%
CYP1A2 inhibition + 0.6945 69.45%
CYP2C8 inhibition - 0.8811 88.11%
CYP inhibitory promiscuity - 0.9368 93.68%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6335 63.35%
Carcinogenicity (trinary) Non-required 0.6496 64.96%
Eye corrosion + 0.9485 94.85%
Eye irritation - 0.7562 75.62%
Skin irritation + 0.7430 74.30%
Skin corrosion + 0.5452 54.52%
Ames mutagenesis - 0.9200 92.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6831 68.31%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.6750 67.50%
skin sensitisation + 0.7997 79.97%
Respiratory toxicity + 0.8667 86.67%
Reproductive toxicity - 0.7520 75.20%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.6870 68.70%
Acute Oral Toxicity (c) III 0.6243 62.43%
Estrogen receptor binding + 0.5265 52.65%
Androgen receptor binding - 0.7691 76.91%
Thyroid receptor binding + 0.6409 64.09%
Glucocorticoid receptor binding - 0.4743 47.43%
Aromatase binding + 0.6512 65.12%
PPAR gamma + 0.7829 78.29%
Honey bee toxicity - 0.9510 95.10%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.6100 61.00%
Fish aquatic toxicity + 0.7710 77.10%

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
CHEMBL4040 P28482 MAP kinase ERK2 96.61% 83.82%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.86% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.26% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.04% 98.95%
CHEMBL221 P23219 Cyclooxygenase-1 86.32% 90.17%
CHEMBL1781 P11387 DNA topoisomerase I 85.33% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.98% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.80% 96.00%

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.
Ximenia americana

Cross-Links

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PubChem 10731060
LOTUS LTS0251162
wikiData Q76415949