Octadec-17-en-9,11,13-triynoic Acid

Details

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Internal ID 29a8bf6c-d7ad-4cd0-a2c7-74aaabde8cae
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name octadec-17-en-9,11,13-triynoic acid
SMILES (Canonical) C=CCCC#CC#CC#CCCCCCCCC(=O)O
SMILES (Isomeric) C=CCCC#CC#CC#CCCCCCCCC(=O)O
InChI InChI=1S/C18H22O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17-18(19)20/h2H,1,3-4,11-17H2,(H,19,20)
InChI Key YESBZXSFUYCBEH-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C18H22O2
Molecular Weight 270.40 g/mol
Exact Mass 270.161979940 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.10
Atomic LogP (AlogP) 3.78
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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17-octadecene-9,11,13-triynoic acid
Octadec-17-en-9,11,13-triynoic Acid
CHEMBL451921
DTXSID301292611
217812-32-3

2D Structure

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2D Structure of Octadec-17-en-9,11,13-triynoic Acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9768 97.68%
Caco-2 - 0.6470 64.70%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Mitochondria 0.4511 45.11%
OATP2B1 inhibitior - 0.8555 85.55%
OATP1B1 inhibitior + 0.8806 88.06%
OATP1B3 inhibitior + 0.8758 87.58%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.7607 76.07%
P-glycoprotein inhibitior - 0.8804 88.04%
P-glycoprotein substrate - 0.9506 95.06%
CYP3A4 substrate - 0.5805 58.05%
CYP2C9 substrate + 0.6200 62.00%
CYP2D6 substrate - 0.8561 85.61%
CYP3A4 inhibition - 0.8839 88.39%
CYP2C9 inhibition - 0.6853 68.53%
CYP2C19 inhibition - 0.9309 93.09%
CYP2D6 inhibition - 0.9609 96.09%
CYP1A2 inhibition + 0.5976 59.76%
CYP2C8 inhibition - 0.8089 80.89%
CYP inhibitory promiscuity - 0.9438 94.38%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6335 63.35%
Carcinogenicity (trinary) Non-required 0.6633 66.33%
Eye corrosion + 0.9524 95.24%
Eye irritation - 0.6111 61.11%
Skin irritation + 0.6947 69.47%
Skin corrosion - 0.6104 61.04%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4040 40.40%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.8371 83.71%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity - 0.8994 89.94%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity + 0.5226 52.26%
Acute Oral Toxicity (c) III 0.4868 48.68%
Estrogen receptor binding - 0.6958 69.58%
Androgen receptor binding - 0.7607 76.07%
Thyroid receptor binding - 0.4905 49.05%
Glucocorticoid receptor binding - 0.5334 53.34%
Aromatase binding - 0.5434 54.34%
PPAR gamma + 0.6219 62.19%
Honey bee toxicity - 0.8704 87.04%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity + 0.8747 87.47%

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 94.13% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.44% 96.09%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 86.74% 83.57%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.30% 91.11%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 85.40% 92.26%
CHEMBL2581 P07339 Cathepsin D 84.97% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 83.20% 97.00%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.73% 95.17%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 80.43% 91.67%

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.
Mitrephora glabra
Orophea enneandra

Cross-Links

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PubChem 10730773
LOTUS LTS0045290
wikiData Q104400192