10,16-Heptadecadien-8-ynoic acid, (E)-

Details

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Internal ID 929cf7e1-32ef-4afb-999c-b76baad50eef
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (10E)-heptadeca-10,16-dien-8-ynoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H26O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15-16-17(18)19/h2,7-8H,1,3-6,11-16H2,(H,18,19)/b8-7+
InChI Key YABWMILQFXOECJ-BQYQJAHWSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26O2
Molecular Weight 262.40 g/mol
Exact Mass 262.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.50
Atomic LogP (AlogP) 4.72
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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10,16-Heptadecadien-8-ynoic acid, (E)-
LMFA01030475
(10E)-heptadeca-10,16-dien-8-ynoic acid
CHEBI:184143
trans-10,16-heptadecadien-8-ynoic acid

2D Structure

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2D Structure of 10,16-Heptadecadien-8-ynoic acid, (E)-

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 - 0.6079 60.79%
Blood Brain Barrier + 0.7000 70.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.4511 45.11%
OATP2B1 inhibitior - 0.8557 85.57%
OATP1B1 inhibitior + 0.8330 83.30%
OATP1B3 inhibitior + 0.8758 87.58%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.5854 58.54%
P-glycoprotein inhibitior - 0.8877 88.77%
P-glycoprotein substrate - 0.9401 94.01%
CYP3A4 substrate - 0.5359 53.59%
CYP2C9 substrate - 0.5976 59.76%
CYP2D6 substrate - 0.8551 85.51%
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 - 0.7703 77.03%
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 + 0.5231 52.31%
Skin irritation + 0.6947 69.47%
Skin corrosion - 0.6104 61.04%
Ames mutagenesis - 0.9100 91.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6805 68.05%
Micronuclear - 0.9800 98.00%
Hepatotoxicity - 0.7625 76.25%
skin sensitisation + 0.8371 83.71%
Respiratory toxicity + 0.7667 76.67%
Reproductive toxicity - 0.8994 89.94%
Mitochondrial toxicity + 0.6500 65.00%
Nephrotoxicity - 0.5695 56.95%
Acute Oral Toxicity (c) III 0.4868 48.68%
Estrogen receptor binding - 0.6265 62.65%
Androgen receptor binding - 0.8247 82.47%
Thyroid receptor binding + 0.7245 72.45%
Glucocorticoid receptor binding - 0.4888 48.88%
Aromatase binding - 0.5965 59.65%
PPAR gamma + 0.7707 77.07%
Honey bee toxicity - 0.8161 81.61%
Biodegradation + 0.5500 55.00%
Crustacea aquatic toxicity + 0.5800 58.00%
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 96.00% 99.17%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 93.26% 91.67%
CHEMBL221 P23219 Cyclooxygenase-1 93.13% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.78% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.04% 96.09%
CHEMBL1781 P11387 DNA topoisomerase I 89.01% 97.00%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 85.44% 92.26%
CHEMBL1829 O15379 Histone deacetylase 3 83.60% 95.00%
CHEMBL2581 P07339 Cathepsin D 83.45% 98.95%
CHEMBL335 P18031 Protein-tyrosine phosphatase 1B 81.86% 95.17%

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.
Jodina rhombifolia

Cross-Links

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PubChem 5312614
LOTUS LTS0174058
wikiData Q76303275