5-Tetradeca-5,8,11,13-tetraen-1-ynoxypent-4-enoic acid

Details

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Internal ID d3ce03f7-34b0-44d1-9b46-f0f6e2d871a2
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Straight chain fatty acids
IUPAC Name 5-tetradeca-5,8,11,13-tetraen-1-ynoxypent-4-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C19H24O3/c1-2-3-4-5-6-7-8-9-10-11-12-14-17-22-18-15-13-16-19(20)21/h2-4,6-7,9-10,15,18H,1,5,8,11-13,16H2,(H,20,21)
InChI Key HNCZZAFOQUEHGF-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C19H24O3
Molecular Weight 300.40 g/mol
Exact Mass 300.17254462 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 4.90
Atomic LogP (AlogP) 4.76
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 11

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Tetradeca-5,8,11,13-tetraen-1-ynoxypent-4-enoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9785 97.85%
Caco-2 - 0.7341 73.41%
Blood Brain Barrier + 0.6000 60.00%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.6063 60.63%
OATP2B1 inhibitior - 0.8584 85.84%
OATP1B1 inhibitior + 0.7879 78.79%
OATP1B3 inhibitior + 0.9270 92.70%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6264 62.64%
P-glycoprotein inhibitior - 0.7251 72.51%
P-glycoprotein substrate - 0.9220 92.20%
CYP3A4 substrate - 0.5050 50.50%
CYP2C9 substrate - 0.5976 59.76%
CYP2D6 substrate - 0.8575 85.75%
CYP3A4 inhibition - 0.7792 77.92%
CYP2C9 inhibition - 0.8208 82.08%
CYP2C19 inhibition - 0.8990 89.90%
CYP2D6 inhibition - 0.9600 96.00%
CYP1A2 inhibition - 0.6871 68.71%
CYP2C8 inhibition - 0.6686 66.86%
CYP inhibitory promiscuity - 0.9375 93.75%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6535 65.35%
Carcinogenicity (trinary) Non-required 0.6700 67.00%
Eye corrosion + 0.9420 94.20%
Eye irritation - 0.7468 74.68%
Skin irritation + 0.5276 52.76%
Skin corrosion - 0.6931 69.31%
Ames mutagenesis - 0.7000 70.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4175 41.75%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.6625 66.25%
skin sensitisation + 0.7803 78.03%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity - 0.9328 93.28%
Mitochondrial toxicity - 0.5375 53.75%
Nephrotoxicity - 0.5873 58.73%
Acute Oral Toxicity (c) III 0.4805 48.05%
Estrogen receptor binding + 0.8418 84.18%
Androgen receptor binding - 0.7843 78.43%
Thyroid receptor binding + 0.6041 60.41%
Glucocorticoid receptor binding + 0.6056 60.56%
Aromatase binding + 0.7522 75.22%
PPAR gamma + 0.8387 83.87%
Honey bee toxicity - 0.7532 75.32%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9197 91.97%

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 93.74% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.42% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 88.32% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.00% 86.33%
CHEMBL1255126 O15151 Protein Mdm4 83.71% 90.20%
CHEMBL2581 P07339 Cathepsin D 82.71% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.58% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.65% 91.11%
CHEMBL1781 P11387 DNA topoisomerase I 81.28% 97.00%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 85093911
LOTUS LTS0030435
wikiData Q104168021