14-Pentadecenoic acid

Details

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Internal ID 7d460a37-657f-4554-b2ea-960fe941d2dc
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name pentadec-14-enoic acid
SMILES (Canonical) C=CCCCCCCCCCCCCC(=O)O
SMILES (Isomeric) C=CCCCCCCCCCCCCC(=O)O
InChI InChI=1S/C15H28O2/c1-2-3-4-5-6-7-8-9-10-11-12-13-14-15(16)17/h2H,1,3-14H2,(H,16,17)
InChI Key CAHZYAQCDBBLER-UHFFFAOYSA-N
Popularity 9 references in papers

Physical and Chemical Properties

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Molecular Formula C15H28O2
Molecular Weight 240.38 g/mol
Exact Mass 240.208930132 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.00
Atomic LogP (AlogP) 4.94
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 13

Synonyms

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pentadec-14-enoic acid
17351-34-7
C15:1n-1
pentadec-14-enoicacid
SCHEMBL3125180
DTXSID90337655
CAHZYAQCDBBLER-UHFFFAOYSA-N
CHEBI:187169
LMFA01030053
MFCD00216550
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 14-Pentadecenoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9812 98.12%
Caco-2 - 0.5316 53.16%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Plasma membrane 0.4568 45.68%
OATP2B1 inhibitior - 0.8530 85.30%
OATP1B1 inhibitior + 0.9300 93.00%
OATP1B3 inhibitior + 0.8638 86.38%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.6820 68.20%
P-glycoprotein inhibitior - 0.9339 93.39%
P-glycoprotein substrate - 0.9873 98.73%
CYP3A4 substrate - 0.7097 70.97%
CYP2C9 substrate + 0.6302 63.02%
CYP2D6 substrate - 0.8602 86.02%
CYP3A4 inhibition - 0.9391 93.91%
CYP2C9 inhibition - 0.8440 84.40%
CYP2C19 inhibition - 0.9539 95.39%
CYP2D6 inhibition - 0.9681 96.81%
CYP1A2 inhibition - 0.5832 58.32%
CYP2C8 inhibition - 0.9507 95.07%
CYP inhibitory promiscuity - 0.9696 96.96%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6535 65.35%
Carcinogenicity (trinary) Non-required 0.6869 68.69%
Eye corrosion + 0.9759 97.59%
Eye irritation + 0.9781 97.81%
Skin irritation + 0.7470 74.70%
Skin corrosion - 0.7110 71.10%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6521 65.21%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7750 77.50%
skin sensitisation + 0.8537 85.37%
Respiratory toxicity + 0.7333 73.33%
Reproductive toxicity - 0.8994 89.94%
Mitochondrial toxicity + 0.6375 63.75%
Nephrotoxicity - 0.6362 63.62%
Acute Oral Toxicity (c) III 0.7880 78.80%
Estrogen receptor binding - 0.7804 78.04%
Androgen receptor binding - 0.9358 93.58%
Thyroid receptor binding + 0.6468 64.68%
Glucocorticoid receptor binding - 0.5621 56.21%
Aromatase binding - 0.7665 76.65%
PPAR gamma + 0.8484 84.84%
Honey bee toxicity - 0.9433 94.33%
Biodegradation + 0.9250 92.50%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.8295 82.95%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
CHEMBL1293235 P02545 Prelamin-A/C 0.8 nM
Potency
via Super-PRED

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL3060 Q9Y345 Glycine transporter 2 94.33% 99.17%
CHEMBL4070 P19784 Casein kinase II alpha (prime) 89.94% 91.67%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.41% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.21% 91.11%
CHEMBL1829 O15379 Histone deacetylase 3 86.08% 95.00%
CHEMBL2581 P07339 Cathepsin D 85.48% 98.95%
CHEMBL1781 P11387 DNA topoisomerase I 84.92% 97.00%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 82.17% 92.26%
CHEMBL221 P23219 Cyclooxygenase-1 82.08% 90.17%

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.
Wurfbainia neoaurantiaca

Cross-Links

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PubChem 543854
NPASS NPC252963