(z)-14-Methyl-9-pentadecenoic acid

Details

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Internal ID 075cfe22-f95a-4e89-9aed-e78ef0982371
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (Z)-14-methylpentadec-9-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H30O2/c1-15(2)13-11-9-7-5-3-4-6-8-10-12-14-16(17)18/h5,7,15H,3-4,6,8-14H2,1-2H3,(H,17,18)/b7-5-
InChI Key YRYADTKRRRPFOA-ALCCZGGFSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C16H30O2
Molecular Weight 254.41 g/mol
Exact Mass 254.224580195 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.90
Atomic LogP (AlogP) 5.18
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (z)-14-Methyl-9-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 + 0.9924 99.24%
Caco-2 + 0.6660 66.60%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5633 56.33%
OATP2B1 inhibitior - 0.8503 85.03%
OATP1B1 inhibitior + 0.8630 86.30%
OATP1B3 inhibitior - 0.2822 28.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.4908 49.08%
P-glycoprotein inhibitior - 0.9380 93.80%
P-glycoprotein substrate - 0.9280 92.80%
CYP3A4 substrate - 0.6392 63.92%
CYP2C9 substrate + 0.6453 64.53%
CYP2D6 substrate - 0.8826 88.26%
CYP3A4 inhibition - 0.9611 96.11%
CYP2C9 inhibition - 0.8970 89.70%
CYP2C19 inhibition - 0.9541 95.41%
CYP2D6 inhibition - 0.9661 96.61%
CYP1A2 inhibition + 0.7074 70.74%
CYP2C8 inhibition - 0.9853 98.53%
CYP inhibitory promiscuity - 0.9587 95.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6515 65.15%
Carcinogenicity (trinary) Non-required 0.7383 73.83%
Eye corrosion + 0.9385 93.85%
Eye irritation + 0.8199 81.99%
Skin irritation + 0.6154 61.54%
Skin corrosion - 0.9655 96.55%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5067 50.67%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6071 60.71%
skin sensitisation + 0.9152 91.52%
Respiratory toxicity + 0.6444 64.44%
Reproductive toxicity - 0.5169 51.69%
Mitochondrial toxicity - 0.5875 58.75%
Nephrotoxicity - 0.8263 82.63%
Acute Oral Toxicity (c) III 0.5896 58.96%
Estrogen receptor binding - 0.8116 81.16%
Androgen receptor binding - 0.8755 87.55%
Thyroid receptor binding + 0.7029 70.29%
Glucocorticoid receptor binding - 0.5336 53.36%
Aromatase binding - 0.8122 81.22%
PPAR gamma + 0.8350 83.50%
Honey bee toxicity - 0.9861 98.61%
Biodegradation + 0.8500 85.00%
Crustacea aquatic toxicity - 0.5300 53.00%
Fish aquatic toxicity + 0.9642 96.42%

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 96.96% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.53% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.65% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 89.67% 96.47%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 89.42% 92.26%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.07% 93.56%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.11% 100.00%
CHEMBL1781 P11387 DNA topoisomerase I 85.55% 97.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.07% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 83.00% 90.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.48% 97.29%
CHEMBL1907 P15144 Aminopeptidase N 81.64% 93.31%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 80.53% 96.00%

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 11414145
LOTUS LTS0176288
wikiData Q105353245