(E)-16-methylheptadec-9-enoic acid

Details

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Internal ID 47dea267-b622-4fed-a7ff-2ffd47ef07d7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (E)-16-methylheptadec-9-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C18H34O2/c1-17(2)15-13-11-9-7-5-3-4-6-8-10-12-14-16-18(19)20/h3,5,17H,4,6-16H2,1-2H3,(H,19,20)/b5-3+
InChI Key OXJKUGPIKSAPTN-HWKANZROSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C18H34O2
Molecular Weight 282.50 g/mol
Exact Mass 282.255880323 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.90
Atomic LogP (AlogP) 5.96
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-16-methylheptadec-9-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 + 0.9924 99.24%
Caco-2 + 0.7994 79.94%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Mitochondria 0.5633 56.33%
OATP2B1 inhibitior - 0.8487 84.87%
OATP1B1 inhibitior + 0.8705 87.05%
OATP1B3 inhibitior - 0.2822 28.22%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5357 53.57%
P-glycoprotein inhibitior - 0.8128 81.28%
P-glycoprotein substrate - 0.9349 93.49%
CYP3A4 substrate - 0.6247 62.47%
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 - 0.9846 98.46%
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 + 0.8992 89.92%
Skin irritation + 0.6154 61.54%
Skin corrosion - 0.9655 96.55%
Ames mutagenesis - 0.9500 95.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7177 71.77%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6446 64.46%
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 - 0.8242 82.42%
Acute Oral Toxicity (c) III 0.5896 58.96%
Estrogen receptor binding - 0.7932 79.32%
Androgen receptor binding - 0.8755 87.55%
Thyroid receptor binding + 0.7729 77.29%
Glucocorticoid receptor binding - 0.6647 66.47%
Aromatase binding - 0.8232 82.32%
PPAR gamma + 0.8429 84.29%
Honey bee toxicity - 0.9854 98.54%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.5200 52.00%
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 97.01% 99.17%
CHEMBL2581 P07339 Cathepsin D 95.51% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.11% 96.09%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 89.38% 92.26%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 89.33% 96.47%
CHEMBL3359 P21462 Formyl peptide receptor 1 88.37% 93.56%
CHEMBL1781 P11387 DNA topoisomerase I 87.96% 97.00%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 86.74% 100.00%
CHEMBL221 P23219 Cyclooxygenase-1 82.57% 90.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 82.48% 97.29%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.96% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.82% 91.11%
CHEMBL1907 P15144 Aminopeptidase N 81.53% 93.31%

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 14123138
LOTUS LTS0063823
wikiData Q105202741