(4S)-4,13-dimethyltetradecanoic acid

Details

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Internal ID c6ce0b90-0f0d-4272-95ab-1ece8dbaaa2d
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (4S)-4,13-dimethyltetradecanoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H32O2/c1-14(2)10-8-6-4-5-7-9-11-15(3)12-13-16(17)18/h14-15H,4-13H2,1-3H3,(H,17,18)/t15-/m0/s1
InChI Key ZYBCRBGIQFSXAT-HNNXBMFYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C16H32O2
Molecular Weight 256.42 g/mol
Exact Mass 256.240230259 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 6.50
Atomic LogP (AlogP) 5.26
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 (4S)-4,13-dimethyltetradecanoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9943 99.43%
Caco-2 + 0.7703 77.03%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.6288 62.88%
OATP2B1 inhibitior - 0.8454 84.54%
OATP1B1 inhibitior + 0.9657 96.57%
OATP1B3 inhibitior + 0.8768 87.68%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.5891 58.91%
P-glycoprotein inhibitior - 0.8977 89.77%
P-glycoprotein substrate - 0.9151 91.51%
CYP3A4 substrate - 0.6365 63.65%
CYP2C9 substrate + 1.0000 100.00%
CYP2D6 substrate - 0.8908 89.08%
CYP3A4 inhibition - 0.9632 96.32%
CYP2C9 inhibition - 0.8974 89.74%
CYP2C19 inhibition - 0.9664 96.64%
CYP2D6 inhibition - 0.9657 96.57%
CYP1A2 inhibition - 0.5185 51.85%
CYP2C8 inhibition - 0.9912 99.12%
CYP inhibitory promiscuity - 0.9844 98.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6115 61.15%
Carcinogenicity (trinary) Non-required 0.7726 77.26%
Eye corrosion + 0.9600 96.00%
Eye irritation + 0.8741 87.41%
Skin irritation - 0.5123 51.23%
Skin corrosion - 0.9439 94.39%
Ames mutagenesis - 0.9600 96.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6168 61.68%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5054 50.54%
skin sensitisation + 0.8125 81.25%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.6134 61.34%
Mitochondrial toxicity - 0.7000 70.00%
Nephrotoxicity - 0.7623 76.23%
Acute Oral Toxicity (c) III 0.8352 83.52%
Estrogen receptor binding - 0.7209 72.09%
Androgen receptor binding - 0.8656 86.56%
Thyroid receptor binding + 0.5714 57.14%
Glucocorticoid receptor binding - 0.7921 79.21%
Aromatase binding - 0.8145 81.45%
PPAR gamma - 0.6000 60.00%
Honey bee toxicity - 0.9894 98.94%
Biodegradation + 0.6750 67.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.8935 89.35%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.72% 96.09%
CHEMBL2581 P07339 Cathepsin D 94.41% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 90.61% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 87.84% 97.29%
CHEMBL5285 Q99683 Mitogen-activated protein kinase kinase kinase 5 87.79% 92.26%
CHEMBL221 P23219 Cyclooxygenase-1 87.04% 90.17%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 85.91% 100.00%
CHEMBL3359 P21462 Formyl peptide receptor 1 85.90% 93.56%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 84.46% 90.71%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 82.30% 96.47%
CHEMBL1907 P15144 Aminopeptidase N 81.81% 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 162938599
LOTUS LTS0266392
wikiData Q105385971