(E,3R,4R,6R,10S)-4,6,10-triethyl-3,6-dihydroxy-8-methyltetradec-7-enoic acid

Details

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Internal ID 29b57887-8b3c-4282-8bf4-67cb6a5662db
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acids and conjugates > Long-chain fatty acids
IUPAC Name (E,3R,4R,6R,10S)-4,6,10-triethyl-3,6-dihydroxy-8-methyltetradec-7-enoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C21H40O4/c1-6-10-11-17(7-2)12-16(5)14-21(25,9-4)15-18(8-3)19(22)13-20(23)24/h14,17-19,22,25H,6-13,15H2,1-5H3,(H,23,24)/b16-14+/t17-,18+,19+,21-/m0/s1
InChI Key IKTPWVGSUROYSG-PTTLPDHWSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C21H40O4
Molecular Weight 356.50 g/mol
Exact Mass 356.29265975 g/mol
Topological Polar Surface Area (TPSA) 77.80 Ų
XlogP 5.60
Atomic LogP (AlogP) 4.93
H-Bond Acceptor 3
H-Bond Donor 3
Rotatable Bonds 14

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E,3R,4R,6R,10S)-4,6,10-triethyl-3,6-dihydroxy-8-methyltetradec-7-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 + 0.9526 95.26%
Caco-2 + 0.7093 70.93%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability - 0.6429 64.29%
Subcellular localzation Mitochondria 0.6314 63.14%
OATP2B1 inhibitior - 0.8592 85.92%
OATP1B1 inhibitior + 0.8653 86.53%
OATP1B3 inhibitior + 0.9101 91.01%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7079 70.79%
P-glycoprotein inhibitior - 0.7843 78.43%
P-glycoprotein substrate - 0.5960 59.60%
CYP3A4 substrate + 0.5423 54.23%
CYP2C9 substrate - 0.5759 57.59%
CYP2D6 substrate - 0.8777 87.77%
CYP3A4 inhibition - 0.8128 81.28%
CYP2C9 inhibition - 0.7581 75.81%
CYP2C19 inhibition - 0.7585 75.85%
CYP2D6 inhibition - 0.9182 91.82%
CYP1A2 inhibition - 0.6280 62.80%
CYP2C8 inhibition - 0.6161 61.61%
CYP inhibitory promiscuity - 0.8143 81.43%
UGT catelyzed - 0.6000 60.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.6659 66.59%
Eye corrosion - 0.9539 95.39%
Eye irritation - 0.9010 90.10%
Skin irritation - 0.5730 57.30%
Skin corrosion - 0.9640 96.40%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4069 40.69%
Micronuclear - 0.9500 95.00%
Hepatotoxicity - 0.5500 55.00%
skin sensitisation - 0.6670 66.70%
Respiratory toxicity - 0.6778 67.78%
Reproductive toxicity - 0.6950 69.50%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity + 0.5112 51.12%
Acute Oral Toxicity (c) III 0.5134 51.34%
Estrogen receptor binding + 0.6027 60.27%
Androgen receptor binding - 0.5754 57.54%
Thyroid receptor binding + 0.7275 72.75%
Glucocorticoid receptor binding + 0.6421 64.21%
Aromatase binding - 0.6037 60.37%
PPAR gamma + 0.6502 65.02%
Honey bee toxicity - 0.9268 92.68%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity + 0.9658 96.58%

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
CHEMBL2581 P07339 Cathepsin D 98.23% 98.95%
CHEMBL4040 P28482 MAP kinase ERK2 96.59% 83.82%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.39% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 95.55% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 92.59% 97.29%
CHEMBL1907 P15144 Aminopeptidase N 91.04% 93.31%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 88.50% 100.00%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.18% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 84.85% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 84.41% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.34% 86.33%
CHEMBL3776 Q14790 Caspase-8 84.29% 97.06%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.86% 91.11%
CHEMBL3359 P21462 Formyl peptide receptor 1 82.82% 93.56%
CHEMBL215 P09917 Arachidonate 5-lipoxygenase 82.62% 92.68%
CHEMBL1293316 Q9HBX9 Relaxin receptor 1 81.62% 82.50%
CHEMBL5163 Q9NY46 Sodium channel protein type III alpha subunit 81.19% 96.90%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.15% 96.00%
CHEMBL256 P0DMS8 Adenosine A3 receptor 81.00% 95.93%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 80.65% 100.00%
CHEMBL4227 P25090 Lipoxin A4 receptor 80.12% 100.00%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 80.01% 85.14%

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 162930736
LOTUS LTS0054047
wikiData Q105114927