ethyl (Z,4R)-4-methylheptadec-6-enoate

Details

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Internal ID c8ef5e9f-fca8-4c31-bbbc-9fb18ae75878
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty acid esters
IUPAC Name ethyl (Z,4R)-4-methylheptadec-6-enoate
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C20H38O2/c1-4-6-7-8-9-10-11-12-13-14-15-16-19(3)17-18-20(21)22-5-2/h14-15,19H,4-13,16-18H2,1-3H3/b15-14-/t19-/m0/s1
InChI Key GAKNGWPTDNFVMV-AVCMKVNGSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C20H38O2
Molecular Weight 310.50 g/mol
Exact Mass 310.287180451 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 7.70
Atomic LogP (AlogP) 6.44
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of ethyl (Z,4R)-4-methylheptadec-6-enoate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9971 99.71%
Caco-2 + 0.8490 84.90%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Plasma membrane 0.4706 47.06%
OATP2B1 inhibitior - 0.8475 84.75%
OATP1B1 inhibitior + 0.8364 83.64%
OATP1B3 inhibitior + 0.8982 89.82%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior + 0.8599 85.99%
P-glycoprotein inhibitior - 0.7373 73.73%
P-glycoprotein substrate - 0.9352 93.52%
CYP3A4 substrate + 0.5294 52.94%
CYP2C9 substrate - 0.8037 80.37%
CYP2D6 substrate - 0.8782 87.82%
CYP3A4 inhibition - 0.9269 92.69%
CYP2C9 inhibition - 0.9261 92.61%
CYP2C19 inhibition - 0.9132 91.32%
CYP2D6 inhibition - 0.9297 92.97%
CYP1A2 inhibition + 0.5070 50.70%
CYP2C8 inhibition - 0.8914 89.14%
CYP inhibitory promiscuity - 0.7472 74.72%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6300 63.00%
Carcinogenicity (trinary) Non-required 0.6381 63.81%
Eye corrosion + 0.9215 92.15%
Eye irritation + 0.7482 74.82%
Skin irritation + 0.5531 55.31%
Skin corrosion - 0.9939 99.39%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7483 74.83%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.5467 54.67%
skin sensitisation + 0.7079 70.79%
Respiratory toxicity - 0.8667 86.67%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 1.0000 100.00%
Nephrotoxicity - 0.6334 63.34%
Acute Oral Toxicity (c) III 0.9084 90.84%
Estrogen receptor binding - 0.8635 86.35%
Androgen receptor binding - 0.8313 83.13%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding - 0.6569 65.69%
Aromatase binding - 0.8208 82.08%
PPAR gamma - 0.6020 60.20%
Honey bee toxicity - 0.9632 96.32%
Biodegradation + 0.6500 65.00%
Crustacea aquatic toxicity + 0.7978 79.78%
Fish aquatic toxicity + 0.9764 97.64%

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
CHEMBL230 P35354 Cyclooxygenase-2 98.96% 89.63%
CHEMBL3060 Q9Y345 Glycine transporter 2 98.10% 99.17%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 96.86% 97.29%
CHEMBL240 Q12809 HERG 95.62% 89.76%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 95.57% 85.94%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.15% 96.09%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 93.01% 96.47%
CHEMBL2581 P07339 Cathepsin D 92.21% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.67% 93.56%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 91.45% 97.21%
CHEMBL3267 P48736 PI3-kinase p110-gamma subunit 88.43% 95.71%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 87.31% 96.95%
CHEMBL2885 P07451 Carbonic anhydrase III 87.14% 87.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.62% 100.00%
CHEMBL3401 O75469 Pregnane X receptor 86.34% 94.73%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.32% 96.00%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 86.14% 92.86%
CHEMBL299 P17252 Protein kinase C alpha 85.79% 98.03%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 85.31% 94.45%
CHEMBL221 P23219 Cyclooxygenase-1 84.91% 90.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.42% 92.08%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 83.74% 100.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.58% 91.81%
CHEMBL5255 O00206 Toll-like receptor 4 83.45% 92.50%
CHEMBL4227 P25090 Lipoxin A4 receptor 82.12% 100.00%
CHEMBL4005 P42336 PI3-kinase p110-alpha subunit 81.83% 97.47%
CHEMBL1781 P11387 DNA topoisomerase I 81.76% 97.00%
CHEMBL1907 P15144 Aminopeptidase N 81.54% 93.31%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 81.51% 90.71%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 81.07% 89.34%
CHEMBL3145 P42338 PI3-kinase p110-beta subunit 81.01% 98.75%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 80.49% 94.33%

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.
Tinospora sinensis

Cross-Links

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PubChem 162870978
LOTUS LTS0181230
wikiData Q105005454