1-Methyloctyl acetate

Details

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Internal ID 2f12ee72-bea9-46ba-92ea-4e107ddd9cc7
Taxonomy Lipids and lipid-like molecules > Fatty Acyls > Fatty alcohol esters
IUPAC Name nonan-2-yl acetate
SMILES (Canonical) CCCCCCCC(C)OC(=O)C
SMILES (Isomeric) CCCCCCCC(C)OC(=O)C
InChI InChI=1S/C11H22O2/c1-4-5-6-7-8-9-10(2)13-11(3)12/h10H,4-9H2,1-3H3
InChI Key GSUGVJOUDSLEBL-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C11H22O2
Molecular Weight 186.29 g/mol
Exact Mass 186.161979940 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 4.00
Atomic LogP (AlogP) 3.30
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 7

Synonyms

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14936-66-4
2-Nonyl acetate
nonan-2-yl acetate
Acetic Acid 2-Nonyl Ester
ACETICACID2-NONYLESTER
2-nonanol, acetate
EINECS 239-010-7
2-Nonanol, 2-acetate
Beta-nonyl acetate
SCHEMBL1301932
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 1-Methyloctyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9960 99.60%
Caco-2 + 0.8827 88.27%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.7286 72.86%
Subcellular localzation Mitochondria 0.4389 43.89%
OATP2B1 inhibitior - 0.8444 84.44%
OATP1B1 inhibitior + 0.9595 95.95%
OATP1B3 inhibitior + 0.9255 92.55%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.9195 91.95%
P-glycoprotein inhibitior - 0.9548 95.48%
P-glycoprotein substrate - 0.8683 86.83%
CYP3A4 substrate - 0.6002 60.02%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8679 86.79%
CYP3A4 inhibition - 0.9505 95.05%
CYP2C9 inhibition - 0.8997 89.97%
CYP2C19 inhibition - 0.9074 90.74%
CYP2D6 inhibition - 0.9345 93.45%
CYP1A2 inhibition - 0.5129 51.29%
CYP2C8 inhibition - 0.9767 97.67%
CYP inhibitory promiscuity - 0.8440 84.40%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5800 58.00%
Carcinogenicity (trinary) Non-required 0.6615 66.15%
Eye corrosion + 0.9652 96.52%
Eye irritation + 0.9397 93.97%
Skin irritation - 0.7278 72.78%
Skin corrosion - 0.9884 98.84%
Ames mutagenesis - 0.9800 98.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5323 53.23%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5983 59.83%
skin sensitisation + 0.7875 78.75%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9875 98.75%
Nephrotoxicity + 0.7384 73.84%
Acute Oral Toxicity (c) III 0.9032 90.32%
Estrogen receptor binding - 0.9181 91.81%
Androgen receptor binding - 0.7500 75.00%
Thyroid receptor binding - 0.7891 78.91%
Glucocorticoid receptor binding - 0.7914 79.14%
Aromatase binding - 0.8659 86.59%
PPAR gamma - 0.8018 80.18%
Honey bee toxicity - 0.9773 97.73%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity + 0.6963 69.63%
Fish aquatic toxicity + 0.9071 90.71%

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 96.63% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 96.01% 96.09%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 95.17% 97.29%
CHEMBL3060 Q9Y345 Glycine transporter 2 93.86% 99.17%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 92.01% 92.86%
CHEMBL3359 P21462 Formyl peptide receptor 1 91.02% 93.56%
CHEMBL240 Q12809 HERG 88.61% 89.76%
CHEMBL253 P34972 Cannabinoid CB2 receptor 88.41% 97.25%
CHEMBL4657 Q6V1X1 Dipeptidyl peptidase VIII 88.15% 97.21%
CHEMBL2885 P07451 Carbonic anhydrase III 88.05% 87.45%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.16% 94.45%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 86.17% 100.00%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 85.14% 96.95%
CHEMBL4040 P28482 MAP kinase ERK2 84.83% 83.82%
CHEMBL230 P35354 Cyclooxygenase-2 84.41% 89.63%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 83.97% 85.94%
CHEMBL1907591 P30926 Neuronal acetylcholine receptor; alpha4/beta4 82.06% 100.00%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 81.41% 91.81%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 80.79% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 80.04% 94.73%

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.
Ruta graveolens

Cross-Links

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PubChem 85788
NPASS NPC72627
LOTUS LTS0211966
wikiData Q82909456