Linalyl acetate, (-)-

Details

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Internal ID 18770f61-c63f-4b35-965a-330a4239b6fa
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name [(3R)-3,7-dimethylocta-1,6-dien-3-yl] acetate
SMILES (Canonical) CC(=CCCC(C)(C=C)OC(=O)C)C
SMILES (Isomeric) CC(=CCC[C@](C)(C=C)OC(=O)C)C
InChI InChI=1S/C12H20O2/c1-6-12(5,14-11(4)13)9-7-8-10(2)3/h6,8H,1,7,9H2,2-5H3/t12-/m0/s1
InChI Key UWKAYLJWKGQEPM-LBPRGKRZSA-N
Popularity 8 references in papers

Physical and Chemical Properties

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Molecular Formula C12H20O2
Molecular Weight 196.29 g/mol
Exact Mass 196.146329876 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 3.30
Atomic LogP (AlogP) 3.24
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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(-)-linalyl acetate
Linalyl acetate, (-)-
16509-46-9
UNII-J7C5I8LV3G
J7C5I8LV3G
L-LINALYL ACETATE
EINECS 240-575-7
[(3R)-3,7-dimethylocta-1,6-dien-3-yl] acetate
1,6-Octadien-3-ol, 3,7-dimethyl-, acetate, (3R)-
R-(-)-LINALYL ACETATE
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Linalyl acetate, (-)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9907 99.07%
Caco-2 + 0.7102 71.02%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.6143 61.43%
Subcellular localzation Mitochondria 0.5406 54.06%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9380 93.80%
OATP1B3 inhibitior + 0.8483 84.83%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8899 88.99%
P-glycoprotein inhibitior - 0.9718 97.18%
P-glycoprotein substrate - 0.9660 96.60%
CYP3A4 substrate - 0.5425 54.25%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.8246 82.46%
CYP2C9 inhibition - 0.8555 85.55%
CYP2C19 inhibition - 0.7144 71.44%
CYP2D6 inhibition - 0.9292 92.92%
CYP1A2 inhibition - 0.6937 69.37%
CYP2C8 inhibition - 0.9523 95.23%
CYP inhibitory promiscuity - 0.7763 77.63%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5200 52.00%
Carcinogenicity (trinary) Warning 0.4855 48.55%
Eye corrosion + 0.5710 57.10%
Eye irritation + 0.9520 95.20%
Skin irritation + 0.8736 87.36%
Skin corrosion - 0.9812 98.12%
Ames mutagenesis - 0.8700 87.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5363 53.63%
Micronuclear - 0.9700 97.00%
Hepatotoxicity - 0.5616 56.16%
skin sensitisation + 0.9075 90.75%
Respiratory toxicity - 0.7778 77.78%
Reproductive toxicity - 0.9667 96.67%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.7521 75.21%
Acute Oral Toxicity (c) IV 0.6409 64.09%
Estrogen receptor binding - 0.9315 93.15%
Androgen receptor binding - 0.9206 92.06%
Thyroid receptor binding - 0.8217 82.17%
Glucocorticoid receptor binding - 0.7858 78.58%
Aromatase binding - 0.8704 87.04%
PPAR gamma - 0.8754 87.54%
Honey bee toxicity - 0.7218 72.18%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9139 91.39%

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
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 91.78% 96.95%
CHEMBL2581 P07339 Cathepsin D 91.05% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.21% 96.09%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 87.78% 89.34%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.04% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 86.11% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.70% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 81.61% 86.33%
CHEMBL2111367 P27986 PI3-kinase p110-alpha/p85-alpha 81.23% 94.33%
CHEMBL3401 O75469 Pregnane X receptor 80.40% 94.73%

Cross-Links

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PubChem 442474
NPASS NPC37947
LOTUS LTS0020520
wikiData Q27147765