(+)-Linalyl acetate

Details

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Internal ID 15a0e930-914c-46fa-a9c9-61a4248b171e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Monoterpenoids > Acyclic monoterpenoids
IUPAC Name [(3S)-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-/m1/s1
InChI Key UWKAYLJWKGQEPM-GFCCVEGCSA-N
Popularity 6 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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(s)-linalyl acetate
Linalyl acetate, (+)-
51685-40-6
UNII-3ID3M89AV9
3ID3M89AV9
(3S)-3,7-dimethylocta-1,6-dien-3-yl acetate
[(3S)-3,7-dimethylocta-1,6-dien-3-yl] acetate
EINECS 257-347-8
(+)-1,5-Dimethyl-1-vinylhex-4-enyl acetate
Coriandrol 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%

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.
Acokanthera oblongifolia
Aglaia meridionalis
Allium ursinum
Ammi majus
Angelica sinensis
Angelica taiwaniana
Arcangelisia gusanlung
Artemisia annua
Artemisia schmidtiana
Asterolasia squamuligera
Bellium bellidioides
Brickellia pendula
Catharanthus roseus
Centaurea calcitrapa
Cinnamomum chekiangense
Citrus deliciosa
Citrus limon
Citrus maxima
Citrus medica
Cladanthus scariosus
Cleidion brevipetiolatum
Conioselinum anthriscoides
Conioselinum smithii
Conioselinum tenuissimum
Copaifera paupera
Crotalaria spectabilis
Cynara humilis
Daucus carota
Delphinium hohenackeri
Elegia deusta
Elettaria cardamomum
Endosamara racemosa
Entandrophragma cylindricum
Erica glauca
Escallonia virgata
Ficus maxima
Garcinia intermedia
Gleichenia polypodioides
Hesperocyparis nevadensis
Jacobaea erratica
Jacobaea vulgaris
Juglans regia
Juniperus communis
Juniperus drupacea
Juniperus thurifera
Kielmeyera coriacea
Kitagawia praeruptora
Lathyrus linifolius
Leptospermum scoparium
Leucas neufliseana
Lithospermum officinale
Litsea glutinosa
Magnolia acuminata
Magnolia officinalis
Monarda fistulosa
Moringa oleifera
Myristica fragrans
Oncosiphon suffruticosus
Onoclea struthiopteris
Ophioglossum vulgatum
Platonia insignis
Plectranthus amboinicus
Plectranthus parishii
Pluchea dioscoridis
Plumbago europaea
Prunella vulgaris
Pyrola rotundifolia
Reissantia indica
Rhodanthe stricta
Salvia munzii
Salvia sclarea
Sarcococca coriacea
Simmondsia chinensis
Solanum villosum
Sophora koreensis
Stevia alpina
Synotis cappa
Syzygium aromaticum
Tabebuia heterophylla
Tabebuia rosea
Tanacetum santolina
Tetradium ruticarpum
Thymus camphoratus
Thymus vulgaris
Timonius kaniensis
Trachelospermum lucidum
Ulmus americana
Wikstroemia chamaedaphne
Wollastonia dentata
Zanthoxylum bungeanum
Zanthoxylum schinifolium
Zanthoxylum simulans
Zingiber officinale

Cross-Links

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PubChem 6999980
NPASS NPC215894
LOTUS LTS0006782
wikiData Q27147766