(2Z,6Z)-Farnesyl acetate

Details

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Internal ID f2d8149f-4a7a-423a-8e89-44951ae6f77e
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name [(2Z,6Z)-3,7,11-trimethyldodeca-2,6,10-trienyl] acetate
SMILES (Canonical) CC(=CCCC(=CCCC(=CCOC(=O)C)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C\CC/C(=C\COC(=O)C)/C)/C)C
InChI InChI=1S/C17H28O2/c1-14(2)8-6-9-15(3)10-7-11-16(4)12-13-19-17(5)18/h8,10,12H,6-7,9,11,13H2,1-5H3/b15-10-,16-12-
InChI Key ZGIGZINMAOQWLX-CYRKZOTCSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C17H28O2
Molecular Weight 264.40 g/mol
Exact Mass 264.208930132 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 5.30
Atomic LogP (AlogP) 4.97
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 8

Synonyms

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all-cis-Farnesyl acetate
6KSQ7YD7EB
Farnesyl acetate, (2Z,6Z)-
24163-97-1
UNII-6KSQ7YD7EB
FEMA No. 4213, (2Z,6Z)-
[(2Z,6Z)-3,7,11-trimethyldodeca-2,6,10-trienyl] acetate
2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl-, acetate, (Z,Z)-
2,6,10-Dodecatrien-1-ol, 3,7,11-trimethyl-, 1-acetate, (2Z,6Z)-
SCHEMBL806928
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (2Z,6Z)-Farnesyl acetate

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9953 99.53%
Caco-2 + 0.8698 86.98%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Mitochondria 0.6095 60.95%
OATP2B1 inhibitior - 0.8528 85.28%
OATP1B1 inhibitior + 0.9427 94.27%
OATP1B3 inhibitior + 0.8637 86.37%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior + 0.7166 71.66%
P-glycoprotein inhibitior - 0.8317 83.17%
P-glycoprotein substrate - 0.9764 97.64%
CYP3A4 substrate - 0.5646 56.46%
CYP2C9 substrate - 0.7977 79.77%
CYP2D6 substrate - 0.8708 87.08%
CYP3A4 inhibition - 0.9647 96.47%
CYP2C9 inhibition - 0.8935 89.35%
CYP2C19 inhibition - 0.8874 88.74%
CYP2D6 inhibition - 0.9361 93.61%
CYP1A2 inhibition - 0.7663 76.63%
CYP2C8 inhibition - 0.9629 96.29%
CYP inhibitory promiscuity - 0.7180 71.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Non-required 0.5291 52.91%
Eye corrosion + 0.7105 71.05%
Eye irritation + 0.7082 70.82%
Skin irritation + 0.8399 83.99%
Skin corrosion - 0.9912 99.12%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6604 66.04%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6000 60.00%
skin sensitisation + 0.5505 55.05%
Respiratory toxicity - 0.9444 94.44%
Reproductive toxicity - 1.0000 100.00%
Mitochondrial toxicity - 0.9625 96.25%
Nephrotoxicity + 0.7427 74.27%
Acute Oral Toxicity (c) III 0.5909 59.09%
Estrogen receptor binding - 0.8072 80.72%
Androgen receptor binding - 0.7930 79.30%
Thyroid receptor binding - 0.6343 63.43%
Glucocorticoid receptor binding - 0.5944 59.44%
Aromatase binding + 0.5959 59.59%
PPAR gamma + 0.5564 55.64%
Honey bee toxicity - 0.8789 87.89%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity - 0.5955 59.55%
Fish aquatic toxicity + 0.9912 99.12%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 92.88% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 92.44% 92.08%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.24% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 84.23% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.79% 94.45%
CHEMBL2581 P07339 Cathepsin D 81.15% 98.95%
CHEMBL340 P08684 Cytochrome P450 3A4 80.41% 91.19%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.11% 91.11%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 80.10% 96.95%

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.
Carapichea ipecacuanha
Citrus maxima

Cross-Links

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PubChem 1551479
NPASS NPC145988
LOTUS LTS0136484
wikiData Q27265064