(E,Z)-farnesol

Details

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Internal ID 226df304-a6a7-4982-89ec-7ed4dafae362
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,6Z)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol
SMILES (Canonical) CC(=CCCC(=CCCC(=CCO)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C\CC/C(=C/CO)/C)/C)C
InChI InChI=1S/C15H26O/c1-13(2)7-5-8-14(3)9-6-10-15(4)11-12-16/h7,9,11,16H,5-6,8,10,12H2,1-4H3/b14-9-,15-11+
InChI Key CRDAMVZIKSXKFV-GNESMGCMSA-N
Popularity 3,186 references in papers

Physical and Chemical Properties

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Molecular Formula C15H26O
Molecular Weight 222.37 g/mol
Exact Mass 222.198365449 g/mol
Topological Polar Surface Area (TPSA) 20.20 Ų
XlogP 4.80
Atomic LogP (AlogP) 4.40
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 7

Synonyms

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(2E,6Z)-farnesol
trans,cis-Farnesol
2-trans,6-cis-farnesol
3879-60-5
2E,6Z-farnesol
Farnesol, (2E,6Z)-
(2E,6Z)-3,7,11-trimethyldodeca-2,6,10-trien-1-ol
Farnesyl alcohol
FEMA No. 2478, (2E,6Z)-
UNII-413TVZ4919
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of (E,Z)-farnesol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9823 98.23%
Caco-2 + 0.9395 93.95%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Lysosomes 0.5576 55.76%
OATP2B1 inhibitior - 0.8517 85.17%
OATP1B1 inhibitior + 0.9449 94.49%
OATP1B3 inhibitior + 0.9480 94.80%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6162 61.62%
P-glycoprotein inhibitior - 0.9566 95.66%
P-glycoprotein substrate - 0.9741 97.41%
CYP3A4 substrate - 0.6422 64.22%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7450 74.50%
CYP3A4 inhibition - 0.9088 90.88%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.9026 90.26%
CYP2D6 inhibition - 0.9230 92.30%
CYP1A2 inhibition - 0.9046 90.46%
CYP2C8 inhibition - 0.9772 97.72%
CYP inhibitory promiscuity - 0.7650 76.50%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.6600 66.00%
Carcinogenicity (trinary) Non-required 0.6507 65.07%
Eye corrosion + 0.5325 53.25%
Eye irritation + 0.8851 88.51%
Skin irritation + 0.8492 84.92%
Skin corrosion - 0.9100 91.00%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4749 47.49%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.9375 93.75%
skin sensitisation + 0.9333 93.33%
Respiratory toxicity - 0.9667 96.67%
Reproductive toxicity - 0.9812 98.12%
Mitochondrial toxicity - 0.9250 92.50%
Nephrotoxicity + 0.6319 63.19%
Acute Oral Toxicity (c) III 0.8552 85.52%
Estrogen receptor binding - 0.8886 88.86%
Androgen receptor binding - 0.8384 83.84%
Thyroid receptor binding - 0.7654 76.54%
Glucocorticoid receptor binding - 0.6535 65.35%
Aromatase binding - 0.7305 73.05%
PPAR gamma + 0.6073 60.73%
Honey bee toxicity - 0.9445 94.45%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity + 0.9500 95.00%

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
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 94.25% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.82% 96.09%
CHEMBL2581 P07339 Cathepsin D 82.45% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.91% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.90% 99.17%

Cross-Links

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PubChem 1549109
NPASS NPC29091
LOTUS LTS0182151
wikiData Q27116653