Methyl farnesoic acid

Details

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Internal ID 36734eed-0f54-4155-aeb9-193767337e49
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name 3,7,11-trimethyltrideca-2,6,10-trienoic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C16H26O2/c1-5-13(2)8-6-9-14(3)10-7-11-15(4)12-16(17)18/h8,10,12H,5-7,9,11H2,1-4H3,(H,17,18)
InChI Key WNJOSMMDGFBJEG-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C16H26O2
Molecular Weight 250.38 g/mol
Exact Mass 250.193280068 g/mol
Topological Polar Surface Area (TPSA) 37.30 Ų
XlogP 5.40
Atomic LogP (AlogP) 4.88
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 8

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Methyl farnesoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9919 99.19%
Caco-2 + 0.9499 94.99%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5714 57.14%
Subcellular localzation Plasma membrane 0.3734 37.34%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9070 90.70%
OATP1B3 inhibitior + 0.8350 83.50%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior + 0.5533 55.33%
P-glycoprotein inhibitior - 0.9306 93.06%
P-glycoprotein substrate - 0.9477 94.77%
CYP3A4 substrate - 0.6284 62.84%
CYP2C9 substrate + 0.6145 61.45%
CYP2D6 substrate - 0.9169 91.69%
CYP3A4 inhibition - 0.8978 89.78%
CYP2C9 inhibition - 0.8480 84.80%
CYP2C19 inhibition - 0.9076 90.76%
CYP2D6 inhibition - 0.9278 92.78%
CYP1A2 inhibition - 0.5793 57.93%
CYP2C8 inhibition - 0.9200 92.00%
CYP inhibitory promiscuity - 0.7545 75.45%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6415 64.15%
Carcinogenicity (trinary) Non-required 0.6409 64.09%
Eye corrosion + 0.6974 69.74%
Eye irritation + 0.6759 67.59%
Skin irritation + 0.6070 60.70%
Skin corrosion - 0.9707 97.07%
Ames mutagenesis - 0.7678 76.78%
Human Ether-a-go-go-Related Gene inhibition + 0.7357 73.57%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.6125 61.25%
skin sensitisation + 0.8078 80.78%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity - 0.7222 72.22%
Mitochondrial toxicity - 0.5750 57.50%
Nephrotoxicity - 0.5931 59.31%
Acute Oral Toxicity (c) III 0.6968 69.68%
Estrogen receptor binding - 0.7279 72.79%
Androgen receptor binding - 0.7188 71.88%
Thyroid receptor binding - 0.6107 61.07%
Glucocorticoid receptor binding - 0.6825 68.25%
Aromatase binding - 0.6801 68.01%
PPAR gamma + 0.7342 73.42%
Honey bee toxicity - 0.9309 93.09%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.9906 99.06%

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 89.56% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.84% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.47% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.40% 98.95%
CHEMBL2061 P19793 Retinoid X receptor alpha 82.39% 91.67%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 129776656
LOTUS LTS0176887
wikiData Q105309115