(4Z,8Z)-5,9,13-trimethyltetradeca-4,8,12-trienoic acid

Details

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Internal ID 1eef74f9-adb0-4b9c-b451-a8b6a679e115
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (4Z,8Z)-5,9,13-trimethyltetradeca-4,8,12-trienoic acid
SMILES (Canonical) CC(=CCCC(=CCCC(=CCCC(=O)O)C)C)C
SMILES (Isomeric) CC(=CCC/C(=C\CC/C(=C\CCC(=O)O)/C)/C)C
InChI InChI=1S/C17H28O2/c1-14(2)8-5-9-15(3)10-6-11-16(4)12-7-13-17(18)19/h8,10,12H,5-7,9,11,13H2,1-4H3,(H,18,19)/b15-10-,16-12-
InChI Key VOKDWPMRYSKGTB-CYRKZOTCSA-N
Popularity 17 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) 37.30 Ų
XlogP 5.40
Atomic LogP (AlogP) 5.27
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 9

Synonyms

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Farnesylacetic acid

2D Structure

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2D Structure of (4Z,8Z)-5,9,13-trimethyltetradeca-4,8,12-trienoic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9951 99.51%
Caco-2 + 0.8615 86.15%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.5126 51.26%
OATP2B1 inhibitior - 0.8518 85.18%
OATP1B1 inhibitior + 0.9262 92.62%
OATP1B3 inhibitior + 0.8524 85.24%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.5560 55.60%
P-glycoprotein inhibitior - 0.8956 89.56%
P-glycoprotein substrate - 0.9826 98.26%
CYP3A4 substrate - 0.6663 66.63%
CYP2C9 substrate + 0.6464 64.64%
CYP2D6 substrate - 0.8876 88.76%
CYP3A4 inhibition - 0.9200 92.00%
CYP2C9 inhibition - 0.8828 88.28%
CYP2C19 inhibition - 0.9361 93.61%
CYP2D6 inhibition - 0.9568 95.68%
CYP1A2 inhibition - 0.6080 60.80%
CYP2C8 inhibition - 0.9871 98.71%
CYP inhibitory promiscuity - 0.9402 94.02%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6315 63.15%
Carcinogenicity (trinary) Non-required 0.7071 70.71%
Eye corrosion + 0.5768 57.68%
Eye irritation + 0.8337 83.37%
Skin irritation + 0.6769 67.69%
Skin corrosion - 0.9574 95.74%
Ames mutagenesis - 0.9000 90.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5798 57.98%
Micronuclear - 1.0000 100.00%
Hepatotoxicity - 0.7000 70.00%
skin sensitisation + 0.7182 71.82%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.7846 78.46%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.4917 49.17%
Acute Oral Toxicity (c) III 0.6201 62.01%
Estrogen receptor binding - 0.7747 77.47%
Androgen receptor binding - 0.8827 88.27%
Thyroid receptor binding - 0.5696 56.96%
Glucocorticoid receptor binding - 0.5111 51.11%
Aromatase binding - 0.5306 53.06%
PPAR gamma + 0.7929 79.29%
Honey bee toxicity - 0.9477 94.77%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity + 0.9666 96.66%

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 93.76% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.46% 96.09%
CHEMBL2581 P07339 Cathepsin D 90.35% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.02% 99.17%
CHEMBL221 P23219 Cyclooxygenase-1 87.01% 90.17%
CHEMBL3401 O75469 Pregnane X receptor 80.73% 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.
Alpinia galanga
Citrus × aurantium
Citrus deliciosa

Cross-Links

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PubChem 6440238
NPASS NPC260501