3,7,11-Trimethyl-2,6,10-triene-1,14-tetradecyl dioic acid

Details

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Internal ID 480a0487-2bd3-43c3-a7d9-60dc1354c018
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesquiterpenoids
IUPAC Name (2E,6E,10E)-3,7,11-trimethyltetradeca-2,6,10-trienedioic acid
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C17H26O4/c1-13(7-5-9-15(3)12-17(20)21)6-4-8-14(2)10-11-16(18)19/h7-8,12H,4-6,9-11H2,1-3H3,(H,18,19)(H,20,21)/b13-7+,14-8+,15-12+
InChI Key RJKAXYAKLYOYFP-NCVGSHPJSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C17H26O4
Molecular Weight 294.40 g/mol
Exact Mass 294.18310931 g/mol
Topological Polar Surface Area (TPSA) 74.60 Ų
XlogP 4.30
Atomic LogP (AlogP) 4.34
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 10

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 3,7,11-Trimethyl-2,6,10-triene-1,14-tetradecyl dioic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9352 93.52%
Caco-2 + 0.7022 70.22%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Mitochondria 0.6641 66.41%
OATP2B1 inhibitior - 0.8543 85.43%
OATP1B1 inhibitior + 0.9058 90.58%
OATP1B3 inhibitior + 0.9163 91.63%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.4521 45.21%
P-glycoprotein inhibitior - 0.8689 86.89%
P-glycoprotein substrate - 0.9539 95.39%
CYP3A4 substrate - 0.6142 61.42%
CYP2C9 substrate + 0.6145 61.45%
CYP2D6 substrate - 0.9169 91.69%
CYP3A4 inhibition - 0.8286 82.86%
CYP2C9 inhibition - 0.9018 90.18%
CYP2C19 inhibition - 0.9306 93.06%
CYP2D6 inhibition - 0.9319 93.19%
CYP1A2 inhibition - 0.7025 70.25%
CYP2C8 inhibition - 0.9671 96.71%
CYP inhibitory promiscuity - 0.9584 95.84%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7315 73.15%
Carcinogenicity (trinary) Non-required 0.7506 75.06%
Eye corrosion - 0.8127 81.27%
Eye irritation + 0.6555 65.55%
Skin irritation - 0.7740 77.40%
Skin corrosion - 0.9840 98.40%
Ames mutagenesis - 0.8100 81.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4281 42.81%
Micronuclear - 0.9600 96.00%
Hepatotoxicity - 0.5750 57.50%
skin sensitisation - 0.6624 66.24%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity - 0.8193 81.93%
Mitochondrial toxicity - 0.5000 50.00%
Nephrotoxicity - 0.5613 56.13%
Acute Oral Toxicity (c) III 0.5541 55.41%
Estrogen receptor binding - 0.6516 65.16%
Androgen receptor binding - 0.7625 76.25%
Thyroid receptor binding + 0.5133 51.33%
Glucocorticoid receptor binding - 0.6134 61.34%
Aromatase binding - 0.6899 68.99%
PPAR gamma + 0.8260 82.60%
Honey bee toxicity - 0.9081 90.81%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity + 0.9880 98.80%

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 88.15% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 87.84% 99.17%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 84.46% 92.08%
CHEMBL2581 P07339 Cathepsin D 81.96% 98.95%

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 156581379
LOTUS LTS0266207
wikiData Q105237549