2,6,10,14-Tetramethyl-7-(3-methylpent-4-enyl)pentadeca-2,5,9,13-tetraene

Details

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Internal ID 004110e2-7b96-49e3-9fc9-73d8bdf605f0
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name 2,6,10,14-tetramethyl-7-(3-methylpent-4-enyl)pentadeca-2,5,9,13-tetraene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H42/c1-9-22(6)16-18-25(24(8)15-11-13-21(4)5)19-17-23(7)14-10-12-20(2)3/h9,12-13,15,17,22,25H,1,10-11,14,16,18-19H2,2-8H3
InChI Key LIGJLBPKCXGAOA-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H42
Molecular Weight 342.60 g/mol
Exact Mass 342.328651340 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 9.90
Atomic LogP (AlogP) 8.59
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 12

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6,10,14-Tetramethyl-7-(3-methylpent-4-enyl)pentadeca-2,5,9,13-tetraene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9860 98.60%
Caco-2 + 0.6382 63.82%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 0.8590 85.90%
OATP1B1 inhibitior + 0.9150 91.50%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8295 82.95%
P-glycoprotein inhibitior + 0.6997 69.97%
P-glycoprotein substrate - 0.8576 85.76%
CYP3A4 substrate - 0.5139 51.39%
CYP2C9 substrate - 0.8110 81.10%
CYP2D6 substrate - 0.7415 74.15%
CYP3A4 inhibition - 0.9627 96.27%
CYP2C9 inhibition - 0.8903 89.03%
CYP2C19 inhibition - 0.8891 88.91%
CYP2D6 inhibition - 0.9474 94.74%
CYP1A2 inhibition - 0.7161 71.61%
CYP2C8 inhibition - 0.9134 91.34%
CYP inhibitory promiscuity - 0.7252 72.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5600 56.00%
Carcinogenicity (trinary) Warning 0.4862 48.62%
Eye corrosion + 0.7167 71.67%
Eye irritation - 0.8852 88.52%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition + 0.8042 80.42%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5963 59.63%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.6000 60.00%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6977 69.77%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding - 0.4779 47.79%
Androgen receptor binding - 0.8458 84.58%
Thyroid receptor binding + 0.6089 60.89%
Glucocorticoid receptor binding + 0.5934 59.34%
Aromatase binding + 0.6245 62.45%
PPAR gamma + 0.8080 80.80%
Honey bee toxicity - 0.8270 82.70%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity + 0.9962 99.62%

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
CHEMBL2581 P07339 Cathepsin D 93.77% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.18% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 88.33% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.08% 94.45%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.19% 93.56%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 83.05% 93.10%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.89% 91.11%

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 73807933
LOTUS LTS0064884
wikiData Q105152170