2,6,10,14-Tetramethyl-9-(3-methylpent-4-enylidene)pentadeca-2,6,13-triene

Details

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Internal ID ddba39b9-8a2b-4d79-a626-c6a8b9656dc3
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name 2,6,10,14-tetramethyl-9-(3-methylpent-4-enylidene)pentadeca-2,6,13-triene
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/h9,12-13,17-18,22,24H,1,10-11,14-16,19H2,2-8H3
InChI Key VDOFLWFFQCRKTK-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 9.80
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-9-(3-methylpent-4-enylidene)pentadeca-2,6,13-triene

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 + 0.6968 69.68%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9199 91.99%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8553 85.53%
P-glycoprotein inhibitior + 0.6270 62.70%
P-glycoprotein substrate - 0.8716 87.16%
CYP3A4 substrate - 0.5361 53.61%
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 - 0.9395 93.95%
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 - 0.8779 87.79%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9308 93.08%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5150 51.50%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity + 0.5070 50.70%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding - 0.5310 53.10%
Androgen receptor binding - 0.6823 68.23%
Thyroid receptor binding + 0.6464 64.64%
Glucocorticoid receptor binding - 0.6346 63.46%
Aromatase binding + 0.5273 52.73%
PPAR gamma + 0.5435 54.35%
Honey bee toxicity - 0.8142 81.42%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.6700 67.00%
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 90.57% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.29% 96.09%
CHEMBL240 Q12809 HERG 89.92% 89.76%
CHEMBL2885 P07451 Carbonic anhydrase III 87.00% 87.45%
CHEMBL3130 O00329 PI3-kinase p110-delta subunit 85.77% 96.47%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 85.03% 83.57%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.85% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.77% 94.45%

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 78409595
LOTUS LTS0264116
wikiData Q105284291