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

Details

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Internal ID a079c514-5973-4d53-b815-e400568ce740
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name 2,6,10,14-tetramethyl-9-(3-methylpent-4-enyl)pentadeca-2,6,10-triene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H44/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/h9,12,15,17,21-22,25H,1,10-11,13-14,16,18-19H2,2-8H3
InChI Key MKKVQZKPCITHAF-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H44
Molecular Weight 344.60 g/mol
Exact Mass 344.344301404 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 10.10
Atomic LogP (AlogP) 8.67
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 13

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-enyl)pentadeca-2,6,10-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 + 0.6295 62.95%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5143 51.43%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 0.8578 85.78%
OATP1B1 inhibitior + 0.9102 91.02%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8084 80.84%
P-glycoprotein inhibitior + 0.5908 59.08%
P-glycoprotein substrate - 0.7606 76.06%
CYP3A4 substrate + 0.5263 52.63%
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 - 0.8963 89.63%
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 - 0.8629 86.29%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.7054 70.54%
Human Ether-a-go-go-Related Gene inhibition + 0.7816 78.16%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5588 55.88%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6072 60.72%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding + 0.5965 59.65%
Androgen receptor binding - 0.8389 83.89%
Thyroid receptor binding + 0.6815 68.15%
Glucocorticoid receptor binding - 0.4649 46.49%
Aromatase binding - 0.5920 59.20%
PPAR gamma + 0.7145 71.45%
Honey bee toxicity - 0.7934 79.34%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.5900 59.00%
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 92.81% 98.95%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.63% 96.09%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 87.02% 94.45%
CHEMBL2107 P61073 C-X-C chemokine receptor type 4 85.21% 93.10%
CHEMBL2885 P07451 Carbonic anhydrase III 82.59% 87.45%
CHEMBL3401 O75469 Pregnane X receptor 82.37% 94.73%
CHEMBL221 P23219 Cyclooxygenase-1 81.85% 90.17%
CHEMBL3359 P21462 Formyl peptide receptor 1 81.76% 93.56%

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 85786781
LOTUS LTS0264205
wikiData Q105166047