2,6,14-Trimethyl-10-methylidene-9-(3-methylpent-4-enyl)pentadec-6-ene

Details

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Internal ID 2b2f8c11-06bd-4684-9a59-e26b7f850952
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Sesterterpenoids
IUPAC Name 2,6,14-trimethyl-10-methylidene-9-(3-methylpent-4-enyl)pentadec-6-ene
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C25H46/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/h9,17,20-22,25H,1,8,10-16,18-19H2,2-7H3
InChI Key BSXYLMVBPPIDSG-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C25H46
Molecular Weight 346.60 g/mol
Exact Mass 346.359951467 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 10.80
Atomic LogP (AlogP) 8.75
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2,6,14-Trimethyl-10-methylidene-9-(3-methylpent-4-enyl)pentadec-6-ene

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 + 0.5608 56.08%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5857 58.57%
Subcellular localzation Nucleus 0.6326 63.26%
OATP2B1 inhibitior - 0.8559 85.59%
OATP1B1 inhibitior + 0.9288 92.88%
OATP1B3 inhibitior + 0.9322 93.22%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.8552 85.52%
P-glycoprotein inhibitior - 0.5489 54.89%
P-glycoprotein substrate - 0.7475 74.75%
CYP3A4 substrate - 0.5000 50.00%
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 - 0.8682 86.82%
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 - 0.8137 81.37%
Skin irritation + 0.8426 84.26%
Skin corrosion - 0.9833 98.33%
Ames mutagenesis - 0.7254 72.54%
Human Ether-a-go-go-Related Gene inhibition + 0.6848 68.48%
Micronuclear - 1.0000 100.00%
Hepatotoxicity + 0.5125 51.25%
skin sensitisation + 0.9235 92.35%
Respiratory toxicity - 0.5889 58.89%
Reproductive toxicity - 0.9778 97.78%
Mitochondrial toxicity - 0.6750 67.50%
Nephrotoxicity - 0.6584 65.84%
Acute Oral Toxicity (c) III 0.9077 90.77%
Estrogen receptor binding + 0.5689 56.89%
Androgen receptor binding - 0.7879 78.79%
Thyroid receptor binding + 0.6197 61.97%
Glucocorticoid receptor binding + 0.5937 59.37%
Aromatase binding - 0.5718 57.18%
PPAR gamma + 0.6187 61.87%
Honey bee toxicity - 0.8316 83.16%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity - 0.6800 68.00%
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 91.56% 98.95%
CHEMBL2885 P07451 Carbonic anhydrase III 91.13% 87.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.72% 96.09%
CHEMBL203 P00533 Epidermal growth factor receptor erbB1 88.19% 97.34%
CHEMBL3401 O75469 Pregnane X receptor 85.76% 94.73%
CHEMBL3892 Q99500 Sphingosine 1-phosphate receptor Edg-3 84.06% 97.29%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.50% 93.56%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 82.31% 94.45%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.18% 91.11%
CHEMBL283 P08254 Matrix metalloproteinase 3 80.83% 97.29%

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 398805
LOTUS LTS0256054
wikiData Q104945459