1-Trimethylsiloxy-3,7,11,15-tetramethyl-2-hexadecene

Details

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Internal ID 9194fdf5-8d92-46c7-9a38-739d0fd29354
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Diterpenoids > Acyclic diterpenoids
IUPAC Name trimethyl-[(E)-3,7,11,15-tetramethylhexadec-2-enoxy]silane
SMILES (Canonical) CC(C)CCCC(C)CCCC(C)CCCC(=CCO[Si](C)(C)C)C
SMILES (Isomeric) CC(C)CCCC(C)CCCC(C)CCC/C(=C/CO[Si](C)(C)C)/C
InChI InChI=1S/C23H48OSi/c1-20(2)12-9-13-21(3)14-10-15-22(4)16-11-17-23(5)18-19-24-25(6,7)8/h18,20-22H,9-17,19H2,1-8H3/b23-18+
InChI Key CKZQZHKPLHXPCT-PTGBLXJZSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C23H48OSi
Molecular Weight 368.70 g/mol
Exact Mass 368.347442685 g/mol
Topological Polar Surface Area (TPSA) 9.20 Ų
XlogP 0.00
Atomic LogP (AlogP) 8.22
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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Phytol, TMS derivative
1-Trimethylsiloxy-3,7,11,15-tetramethyl-2-hexadecene
CKZQZHKPLHXPCT-PTGBLXJZSA-N
[(3,7,11,15-Tetramethyl-2-hexadecenyl)oxy]trimethylsilane
(2E)-3,7,11,15-Tetramethyl-2-hexadecenyl trimethylsilyl ether #
57397-39-4

2D Structure

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2D Structure of 1-Trimethylsiloxy-3,7,11,15-tetramethyl-2-hexadecene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8587 85.87%
Caco-2 + 0.7043 70.43%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability - 0.5286 52.86%
Subcellular localzation Lysosomes 0.4330 43.30%
OATP2B1 inhibitior - 0.8514 85.14%
OATP1B1 inhibitior + 0.9485 94.85%
OATP1B3 inhibitior + 0.9308 93.08%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.5764 57.64%
P-glycoprotein inhibitior - 0.7553 75.53%
P-glycoprotein substrate - 0.8121 81.21%
CYP3A4 substrate - 0.5326 53.26%
CYP2C9 substrate - 0.6000 60.00%
CYP2D6 substrate - 0.7344 73.44%
CYP3A4 inhibition - 0.9575 95.75%
CYP2C9 inhibition - 0.8677 86.77%
CYP2C19 inhibition - 0.8164 81.64%
CYP2D6 inhibition - 0.9225 92.25%
CYP1A2 inhibition - 0.8042 80.42%
CYP2C8 inhibition - 0.8946 89.46%
CYP inhibitory promiscuity - 0.8950 89.50%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6100 61.00%
Carcinogenicity (trinary) Non-required 0.5516 55.16%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.5384 53.84%
Skin irritation - 0.6243 62.43%
Skin corrosion - 0.9079 90.79%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5270 52.70%
Micronuclear - 0.8300 83.00%
Hepatotoxicity - 0.5821 58.21%
skin sensitisation - 0.5425 54.25%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity - 0.9034 90.34%
Mitochondrial toxicity - 0.7625 76.25%
Nephrotoxicity + 0.4795 47.95%
Acute Oral Toxicity (c) III 0.6957 69.57%
Estrogen receptor binding - 0.6447 64.47%
Androgen receptor binding - 0.8241 82.41%
Thyroid receptor binding + 0.6037 60.37%
Glucocorticoid receptor binding - 0.6063 60.63%
Aromatase binding - 0.5807 58.07%
PPAR gamma - 0.5263 52.63%
Honey bee toxicity - 0.9360 93.60%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity + 0.9528 95.28%

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
CHEMBL2039 P27338 Monoamine oxidase B 95.16% 92.51%
CHEMBL3401 O75469 Pregnane X receptor 90.35% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.55% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.30% 96.09%
CHEMBL2581 P07339 Cathepsin D 87.35% 98.95%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 84.90% 94.45%
CHEMBL1907 P15144 Aminopeptidase N 84.53% 93.31%
CHEMBL3359 P21462 Formyl peptide receptor 1 80.74% 93.56%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Artemisia annua
Artemisia carvifolia

Cross-Links

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PubChem 5372684
NPASS NPC11397