Hexadecanoic acid, trimethylsilyl ester

Details

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Internal ID 5aa682f8-1ac5-4e78-85c8-59cb3f5af1ed
Taxonomy Organometallic compounds > Organometalloid compounds > Organosilicon compounds > Trimethylsilyl esters
IUPAC Name trimethylsilyl hexadecanoate
SMILES (Canonical) CCCCCCCCCCCCCCCC(=O)O[Si](C)(C)C
SMILES (Isomeric) CCCCCCCCCCCCCCCC(=O)O[Si](C)(C)C
InChI InChI=1S/C19H40O2Si/c1-5-6-7-8-9-10-11-12-13-14-15-16-17-18-19(20)21-22(2,3)4/h5-18H2,1-4H3
InChI Key HKNNSWCACQFVIK-UHFFFAOYSA-N
Popularity 12 references in papers

Physical and Chemical Properties

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Molecular Formula C19H40O2Si
Molecular Weight 328.60 g/mol
Exact Mass 328.27975705 g/mol
Topological Polar Surface Area (TPSA) 26.30 Ų
XlogP 0.00
Atomic LogP (AlogP) 6.85
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 15

Synonyms

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Trimethylsilyl palmitate
Palmitic acid, trimethylsilyl ester
55520-89-3
trimethylsilyl hexadecanoate
Palmitic acid, TMS
palmitic acid tms ester
Hexadecanoic acid, TMS
Trimethylsilyl palmitate #
Hexadecanoic acid, TMS ester
Palmitic Acid, TMS derivative
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of Hexadecanoic acid, trimethylsilyl ester

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8967 89.67%
Caco-2 + 0.7679 76.79%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability - 0.6000 60.00%
Subcellular localzation Plasma membrane 0.4271 42.71%
OATP2B1 inhibitior - 0.8490 84.90%
OATP1B1 inhibitior + 0.9323 93.23%
OATP1B3 inhibitior + 0.9309 93.09%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.6040 60.40%
P-glycoprotein inhibitior - 0.8071 80.71%
P-glycoprotein substrate - 0.9480 94.80%
CYP3A4 substrate - 0.6202 62.02%
CYP2C9 substrate - 0.6061 60.61%
CYP2D6 substrate - 0.8514 85.14%
CYP3A4 inhibition - 0.9544 95.44%
CYP2C9 inhibition - 0.8582 85.82%
CYP2C19 inhibition - 0.8526 85.26%
CYP2D6 inhibition - 0.9192 91.92%
CYP1A2 inhibition - 0.7064 70.64%
CYP2C8 inhibition - 0.8472 84.72%
CYP inhibitory promiscuity - 0.9611 96.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5100 51.00%
Carcinogenicity (trinary) Non-required 0.6549 65.49%
Eye corrosion + 0.8632 86.32%
Eye irritation + 0.9581 95.81%
Skin irritation - 0.8472 84.72%
Skin corrosion - 0.9636 96.36%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5697 56.97%
Micronuclear - 0.8500 85.00%
Hepatotoxicity + 0.6339 63.39%
skin sensitisation - 0.7095 70.95%
Respiratory toxicity - 0.8556 85.56%
Reproductive toxicity - 0.8531 85.31%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7010 70.10%
Acute Oral Toxicity (c) III 0.6239 62.39%
Estrogen receptor binding - 0.7164 71.64%
Androgen receptor binding - 0.8823 88.23%
Thyroid receptor binding - 0.5539 55.39%
Glucocorticoid receptor binding - 0.7950 79.50%
Aromatase binding - 0.6793 67.93%
PPAR gamma + 0.5207 52.07%
Honey bee toxicity - 0.9936 99.36%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.8268 82.68%
Fish aquatic toxicity + 0.9189 91.89%

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
CHEMBL3060 Q9Y345 Glycine transporter 2 96.48% 99.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 95.11% 96.09%
CHEMBL230 P35354 Cyclooxygenase-2 93.39% 89.63%
CHEMBL2581 P07339 Cathepsin D 89.36% 98.95%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 89.25% 92.08%
CHEMBL2265 P23141 Acyl coenzyme A:cholesterol acyltransferase 86.27% 85.94%
CHEMBL2955 O95136 Sphingosine 1-phosphate receptor Edg-5 83.65% 92.86%
CHEMBL5043 Q6P179 Endoplasmic reticulum aminopeptidase 2 83.10% 91.81%
CHEMBL2274 Q9H228 Sphingosine 1-phosphate receptor Edg-8 82.28% 100.00%
CHEMBL5255 O00206 Toll-like receptor 4 82.21% 92.50%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.82% 86.33%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.57% 99.23%

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
Polygonatum odoratum

Cross-Links

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PubChem 521638
NPASS NPC86807