(31-Methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,10,12,14,16,18,20,22,24,26,28-undecaen-2-yl)oxy-trimethylsilane

Details

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Internal ID 237fb3af-bb96-4a30-870f-d180b98f2ae6
Taxonomy Lipids and lipid-like molecules > Prenol lipids > Tetraterpenoids > Carotenoids > Xanthophylls
IUPAC Name (31-methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,10,12,14,16,18,20,22,24,26,28-undecaen-2-yl)oxy-trimethylsilane
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C44H70O2Si/c1-37(25-17-27-39(3)29-19-31-41(5)33-21-35-43(7,8)45-11)23-15-16-24-38(2)26-18-28-40(4)30-20-32-42(6)34-22-36-44(9,10)46-47(12,13)14/h15-19,21,23-29,31-33H,20,22,30,34-36H2,1-14H3
InChI Key AEPCBQRPKAZQMS-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C44H70O2Si
Molecular Weight 659.10 g/mol
Exact Mass 658.51450801 g/mol
Topological Polar Surface Area (TPSA) 18.50 Ų
XlogP 0.00
Atomic LogP (AlogP) 13.84
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 21

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (31-Methoxy-2,6,10,14,19,23,27,31-octamethyldotriaconta-6,10,12,14,16,18,20,22,24,26,28-undecaen-2-yl)oxy-trimethylsilane

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9223 92.23%
Caco-2 - 0.8036 80.36%
Blood Brain Barrier + 0.8750 87.50%
Human oral bioavailability - 0.5571 55.71%
Subcellular localzation Mitochondria 0.4634 46.34%
OATP2B1 inhibitior + 0.5705 57.05%
OATP1B1 inhibitior + 0.8332 83.32%
OATP1B3 inhibitior + 0.9317 93.17%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior + 0.9971 99.71%
P-glycoprotein inhibitior + 0.8209 82.09%
P-glycoprotein substrate - 0.6002 60.02%
CYP3A4 substrate + 0.6475 64.75%
CYP2C9 substrate - 0.8027 80.27%
CYP2D6 substrate - 0.7638 76.38%
CYP3A4 inhibition - 0.8973 89.73%
CYP2C9 inhibition - 0.8284 82.84%
CYP2C19 inhibition - 0.7377 73.77%
CYP2D6 inhibition - 0.9139 91.39%
CYP1A2 inhibition - 0.7463 74.63%
CYP2C8 inhibition + 0.4860 48.60%
CYP inhibitory promiscuity - 0.8711 87.11%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5000 50.00%
Carcinogenicity (trinary) Non-required 0.5713 57.13%
Eye corrosion - 0.7047 70.47%
Eye irritation - 0.9004 90.04%
Skin irritation - 0.6693 66.93%
Skin corrosion - 0.9695 96.95%
Ames mutagenesis - 0.6000 60.00%
Human Ether-a-go-go-Related Gene inhibition + 0.9240 92.40%
Micronuclear - 0.8600 86.00%
Hepatotoxicity - 0.6298 62.98%
skin sensitisation + 0.5000 50.00%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity - 0.9556 95.56%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity + 0.6432 64.32%
Acute Oral Toxicity (c) III 0.6053 60.53%
Estrogen receptor binding + 0.8445 84.45%
Androgen receptor binding + 0.6542 65.42%
Thyroid receptor binding + 0.7002 70.02%
Glucocorticoid receptor binding + 0.7038 70.38%
Aromatase binding - 0.5262 52.62%
PPAR gamma + 0.7337 73.37%
Honey bee toxicity - 0.8189 81.89%
Biodegradation - 0.8500 85.00%
Crustacea aquatic toxicity + 0.6500 65.00%
Fish aquatic toxicity + 0.8190 81.90%

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 91.76% 99.17%
CHEMBL2815 P04629 Nerve growth factor receptor Trk-A 90.80% 87.16%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.44% 86.33%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.77% 96.09%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.31% 92.08%
CHEMBL3401 O75469 Pregnane X receptor 87.96% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 82.77% 91.11%
CHEMBL2581 P07339 Cathepsin D 82.55% 98.95%
CHEMBL1293267 Q9HC97 G-protein coupled receptor 35 80.49% 89.34%

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 162965090
LOTUS LTS0235751
wikiData Q104910309