alpha-(Trimethylsilyl)stilbene

Details

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Internal ID dd7b0d92-3c57-4d0b-a151-8be55d8fb27a
Taxonomy Phenylpropanoids and polyketides > Stilbenes
IUPAC Name [(Z)-1,2-diphenylethenyl]-trimethylsilane
SMILES (Canonical) C[Si](C)(C)C(=CC1=CC=CC=C1)C2=CC=CC=C2
SMILES (Isomeric) C[Si](C)(C)/C(=C\C1=CC=CC=C1)/C2=CC=CC=C2
InChI InChI=1S/C17H20Si/c1-18(2,3)17(16-12-8-5-9-13-16)14-15-10-6-4-7-11-15/h4-14H,1-3H3/b17-14-
InChI Key VGTMRFDPRSLOHW-VKAVYKQESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H20Si
Molecular Weight 252.42 g/mol
Exact Mass 252.133427172 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 5.10
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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[(Z)-1,2-Diphenyleth-1-enyl]-trimethylsilan
[(Z)-1,2-Diphenylethenyl](trimethyl)silane #

2D Structure

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2D Structure of alpha-(Trimethylsilyl)stilbene

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8906 89.06%
Caco-2 + 0.9311 93.11%
Blood Brain Barrier + 0.8000 80.00%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.6218 62.18%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9243 92.43%
OATP1B3 inhibitior + 0.9427 94.27%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9594 95.94%
P-glycoprotein substrate - 0.9786 97.86%
CYP3A4 substrate - 0.7507 75.07%
CYP2C9 substrate - 0.8281 82.81%
CYP2D6 substrate - 0.7220 72.20%
CYP3A4 inhibition - 0.8037 80.37%
CYP2C9 inhibition - 0.7789 77.89%
CYP2C19 inhibition - 0.7287 72.87%
CYP2D6 inhibition - 0.8866 88.66%
CYP1A2 inhibition - 0.6847 68.47%
CYP2C8 inhibition - 0.6904 69.04%
CYP inhibitory promiscuity + 0.6061 60.61%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6120 61.20%
Carcinogenicity (trinary) Non-required 0.5015 50.15%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.8689 86.89%
Skin irritation - 0.6853 68.53%
Skin corrosion - 0.8998 89.98%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.6969 69.69%
Micronuclear - 0.7941 79.41%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.7664 76.64%
Respiratory toxicity - 0.8111 81.11%
Reproductive toxicity - 0.5667 56.67%
Mitochondrial toxicity - 0.7496 74.96%
Nephrotoxicity + 0.5071 50.71%
Acute Oral Toxicity (c) III 0.6810 68.10%
Estrogen receptor binding + 0.8290 82.90%
Androgen receptor binding + 0.6674 66.74%
Thyroid receptor binding - 0.6326 63.26%
Glucocorticoid receptor binding - 0.7752 77.52%
Aromatase binding + 0.8575 85.75%
PPAR gamma + 0.6047 60.47%
Honey bee toxicity - 0.9846 98.46%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity + 0.6800 68.00%
Fish aquatic toxicity + 0.9884 98.84%

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
CHEMBL1293249 Q13887 Kruppel-like factor 5 94.83% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 91.08% 94.73%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.47% 95.56%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 89.52% 94.62%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 88.09% 87.67%
CHEMBL1951 P21397 Monoamine oxidase A 87.01% 91.49%
CHEMBL221 P23219 Cyclooxygenase-1 82.86% 90.17%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.54% 93.81%
CHEMBL1821 P08173 Muscarinic acetylcholine receptor M4 80.33% 94.08%

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.
Conioselinum anthriscoides
Conioselinum officinale

Cross-Links

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PubChem 5372072
NPASS NPC161952