Cyclopentane, (1-phenyl-1-trimethylsilylmethylene,-

Details

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Internal ID 18517249-d77f-4ab1-a93e-389514dea948
Taxonomy Benzenoids > Benzene and substituted derivatives
IUPAC Name [cyclopentylidene(phenyl)methyl]-trimethylsilane
SMILES (Canonical) C[Si](C)(C)C(=C1CCCC1)C2=CC=CC=C2
SMILES (Isomeric) C[Si](C)(C)C(=C1CCCC1)C2=CC=CC=C2
InChI InChI=1S/C15H22Si/c1-16(2,3)15(14-11-7-8-12-14)13-9-5-4-6-10-13/h4-6,9-10H,7-8,11-12H2,1-3H3
InChI Key VYENQJYFQHBPSI-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C15H22Si
Molecular Weight 230.42 g/mol
Exact Mass 230.149077236 g/mol
Topological Polar Surface Area (TPSA) 0.00 Ų
XlogP 0.00
Atomic LogP (AlogP) 4.89
H-Bond Acceptor 0
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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VYENQJYFQHBPSI-UHFFFAOYSA-N
[Cyclopentylidene(phenyl)methyl](trimethyl)silane #

2D Structure

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2D Structure of Cyclopentane, (1-phenyl-1-trimethylsilylmethylene,-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8333 83.33%
Caco-2 + 0.9671 96.71%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.8429 84.29%
Subcellular localzation Lysosomes 0.4334 43.34%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9649 96.49%
OATP1B3 inhibitior + 0.9386 93.86%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8568 85.68%
P-glycoprotein inhibitior - 0.9770 97.70%
P-glycoprotein substrate - 0.9784 97.84%
CYP3A4 substrate - 0.7552 75.52%
CYP2C9 substrate - 0.6624 66.24%
CYP2D6 substrate + 0.3460 34.60%
CYP3A4 inhibition - 0.8234 82.34%
CYP2C9 inhibition - 0.8257 82.57%
CYP2C19 inhibition - 0.7832 78.32%
CYP2D6 inhibition - 0.9015 90.15%
CYP1A2 inhibition - 0.6765 67.65%
CYP2C8 inhibition - 0.7460 74.60%
CYP inhibitory promiscuity - 0.6169 61.69%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7120 71.20%
Carcinogenicity (trinary) Non-required 0.4765 47.65%
Eye corrosion - 0.6410 64.10%
Eye irritation + 0.8120 81.20%
Skin irritation - 0.5827 58.27%
Skin corrosion - 0.9264 92.64%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.3940 39.40%
Micronuclear - 0.8400 84.00%
Hepatotoxicity + 0.6303 63.03%
skin sensitisation + 0.6138 61.38%
Respiratory toxicity + 0.5667 56.67%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.6786 67.86%
Nephrotoxicity - 0.7485 74.85%
Acute Oral Toxicity (c) III 0.7644 76.44%
Estrogen receptor binding - 0.7956 79.56%
Androgen receptor binding - 0.6641 66.41%
Thyroid receptor binding - 0.7275 72.75%
Glucocorticoid receptor binding - 0.8527 85.27%
Aromatase binding - 0.8500 85.00%
PPAR gamma - 0.5975 59.75%
Honey bee toxicity - 0.9920 99.20%
Biodegradation - 0.7500 75.00%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity + 0.9707 97.07%

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 93.29% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.67% 95.56%
CHEMBL1293294 P51151 Ras-related protein Rab-9A 90.60% 87.67%
CHEMBL1951 P21397 Monoamine oxidase A 85.60% 91.49%
CHEMBL2581 P07339 Cathepsin D 84.88% 98.95%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 84.30% 91.11%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 83.39% 95.50%
CHEMBL3401 O75469 Pregnane X receptor 82.22% 94.73%
CHEMBL3902 P09211 Glutathione S-transferase Pi 80.28% 93.81%

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.
Curcuma kwangsiensis
Curcuma phaeocaulis
Curcuma wenyujin
Curcuma zedoaria

Cross-Links

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PubChem 611945
NPASS NPC27396