N-(2-methylsulfanylethenyl)-3-phenylprop-2-enamide

Details

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Internal ID dfec9d1e-e89f-4ebe-9b4e-71d5d7aa8c8e
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name N-(2-methylsulfanylethenyl)-3-phenylprop-2-enamide
SMILES (Canonical) CSC=CNC(=O)C=CC1=CC=CC=C1
SMILES (Isomeric) CSC=CNC(=O)C=CC1=CC=CC=C1
InChI InChI=1S/C12H13NOS/c1-15-10-9-13-12(14)8-7-11-5-3-2-4-6-11/h2-10H,1H3,(H,13,14)
InChI Key UZYLTVKDCGMZIY-UHFFFAOYSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C12H13NOS
Molecular Weight 219.30 g/mol
Exact Mass 219.07178521 g/mol
Topological Polar Surface Area (TPSA) 54.40 Ų
XlogP 2.30
Atomic LogP (AlogP) 2.65
H-Bond Acceptor 2
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of N-(2-methylsulfanylethenyl)-3-phenylprop-2-enamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9387 93.87%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5429 54.29%
Subcellular localzation Mitochondria 0.3624 36.24%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9214 92.14%
OATP1B3 inhibitior + 0.9597 95.97%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.5000 50.00%
P-glycoprotein inhibitior - 0.9613 96.13%
P-glycoprotein substrate - 0.9112 91.12%
CYP3A4 substrate - 0.6374 63.74%
CYP2C9 substrate - 0.8004 80.04%
CYP2D6 substrate - 0.8449 84.49%
CYP3A4 inhibition - 0.8780 87.80%
CYP2C9 inhibition - 0.7875 78.75%
CYP2C19 inhibition - 0.7681 76.81%
CYP2D6 inhibition - 0.9400 94.00%
CYP1A2 inhibition - 0.5848 58.48%
CYP2C8 inhibition - 0.7127 71.27%
CYP inhibitory promiscuity - 0.6780 67.80%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6520 65.20%
Carcinogenicity (trinary) Non-required 0.5945 59.45%
Eye corrosion + 0.5285 52.85%
Eye irritation + 0.7822 78.22%
Skin irritation - 0.6689 66.89%
Skin corrosion - 0.9693 96.93%
Ames mutagenesis - 0.7300 73.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6543 65.43%
Micronuclear + 0.6000 60.00%
Hepatotoxicity - 0.5277 52.77%
skin sensitisation - 0.7341 73.41%
Respiratory toxicity - 0.6333 63.33%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity + 0.5333 53.33%
Acute Oral Toxicity (c) III 0.9308 93.08%
Estrogen receptor binding + 0.6765 67.65%
Androgen receptor binding - 0.4869 48.69%
Thyroid receptor binding - 0.5816 58.16%
Glucocorticoid receptor binding - 0.6481 64.81%
Aromatase binding + 0.8829 88.29%
PPAR gamma - 0.5785 57.85%
Honey bee toxicity - 0.9109 91.09%
Biodegradation - 0.8000 80.00%
Crustacea aquatic toxicity - 0.5500 55.00%
Fish aquatic toxicity - 0.4141 41.41%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.12% 95.56%
CHEMBL221 P23219 Cyclooxygenase-1 90.26% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 89.63% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.74% 91.11%
CHEMBL2581 P07339 Cathepsin D 86.25% 98.95%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 86.16% 96.00%
CHEMBL5028 O14672 ADAM10 84.52% 97.50%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.13% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 82.47% 94.73%

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.
Glycosmis mauritiana

Cross-Links

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PubChem 163020140
LOTUS LTS0194437
wikiData Q105282538