(E)-N-methyl-N-(2-methylsulfanylethyl)-3-phenylprop-2-enamide

Details

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Internal ID 1aa739f3-90d9-4412-a4a2-872bb3357b8a
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives
IUPAC Name (E)-N-methyl-N-(2-methylsulfanylethyl)-3-phenylprop-2-enamide
SMILES (Canonical) CN(CCSC)C(=O)C=CC1=CC=CC=C1
SMILES (Isomeric) CN(CCSC)C(=O)/C=C/C1=CC=CC=C1
InChI InChI=1S/C13H17NOS/c1-14(10-11-16-2)13(15)9-8-12-6-4-3-5-7-12/h3-9H,10-11H2,1-2H3/b9-8+
InChI Key XFYGGQGDUBKTFT-CMDGGOBGSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C13H17NOS
Molecular Weight 235.35 g/mol
Exact Mass 235.10308534 g/mol
Topological Polar Surface Area (TPSA) 45.60 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.52
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-N-methyl-N-(2-methylsulfanylethyl)-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 + 0.9770 97.70%
Caco-2 + 0.9611 96.11%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability - 0.5000 50.00%
Subcellular localzation Plasma membrane 0.3541 35.41%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8637 86.37%
OATP1B3 inhibitior + 0.9482 94.82%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.5000 50.00%
BSEP inhibitior - 0.6400 64.00%
P-glycoprotein inhibitior - 0.9739 97.39%
P-glycoprotein substrate - 0.8861 88.61%
CYP3A4 substrate - 0.5343 53.43%
CYP2C9 substrate + 0.6000 60.00%
CYP2D6 substrate - 0.8547 85.47%
CYP3A4 inhibition - 0.9775 97.75%
CYP2C9 inhibition - 0.9071 90.71%
CYP2C19 inhibition - 0.7959 79.59%
CYP2D6 inhibition - 0.9145 91.45%
CYP1A2 inhibition - 0.5431 54.31%
CYP2C8 inhibition - 0.7440 74.40%
CYP inhibitory promiscuity - 0.9144 91.44%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8200 82.00%
Carcinogenicity (trinary) Non-required 0.7499 74.99%
Eye corrosion - 0.9509 95.09%
Eye irritation - 0.7068 70.68%
Skin irritation + 0.6181 61.81%
Skin corrosion - 0.7053 70.53%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition + 0.7108 71.08%
Micronuclear - 0.6300 63.00%
Hepatotoxicity - 0.7573 75.73%
skin sensitisation - 0.7167 71.67%
Respiratory toxicity + 0.7000 70.00%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity + 0.7875 78.75%
Nephrotoxicity - 0.6900 69.00%
Acute Oral Toxicity (c) III 0.6209 62.09%
Estrogen receptor binding - 0.7374 73.74%
Androgen receptor binding - 0.5472 54.72%
Thyroid receptor binding + 0.5902 59.02%
Glucocorticoid receptor binding - 0.7738 77.38%
Aromatase binding + 0.7888 78.88%
PPAR gamma - 0.7669 76.69%
Honey bee toxicity - 0.9420 94.20%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.5800 58.00%
Fish aquatic toxicity - 0.3654 36.54%

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
CHEMBL2581 P07339 Cathepsin D 94.91% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.24% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.43% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 91.40% 96.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 89.40% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 89.20% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.37% 86.33%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.42% 99.17%
CHEMBL3401 O75469 Pregnane X receptor 82.23% 94.73%
CHEMBL2288 Q13526 Peptidyl-prolyl cis-trans isomerase NIMA-interacting 1 81.80% 91.71%

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.
Euphorbia hirta
Glycosmis cyanocarpa

Cross-Links

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PubChem 21762182
NPASS NPC79653
LOTUS LTS0071918
wikiData Q105327383