(E)-4-(2-methylphenyl)but-3-enamide

Details

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Internal ID f5a35471-dafc-4eb0-8276-3e1a272be29a
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name (E)-4-(2-methylphenyl)but-3-enamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C11H13NO/c1-9-5-2-3-6-10(9)7-4-8-11(12)13/h2-7H,8H2,1H3,(H2,12,13)/b7-4+
InChI Key MZTAQNGQEGPSFO-QPJJXVBHSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C11H13NO
Molecular Weight 175.23 g/mol
Exact Mass 175.099714038 g/mol
Topological Polar Surface Area (TPSA) 43.10 Ų
XlogP 1.70
Atomic LogP (AlogP) 1.88
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-4-(2-methylphenyl)but-3-enamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9561 95.61%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.4386 43.86%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9297 92.97%
OATP1B3 inhibitior + 0.9564 95.64%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.7220 72.20%
P-glycoprotein inhibitior - 0.9784 97.84%
P-glycoprotein substrate - 0.9275 92.75%
CYP3A4 substrate - 0.6432 64.32%
CYP2C9 substrate - 0.8054 80.54%
CYP2D6 substrate - 0.8366 83.66%
CYP3A4 inhibition - 0.7802 78.02%
CYP2C9 inhibition - 0.7678 76.78%
CYP2C19 inhibition + 0.5452 54.52%
CYP2D6 inhibition - 0.8397 83.97%
CYP1A2 inhibition + 0.5089 50.89%
CYP2C8 inhibition - 0.9276 92.76%
CYP inhibitory promiscuity - 0.6323 63.23%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6000 60.00%
Carcinogenicity (trinary) Non-required 0.7156 71.56%
Eye corrosion - 0.9252 92.52%
Eye irritation + 0.9542 95.42%
Skin irritation - 0.6919 69.19%
Skin corrosion - 0.9587 95.87%
Ames mutagenesis - 0.5900 59.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7175 71.75%
Micronuclear + 0.6000 60.00%
Hepatotoxicity + 0.5586 55.86%
skin sensitisation - 0.7456 74.56%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity - 0.7774 77.74%
Acute Oral Toxicity (c) III 0.8102 81.02%
Estrogen receptor binding - 0.7963 79.63%
Androgen receptor binding - 0.8595 85.95%
Thyroid receptor binding - 0.7923 79.23%
Glucocorticoid receptor binding - 0.5949 59.49%
Aromatase binding + 0.5381 53.81%
PPAR gamma - 0.7845 78.45%
Honey bee toxicity - 0.9927 99.27%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.6195 61.95%

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
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 94.83% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.41% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.58% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 89.09% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.86% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 88.46% 94.73%
CHEMBL2581 P07339 Cathepsin D 87.57% 98.95%
CHEMBL230 P35354 Cyclooxygenase-2 85.50% 89.63%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.92% 96.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.20% 99.17%

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 68613376
LOTUS LTS0070156
wikiData Q105176028