(E)-4-phenylbut-3-enamide

Details

Top
Internal ID 612d6354-719a-43d7-b9a7-00fd5bc8249e
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name (E)-4-phenylbut-3-enamide
SMILES (Canonical) C1=CC=C(C=C1)C=CCC(=O)N
SMILES (Isomeric) C1=CC=C(C=C1)/C=C/CC(=O)N
InChI InChI=1S/C10H11NO/c11-10(12)8-4-7-9-5-2-1-3-6-9/h1-7H,8H2,(H2,11,12)/b7-4+
InChI Key MLLQDAULRWHYJT-QPJJXVBHSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

Top
Molecular Formula C10H11NO
Molecular Weight 161.20 g/mol
Exact Mass 161.084063974 g/mol
Topological Polar Surface Area (TPSA) 43.10 Ų
XlogP 1.60
Atomic LogP (AlogP) 1.58
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 3

Synonyms

Top
MLLQDAULRWHYJT-QPJJXVBHSA-N

2D Structure

Top
2D Structure of (E)-4-phenylbut-3-enamide

3D Structure

Top

ADMET Properties (via admetSAR 2)

Top
Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 1.0000 100.00%
Caco-2 + 0.9520 95.20%
Blood Brain Barrier + 1.0000 100.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Lysosomes 0.4444 44.44%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9347 93.47%
OATP1B3 inhibitior + 0.9547 95.47%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8500 85.00%
BSEP inhibitior - 0.8762 87.62%
P-glycoprotein inhibitior - 0.9847 98.47%
P-glycoprotein substrate - 0.9754 97.54%
CYP3A4 substrate - 0.7595 75.95%
CYP2C9 substrate - 0.6171 61.71%
CYP2D6 substrate - 0.8066 80.66%
CYP3A4 inhibition - 0.8505 85.05%
CYP2C9 inhibition - 0.7440 74.40%
CYP2C19 inhibition - 0.6038 60.38%
CYP2D6 inhibition - 0.8183 81.83%
CYP1A2 inhibition + 0.5101 51.01%
CYP2C8 inhibition - 0.9073 90.73%
CYP inhibitory promiscuity - 0.7051 70.51%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Non-required 0.6476 64.76%
Eye corrosion - 0.8177 81.77%
Eye irritation + 0.9007 90.07%
Skin irritation - 0.6305 63.05%
Skin corrosion - 0.8781 87.81%
Ames mutagenesis - 0.7240 72.40%
Human Ether-a-go-go-Related Gene inhibition - 0.8355 83.55%
Micronuclear + 0.6100 61.00%
Hepatotoxicity + 0.5034 50.34%
skin sensitisation - 0.8034 80.34%
Respiratory toxicity + 0.5111 51.11%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity + 0.5125 51.25%
Nephrotoxicity - 0.7650 76.50%
Acute Oral Toxicity (c) III 0.8480 84.80%
Estrogen receptor binding - 0.8370 83.70%
Androgen receptor binding - 0.6567 65.67%
Thyroid receptor binding - 0.8354 83.54%
Glucocorticoid receptor binding - 0.5819 58.19%
Aromatase binding + 0.6342 63.42%
PPAR gamma - 0.7488 74.88%
Honey bee toxicity - 0.9841 98.41%
Biodegradation - 0.7000 70.00%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.8078 80.78%

Targets

Top

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 95.37% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.52% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 90.51% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 90.39% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.04% 95.56%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.63% 99.17%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 83.43% 96.95%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 81.94% 94.62%

Plants that contains it

Top
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.
There are no matching plants.

Cross-Links

Top
PubChem 14386648
LOTUS LTS0164368
wikiData Q105166817