N-(2-Hydroxyethyl)-3-phenyl-2-propenamide

Details

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Internal ID b52b198a-a17b-42f8-8c9c-52f8d634a4df
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid amides
IUPAC Name N-(2-hydroxyethyl)-3-phenylprop-2-enamide
SMILES (Canonical) C1=CC=C(C=C1)C=CC(=O)NCCO
SMILES (Isomeric) C1=CC=C(C=C1)C=CC(=O)NCCO
InChI InChI=1S/C11H13NO2/c13-9-8-12-11(14)7-6-10-4-2-1-3-5-10/h1-7,13H,8-9H2,(H,12,14)
InChI Key OSCTXCOERRNGLW-UHFFFAOYSA-N
Popularity 4 references in papers

Physical and Chemical Properties

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Molecular Formula C11H13NO2
Molecular Weight 191.23 g/mol
Exact Mass 191.094628657 g/mol
Topological Polar Surface Area (TPSA) 49.30 Ų
XlogP 0.90
Atomic LogP (AlogP) 0.81
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 4

Synonyms

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N-(2-Hydroxyethyl)-3-phenylpropenamide
Srilane; Brolitene
N-(2-Hydroxyethyl)-3-phenyl-2-propenamide
NCIOpen2_000059
CBDivE_015640
n-(2-hydroxyethyl) cinnamamide
BCP21372
Q682532

2D Structure

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2D Structure of N-(2-Hydroxyethyl)-3-phenyl-2-propenamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9877 98.77%
Caco-2 + 0.8193 81.93%
Blood Brain Barrier + 0.6500 65.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.5996 59.96%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9301 93.01%
OATP1B3 inhibitior + 0.9507 95.07%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.8669 86.69%
P-glycoprotein inhibitior - 0.9902 99.02%
P-glycoprotein substrate - 0.8488 84.88%
CYP3A4 substrate - 0.7267 72.67%
CYP2C9 substrate - 0.8003 80.03%
CYP2D6 substrate - 0.8474 84.74%
CYP3A4 inhibition - 0.8117 81.17%
CYP2C9 inhibition - 0.7127 71.27%
CYP2C19 inhibition - 0.6716 67.16%
CYP2D6 inhibition - 0.8545 85.45%
CYP1A2 inhibition - 0.6627 66.27%
CYP2C8 inhibition - 0.6618 66.18%
CYP inhibitory promiscuity - 0.9232 92.32%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.7360 73.60%
Eye corrosion - 0.9108 91.08%
Eye irritation + 0.8251 82.51%
Skin irritation - 0.8183 81.83%
Skin corrosion - 0.9657 96.57%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6403 64.03%
Micronuclear - 0.5900 59.00%
Hepatotoxicity - 0.7340 73.40%
skin sensitisation - 0.9014 90.14%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity + 0.6000 60.00%
Nephrotoxicity - 0.6899 68.99%
Acute Oral Toxicity (c) III 0.8392 83.92%
Estrogen receptor binding - 0.7933 79.33%
Androgen receptor binding + 0.5669 56.69%
Thyroid receptor binding - 0.6514 65.14%
Glucocorticoid receptor binding - 0.7312 73.12%
Aromatase binding + 0.8017 80.17%
PPAR gamma - 0.5400 54.00%
Honey bee toxicity - 0.9746 97.46%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6800 68.00%
Fish aquatic toxicity - 0.9367 93.67%

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 94.84% 91.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 92.72% 96.00%
CHEMBL2581 P07339 Cathepsin D 91.74% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 90.21% 95.56%
CHEMBL2563 Q9UQL6 Histone deacetylase 5 87.77% 89.67%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.86% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 85.75% 90.17%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.58% 96.09%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.65% 99.17%
CHEMBL5028 O14672 ADAM10 82.34% 97.50%
CHEMBL5701 Q9H2K8 Serine/threonine-protein kinase TAO3 81.46% 96.67%

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.
Bupleurum falcatum
Bupleurum rotundifolium
Erythrophleum chlorostachys

Cross-Links

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PubChem 23397
LOTUS LTS0134852
wikiData Q105345940