Cinnamic Acid Amide

Details

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Internal ID 18f49c90-573a-495b-b82b-96010f725470
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid amides
IUPAC Name 3-phenylprop-2-enamide
SMILES (Canonical) C1=CC=C(C=C1)C=CC(=O)N
SMILES (Isomeric) C1=CC=C(C=C1)C=CC(=O)N
InChI InChI=1S/C9H9NO/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H2,10,11)
InChI Key APEJMQOBVMLION-UHFFFAOYSA-N
Popularity 92 references in papers

Physical and Chemical Properties

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Molecular Formula C9H9NO
Molecular Weight 147.17 g/mol
Exact Mass 147.068413911 g/mol
Topological Polar Surface Area (TPSA) 43.10 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.19
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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SCHEMBL159753
SCHEMBL1821026
APEJMQOBVMLION-UHFFFAOYSA-N
AKOS022259532
SY006676
FT-0623828
FT-0647828
Q204165

2D Structure

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2D Structure of Cinnamic Acid Amide

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 + 0.9545 95.45%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Lysosomes 0.4109 41.09%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9726 97.26%
OATP1B3 inhibitior + 0.9601 96.01%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.8455 84.55%
P-glycoprotein inhibitior - 0.9890 98.90%
P-glycoprotein substrate - 0.9842 98.42%
CYP3A4 substrate - 0.8030 80.30%
CYP2C9 substrate - 0.6104 61.04%
CYP2D6 substrate - 0.8537 85.37%
CYP3A4 inhibition - 0.9404 94.04%
CYP2C9 inhibition - 0.8270 82.70%
CYP2C19 inhibition - 0.8296 82.96%
CYP2D6 inhibition - 0.9058 90.58%
CYP1A2 inhibition - 0.8163 81.63%
CYP2C8 inhibition - 0.7725 77.25%
CYP inhibitory promiscuity - 0.8726 87.26%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) + 0.5300 53.00%
Carcinogenicity (trinary) Non-required 0.4313 43.13%
Eye corrosion + 0.7486 74.86%
Eye irritation + 0.9891 98.91%
Skin irritation - 0.6173 61.73%
Skin corrosion - 0.9537 95.37%
Ames mutagenesis - 0.9570 95.70%
Human Ether-a-go-go-Related Gene inhibition - 0.7855 78.55%
Micronuclear + 0.6500 65.00%
Hepatotoxicity + 0.5356 53.56%
skin sensitisation - 0.7336 73.36%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity + 0.5625 56.25%
Nephrotoxicity - 0.7198 71.98%
Acute Oral Toxicity (c) III 0.9313 93.13%
Estrogen receptor binding - 0.8278 82.78%
Androgen receptor binding + 0.5556 55.56%
Thyroid receptor binding - 0.7333 73.33%
Glucocorticoid receptor binding - 0.6250 62.50%
Aromatase binding + 0.5644 56.44%
PPAR gamma - 0.7976 79.76%
Honey bee toxicity - 0.9737 97.37%
Biodegradation - 0.6750 67.50%
Crustacea aquatic toxicity - 0.7200 72.00%
Fish aquatic toxicity - 0.5349 53.49%

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 92.36% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.63% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 91.48% 86.33%
CHEMBL221 P23219 Cyclooxygenase-1 90.37% 90.17%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 89.71% 96.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 83.59% 96.09%
CHEMBL2035 P08912 Muscarinic acetylcholine receptor M5 82.84% 94.62%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 82.14% 95.50%

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.
Aristolochia kaempferi
Haplophyllum ramosissimum
Penstemon whippleanus
Reseda luteola
Verbascum pseudonobile

Cross-Links

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PubChem 12135
LOTUS LTS0266580
wikiData Q204165