Lansiumamide A

Details

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Internal ID aa16c914-20bf-438a-b6bb-7ba669fcfa65
Taxonomy Phenylpropanoids and polyketides > Cinnamic acids and derivatives > Cinnamic acid amides
IUPAC Name (E)-3-phenyl-N-[(Z)-2-phenylethenyl]prop-2-enamide
SMILES (Canonical) C1=CC=C(C=C1)C=CC(=O)NC=CC2=CC=CC=C2
SMILES (Isomeric) C1=CC=C(C=C1)/C=C/C(=O)N/C=C\C2=CC=CC=C2
InChI InChI=1S/C17H15NO/c19-17(12-11-15-7-3-1-4-8-15)18-14-13-16-9-5-2-6-10-16/h1-14H,(H,18,19)/b12-11+,14-13-
InChI Key DAZFHZLCFLDNPG-WCYNZMGESA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H15NO
Molecular Weight 249.31 g/mol
Exact Mass 249.115364102 g/mol
Topological Polar Surface Area (TPSA) 29.10 Ų
XlogP 3.60
Atomic LogP (AlogP) 3.49
H-Bond Acceptor 1
H-Bond Donor 1
Rotatable Bonds 4

Synonyms

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N-cis-Styrylcinnamamide
CHEBI:180742
DTXSID401219979
121817-36-5
(E)-3-phenyl-N-[(Z)-2-phenylethenyl]prop-2-enamide
(2E)-3-Phenyl-N-[(1Z)-2-phenylethenyl]-2-propenamide
(2E)-3-phenyl-N-[(Z)-2-phenylethenyl]prop-2-enamide

2D Structure

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2D Structure of Lansiumamide A

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9964 99.64%
Caco-2 + 0.8963 89.63%
Blood Brain Barrier + 0.9750 97.50%
Human oral bioavailability + 0.5714 57.14%
Subcellular localzation Plasma membrane 0.4523 45.23%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9467 94.67%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior + 0.5567 55.67%
P-glycoprotein inhibitior - 0.9471 94.71%
P-glycoprotein substrate - 0.9720 97.20%
CYP3A4 substrate - 0.7085 70.85%
CYP2C9 substrate - 0.8005 80.05%
CYP2D6 substrate - 0.8444 84.44%
CYP3A4 inhibition - 0.7857 78.57%
CYP2C9 inhibition - 0.5252 52.52%
CYP2C19 inhibition + 0.6444 64.44%
CYP2D6 inhibition - 0.8623 86.23%
CYP1A2 inhibition + 0.5723 57.23%
CYP2C8 inhibition - 0.7023 70.23%
CYP inhibitory promiscuity + 0.7030 70.30%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.5400 54.00%
Carcinogenicity (trinary) Danger 0.4815 48.15%
Eye corrosion - 0.7175 71.75%
Eye irritation + 0.9533 95.33%
Skin irritation - 0.7332 73.32%
Skin corrosion - 0.9900 99.00%
Ames mutagenesis - 0.6400 64.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5706 57.06%
Micronuclear + 0.5700 57.00%
Hepatotoxicity - 0.5652 56.52%
skin sensitisation - 0.7185 71.85%
Respiratory toxicity - 0.7000 70.00%
Reproductive toxicity - 0.5889 58.89%
Mitochondrial toxicity + 0.6250 62.50%
Nephrotoxicity - 0.5709 57.09%
Acute Oral Toxicity (c) III 0.8816 88.16%
Estrogen receptor binding + 0.9210 92.10%
Androgen receptor binding + 0.6558 65.58%
Thyroid receptor binding - 0.6696 66.96%
Glucocorticoid receptor binding - 0.6086 60.86%
Aromatase binding + 0.8782 87.82%
PPAR gamma - 0.5765 57.65%
Honey bee toxicity - 0.9366 93.66%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity - 0.6000 60.00%
Fish aquatic toxicity + 0.8955 89.55%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.63% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.50% 91.11%
CHEMBL221 P23219 Cyclooxygenase-1 87.92% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 87.29% 86.33%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.72% 96.00%
CHEMBL5028 O14672 ADAM10 81.29% 97.50%

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.
Clausena lansium

Cross-Links

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PubChem 11414008
LOTUS LTS0102230
wikiData Q76421502