(E)-N-(2-hydroxy-5-oxocyclopenten-1-yl)-5-(2-methylphenyl)pent-4-enamide

Details

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Internal ID 1cc1f62c-ed6d-4a3e-b304-1e0bc20c5684
Taxonomy Benzenoids > Benzene and substituted derivatives > Styrenes
IUPAC Name (E)-N-(2-hydroxy-5-oxocyclopenten-1-yl)-5-(2-methylphenyl)pent-4-enamide
SMILES (Canonical) CC1=CC=CC=C1C=CCCC(=O)NC2=C(CCC2=O)O
SMILES (Isomeric) CC1=CC=CC=C1/C=C/CCC(=O)NC2=C(CCC2=O)O
InChI InChI=1S/C17H19NO3/c1-12-6-2-3-7-13(12)8-4-5-9-16(21)18-17-14(19)10-11-15(17)20/h2-4,6-8,19H,5,9-11H2,1H3,(H,18,21)/b8-4+
InChI Key YABYTVNSTSAIEE-XBXARRHUSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C17H19NO3
Molecular Weight 285.34 g/mol
Exact Mass 285.13649347 g/mol
Topological Polar Surface Area (TPSA) 66.40 Ų
XlogP 2.20
Atomic LogP (AlogP) 3.04
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 5

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of (E)-N-(2-hydroxy-5-oxocyclopenten-1-yl)-5-(2-methylphenyl)pent-4-enamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9614 96.14%
Caco-2 - 0.6219 62.19%
Blood Brain Barrier + 0.5250 52.50%
Human oral bioavailability + 0.5286 52.86%
Subcellular localzation Mitochondria 0.8697 86.97%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8908 89.08%
OATP1B3 inhibitior + 0.9519 95.19%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.5572 55.72%
P-glycoprotein inhibitior - 0.8827 88.27%
P-glycoprotein substrate - 0.7985 79.85%
CYP3A4 substrate + 0.5407 54.07%
CYP2C9 substrate - 0.7869 78.69%
CYP2D6 substrate - 0.8738 87.38%
CYP3A4 inhibition - 0.8183 81.83%
CYP2C9 inhibition - 0.8029 80.29%
CYP2C19 inhibition - 0.6678 66.78%
CYP2D6 inhibition - 0.9145 91.45%
CYP1A2 inhibition - 0.7896 78.96%
CYP2C8 inhibition - 0.7327 73.27%
CYP inhibitory promiscuity - 0.7763 77.63%
UGT catelyzed + 0.9000 90.00%
Carcinogenicity (binary) - 0.8111 81.11%
Carcinogenicity (trinary) Non-required 0.6891 68.91%
Eye corrosion - 0.9891 98.91%
Eye irritation - 0.9099 90.99%
Skin irritation - 0.7887 78.87%
Skin corrosion - 0.9397 93.97%
Ames mutagenesis - 0.5300 53.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4465 44.65%
Micronuclear + 0.7200 72.00%
Hepatotoxicity + 0.5321 53.21%
skin sensitisation - 0.8480 84.80%
Respiratory toxicity + 0.6000 60.00%
Reproductive toxicity + 0.9778 97.78%
Mitochondrial toxicity + 0.8125 81.25%
Nephrotoxicity - 0.6493 64.93%
Acute Oral Toxicity (c) III 0.6959 69.59%
Estrogen receptor binding + 0.7578 75.78%
Androgen receptor binding - 0.7840 78.40%
Thyroid receptor binding - 0.5000 50.00%
Glucocorticoid receptor binding + 0.5779 57.79%
Aromatase binding + 0.6453 64.53%
PPAR gamma + 0.7805 78.05%
Honey bee toxicity - 0.9718 97.18%
Biodegradation - 0.7750 77.50%
Crustacea aquatic toxicity - 0.5400 54.00%
Fish aquatic toxicity - 0.3924 39.24%

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 97.45% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 96.81% 95.56%
CHEMBL2581 P07339 Cathepsin D 92.29% 98.95%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 89.74% 99.23%
CHEMBL3060 Q9Y345 Glycine transporter 2 89.58% 99.17%
CHEMBL230 P35354 Cyclooxygenase-2 86.67% 89.63%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.92% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 83.94% 94.73%
CHEMBL1806 P11388 DNA topoisomerase II alpha 83.02% 89.00%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 82.03% 96.00%
CHEMBL5028 O14672 ADAM10 81.00% 97.50%

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 155563894
LOTUS LTS0235234
wikiData Q105345311