4-benzyl-6-oxo-1H-pyridine-3-carboxamide

Details

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Internal ID f4918cbe-6998-4d42-98d3-e7d51b7c11aa
Taxonomy Organoheterocyclic compounds > Pyridines and derivatives > Pyridinecarboxylic acids and derivatives > Pyridinecarboxamides > Nicotinamides
IUPAC Name 4-benzyl-6-oxo-1H-pyridine-3-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C13H12N2O2/c14-13(17)11-8-15-12(16)7-10(11)6-9-4-2-1-3-5-9/h1-5,7-8H,6H2,(H2,14,17)(H,15,16)
InChI Key LMBDGTRVHLFFEW-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C13H12N2O2
Molecular Weight 228.25 g/mol
Exact Mass 228.089877630 g/mol
Topological Polar Surface Area (TPSA) 72.20 Ų
XlogP 0.30
Atomic LogP (AlogP) 1.06
H-Bond Acceptor 2
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-benzyl-6-oxo-1H-pyridine-3-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9528 95.28%
Caco-2 + 0.4926 49.26%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.5731 57.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9406 94.06%
OATP1B3 inhibitior + 0.9441 94.41%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.8750 87.50%
BSEP inhibitior - 0.6414 64.14%
P-glycoprotein inhibitior - 0.9573 95.73%
P-glycoprotein substrate - 0.8234 82.34%
CYP3A4 substrate - 0.6679 66.79%
CYP2C9 substrate + 0.6063 60.63%
CYP2D6 substrate - 0.8694 86.94%
CYP3A4 inhibition - 0.6944 69.44%
CYP2C9 inhibition - 0.8158 81.58%
CYP2C19 inhibition - 0.9286 92.86%
CYP2D6 inhibition - 0.9370 93.70%
CYP1A2 inhibition - 0.5679 56.79%
CYP2C8 inhibition - 0.7946 79.46%
CYP inhibitory promiscuity - 0.6307 63.07%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8800 88.00%
Carcinogenicity (trinary) Non-required 0.5965 59.65%
Eye corrosion - 0.9945 99.45%
Eye irritation - 0.9560 95.60%
Skin irritation - 0.8502 85.02%
Skin corrosion - 0.9672 96.72%
Ames mutagenesis - 0.8170 81.70%
Human Ether-a-go-go-Related Gene inhibition - 0.6568 65.68%
Micronuclear + 0.8500 85.00%
Hepatotoxicity + 0.6232 62.32%
skin sensitisation - 0.8851 88.51%
Respiratory toxicity + 0.7556 75.56%
Reproductive toxicity + 0.7444 74.44%
Mitochondrial toxicity + 0.6125 61.25%
Nephrotoxicity - 0.8487 84.87%
Acute Oral Toxicity (c) III 0.6586 65.86%
Estrogen receptor binding + 0.7200 72.00%
Androgen receptor binding + 0.5239 52.39%
Thyroid receptor binding - 0.5249 52.49%
Glucocorticoid receptor binding + 0.7571 75.71%
Aromatase binding + 0.9132 91.32%
PPAR gamma + 0.5174 51.74%
Honey bee toxicity - 0.9304 93.04%
Biodegradation - 0.8750 87.50%
Crustacea aquatic toxicity - 0.7000 70.00%
Fish aquatic toxicity - 0.6815 68.15%

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 96.18% 91.11%
CHEMBL2581 P07339 Cathepsin D 96.04% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 93.63% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 93.32% 96.09%
CHEMBL221 P23219 Cyclooxygenase-1 89.93% 90.17%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.16% 86.33%
CHEMBL3091268 Q92753 Nuclear receptor ROR-beta 87.68% 95.50%
CHEMBL2535 P11166 Glucose transporter 83.91% 98.75%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 80.21% 94.45%

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 11447516
LOTUS LTS0228985
wikiData Q105153828