6-Oxo-2,3-dihydropyran-4-carboxamide

Details

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Internal ID 82350d94-05a6-4f26-864e-8efb64418efe
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives > Dihydropyranones
IUPAC Name 6-oxo-2,3-dihydropyran-4-carboxamide
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H7NO3/c7-6(9)4-1-2-10-5(8)3-4/h3H,1-2H2,(H2,7,9)
InChI Key GFRDFIQEUBNRHA-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H7NO3
Molecular Weight 141.12 g/mol
Exact Mass 141.042593085 g/mol
Topological Polar Surface Area (TPSA) 69.40 Ų
XlogP -0.70
Atomic LogP (AlogP) -0.66
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 6-Oxo-2,3-dihydropyran-4-carboxamide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9805 98.05%
Caco-2 + 0.5167 51.67%
Blood Brain Barrier + 0.7750 77.50%
Human oral bioavailability + 0.7286 72.86%
Subcellular localzation Mitochondria 0.7168 71.68%
OATP2B1 inhibitior - 0.8600 86.00%
OATP1B1 inhibitior + 0.9781 97.81%
OATP1B3 inhibitior + 0.9508 95.08%
MATE1 inhibitior - 0.9218 92.18%
OCT2 inhibitior - 0.9000 90.00%
BSEP inhibitior - 0.9480 94.80%
P-glycoprotein inhibitior - 0.9883 98.83%
P-glycoprotein substrate - 0.9556 95.56%
CYP3A4 substrate - 0.7213 72.13%
CYP2C9 substrate + 0.5799 57.99%
CYP2D6 substrate - 0.8804 88.04%
CYP3A4 inhibition - 0.9700 97.00%
CYP2C9 inhibition - 0.8395 83.95%
CYP2C19 inhibition - 0.7786 77.86%
CYP2D6 inhibition - 0.9047 90.47%
CYP1A2 inhibition - 0.8264 82.64%
CYP2C8 inhibition - 0.9897 98.97%
CYP inhibitory promiscuity - 0.9787 97.87%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.9228 92.28%
Carcinogenicity (trinary) Non-required 0.5743 57.43%
Eye corrosion - 0.9382 93.82%
Eye irritation + 0.9585 95.85%
Skin irritation - 0.7331 73.31%
Skin corrosion - 0.9167 91.67%
Ames mutagenesis - 0.6454 64.54%
Human Ether-a-go-go-Related Gene inhibition - 0.7299 72.99%
Micronuclear - 0.5000 50.00%
Hepatotoxicity + 0.7500 75.00%
skin sensitisation - 0.8800 88.00%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity + 0.6625 66.25%
Nephrotoxicity - 0.5529 55.29%
Acute Oral Toxicity (c) III 0.5858 58.58%
Estrogen receptor binding - 0.9171 91.71%
Androgen receptor binding - 0.5074 50.74%
Thyroid receptor binding - 0.8283 82.83%
Glucocorticoid receptor binding - 0.8006 80.06%
Aromatase binding - 0.8237 82.37%
PPAR gamma - 0.6607 66.07%
Honey bee toxicity - 0.9446 94.46%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.8000 80.00%
Fish aquatic toxicity - 0.7771 77.71%

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 96.90% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.27% 85.14%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.82% 94.45%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 87.97% 96.09%
CHEMBL4040 P28482 MAP kinase ERK2 87.28% 83.82%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.58% 95.56%
CHEMBL3830 Q2M2I8 Adaptor-associated kinase 80.38% 83.10%
CHEMBL1994 P08235 Mineralocorticoid receptor 80.33% 100.00%

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.
Gentiana cruciata

Cross-Links

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PubChem 55282040
LOTUS LTS0039282
wikiData Q105007742