3-hydroxy-2H-pyran-2-one

Details

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Internal ID 58fb872d-2ec4-4452-8cca-97fad2798c41
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-hydroxypyran-2-one
SMILES (Canonical) C1=COC(=O)C(=C1)O
SMILES (Isomeric) C1=COC(=O)C(=C1)O
InChI InChI=1S/C5H4O3/c6-4-2-1-3-8-5(4)7/h1-3,6H
InChI Key LIPRKYKMVQPYPG-UHFFFAOYSA-N
Popularity 129 references in papers

Physical and Chemical Properties

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Molecular Formula C5H4O3
Molecular Weight 112.08 g/mol
Exact Mass 112.016043985 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP 0.60
Atomic LogP (AlogP) 0.35
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 0

Synonyms

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496-64-0
3-Hydroxy-2-pyrone
3-Hydroxypyrone
3-hydroxypyran-2-one
3-hydroxy-2-pyranone
2H-pyran-2-one, 3-hydroxy-
2H-Pyran-4-one, 3-hydroxy-
WBW7DM4PJL
MFCD01318559
hydroxypyrone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 3-hydroxy-2H-pyran-2-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9814 98.14%
Caco-2 + 0.7277 72.77%
Blood Brain Barrier - 0.7250 72.50%
Human oral bioavailability + 0.8286 82.86%
Subcellular localzation Mitochondria 0.8791 87.91%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9485 94.85%
OATP1B3 inhibitior + 0.9664 96.64%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9682 96.82%
P-glycoprotein inhibitior - 0.9846 98.46%
P-glycoprotein substrate - 0.9949 99.49%
CYP3A4 substrate - 0.7456 74.56%
CYP2C9 substrate - 0.8260 82.60%
CYP2D6 substrate - 0.8533 85.33%
CYP3A4 inhibition - 0.9753 97.53%
CYP2C9 inhibition - 0.9486 94.86%
CYP2C19 inhibition - 0.9487 94.87%
CYP2D6 inhibition - 0.9688 96.88%
CYP1A2 inhibition - 0.9556 95.56%
CYP2C8 inhibition - 0.9736 97.36%
CYP inhibitory promiscuity - 0.9407 94.07%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8715 87.15%
Carcinogenicity (trinary) Non-required 0.6413 64.13%
Eye corrosion + 0.6471 64.71%
Eye irritation + 0.9893 98.93%
Skin irritation + 0.9344 93.44%
Skin corrosion - 0.8393 83.93%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.9013 90.13%
Micronuclear + 0.7340 73.40%
Hepatotoxicity + 0.8033 80.33%
skin sensitisation + 0.6011 60.11%
Respiratory toxicity - 0.5444 54.44%
Reproductive toxicity + 0.5889 58.89%
Mitochondrial toxicity - 0.7750 77.50%
Nephrotoxicity + 0.6463 64.63%
Acute Oral Toxicity (c) III 0.5499 54.99%
Estrogen receptor binding - 0.8957 89.57%
Androgen receptor binding - 0.8829 88.29%
Thyroid receptor binding - 0.8257 82.57%
Glucocorticoid receptor binding - 0.8598 85.98%
Aromatase binding - 0.8422 84.22%
PPAR gamma - 0.8192 81.92%
Honey bee toxicity - 0.9781 97.81%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity + 0.6781 67.81%

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 97.02% 91.11%
CHEMBL1951 P21397 Monoamine oxidase A 92.67% 91.49%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.83% 95.56%
CHEMBL2581 P07339 Cathepsin D 86.13% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 83.81% 94.73%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 82.18% 99.23%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.62% 94.00%
CHEMBL1806 P11388 DNA topoisomerase II alpha 80.37% 89.00%

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.
Actinidia chinensis

Cross-Links

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PubChem 68130
LOTUS LTS0255301
wikiData Q72481657