InChI=1/C6H6O4/c1-9-5-3-10-2-4(7)6(5)8/h2-3,7H,1H

Details

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Internal ID ebb7dc4f-2018-4796-9bc8-3a7114d80d3c
Taxonomy Organoheterocyclic compounds > Pyrans > Pyranones and derivatives
IUPAC Name 3-hydroxy-5-methoxypyran-4-one
SMILES (Canonical) COC1=COC=C(C1=O)O
SMILES (Isomeric) COC1=COC=C(C1=O)O
InChI InChI=1S/C6H6O4/c1-9-5-3-10-2-4(7)6(5)8/h2-3,7H,1H3
InChI Key YADGBDNJZIOCBO-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O4
Molecular Weight 142.11 g/mol
Exact Mass 142.02660867 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP 0.20
Atomic LogP (AlogP) 0.35
H-Bond Acceptor 4
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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RefChem:913419
5-OH-3-MeO-4-pyran-4-one
274925-13-2
InChI=1/C6H6O4/c1-9-5-3-10-2-4(7)6(5)8/h2-3,7H,1H

2D Structure

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2D Structure of InChI=1/C6H6O4/c1-9-5-3-10-2-4(7)6(5)8/h2-3,7H,1H

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9580 95.80%
Caco-2 - 0.5614 56.14%
Blood Brain Barrier - 0.5500 55.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.8331 83.31%
OATP2B1 inhibitior - 0.8680 86.80%
OATP1B1 inhibitior + 0.9474 94.74%
OATP1B3 inhibitior + 0.9944 99.44%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9561 95.61%
P-glycoprotein inhibitior - 0.9665 96.65%
P-glycoprotein substrate - 0.9802 98.02%
CYP3A4 substrate - 0.6447 64.47%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7621 76.21%
CYP3A4 inhibition - 0.8794 87.94%
CYP2C9 inhibition - 0.9774 97.74%
CYP2C19 inhibition - 0.5359 53.59%
CYP2D6 inhibition - 0.9366 93.66%
CYP1A2 inhibition + 0.5107 51.07%
CYP2C8 inhibition - 0.9287 92.87%
CYP inhibitory promiscuity - 0.7258 72.58%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8751 87.51%
Carcinogenicity (trinary) Non-required 0.6371 63.71%
Eye corrosion + 0.6066 60.66%
Eye irritation + 0.9768 97.68%
Skin irritation + 0.6964 69.64%
Skin corrosion - 0.9431 94.31%
Ames mutagenesis - 0.8600 86.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7578 75.78%
Micronuclear + 0.8040 80.40%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation - 0.8385 83.85%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.7778 77.78%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.7655 76.55%
Acute Oral Toxicity (c) III 0.8227 82.27%
Estrogen receptor binding - 0.9539 95.39%
Androgen receptor binding - 0.8102 81.02%
Thyroid receptor binding - 0.8160 81.60%
Glucocorticoid receptor binding - 0.9685 96.85%
Aromatase binding - 0.8730 87.30%
PPAR gamma - 0.8980 89.80%
Honey bee toxicity - 0.9238 92.38%
Biodegradation + 0.6250 62.50%
Crustacea aquatic toxicity - 0.6049 60.49%
Fish aquatic toxicity - 0.5733 57.33%

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 94.06% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 91.43% 95.56%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 88.32% 85.14%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 88.22% 94.00%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 84.35% 96.09%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.14% 86.33%
CHEMBL2581 P07339 Cathepsin D 83.76% 98.95%

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.
Haloxylon salicornicum

Cross-Links

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PubChem 10701923
LOTUS LTS0208164
wikiData Q105345331