(2R)-2-hydroxy-3-methoxy-2H-furan-5-one

Details

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Internal ID e42d4e91-e007-4457-84d0-9c4e940d5d70
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (2R)-2-hydroxy-3-methoxy-2H-furan-5-one
SMILES (Canonical) COC1=CC(=O)OC1O
SMILES (Isomeric) COC1=CC(=O)O[C@H]1O
InChI InChI=1S/C5H6O4/c1-8-3-2-4(6)9-5(3)7/h2,5,7H,1H3/t5-/m1/s1
InChI Key ZFBPPZVSMKOHMW-RXMQYKEDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6O4
Molecular Weight 130.10 g/mol
Exact Mass 130.02660867 g/mol
Topological Polar Surface Area (TPSA) 55.80 Ų
XlogP -0.60
Atomic LogP (AlogP) -0.61
H-Bond Acceptor 4
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 (2R)-2-hydroxy-3-methoxy-2H-furan-5-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9690 96.90%
Caco-2 + 0.5115 51.15%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.7027 70.27%
OATP2B1 inhibitior - 0.8622 86.22%
OATP1B1 inhibitior + 0.9442 94.42%
OATP1B3 inhibitior + 0.9727 97.27%
MATE1 inhibitior - 0.7600 76.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9597 95.97%
P-glycoprotein inhibitior - 0.9641 96.41%
P-glycoprotein substrate - 0.9781 97.81%
CYP3A4 substrate - 0.6497 64.97%
CYP2C9 substrate - 0.8241 82.41%
CYP2D6 substrate - 0.8854 88.54%
CYP3A4 inhibition - 0.9630 96.30%
CYP2C9 inhibition - 0.9602 96.02%
CYP2C19 inhibition - 0.7401 74.01%
CYP2D6 inhibition - 0.9587 95.87%
CYP1A2 inhibition - 0.6442 64.42%
CYP2C8 inhibition - 0.9864 98.64%
CYP inhibitory promiscuity - 0.7379 73.79%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8528 85.28%
Carcinogenicity (trinary) Danger 0.4403 44.03%
Eye corrosion - 0.6802 68.02%
Eye irritation + 0.9391 93.91%
Skin irritation - 0.5878 58.78%
Skin corrosion - 0.9008 90.08%
Ames mutagenesis - 0.7200 72.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8600 86.00%
Micronuclear + 0.6400 64.00%
Hepatotoxicity + 0.6677 66.77%
skin sensitisation - 0.8438 84.38%
Respiratory toxicity - 0.6556 65.56%
Reproductive toxicity - 0.5556 55.56%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.5967 59.67%
Acute Oral Toxicity (c) IV 0.4827 48.27%
Estrogen receptor binding - 0.8011 80.11%
Androgen receptor binding - 0.7511 75.11%
Thyroid receptor binding - 0.8389 83.89%
Glucocorticoid receptor binding - 0.9030 90.30%
Aromatase binding - 0.8476 84.76%
PPAR gamma - 0.7767 77.67%
Honey bee toxicity - 0.8948 89.48%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.5700 57.00%
Fish aquatic toxicity - 0.4357 43.57%

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 89.72% 91.11%
CHEMBL4261 Q16665 Hypoxia-inducible factor 1 alpha 89.10% 85.14%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 87.84% 95.56%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.88% 96.09%
CHEMBL2581 P07339 Cathepsin D 81.88% 98.95%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 81.53% 94.00%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 80.60% 99.23%

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.
Narthecium ossifragum

Cross-Links

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PubChem 163086510
LOTUS LTS0213126
wikiData Q105373969