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

Details

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Internal ID f4a53bb9-5526-4448-a6ea-3859615ecc43
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name (2R)-2-hydroxy-3-(hydroxymethyl)-2H-furan-5-one
SMILES (Canonical) C1=C(C(OC1=O)O)CO
SMILES (Isomeric) C1=C([C@@H](OC1=O)O)CO
InChI InChI=1S/C5H6O4/c6-2-3-1-4(7)9-5(3)8/h1,5-6,8H,2H2/t5-/m1/s1
InChI Key MSBIGIDBOKJKCS-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) 66.80 Ų
XlogP -1.10
Atomic LogP (AlogP) -1.22
H-Bond Acceptor 4
H-Bond Donor 2
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-(hydroxymethyl)-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 + 0.9189 91.89%
Caco-2 - 0.6934 69.34%
Blood Brain Barrier + 0.6178 61.78%
Human oral bioavailability + 0.6286 62.86%
Subcellular localzation Mitochondria 0.6145 61.45%
OATP2B1 inhibitior - 0.8597 85.97%
OATP1B1 inhibitior + 0.9213 92.13%
OATP1B3 inhibitior + 0.9494 94.94%
MATE1 inhibitior - 0.8200 82.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9750 97.50%
P-glycoprotein inhibitior - 0.9790 97.90%
P-glycoprotein substrate - 0.9710 97.10%
CYP3A4 substrate - 0.7024 70.24%
CYP2C9 substrate - 0.6272 62.72%
CYP2D6 substrate - 0.8863 88.63%
CYP3A4 inhibition - 0.9649 96.49%
CYP2C9 inhibition - 0.8926 89.26%
CYP2C19 inhibition - 0.8627 86.27%
CYP2D6 inhibition - 0.9488 94.88%
CYP1A2 inhibition - 0.7953 79.53%
CYP2C8 inhibition - 0.9927 99.27%
CYP inhibitory promiscuity - 0.8161 81.61%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9128 91.28%
Carcinogenicity (trinary) Non-required 0.6642 66.42%
Eye corrosion - 0.9132 91.32%
Eye irritation + 0.9104 91.04%
Skin irritation - 0.5566 55.66%
Skin corrosion - 0.8374 83.74%
Ames mutagenesis + 0.5100 51.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8836 88.36%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation - 0.8317 83.17%
Respiratory toxicity + 0.5222 52.22%
Reproductive toxicity + 0.5111 51.11%
Mitochondrial toxicity - 0.6500 65.00%
Nephrotoxicity + 0.4778 47.78%
Acute Oral Toxicity (c) III 0.5738 57.38%
Estrogen receptor binding - 0.8020 80.20%
Androgen receptor binding - 0.8042 80.42%
Thyroid receptor binding - 0.7650 76.50%
Glucocorticoid receptor binding - 0.6474 64.74%
Aromatase binding - 0.8072 80.72%
PPAR gamma - 0.7475 74.75%
Honey bee toxicity - 0.8799 87.99%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity + 0.7323 73.23%

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 88.24% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.97% 97.09%
CHEMBL226 P30542 Adenosine A1 receptor 86.24% 95.93%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 84.73% 86.92%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.64% 97.25%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 80.99% 95.56%

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.
Brachystemma calycinum

Cross-Links

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PubChem 162867978
LOTUS LTS0243951
wikiData Q105171068