4-Hydroxy-5-(hydroxymethyl)oxolan-2-one

Details

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Internal ID 45de9ece-aa53-4c90-810f-12a93561ec72
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 4-hydroxy-5-(hydroxymethyl)oxolan-2-one
SMILES (Canonical) C1C(C(OC1=O)CO)O
SMILES (Isomeric) C1C(C(OC1=O)CO)O
InChI InChI=1S/C5H8O4/c6-2-4-3(7)1-5(8)9-4/h3-4,6-7H,1-2H2
InChI Key YIXDEYPPAGPYDP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C5H8O4
Molecular Weight 132.11 g/mol
Exact Mass 132.04225873 g/mol
Topological Polar Surface Area (TPSA) 66.80 Ų
XlogP -0.90
Atomic LogP (AlogP) -1.34
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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4-hydroxy-5-(hydroxymethyl)oxolan-2-one
SCHEMBL9130905
4,5-Dihydro-4-hydroxy-5-(hydroxymethyl)-2(3H)-furanone
CHEBI:173532
BCP18088
PB47697
LS-13053
SY099138
FT-0770508
FT-0773511

2D Structure

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2D Structure of 4-Hydroxy-5-(hydroxymethyl)oxolan-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 + 0.6192 61.92%
Caco-2 - 0.8506 85.06%
Blood Brain Barrier - 0.5250 52.50%
Human oral bioavailability + 0.6143 61.43%
Subcellular localzation Mitochondria 0.6987 69.87%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9274 92.74%
OATP1B3 inhibitior + 0.9465 94.65%
MATE1 inhibitior - 1.0000 100.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9770 97.70%
P-glycoprotein inhibitior - 0.9801 98.01%
P-glycoprotein substrate - 0.9801 98.01%
CYP3A4 substrate - 0.7149 71.49%
CYP2C9 substrate - 0.8047 80.47%
CYP2D6 substrate - 0.8332 83.32%
CYP3A4 inhibition - 0.9710 97.10%
CYP2C9 inhibition - 0.9487 94.87%
CYP2C19 inhibition - 0.9319 93.19%
CYP2D6 inhibition - 0.9607 96.07%
CYP1A2 inhibition - 0.9443 94.43%
CYP2C8 inhibition - 0.9956 99.56%
CYP inhibitory promiscuity - 0.9630 96.30%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 1.0000 100.00%
Carcinogenicity (trinary) Non-required 0.7559 75.59%
Eye corrosion - 0.9788 97.88%
Eye irritation + 0.9058 90.58%
Skin irritation - 0.7859 78.59%
Skin corrosion - 0.9279 92.79%
Ames mutagenesis - 0.6100 61.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7738 77.38%
Micronuclear - 0.8126 81.26%
Hepatotoxicity + 0.5165 51.65%
skin sensitisation - 0.9476 94.76%
Respiratory toxicity - 0.6444 64.44%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity + 0.7135 71.35%
Acute Oral Toxicity (c) III 0.4726 47.26%
Estrogen receptor binding - 0.9241 92.41%
Androgen receptor binding - 0.8047 80.47%
Thyroid receptor binding - 0.8546 85.46%
Glucocorticoid receptor binding - 0.7726 77.26%
Aromatase binding - 0.8469 84.69%
PPAR gamma - 0.8359 83.59%
Honey bee toxicity - 0.9108 91.08%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.6700 67.00%
Fish aquatic toxicity - 0.6710 67.10%

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 91.52% 91.11%
CHEMBL3137262 O60341 LSD1/CoREST complex 87.67% 97.09%
CHEMBL2996 Q05655 Protein kinase C delta 84.44% 97.79%
CHEMBL2581 P07339 Cathepsin D 83.86% 98.95%
CHEMBL253 P34972 Cannabinoid CB2 receptor 82.63% 97.25%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 82.37% 96.09%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.15% 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.
Clematis hexapetala
Cnidium monnieri
Helianthus annuus

Cross-Links

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PubChem 4635870
LOTUS LTS0037676
wikiData Q105233364