(R)-3-Hydroxy-5-oxotetrahydrofuran-3-carboxylic acid

Details

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Internal ID 466e2939-4703-45b0-9af1-2a510cd5df66
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name (3R)-3-hydroxy-5-oxooxolane-3-carboxylic acid
SMILES (Canonical) C1C(=O)OCC1(C(=O)O)O
SMILES (Isomeric) C1C(=O)OC[C@]1(C(=O)O)O
InChI InChI=1S/C5H6O5/c6-3-1-5(9,2-10-3)4(7)8/h9H,1-2H2,(H,7,8)/t5-/m1/s1
InChI Key VCYINFNRMDFDMP-RXMQYKEDSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6O5
Molecular Weight 146.10 g/mol
Exact Mass 146.02152329 g/mol
Topological Polar Surface Area (TPSA) 83.80 Ų
XlogP -1.40
Atomic LogP (AlogP) -1.25
H-Bond Acceptor 4
H-Bond Donor 2
Rotatable Bonds 1

Synonyms

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(R)-3-Hydroxy-5-oxotetrahydrofuran-3-carboxylic acid

2D Structure

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2D Structure of (R)-3-Hydroxy-5-oxotetrahydrofuran-3-carboxylic acid

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.8359 83.59%
Caco-2 - 0.7363 73.63%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6571 65.71%
Subcellular localzation Mitochondria 0.7878 78.78%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.9723 97.23%
OATP1B3 inhibitior + 0.9478 94.78%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9543 95.43%
P-glycoprotein inhibitior - 0.9867 98.67%
P-glycoprotein substrate - 0.9742 97.42%
CYP3A4 substrate - 0.7039 70.39%
CYP2C9 substrate - 0.5979 59.79%
CYP2D6 substrate - 0.8635 86.35%
CYP3A4 inhibition - 0.9733 97.33%
CYP2C9 inhibition - 0.9516 95.16%
CYP2C19 inhibition - 0.9448 94.48%
CYP2D6 inhibition - 0.9598 95.98%
CYP1A2 inhibition - 0.9309 93.09%
CYP2C8 inhibition - 0.9854 98.54%
CYP inhibitory promiscuity - 0.9953 99.53%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9500 95.00%
Carcinogenicity (trinary) Non-required 0.6350 63.50%
Eye corrosion - 0.9017 90.17%
Eye irritation + 0.9764 97.64%
Skin irritation - 0.7568 75.68%
Skin corrosion - 0.7981 79.81%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8221 82.21%
Micronuclear - 0.5926 59.26%
Hepatotoxicity + 0.5875 58.75%
skin sensitisation - 0.9214 92.14%
Respiratory toxicity - 0.5667 56.67%
Reproductive toxicity - 0.6667 66.67%
Mitochondrial toxicity - 0.7125 71.25%
Nephrotoxicity + 0.8307 83.07%
Acute Oral Toxicity (c) III 0.5745 57.45%
Estrogen receptor binding - 0.7903 79.03%
Androgen receptor binding - 0.8077 80.77%
Thyroid receptor binding - 0.8687 86.87%
Glucocorticoid receptor binding - 0.7692 76.92%
Aromatase binding - 0.8210 82.10%
PPAR gamma - 0.6496 64.96%
Honey bee toxicity - 0.9657 96.57%
Biodegradation + 0.8000 80.00%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.6777 67.77%

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
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 88.50% 94.45%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 86.06% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.78% 91.11%
CHEMBL3038477 P67870 Casein kinase II alpha/beta 84.04% 99.23%
CHEMBL4303 P08238 Heat shock protein HSP 90-beta 81.09% 96.77%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
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There are no matching plants.

Cross-Links

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PubChem 45084685
LOTUS LTS0257743
wikiData Q105284026