5-(hydroxymethyl)-2(5H)-furanone

Details

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Internal ID 4fb66589-d51a-446b-b3bd-b275e4fbf618
Taxonomy Organoheterocyclic compounds > Dihydrofurans > Furanones > Butenolides
IUPAC Name 2-(hydroxymethyl)-2H-furan-5-one
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C5H6O3/c6-3-4-1-2-5(7)8-4/h1-2,4,6H,3H2
InChI Key AWNLUIGMHSSXHB-UHFFFAOYSA-N
Popularity 5 references in papers

Physical and Chemical Properties

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Molecular Formula C5H6O3
Molecular Weight 114.10 g/mol
Exact Mass 114.031694049 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP -0.40
Atomic LogP (AlogP) -0.54
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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10374-60-4
DTXSID70276396
RefChem:1072555
DTXCID70227702
2-(hydroxymethyl)-2H-furan-5-one
2(5H)-Furanone, 5-(hydroxymethyl)-
L-ERYTHRO-ASCORBATE
(S)-(-)-5-(HYDROXYMETHYL)-2(5H)-FURANONE
5-(Hydroxymethyl)furan-2(5H)-one
(S)-5-Hydroxymethyl-2(5H)-furanone
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 5-(hydroxymethyl)-2(5H)-furanone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9873 98.73%
Caco-2 + 0.5000 50.00%
Blood Brain Barrier + 0.7250 72.50%
Human oral bioavailability + 0.7143 71.43%
Subcellular localzation Mitochondria 0.7142 71.42%
OATP2B1 inhibitior - 0.8630 86.30%
OATP1B1 inhibitior + 0.8843 88.43%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9000 90.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9589 95.89%
P-glycoprotein inhibitior - 0.9858 98.58%
P-glycoprotein substrate - 0.9816 98.16%
CYP3A4 substrate - 0.7220 72.20%
CYP2C9 substrate - 0.8148 81.48%
CYP2D6 substrate - 0.8902 89.02%
CYP3A4 inhibition - 0.9813 98.13%
CYP2C9 inhibition - 0.9680 96.80%
CYP2C19 inhibition - 0.9260 92.60%
CYP2D6 inhibition - 0.9661 96.61%
CYP1A2 inhibition - 0.8417 84.17%
CYP2C8 inhibition - 0.9855 98.55%
CYP inhibitory promiscuity - 0.9225 92.25%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9144 91.44%
Carcinogenicity (trinary) Non-required 0.5721 57.21%
Eye corrosion + 0.6032 60.32%
Eye irritation + 0.9150 91.50%
Skin irritation + 0.5603 56.03%
Skin corrosion + 0.6610 66.10%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8606 86.06%
Micronuclear - 0.7441 74.41%
Hepatotoxicity + 0.6158 61.58%
skin sensitisation - 0.6417 64.17%
Respiratory toxicity - 0.5778 57.78%
Reproductive toxicity - 0.6444 64.44%
Mitochondrial toxicity - 0.7500 75.00%
Nephrotoxicity + 0.6202 62.02%
Acute Oral Toxicity (c) III 0.5036 50.36%
Estrogen receptor binding - 0.9404 94.04%
Androgen receptor binding - 0.8407 84.07%
Thyroid receptor binding - 0.9025 90.25%
Glucocorticoid receptor binding - 0.8372 83.72%
Aromatase binding - 0.8739 87.39%
PPAR gamma - 0.8340 83.40%
Honey bee toxicity - 0.9420 94.20%
Biodegradation + 0.7750 77.50%
Crustacea aquatic toxicity - 0.7600 76.00%
Fish aquatic toxicity - 0.8635 86.35%

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 93.18% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 84.73% 95.56%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.67% 86.92%
CHEMBL2581 P07339 Cathepsin D 82.07% 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.
Patrinia scabiosifolia
Patrinia villosa

Cross-Links

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PubChem 144863
NPASS NPC155183