5-(hydroxymethyl)dihydrofuran-2(3H)-one

Details

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Internal ID 27544fc8-0121-4ad2-b9ee-c3137d239880
Taxonomy Organoheterocyclic compounds > Lactones > Gamma butyrolactones
IUPAC Name 5-(hydroxymethyl)oxolan-2-one
SMILES (Canonical) C1CC(=O)OC1CO
SMILES (Isomeric) C1CC(=O)OC1CO
InChI InChI=1S/C5H8O3/c6-3-4-1-2-5(7)8-4/h4,6H,1-3H2
InChI Key NSISJFFVIMQBRN-UHFFFAOYSA-N
Popularity 19 references in papers

Physical and Chemical Properties

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Molecular Formula C5H8O3
Molecular Weight 116.11 g/mol
Exact Mass 116.047344113 g/mol
Topological Polar Surface Area (TPSA) 46.50 Ų
XlogP -0.40
Atomic LogP (AlogP) -0.32
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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10374-51-3
5-(hydroxymethyl)oxolan-2-one
5-Hydroxymethyl-dihydro-furan-2-one
2(3H)-Furanone, dihydro-5-(hydroxymethyl)-
5-(Hydroxymethyl)dihydro-2(3H)-furanone
5-Hydroxymethyldihydrofuran-2-one
5-(Hydroxymethyl)oxolane-2-one
MFCD00506240
NSC 128380
(R)-(-)-Dihydro-5-(hydroxymethyl)-2(3H)-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)dihydrofuran-2(3H)-one

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9650 96.50%
Caco-2 - 0.6374 63.74%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.6714 67.14%
Subcellular localzation Mitochondria 0.8511 85.11%
OATP2B1 inhibitior - 0.8444 84.44%
OATP1B1 inhibitior + 0.9485 94.85%
OATP1B3 inhibitior + 0.9481 94.81%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.7000 70.00%
BSEP inhibitior - 0.9631 96.31%
P-glycoprotein inhibitior - 0.9897 98.97%
P-glycoprotein substrate - 0.9906 99.06%
CYP3A4 substrate - 0.7163 71.63%
CYP2C9 substrate - 0.8062 80.62%
CYP2D6 substrate - 0.8327 83.27%
CYP3A4 inhibition - 0.9803 98.03%
CYP2C9 inhibition - 0.8350 83.50%
CYP2C19 inhibition - 0.8096 80.96%
CYP2D6 inhibition - 0.9657 96.57%
CYP1A2 inhibition - 0.8757 87.57%
CYP2C8 inhibition - 0.9847 98.47%
CYP inhibitory promiscuity - 0.9556 95.56%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.9800 98.00%
Carcinogenicity (trinary) Non-required 0.6859 68.59%
Eye corrosion + 0.5000 50.00%
Eye irritation + 0.9700 97.00%
Skin irritation - 0.7013 70.13%
Skin corrosion - 0.6836 68.36%
Ames mutagenesis - 0.7640 76.40%
Human Ether-a-go-go-Related Gene inhibition - 0.7623 76.23%
Micronuclear - 0.9800 98.00%
Hepatotoxicity + 0.5625 56.25%
skin sensitisation - 0.9202 92.02%
Respiratory toxicity - 0.7333 73.33%
Reproductive toxicity - 0.5098 50.98%
Mitochondrial toxicity - 0.7250 72.50%
Nephrotoxicity + 0.4804 48.04%
Acute Oral Toxicity (c) III 0.7714 77.14%
Estrogen receptor binding - 0.9419 94.19%
Androgen receptor binding - 0.9185 91.85%
Thyroid receptor binding - 0.9257 92.57%
Glucocorticoid receptor binding - 0.8587 85.87%
Aromatase binding - 0.8358 83.58%
PPAR gamma - 0.8457 84.57%
Honey bee toxicity - 0.9602 96.02%
Biodegradation + 0.9500 95.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.8051 80.51%

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
CHEMBL3137262 O60341 LSD1/CoREST complex 90.22% 97.09%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.10% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.07% 95.56%
CHEMBL5608 Q16288 NT-3 growth factor receptor 80.62% 95.89%

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.
Ranunculus ternatus
Trivalvaria costata

Cross-Links

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PubChem 98431
NPASS NPC32472