2(5H)-Furanone, 5-(hydroxymethylene)-

Details

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Internal ID 99223f1f-322c-43a8-8221-1f98870462d0
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 5-hydroxyfuran-2-carbaldehyde
SMILES (Canonical) C1=C(OC(=C1)O)C=O
SMILES (Isomeric) C1=C(OC(=C1)O)C=O
InChI InChI=1S/C5H4O3/c6-3-4-1-2-5(7)8-4/h1-3,7H
InChI Key QVYAWBLDJPTXHS-UHFFFAOYSA-N
Popularity 6 references in papers

Physical and Chemical Properties

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Molecular Formula C5H4O3
Molecular Weight 112.08 g/mol
Exact Mass 112.016043985 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP 0.80
Atomic LogP (AlogP) 0.80
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 1

Synonyms

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107997-80-8
2(5H)-Furanone, 5-(hydroxymethylene)-
5-hydroxyfurfural
5-(Hydroxymethylene)-2(5H)-furanone
107997-81-9
SCHEMBL529291
5-hydroxymethylene-2(5h)-furanone
AKOS017668442

2D Structure

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2D Structure of 2(5H)-Furanone, 5-(hydroxymethylene)-

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9914 99.14%
Caco-2 + 0.7468 74.68%
Blood Brain Barrier - 0.6250 62.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7782 77.82%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8600 86.00%
OATP1B3 inhibitior + 0.9297 92.97%
MATE1 inhibitior - 0.8800 88.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9817 98.17%
P-glycoprotein inhibitior - 0.9827 98.27%
P-glycoprotein substrate - 0.9921 99.21%
CYP3A4 substrate - 0.7529 75.29%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7846 78.46%
CYP3A4 inhibition - 0.9590 95.90%
CYP2C9 inhibition - 0.9649 96.49%
CYP2C19 inhibition - 0.9315 93.15%
CYP2D6 inhibition - 0.9568 95.68%
CYP1A2 inhibition - 0.7268 72.68%
CYP2C8 inhibition - 0.9498 94.98%
CYP inhibitory promiscuity - 0.9169 91.69%
UGT catelyzed + 0.8000 80.00%
Carcinogenicity (binary) - 0.8417 84.17%
Carcinogenicity (trinary) Warning 0.4643 46.43%
Eye corrosion + 0.8462 84.62%
Eye irritation + 0.9948 99.48%
Skin irritation + 0.8465 84.65%
Skin corrosion - 0.5590 55.90%
Ames mutagenesis - 0.8500 85.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8393 83.93%
Micronuclear + 0.6481 64.81%
Hepatotoxicity + 0.8250 82.50%
skin sensitisation + 0.5099 50.99%
Respiratory toxicity - 0.7667 76.67%
Reproductive toxicity - 0.5000 50.00%
Mitochondrial toxicity - 0.6000 60.00%
Nephrotoxicity + 0.6303 63.03%
Acute Oral Toxicity (c) II 0.4485 44.85%
Estrogen receptor binding - 0.9008 90.08%
Androgen receptor binding - 0.8493 84.93%
Thyroid receptor binding - 0.8692 86.92%
Glucocorticoid receptor binding - 0.8792 87.92%
Aromatase binding - 0.8516 85.16%
PPAR gamma - 0.7833 78.33%
Honey bee toxicity - 0.9634 96.34%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity - 0.7400 74.00%
Fish aquatic toxicity - 0.4468 44.68%

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
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 94.41% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 92.26% 91.11%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 89.86% 98.11%
CHEMBL1293255 P15428 15-hydroxyprostaglandin dehydrogenase [NAD+] 85.91% 83.57%

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.
Mikania microptera
Peristeria elata

Cross-Links

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PubChem 135697
LOTUS LTS0138329
wikiData Q104254058