2-Furyl hydroxymethyl ketone

Details

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Internal ID 5bbe4942-ad70-481b-9c27-d663bb3b2891
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aryl ketones > Aryl alkyl ketones
IUPAC Name 1-(furan-2-yl)-2-hydroxyethanone
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C6H6O3/c7-4-5(8)6-2-1-3-9-6/h1-3,7H,4H2
InChI Key RSZZMVPSHLKFQY-UHFFFAOYSA-N
Popularity 68 references in papers

Physical and Chemical Properties

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Molecular Formula C6H6O3
Molecular Weight 126.11 g/mol
Exact Mass 126.031694049 g/mol
Topological Polar Surface Area (TPSA) 50.40 Ų
XlogP -0.10
Atomic LogP (AlogP) 0.45
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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Furyl hydroxymethyl ketone
1-(furan-2-yl)-2-hydroxyethanone
Ethanone, 1-(2-furanyl)-2-hydroxy-
2-Furyl hydroxymethyl ketone
2-(Hydroxyacetyl)furan
UNII-9U7H4P11RD
9U7H4P11RD
1-(2-FURANYL)-2-HYDROXYETHANONE
RefChem:87234
RSZZMVPSHLKFQY-UHFFFAOYSA-N
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Furyl hydroxymethyl ketone

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9849 98.49%
Caco-2 + 0.8130 81.30%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7415 74.15%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9371 93.71%
OATP1B3 inhibitior + 0.9572 95.72%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9386 93.86%
P-glycoprotein inhibitior - 0.9842 98.42%
P-glycoprotein substrate - 0.9803 98.03%
CYP3A4 substrate - 0.7114 71.14%
CYP2C9 substrate - 0.8060 80.60%
CYP2D6 substrate - 0.8128 81.28%
CYP3A4 inhibition - 0.9856 98.56%
CYP2C9 inhibition - 0.9077 90.77%
CYP2C19 inhibition - 0.7752 77.52%
CYP2D6 inhibition - 0.9641 96.41%
CYP1A2 inhibition - 0.5440 54.40%
CYP2C8 inhibition - 0.9573 95.73%
CYP inhibitory promiscuity - 0.8283 82.83%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Danger 0.4654 46.54%
Eye corrosion + 0.5651 56.51%
Eye irritation + 0.9939 99.39%
Skin irritation + 0.7112 71.12%
Skin corrosion + 0.5209 52.09%
Ames mutagenesis - 0.7700 77.00%
Human Ether-a-go-go-Related Gene inhibition - 0.8344 83.44%
Micronuclear - 0.7400 74.00%
Hepatotoxicity - 0.5426 54.26%
skin sensitisation - 0.5902 59.02%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity + 0.5613 56.13%
Acute Oral Toxicity (c) III 0.7337 73.37%
Estrogen receptor binding - 0.9406 94.06%
Androgen receptor binding - 0.9084 90.84%
Thyroid receptor binding - 0.8603 86.03%
Glucocorticoid receptor binding - 0.8692 86.92%
Aromatase binding - 0.8289 82.89%
PPAR gamma - 0.8362 83.62%
Honey bee toxicity - 0.9757 97.57%
Biodegradation + 0.7500 75.00%
Crustacea aquatic toxicity - 0.7500 75.00%
Fish aquatic toxicity - 0.9246 92.46%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.26% 96.09%
CHEMBL3401 O75469 Pregnane X receptor 85.58% 94.73%
CHEMBL2581 P07339 Cathepsin D 85.01% 98.95%
CHEMBL3060 Q9Y345 Glycine transporter 2 84.13% 99.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.39% 91.11%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 82.74% 95.56%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.75% 86.33%

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 519466
LOTUS LTS0241920
wikiData Q27273231