4-(Hydroxymethyl)furan-2-carbaldehyde

Details

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Internal ID 108f47c8-e6e6-4d24-a266-e5d94e21be49
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 4-(hydroxymethyl)furan-2-carbaldehyde
SMILES (Canonical) C1=C(OC=C1CO)C=O
SMILES (Isomeric) C1=C(OC=C1CO)C=O
InChI InChI=1S/C6H6O3/c7-2-5-1-6(3-8)9-4-5/h1,3-4,7H,2H2
InChI Key GYQBROOJXNICMZ-UHFFFAOYSA-N
Popularity 11 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) 0.58
H-Bond Acceptor 3
H-Bond Donor 1
Rotatable Bonds 2

Synonyms

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158360-01-1
4-(Hydroxymethyl)-2-furancarboxaldehyde
4-Hydroxymethylfurfural
2-Furancarboxaldehyde, 4-(hydroxymethyl)-
4-(Hydroxymethyl)furfural
SCHEMBL934450
DTXSID80415739
AMY41823
4-hydroxymethyl-furan-2-carbaldehyde
MFCD14584441
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 4-(Hydroxymethyl)furan-2-carbaldehyde

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9853 98.53%
Caco-2 + 0.7914 79.14%
Blood Brain Barrier + 0.7500 75.00%
Human oral bioavailability + 0.5857 58.57%
Subcellular localzation Mitochondria 0.7271 72.71%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8458 84.58%
OATP1B3 inhibitior + 0.9577 95.77%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 1.0000 100.00%
BSEP inhibitior - 0.9357 93.57%
P-glycoprotein inhibitior - 0.9820 98.20%
P-glycoprotein substrate - 0.9863 98.63%
CYP3A4 substrate - 0.7265 72.65%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7912 79.12%
CYP3A4 inhibition - 0.9828 98.28%
CYP2C9 inhibition - 0.9037 90.37%
CYP2C19 inhibition - 0.7786 77.86%
CYP2D6 inhibition - 0.9564 95.64%
CYP1A2 inhibition + 0.5388 53.88%
CYP2C8 inhibition - 0.9609 96.09%
CYP inhibitory promiscuity - 0.7897 78.97%
UGT catelyzed + 0.7000 70.00%
Carcinogenicity (binary) - 0.8100 81.00%
Carcinogenicity (trinary) Non-required 0.4136 41.36%
Eye corrosion + 0.5603 56.03%
Eye irritation + 1.0000 100.00%
Skin irritation + 0.7585 75.85%
Skin corrosion - 0.5699 56.99%
Ames mutagenesis - 0.6500 65.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7926 79.26%
Micronuclear - 0.6800 68.00%
Hepatotoxicity - 0.6947 69.47%
skin sensitisation - 0.5514 55.14%
Respiratory toxicity + 0.5444 54.44%
Reproductive toxicity + 0.6778 67.78%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6481 64.81%
Acute Oral Toxicity (c) III 0.7066 70.66%
Estrogen receptor binding - 0.8590 85.90%
Androgen receptor binding - 0.7650 76.50%
Thyroid receptor binding - 0.8370 83.70%
Glucocorticoid receptor binding - 0.7809 78.09%
Aromatase binding - 0.7023 70.23%
PPAR gamma - 0.8558 85.58%
Honey bee toxicity - 0.9331 93.31%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.7100 71.00%
Fish aquatic toxicity - 0.8539 85.39%

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 89.44% 95.56%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 87.55% 91.11%
CHEMBL3401 O75469 Pregnane X receptor 86.56% 94.73%
CHEMBL3060 Q9Y345 Glycine transporter 2 86.01% 99.17%
CHEMBL2581 P07339 Cathepsin D 83.21% 98.95%
CHEMBL4016 P42262 Glutamate receptor ionotropic, AMPA 2 82.89% 86.92%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.43% 94.45%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.18% 86.33%

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.
Artemisia capillaris
Phlomoides umbrosa

Cross-Links

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PubChem 5318289
NPASS NPC311211