5-(Methoxymethyl)-2-furaldehyde

Details

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Internal ID ab71e42e-d332-46f0-845f-e8a572121ff8
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 5-(methoxymethyl)furan-2-carbaldehyde
SMILES (Canonical) COCC1=CC=C(O1)C=O
SMILES (Isomeric) COCC1=CC=C(O1)C=O
InChI InChI=1S/C7H8O3/c1-9-5-7-3-2-6(4-8)10-7/h2-4H,5H2,1H3
InChI Key ASHVULSQMDWKFO-UHFFFAOYSA-N
Popularity 18 references in papers

Physical and Chemical Properties

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Molecular Formula C7H8O3
Molecular Weight 140.14 g/mol
Exact Mass 140.047344113 g/mol
Topological Polar Surface Area (TPSA) 39.40 Ų
XlogP 0.00
Atomic LogP (AlogP) 1.24
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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5-(methoxymethyl)furan-2-carbaldehyde
5-(METHOXYMETHYL)-2-FURALDEHYDE
5-(Methoxymethyl)-2-furancarboxaldehyde
2-Furancarboxaldehyde, 5-(methoxymethyl)-
5-methoxymethylfurfural
5-Methoxymethylfuran-2-carbaldehyde
5XBV4H5CX7
MFCD02253954
EC 700-511-5
5-Methoxymethyl furfural
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-(Methoxymethyl)-2-furaldehyde

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 + 0.6284 62.84%
Blood Brain Barrier + 0.8250 82.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Mitochondria 0.7463 74.63%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8827 88.27%
OATP1B3 inhibitior + 0.9548 95.48%
MATE1 inhibitior - 0.9600 96.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9243 92.43%
P-glycoprotein inhibitior - 0.9799 97.99%
P-glycoprotein substrate - 0.9613 96.13%
CYP3A4 substrate - 0.6366 63.66%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7906 79.06%
CYP3A4 inhibition - 0.9869 98.69%
CYP2C9 inhibition - 0.8104 81.04%
CYP2C19 inhibition - 0.6570 65.70%
CYP2D6 inhibition - 0.9431 94.31%
CYP1A2 inhibition + 0.6233 62.33%
CYP2C8 inhibition - 0.8382 83.82%
CYP inhibitory promiscuity - 0.7143 71.43%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7517 75.17%
Carcinogenicity (trinary) Non-required 0.4002 40.02%
Eye corrosion + 0.5870 58.70%
Eye irritation + 0.9900 99.00%
Skin irritation - 0.6193 61.93%
Skin corrosion - 0.8422 84.22%
Ames mutagenesis - 0.6778 67.78%
Human Ether-a-go-go-Related Gene inhibition - 0.7059 70.59%
Micronuclear - 0.7467 74.67%
Hepatotoxicity + 0.6460 64.60%
skin sensitisation + 0.9334 93.34%
Respiratory toxicity - 0.7222 72.22%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.8500 85.00%
Nephrotoxicity + 0.7548 75.48%
Acute Oral Toxicity (c) III 0.5259 52.59%
Estrogen receptor binding - 0.9375 93.75%
Androgen receptor binding - 0.8318 83.18%
Thyroid receptor binding - 0.9187 91.87%
Glucocorticoid receptor binding - 0.8574 85.74%
Aromatase binding - 0.8923 89.23%
PPAR gamma - 0.8231 82.31%
Honey bee toxicity - 0.8862 88.62%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.6100 61.00%
Fish aquatic toxicity - 0.7970 79.70%

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 91.86% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 86.80% 94.73%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 86.12% 96.09%
CHEMBL2581 P07339 Cathepsin D 86.06% 98.95%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.91% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.61% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 82.80% 99.17%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 81.81% 94.45%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 81.06% 96.00%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.15% 94.00%

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.
Asparagus cochinchinensis
Codonopsis pilosula
Jaborosa magellanica
Murraya paniculata

Cross-Links

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PubChem 74711
NPASS NPC215377
LOTUS LTS0068028
wikiData Q6555445