5-Methoxyfuran-2-carbaldehyde

Details

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Internal ID 7f30ad3c-f1b1-4cc1-bd54-7ee8d2e3012d
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Alkyl aryl ethers
IUPAC Name 5-methoxyfuran-2-carbaldehyde
SMILES (Canonical) COC1=CC=C(O1)C=O
SMILES (Isomeric) COC1=CC=C(O1)C=O
InChI InChI=1S/C6H6O3/c1-8-6-3-2-5(4-7)9-6/h2-4H,1H3
InChI Key RJGBSYZFOCAGQY-UHFFFAOYSA-N
Popularity 12 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) 39.40 Ų
XlogP 1.10
Atomic LogP (AlogP) 1.10
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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21300-07-2
5-methoxyfurfural
5-Methoxyfuraldehyde
2-Furancarboxaldehyde, 5-methoxy-
5-methoxy-furan-2-carbaldehyde
SCHEMBL54493
DTXSID00274481
RJGBSYZFOCAGQY-UHFFFAOYSA-N
AKOS017669778
AT17092
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-Methoxyfuran-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 + 0.9941 99.41%
Caco-2 + 0.7786 77.86%
Blood Brain Barrier + 0.5750 57.50%
Human oral bioavailability + 0.7000 70.00%
Subcellular localzation Mitochondria 0.7802 78.02%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9193 91.93%
OATP1B3 inhibitior + 0.9627 96.27%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9561 95.61%
P-glycoprotein inhibitior - 0.9775 97.75%
P-glycoprotein substrate - 0.9788 97.88%
CYP3A4 substrate - 0.6676 66.76%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.7494 74.94%
CYP3A4 inhibition - 0.9697 96.97%
CYP2C9 inhibition - 0.8938 89.38%
CYP2C19 inhibition - 0.5644 56.44%
CYP2D6 inhibition - 0.9326 93.26%
CYP1A2 inhibition + 0.8174 81.74%
CYP2C8 inhibition - 0.9453 94.53%
CYP inhibitory promiscuity - 0.6470 64.70%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7967 79.67%
Carcinogenicity (trinary) Warning 0.5626 56.26%
Eye corrosion + 0.8715 87.15%
Eye irritation + 0.9958 99.58%
Skin irritation + 0.5513 55.13%
Skin corrosion - 0.8568 85.68%
Ames mutagenesis - 0.8900 89.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6055 60.55%
Micronuclear + 0.6281 62.81%
Hepatotoxicity + 0.5534 55.34%
skin sensitisation - 0.7224 72.24%
Respiratory toxicity - 0.8000 80.00%
Reproductive toxicity + 0.6222 62.22%
Mitochondrial toxicity - 0.8000 80.00%
Nephrotoxicity + 0.6783 67.83%
Acute Oral Toxicity (c) III 0.5150 51.50%
Estrogen receptor binding - 0.9092 90.92%
Androgen receptor binding - 0.8480 84.80%
Thyroid receptor binding - 0.8689 86.89%
Glucocorticoid receptor binding - 0.9033 90.33%
Aromatase binding - 0.9058 90.58%
PPAR gamma - 0.8793 87.93%
Honey bee toxicity - 0.8960 89.60%
Biodegradation + 0.6000 60.00%
Crustacea aquatic toxicity - 0.5100 51.00%
Fish aquatic toxicity - 0.4868 48.68%

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 93.67% 95.56%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.67% 96.00%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.24% 94.80%
CHEMBL3401 O75469 Pregnane X receptor 84.00% 94.73%
CHEMBL4203 Q9HAZ1 Dual specificity protein kinase CLK4 83.57% 94.45%
CHEMBL3492 P49721 Proteasome Macropain subunit 82.93% 90.24%
CHEMBL1293249 Q13887 Kruppel-like factor 5 82.49% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 81.31% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 80.71% 96.09%

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.
Codonopsis pilosula
Crocus sativus
Eleutherococcus sessiliflorus
Murraya paniculata

Cross-Links

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PubChem 6208
NPASS NPC142691
LOTUS LTS0259435
wikiData Q82003830