5-Methoxy-3-methylfuran-2-carbaldehyde

Details

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Internal ID 9dc6eee6-0400-45be-9c30-34a4680fcd6b
Taxonomy Organic oxygen compounds > Organooxygen compounds > Ethers > Alkyl aryl ethers
IUPAC Name 5-methoxy-3-methylfuran-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H8O3/c1-5-3-7(9-2)10-6(5)4-8/h3-4H,1-2H3
InChI Key BKLBPCONKWNEGL-UHFFFAOYSA-N
Popularity 2 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 1.50
Atomic LogP (AlogP) 1.41
H-Bond Acceptor 3
H-Bond Donor 0
Rotatable Bonds 2

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 5-Methoxy-3-methylfuran-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 + 0.9927 99.27%
Caco-2 + 0.7120 71.20%
Blood Brain Barrier + 0.6250 62.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.8104 81.04%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8798 87.98%
OATP1B3 inhibitior + 0.9680 96.80%
MATE1 inhibitior - 0.9400 94.00%
OCT2 inhibitior - 0.9250 92.50%
BSEP inhibitior - 0.9507 95.07%
P-glycoprotein inhibitior - 0.9500 95.00%
P-glycoprotein substrate - 0.9775 97.75%
CYP3A4 substrate - 0.6390 63.90%
CYP2C9 substrate - 0.8021 80.21%
CYP2D6 substrate - 0.8203 82.03%
CYP3A4 inhibition - 0.9368 93.68%
CYP2C9 inhibition - 0.8854 88.54%
CYP2C19 inhibition + 0.6169 61.69%
CYP2D6 inhibition - 0.9442 94.42%
CYP1A2 inhibition + 0.8564 85.64%
CYP2C8 inhibition - 0.8803 88.03%
CYP inhibitory promiscuity + 0.5356 53.56%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8550 85.50%
Carcinogenicity (trinary) Non-required 0.4412 44.12%
Eye corrosion + 0.6611 66.11%
Eye irritation + 0.9911 99.11%
Skin irritation - 0.5601 56.01%
Skin corrosion - 0.9228 92.28%
Ames mutagenesis - 0.8300 83.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5439 54.39%
Micronuclear + 0.5459 54.59%
Hepatotoxicity - 0.5466 54.66%
skin sensitisation - 0.7363 73.63%
Respiratory toxicity - 0.8222 82.22%
Reproductive toxicity + 0.5778 57.78%
Mitochondrial toxicity - 0.8375 83.75%
Nephrotoxicity + 0.5335 53.35%
Acute Oral Toxicity (c) III 0.4750 47.50%
Estrogen receptor binding - 0.9419 94.19%
Androgen receptor binding - 0.6873 68.73%
Thyroid receptor binding - 0.8395 83.95%
Glucocorticoid receptor binding - 0.9066 90.66%
Aromatase binding - 0.8701 87.01%
PPAR gamma - 0.9055 90.55%
Honey bee toxicity - 0.8645 86.45%
Biodegradation - 0.5250 52.50%
Crustacea aquatic toxicity + 0.5200 52.00%
Fish aquatic toxicity + 0.7731 77.31%

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 93.21% 95.56%
CHEMBL3401 O75469 Pregnane X receptor 91.37% 94.73%
CHEMBL1163101 O75460 Serine/threonine-protein kinase/endoribonuclease IRE1 87.65% 98.11%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 87.64% 96.00%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.01% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 85.10% 86.33%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 85.02% 93.65%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.12% 94.80%
CHEMBL2635 P51452 Dual specificity protein phosphatase 3 80.05% 94.00%

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 87265205
LOTUS LTS0111119
wikiData Q104937668