3-Methyl-5-(2-methylpropyl)furan-2-carbaldehyde

Details

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Internal ID 6321c0be-ab1a-40e5-94e3-85c79e63cd06
Taxonomy Organic oxygen compounds > Organooxygen compounds > Carbonyl compounds > Aldehydes > Aryl-aldehydes
IUPAC Name 3-methyl-5-(2-methylpropyl)furan-2-carbaldehyde
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H14O2/c1-7(2)4-9-5-8(3)10(6-11)12-9/h5-7H,4H2,1-3H3
InChI Key QMLNYDORMWTLNR-UHFFFAOYSA-N
Popularity 2 references in papers

Physical and Chemical Properties

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Molecular Formula C10H14O2
Molecular Weight 166.22 g/mol
Exact Mass 166.099379685 g/mol
Topological Polar Surface Area (TPSA) 30.20 Ų
XlogP 2.80
Atomic LogP (AlogP) 2.60
H-Bond Acceptor 2
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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90052-91-8
DTXSID30849166

2D Structure

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2D Structure of 3-Methyl-5-(2-methylpropyl)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 + 0.9923 99.23%
Caco-2 + 0.9033 90.33%
Blood Brain Barrier + 0.8500 85.00%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Mitochondria 0.7031 70.31%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.8353 83.53%
OATP1B3 inhibitior + 0.9517 95.17%
MATE1 inhibitior - 0.7800 78.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.8502 85.02%
P-glycoprotein inhibitior - 0.9651 96.51%
P-glycoprotein substrate - 0.9442 94.42%
CYP3A4 substrate - 0.7048 70.48%
CYP2C9 substrate - 1.0000 100.00%
CYP2D6 substrate - 0.8081 80.81%
CYP3A4 inhibition - 0.9266 92.66%
CYP2C9 inhibition - 0.7663 76.63%
CYP2C19 inhibition - 0.5841 58.41%
CYP2D6 inhibition - 0.9082 90.82%
CYP1A2 inhibition + 0.6232 62.32%
CYP2C8 inhibition - 0.9238 92.38%
CYP inhibitory promiscuity - 0.5297 52.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7000 70.00%
Carcinogenicity (trinary) Non-required 0.3980 39.80%
Eye corrosion - 0.6908 69.08%
Eye irritation + 0.9410 94.10%
Skin irritation - 0.5459 54.59%
Skin corrosion - 0.9384 93.84%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6516 65.16%
Micronuclear - 0.7400 74.00%
Hepatotoxicity + 0.6000 60.00%
skin sensitisation + 0.9083 90.83%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.5444 54.44%
Mitochondrial toxicity - 0.8625 86.25%
Nephrotoxicity - 0.6572 65.72%
Acute Oral Toxicity (c) III 0.6587 65.87%
Estrogen receptor binding - 0.9744 97.44%
Androgen receptor binding - 0.6359 63.59%
Thyroid receptor binding - 0.8841 88.41%
Glucocorticoid receptor binding - 0.7959 79.59%
Aromatase binding - 0.8274 82.74%
PPAR gamma - 0.8787 87.87%
Honey bee toxicity - 0.9387 93.87%
Biodegradation - 0.6500 65.00%
Crustacea aquatic toxicity - 0.6200 62.00%
Fish aquatic toxicity - 0.4072 40.72%

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
CHEMBL3401 O75469 Pregnane X receptor 94.76% 94.73%
CHEMBL2581 P07339 Cathepsin D 93.19% 98.95%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 92.58% 95.56%
CHEMBL3492 P49721 Proteasome Macropain subunit 87.59% 90.24%
CHEMBL1075094 Q16236 Nuclear factor erythroid 2-related factor 2 85.01% 96.00%
CHEMBL5845 P23415 Glycine receptor subunit alpha-1 83.38% 90.71%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 83.06% 94.80%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 80.66% 93.65%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.55% 86.33%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 80.00% 91.11%

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.
Tagetes minuta

Cross-Links

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PubChem 71430550
LOTUS LTS0100017
wikiData Q82841877