2-Butyl-4-methylfuran

Details

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Internal ID ea81ba52-0b2d-4237-95a0-c63b61163a28
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-butyl-4-methylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C9H14O/c1-3-4-5-9-6-8(2)7-10-9/h6-7H,3-5H2,1-2H3
InChI Key VGRKACDKLYAZJN-UHFFFAOYSA-N
Popularity 3 references in papers

Physical and Chemical Properties

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Molecular Formula C9H14O
Molecular Weight 138.21 g/mol
Exact Mass 138.104465066 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.93
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 2-Butyl-4-methylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9944 99.44%
Caco-2 + 0.9515 95.15%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6857 68.57%
Subcellular localzation Lysosomes 0.3517 35.17%
OATP2B1 inhibitior - 0.8521 85.21%
OATP1B1 inhibitior + 0.8875 88.75%
OATP1B3 inhibitior + 0.9496 94.96%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8000 80.00%
BSEP inhibitior - 0.8789 87.89%
P-glycoprotein inhibitior - 0.9850 98.50%
P-glycoprotein substrate - 0.8852 88.52%
CYP3A4 substrate - 0.6770 67.70%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.6668 66.68%
CYP3A4 inhibition - 0.9508 95.08%
CYP2C9 inhibition - 0.8673 86.73%
CYP2C19 inhibition - 0.6342 63.42%
CYP2D6 inhibition - 0.8966 89.66%
CYP1A2 inhibition + 0.5804 58.04%
CYP2C8 inhibition - 0.8320 83.20%
CYP inhibitory promiscuity - 0.6597 65.97%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8300 83.00%
Carcinogenicity (trinary) Non-required 0.3960 39.60%
Eye corrosion + 0.6420 64.20%
Eye irritation + 0.9034 90.34%
Skin irritation + 0.7384 73.84%
Skin corrosion - 0.9147 91.47%
Ames mutagenesis - 0.7900 79.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5774 57.74%
Micronuclear - 0.9100 91.00%
Hepatotoxicity + 0.6250 62.50%
skin sensitisation + 0.7343 73.43%
Respiratory toxicity - 0.7444 74.44%
Reproductive toxicity - 0.5531 55.31%
Mitochondrial toxicity - 0.9000 90.00%
Nephrotoxicity + 0.5087 50.87%
Acute Oral Toxicity (c) III 0.6489 64.89%
Estrogen receptor binding - 0.9395 93.95%
Androgen receptor binding - 0.6321 63.21%
Thyroid receptor binding - 0.8220 82.20%
Glucocorticoid receptor binding - 0.7778 77.78%
Aromatase binding - 0.8459 84.59%
PPAR gamma - 0.8154 81.54%
Honey bee toxicity - 0.9876 98.76%
Biodegradation + 0.5250 52.50%
Crustacea aquatic toxicity + 0.5100 51.00%
Fish aquatic toxicity - 0.5249 52.49%

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
CHEMBL2581 P07339 Cathepsin D 93.94% 98.95%
CHEMBL3401 O75469 Pregnane X receptor 91.74% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 88.54% 92.08%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.01% 86.33%
CHEMBL4481 P35228 Nitric oxide synthase, inducible 84.43% 94.80%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.62% 91.11%
CHEMBL3060 Q9Y345 Glycine transporter 2 83.55% 99.17%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 81.42% 93.65%
CHEMBL4835 P00338 L-lactate dehydrogenase A chain 81.33% 95.34%
CHEMBL230 P35354 Cyclooxygenase-2 80.31% 89.63%
CHEMBL1907 P15144 Aminopeptidase N 80.14% 93.31%

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.
Gossypium hirsutum

Cross-Links

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PubChem 13197868
LOTUS LTS0027872
wikiData Q105256691