2-Butylfuran

Details

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Internal ID c6b7cf85-ff04-4991-b69e-dd78f3afa2fe
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-butylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C8H12O/c1-2-3-5-8-6-4-7-9-8/h4,6-7H,2-3,5H2,1H3
InChI Key NWZIYQNUCXUJJJ-UHFFFAOYSA-N
Popularity 85 references in papers

Physical and Chemical Properties

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Molecular Formula C8H12O
Molecular Weight 124.18 g/mol
Exact Mass 124.088815002 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 3.10
Atomic LogP (AlogP) 2.62
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 3

Synonyms

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Furan, 2-butyl-
2-n-Butylfuran
2-n-Butyl furan
2-butyl-furan
UNII-81JV9ZYK0D
81JV9ZYK0D
EINECS 224-732-7
2-BUTYLFURAN [FHFI]
DTXSID8073340
FEMA NO. 4081
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2-Butylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9954 99.54%
Caco-2 + 0.9276 92.76%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.6429 64.29%
Subcellular localzation Plasma membrane 0.3819 38.19%
OATP2B1 inhibitior - 0.8594 85.94%
OATP1B1 inhibitior + 0.8984 89.84%
OATP1B3 inhibitior + 0.9569 95.69%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.8250 82.50%
BSEP inhibitior - 0.9248 92.48%
P-glycoprotein inhibitior - 0.9895 98.95%
P-glycoprotein substrate - 0.8677 86.77%
CYP3A4 substrate - 0.7024 70.24%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.6668 66.68%
CYP3A4 inhibition - 0.9648 96.48%
CYP2C9 inhibition - 0.8569 85.69%
CYP2C19 inhibition - 0.5000 50.00%
CYP2D6 inhibition - 0.9181 91.81%
CYP1A2 inhibition + 0.6323 63.23%
CYP2C8 inhibition - 0.7858 78.58%
CYP inhibitory promiscuity - 0.6108 61.08%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.8400 84.00%
Carcinogenicity (trinary) Warning 0.4110 41.10%
Eye corrosion + 0.8264 82.64%
Eye irritation + 0.9552 95.52%
Skin irritation + 0.8412 84.12%
Skin corrosion - 0.8984 89.84%
Ames mutagenesis - 0.7800 78.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6112 61.12%
Micronuclear - 0.8800 88.00%
Hepatotoxicity + 0.5250 52.50%
skin sensitisation + 0.6495 64.95%
Respiratory toxicity - 0.5556 55.56%
Reproductive toxicity + 0.5333 53.33%
Mitochondrial toxicity - 0.8750 87.50%
Nephrotoxicity + 0.5527 55.27%
Acute Oral Toxicity (c) III 0.7341 73.41%
Estrogen receptor binding - 0.9283 92.83%
Androgen receptor binding - 0.8465 84.65%
Thyroid receptor binding - 0.8786 87.86%
Glucocorticoid receptor binding - 0.7290 72.90%
Aromatase binding - 0.8267 82.67%
PPAR gamma - 0.7997 79.97%
Honey bee toxicity - 0.9937 99.37%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity + 0.6400 64.00%
Fish aquatic toxicity - 0.5982 59.82%

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 93.88% 98.95%
CHEMBL240 Q12809 HERG 92.78% 89.76%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 91.56% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 88.07% 86.33%
CHEMBL3401 O75469 Pregnane X receptor 88.06% 94.73%
CHEMBL4769 O95749 Geranylgeranyl pyrophosphate synthetase 86.06% 92.08%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 85.14% 96.09%
CHEMBL255 P29275 Adenosine A2b receptor 82.51% 98.59%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 82.36% 93.65%
CHEMBL1907 P15144 Aminopeptidase N 80.60% 93.31%
CHEMBL3060 Q9Y345 Glycine transporter 2 80.43% 99.17%

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.
Chrysopogon zizanioides

Cross-Links

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PubChem 20534
NPASS NPC155718
LOTUS LTS0235847
wikiData Q27161938