2-(1-Methylethyl)furan

Details

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Internal ID c16458f3-b2a9-4ac8-b41a-3bca6961c056
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-propan-2-ylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10O/c1-6(2)7-4-3-5-8-7/h3-6H,1-2H3
InChI Key AFOPCURQYRRFRQ-UHFFFAOYSA-N
Popularity 11 references in papers

Physical and Chemical Properties

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Molecular Formula C7H10O
Molecular Weight 110.15 g/mol
Exact Mass 110.073164938 g/mol
Topological Polar Surface Area (TPSA) 13.10 Ų
XlogP 2.10
Atomic LogP (AlogP) 2.40
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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10599-59-4
2-propan-2-ylfuran
2-(propan-2-yl)furan
B44A434J7U
Furan, (1-methylethyl)-
isopropylfuran
2-isopropyl-furan
2-propan-2-yluran
SCHEMBL80874
UNII-B44A434J7U
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-(1-Methylethyl)furan

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9922 99.22%
Caco-2 + 0.7646 76.46%
Blood Brain Barrier + 0.9250 92.50%
Human oral bioavailability + 0.8143 81.43%
Subcellular localzation Mitochondria 0.5152 51.52%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9567 95.67%
OATP1B3 inhibitior + 0.9654 96.54%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9563 95.63%
P-glycoprotein inhibitior - 0.9862 98.62%
P-glycoprotein substrate - 0.9760 97.60%
CYP3A4 substrate - 0.7801 78.01%
CYP2C9 substrate - 0.5918 59.18%
CYP2D6 substrate - 0.7370 73.70%
CYP3A4 inhibition - 0.9823 98.23%
CYP2C9 inhibition - 0.9011 90.11%
CYP2C19 inhibition - 0.7583 75.83%
CYP2D6 inhibition - 0.9015 90.15%
CYP1A2 inhibition - 0.5375 53.75%
CYP2C8 inhibition - 0.9865 98.65%
CYP inhibitory promiscuity - 0.6552 65.52%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7117 71.17%
Carcinogenicity (trinary) Warning 0.4683 46.83%
Eye corrosion + 0.9416 94.16%
Eye irritation + 0.9782 97.82%
Skin irritation + 0.7039 70.39%
Skin corrosion - 0.9481 94.81%
Ames mutagenesis - 0.9400 94.00%
Human Ether-a-go-go-Related Gene inhibition - 0.6083 60.83%
Micronuclear - 0.7200 72.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.5697 56.97%
Respiratory toxicity + 0.5778 57.78%
Reproductive toxicity + 0.6556 65.56%
Mitochondrial toxicity - 0.7050 70.50%
Nephrotoxicity + 0.5814 58.14%
Acute Oral Toxicity (c) III 0.5057 50.57%
Estrogen receptor binding - 0.9395 93.95%
Androgen receptor binding - 0.8985 89.85%
Thyroid receptor binding - 0.8802 88.02%
Glucocorticoid receptor binding - 0.8760 87.60%
Aromatase binding - 0.8678 86.78%
PPAR gamma - 0.9132 91.32%
Honey bee toxicity - 0.9754 97.54%
Biodegradation - 0.6000 60.00%
Crustacea aquatic toxicity + 0.6900 69.00%
Fish aquatic toxicity - 0.6785 67.85%

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 88.73% 94.73%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 86.37% 91.11%
CHEMBL2581 P07339 Cathepsin D 85.71% 98.95%
CHEMBL3359 P21462 Formyl peptide receptor 1 83.43% 93.56%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.58% 95.56%

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.
Hypericum brasiliense

Cross-Links

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PubChem 12200728
LOTUS LTS0031604
wikiData Q105169477