2-Ethyl-5-methylfuran

Details

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Internal ID e0afffd7-605f-4873-bcb0-a8c9a34678df
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2-ethyl-5-methylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10O/c1-3-7-5-4-6(2)8-7/h4-5H,3H2,1-2H3
InChI Key NBXLPPVOZWYADY-UHFFFAOYSA-N
Popularity 35 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 2.20
Atomic LogP (AlogP) 2.15
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 1

Synonyms

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1703-52-2
Furan, 2-ethyl-5-methyl-
2-Methyl-5-ethylfuran
2-Ethyl-5-methyl-furan
PG4BLD3EJI
EINECS 216-937-5
UNII-PG4BLD3EJI
2-ethyl-5-methyl furan
furan, 2-methyl, 5-ethyl
SCHEMBL144611
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-Ethyl-5-methylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9934 99.34%
Caco-2 + 0.8532 85.32%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Mitochondria 0.4380 43.80%
OATP2B1 inhibitior - 0.8691 86.91%
OATP1B1 inhibitior + 0.9311 93.11%
OATP1B3 inhibitior + 0.9493 94.93%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9750 97.50%
BSEP inhibitior - 0.9207 92.07%
P-glycoprotein inhibitior - 0.9806 98.06%
P-glycoprotein substrate - 0.9549 95.49%
CYP3A4 substrate - 0.7752 77.52%
CYP2C9 substrate - 0.8046 80.46%
CYP2D6 substrate - 0.6668 66.68%
CYP3A4 inhibition - 0.9558 95.58%
CYP2C9 inhibition - 0.8215 82.15%
CYP2C19 inhibition - 0.5596 55.96%
CYP2D6 inhibition - 0.9022 90.22%
CYP1A2 inhibition + 0.5157 51.57%
CYP2C8 inhibition - 0.9135 91.35%
CYP inhibitory promiscuity + 0.5000 50.00%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.6200 62.00%
Carcinogenicity (trinary) Warning 0.3936 39.36%
Eye corrosion + 0.7624 76.24%
Eye irritation + 0.9620 96.20%
Skin irritation + 0.6977 69.77%
Skin corrosion - 0.9312 93.12%
Ames mutagenesis - 0.7637 76.37%
Human Ether-a-go-go-Related Gene inhibition - 0.6877 68.77%
Micronuclear - 0.7600 76.00%
Hepatotoxicity + 0.6625 66.25%
skin sensitisation + 0.8017 80.17%
Respiratory toxicity - 0.6111 61.11%
Reproductive toxicity + 0.5024 50.24%
Mitochondrial toxicity - 0.8250 82.50%
Nephrotoxicity - 0.6706 67.06%
Acute Oral Toxicity (c) III 0.6599 65.99%
Estrogen receptor binding - 0.9640 96.40%
Androgen receptor binding - 0.8624 86.24%
Thyroid receptor binding - 0.9133 91.33%
Glucocorticoid receptor binding - 0.8619 86.19%
Aromatase binding - 0.8831 88.31%
PPAR gamma - 0.8879 88.79%
Honey bee toxicity - 0.9749 97.49%
Biodegradation - 0.5750 57.50%
Crustacea aquatic toxicity + 0.5500 55.00%
Fish aquatic toxicity - 0.7903 79.03%

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 90.66% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 88.43% 93.65%
CHEMBL2581 P07339 Cathepsin D 84.54% 98.95%
CHEMBL3492 P49721 Proteasome Macropain subunit 80.76% 90.24%

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 74346
LOTUS LTS0009759
wikiData Q27160507