2,3,5-Trimethylfuran

Details

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Internal ID e8b67702-6f02-4cf1-b675-2684bebc7312
Taxonomy Organoheterocyclic compounds > Heteroaromatic compounds
IUPAC Name 2,3,5-trimethylfuran
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C7H10O/c1-5-4-6(2)8-7(5)3/h4H,1-3H3
InChI Key NJXZFRUNHWKHEC-UHFFFAOYSA-N
Popularity 15 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) 2.20
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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10504-04-8
Furan, 2,3,5-trimethyl-
MFCD03931179
2,3,5-Trimethyl-Furan
2,3,5-trimethyluran
2,3,5-Trimethylfuran #
SCHEMBL182910
SCHEMBL10768398
DTXSID10146923
CHEBI:189311
There are more than 10 synonyms. If you wish to see them all click here.

2D Structure

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2D Structure of 2,3,5-Trimethylfuran

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9925 99.25%
Caco-2 + 0.8182 81.82%
Blood Brain Barrier + 0.9500 95.00%
Human oral bioavailability + 0.7714 77.14%
Subcellular localzation Mitochondria 0.5972 59.72%
OATP2B1 inhibitior - 1.0000 100.00%
OATP1B1 inhibitior + 0.9637 96.37%
OATP1B3 inhibitior + 0.9675 96.75%
MATE1 inhibitior - 0.9200 92.00%
OCT2 inhibitior - 0.9500 95.00%
BSEP inhibitior - 0.9112 91.12%
P-glycoprotein inhibitior - 0.9733 97.33%
P-glycoprotein substrate - 0.9797 97.97%
CYP3A4 substrate - 0.7595 75.95%
CYP2C9 substrate - 0.8120 81.20%
CYP2D6 substrate - 0.7610 76.10%
CYP3A4 inhibition - 0.9603 96.03%
CYP2C9 inhibition - 0.8863 88.63%
CYP2C19 inhibition - 0.6780 67.80%
CYP2D6 inhibition - 0.9257 92.57%
CYP1A2 inhibition + 0.7057 70.57%
CYP2C8 inhibition - 0.9486 94.86%
CYP inhibitory promiscuity + 0.5962 59.62%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7200 72.00%
Carcinogenicity (trinary) Warning 0.4318 43.18%
Eye corrosion + 0.7288 72.88%
Eye irritation + 0.9781 97.81%
Skin irritation + 0.6608 66.08%
Skin corrosion - 0.9495 94.95%
Ames mutagenesis - 0.6600 66.00%
Human Ether-a-go-go-Related Gene inhibition - 0.7803 78.03%
Micronuclear - 0.7100 71.00%
Hepatotoxicity + 0.7000 70.00%
skin sensitisation + 0.6526 65.26%
Respiratory toxicity - 0.8778 87.78%
Reproductive toxicity - 0.5222 52.22%
Mitochondrial toxicity - 0.6875 68.75%
Nephrotoxicity - 0.5820 58.20%
Acute Oral Toxicity (c) II 0.5962 59.62%
Estrogen receptor binding - 0.9030 90.30%
Androgen receptor binding - 0.7820 78.20%
Thyroid receptor binding - 0.7948 79.48%
Glucocorticoid receptor binding - 0.8593 85.93%
Aromatase binding - 0.7595 75.95%
PPAR gamma - 0.8866 88.66%
Honey bee toxicity - 0.9713 97.13%
Biodegradation - 0.7250 72.50%
Crustacea aquatic toxicity + 0.7100 71.00%
Fish aquatic toxicity - 0.5053 50.53%

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 91.24% 94.73%
CHEMBL5409 Q8TDU6 G-protein coupled bile acid receptor 1 86.55% 93.65%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 85.68% 91.11%
CHEMBL1293249 Q13887 Kruppel-like factor 5 84.08% 86.33%
CHEMBL3108638 O15164 Transcription intermediary factor 1-alpha 81.89% 95.56%

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 517859
LOTUS LTS0155533
wikiData Q75069202