4-Ethyltetrahydro-3-methyl-5-propylfuran-2,3-diol

Details

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Internal ID 70845a19-c297-4734-beae-6c5d568b7c09
Taxonomy Organoheterocyclic compounds > Tetrahydrofurans
IUPAC Name 4-ethyl-3-methyl-5-propyloxolane-2,3-diol
SMILES (Canonical)
SMILES (Isomeric)
InChI InChI=1S/C10H20O3/c1-4-6-8-7(5-2)10(3,12)9(11)13-8/h7-9,11-12H,4-6H2,1-3H3
InChI Key FSFWUMOVZGOJDP-UHFFFAOYSA-N
Popularity 1 reference in papers

Physical and Chemical Properties

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Molecular Formula C10H20O3
Molecular Weight 188.26 g/mol
Exact Mass 188.14124450 g/mol
Topological Polar Surface Area (TPSA) 49.70 Ų
XlogP 1.40
Atomic LogP (AlogP) 1.28
H-Bond Acceptor 3
H-Bond Donor 2
Rotatable Bonds 3

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of 4-Ethyltetrahydro-3-methyl-5-propylfuran-2,3-diol

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9204 92.04%
Caco-2 + 0.5291 52.91%
Blood Brain Barrier + 0.5500 55.00%
Human oral bioavailability + 0.5143 51.43%
Subcellular localzation Mitochondria 0.6428 64.28%
OATP2B1 inhibitior - 0.8374 83.74%
OATP1B1 inhibitior + 0.9016 90.16%
OATP1B3 inhibitior + 0.9199 91.99%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.7750 77.50%
BSEP inhibitior - 0.9178 91.78%
P-glycoprotein inhibitior - 0.9496 94.96%
P-glycoprotein substrate - 0.8811 88.11%
CYP3A4 substrate - 0.5278 52.78%
CYP2C9 substrate - 0.8042 80.42%
CYP2D6 substrate - 0.8198 81.98%
CYP3A4 inhibition - 0.6145 61.45%
CYP2C9 inhibition - 0.7101 71.01%
CYP2C19 inhibition - 0.5988 59.88%
CYP2D6 inhibition - 0.9406 94.06%
CYP1A2 inhibition - 0.6914 69.14%
CYP2C8 inhibition - 0.9350 93.50%
CYP inhibitory promiscuity - 0.8973 89.73%
UGT catelyzed - 0.5000 50.00%
Carcinogenicity (binary) - 0.9300 93.00%
Carcinogenicity (trinary) Non-required 0.6223 62.23%
Eye corrosion - 0.9748 97.48%
Eye irritation - 0.5768 57.68%
Skin irritation - 0.5925 59.25%
Skin corrosion - 0.8911 89.11%
Ames mutagenesis - 0.5500 55.00%
Human Ether-a-go-go-Related Gene inhibition - 0.5653 56.53%
Micronuclear - 0.9100 91.00%
Hepatotoxicity - 0.5119 51.19%
skin sensitisation - 0.7385 73.85%
Respiratory toxicity - 0.6222 62.22%
Reproductive toxicity - 0.5333 53.33%
Mitochondrial toxicity + 0.5375 53.75%
Nephrotoxicity + 0.5805 58.05%
Acute Oral Toxicity (c) III 0.5181 51.81%
Estrogen receptor binding - 0.6888 68.88%
Androgen receptor binding - 0.7893 78.93%
Thyroid receptor binding - 0.6689 66.89%
Glucocorticoid receptor binding - 0.8493 84.93%
Aromatase binding - 0.8671 86.71%
PPAR gamma - 0.7223 72.23%
Honey bee toxicity - 0.9241 92.41%
Biodegradation - 0.6250 62.50%
Crustacea aquatic toxicity - 0.6732 67.32%
Fish aquatic toxicity + 0.9023 90.23%

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
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 94.90% 96.09%
CHEMBL253 P34972 Cannabinoid CB2 receptor 91.70% 97.25%
CHEMBL226 P30542 Adenosine A1 receptor 89.03% 95.93%
CHEMBL206 P03372 Estrogen receptor alpha 84.88% 97.64%
CHEMBL4793 Q86TI2 Dipeptidyl peptidase IX 84.36% 96.95%
CHEMBL221 P23219 Cyclooxygenase-1 83.49% 90.17%
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 83.28% 91.11%
CHEMBL299 P17252 Protein kinase C alpha 82.38% 98.03%

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 129853792
LOTUS LTS0043884
wikiData Q104166734