Diethone

CAS: 1149-23-1

Ref. 3D-FD00103

Product Information

• Name: Diethone
• Synonyms: 3,5-Dicarbethoxy-2,6-dimethyl-1,4-dihydropyridineDiludine, 1,4-Dihydro-2,6-dimethyl-3,5-pyridinedicarboxylic acid diethyl ester, 1,4-Dihydro-3,5-dicarboxylic acid diethyl ester-2,6-dimethylpyridine, 2,6-Dimethyl-1,4-dihydropyridine-3,5-dicarboxylic acid diethyl ester, 2,6-Dimethyl-3,5-di(carboethoxy)-1,4-dihydropyridine, 2,6-Dimethyl-3,5-dicarbethoxy-1,4-dihydropyridine, 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridin, 2,6-Dimethyl-3,5-diethoxycarbonyl-1,4-dihydropyridine, 3,5-Bis(ethoxycarbonyl)-1,4-dihydro-2,6-dimethylpyridine, 3,5-Bis(ethoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine, 3,5-Dicarbethoxy-2,6-dimethyl-1,4-dihydropyridine, 3,5-Dicarboethoxy-2,6-dimethyl-1,4-dihydropyridine, 3,5-Diethoxycarbonyl-1,4-dihydro-2,6-dimethylpyridine, 3,5-Diethoxycarbonyl-2,6-dimethyl-1,4-dihydropyridine, 3,5-Diethyl 2,6-dimethyl-1,4-dihydropyridine-3,5-dicarboxylate, 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-, 3,5-diethyl ester, 3,5-Pyridinedicarboxylic acid, 1,4-dihydro-2,6-dimethyl-, diethyl ester, Diethyl 2,6-Dimethyl-1,4-Dihydropyridine-3,5-Dicarboxylate, Diethyl-1,4-dihydro-2,6-dimethyl-3,5-pyridinedicarboxylate, Diludin, Diludine, Ethidine, Hantzsch ester, Hantzsch's dihydropyridine, NSC 120573, NSC 3344, Rr 116

Description

Diethone is a chemical compound that has been found to have a variety of biological effects. It has been shown to inhibit the activity of enzymes, such as phospholipase A2, cyclooxygenase-1 and -2, lipoxygenase-1 and -2, and glutathione S-transferases. In addition, diethone inhibits the synthesis of prostaglandins and leukotrienes. Diethone also has various physiological functions in humans. It is an eye irritant that can cause conjunctivitis and corneal damage if it comes into contact with the eye. Diethone also inhibits toll-like receptor (TLR) signaling in macrophages and myeloid cells, which may be due to its ability to inhibit NF-κβ activation. Diethone is also involved in metabolic disorders such as bowel disease or liver disease. This compound is metabolized by rat liver microsomes and produces a number of

• Brand: Biosynth

Chemical properties

• Molecular weight: 253.29 g/mol
• Formula: C₁₃H₁₉NO₄
• Purity: Min. 95%
• Color/Form: Yellow Powder
• InChI: InChI=1S/C13H19NO4/c1-5-17-12(15)10-7-11(13(16)18-6-2)9(4)14-8(10)3/h14H,5-7H2,1-4H3
• InChI key: InChIKey=LJXTYJXBORAIHX-UHFFFAOYSA-N
• SMILES: CCOC(=O)C1=C(C)NC(C)=C(C(=O)OCC)C1