MD001

• 常用名: MD001
• 英文名: MD001
• CAS号: 2254605-76-8
• 分子量: 398.407
• 密度: 1.4±0.1 g/cm3
• 沸点: 575.1±45.0 °C at 760 mmHg
• 分子式: C₂₅H₁₈O₅
• 熔点: N/A
• 闪点: 199.1±22.2 °C

MD001用途

MD001 is a dual agonist of peroxisome proliferator-activated receptor α (PPARα) and PPARγ. It binds to PPARα and PPARγ but does not bind to PPARβ/δ. It increases transcriptional activity of PPARα and PPARγ and glucose consumption. MD001 decreases levels of glucose, insulin, free fatty acids, triglycerides, LDL, alanine aminotransferase (ALT), and aspartate aminotransferase (AST) in blood and reduces the size and number of hepatic lipid droplets in diabetic db/db mice.

MD001名称

• 英文名: MD001

MD001物理化学性质

• 密度: 1.4±0.1 g/cm3
• 沸点: 575.1±45.0 °C at 760 mmHg
• 分子式: C₂₅H₁₈O₅
• 分子量: 398.407
• 闪点: 199.1±22.2 °C
• 精确质量: 398.115417
• LogP: 6.14
• 蒸汽压: 0.0±1.6 mmHg at 25°C
• 折射率: 1.704

MD001英文别名

• 2H-1-Benzopyran-2-one, 5,7-dihydroxy-8-methyl-3-[(2E)-1-oxo-3-phenyl-2-propen-1-yl]-4-phenyl-
• MD001
• 5,7-Dihydroxy-8-methyl-4-phenyl-3-[(2E)-3-phenyl-2-propenoyl]-2H-chromen-2-one