In this article we will explore the fascinating world of Meciadanol, a topic that has piqued the interest of many people over the years. Meciadanol has been the subject of numerous studies and research, and its relevance has remained over time. From its origins to its impact on today's society, Meciadanol has left a significant mark on different aspects of daily life. Through this article, we will delve into the different aspects that make Meciadanol such a relevant and interesting topic, examining its evolution over time and its influence in different areas. Get ready to immerse yourself in the exciting universe of Meciadanol!
![]() | |
Names | |
---|---|
IUPAC name
3-Methoxyflavan-3′,4′,5,7-tetrol
| |
Systematic IUPAC name
(2R,3S)-2-(3,4-Dihydroxyphenyl)-3-methoxy-3,4-dihydro-2H-1-benzopyran-5,7-diol | |
Other names
3-O-Methylcatechin
Meciadanolum 3',4',5,7-Tetrahydroxy-3-methoxyflavan (2R,3S)-2-(3,4-Dihydroxyphenyl)-3-methoxy-5,7-chromandiol | |
Identifiers | |
3D model (JSmol)
|
|
ChemSpider | |
ECHA InfoCard | 100.059.719 |
PubChem CID
|
|
UNII | |
CompTox Dashboard (EPA)
|
|
| |
| |
Properties | |
C16H16O6 | |
Molar mass | 304.298 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa).
|
Meciadanol is a synthetic O-methylated flavanol. It is the 3-O-methylation of catechin.
It inhibits histidine decarboxylase in rats.[1]