5-Methyl-7-methoxyisoflavone
Appearance
Names | |
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IUPAC name
7-Methoxy-5-methylisoflavone
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Systematic IUPAC name
7-Methoxy-5-methyl-3-phenyl-4H-1-benzopyran-4-one | |
Other names
Methoxyisoflavone
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Identifiers | |
3D model (JSmol)
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ChemSpider | |
ECHA InfoCard | 100.126.888 |
PubChem CID
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UNII | |
CompTox Dashboard (EPA)
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Properties | |
C17H14O3 | |
Molar mass | 266.296 g·mol−1 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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5-Methyl-7-methoxyisoflavone, commonly referred to simply as methoxyisoflavone, is a chemical compound marketed as a bodybuilding supplement. However, there is no meaningful clinical evidence to support its usefulness.[1][2] A study published in 2006 examined the effect of methoxyflavone on training adaptations and markers of muscle anabolism and catabolism. No measurable effects were observed in athletic performance or in levels of testosterone and cortisol.[3]
Consumption of 5-methyl-7-methoxyisoflavone can produce false positive results in urinary tests for cannabinoid use.[4][5]
References
[edit]- ^ "Methoxyisoflavone". NYU Langone Medical Center. July 2012. Archived from the original on August 19, 2014.
There is no meaningful evidence to indicate that methoxyisoflavone is useful as a sports supplement.
- ^ "Methoxyisoflavone". EBSCO CAM Review Board. Retrieved April 15, 2015.
- ^ Wilborn, Colin D; Taylor, Lemuel W; Campbell, Bill I; Kerksick, Chad; Rasmussen, Chris J; Greenwood, Michael; Kreider, Richard B (2006). "Effects of Methoxyisoflavone, Ecdysterone, and Sulfo-Polysaccharide Supplementation on Training Adaptations in Resistance-Trained Males". Journal of the International Society of Sports Nutrition. 3 (2): 19–27. CiteSeerX 10.1.1.274.1063. doi:10.1186/1550-2783-3-2-19. PMC 2129166. PMID 18500969.
- ^ Lecompte, Yannick; Perrin, Martine; Daude, Bernard; Arpino, Patrick (2012). "Méthoxyisoflavone et dépistage du cannabis dans les urines : mise en évidence d'une réaction croisée peu connue" [Methoxyisoflavone and urine cannabinoid screening: evidence of a poorly known cross-reactivity]. Annales de Toxicologie Analytique (in French). 24 (1): 49–58. doi:10.1051/ata/2012002.
- ^ Lecompte, Yannick; Rosset, Martine; Richeval, Camille; Humbert, Luc; Arpino, Patrick (2014). "UPLC-ESI-Q-TOF-MSE identification of urinary metabolites of the emerging sport nutrition supplement methoxyisoflavone in human subjects". Journal of Pharmaceutical and Biomedical Analysis. 96: 127–134. doi:10.1016/j.jpba.2014.03.031. PMID 24742771.
External links
[edit]- Hu, Wei-Xiao; Qian, Hong-Sheng; Rao, Guo-Wu (2004). "Structure of 5-methyl-7-methoxy-isoflavone". Journal of Chemical Crystallography. 34 (11): 793. Bibcode:2004JCCry..34..793H. doi:10.1007/s10870-004-7655-y. S2CID 96359776.