5-Methyl-7-methoxyisoflavone MedChemExpress (MCE)

Product Name	5-Methyl-7-methoxyisoflavone
Synonyms	5-Methyl-7-methoxyis 5-Methyl-7-methoxyisoflavone 5-METHYL-7-METHOXYISOFLAVONE 7-METHOXY-5-METHYLISOFLAVONE 5-methyl-7-methoxy-Isoflavone METHYL-7-METHOXY-ISOFLAVONE, 5- 7-methoxy-5-methyl-3-phenyl-4H-chromen-4-one Synonyms 5-Methyl-7-methoxyis 5-Methyl-7-methoxyisoflavone 5-METHYL-7-METHOXYISOFLAVONE 7-METHOXY-5-METHYLISOFLAVONE 5-methyl-7-methoxy-Isoflavone METHYL-7-METHOXY-ISOFLAVONE, 5- 7-methoxy-5-methyl-3-phenyl-4H-chromen-4-one 7-methoxy-5-methyl-3-phenyl-1-benzopyran-4-one
CAS	82517-12-2
EINECS	617-342-7
Chemical Formula	C17H14O3
Molecular Weight	266.29
inchi	InChI=1/C17H14O3/c1-11-8-13(19-2)9-15-16(11)17(18)14(10-20-15)12-6-4-3-5-7-12/h3-10H,1-2H3
Package	10 mM * 1 mL;5 mg;10 mg;25 mg;50 mg;100 mg
Price	Get quote
Descriptions	5-Methyl-7-methoxyisoflavone 5-Methyl-7-methoxyisoflavone MedChemExpress (MCE) HY-N1993 82517-12-2 99.78% Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year Room temperature in continental US Descriptions 5-Methyl-7-methoxyisoflavone 5-Methyl-7-methoxyisoflavone MedChemExpress (MCE) HY-N1993 82517-12-2 99.78% Powder -20°C 3 years 4°C 2 years In solvent -80°C 2 years -20°C 1 year Room temperature in continental US may vary elsewhere. 5-Methyl-7-methoxyisoflavone is an orally active anti-oxidant with remyelinating activity. 5-Methyl-7-methoxyisoflavone inhibits the enzyme aromatase, interfering with the normal metabolic pathways of testosterone. 5-Methyl-7-methoxyisoflavone is a non-steroidal anabolic isoflavone, used as a anabolic agent. 5-Methyl-7-methoxyisoflavone shows better potency increasing muscle mass and endurance than Ipriflavone (HY-N0094). 5-Methyl-7-methoxyisoflavone can be used for fat loss besides the maintenance of low cholesterol level and strengthen bones. \| \| \| \| \| \| \| \| \| \| [1]. Ningbo Gong, et al. Concomitant polymorphs of methoxyflavone (5-methyl-7-methoxyflavone). RSC Adv., 2016, 6, 38709-38715. [2]. Agresti C, et al. Oxidative status in multiple sclerosis and off-targets of antioxidants: the case of edaravone[J]. Current Medicinal Chemistry, 2020, 27(13): 2095-2105. [Content Brief] [3]. Iannone M, et al. An investigation on the metabolic pathways of synthetic isoflavones by gas chromatography coupled to high accuracy mass spectrometry. Rapid Commun Mass Spectrom. 2019 Oct 15 33(19):1485-1493. [Content Brief] [4]. Lecompte Y, et al. UPLC-ESI-Q-TOF-MS(E) identification of urinary metabolites of the emerging sport nutrition supplement methoxyisoflavone in human subjects. J Pharm Biomed Anal. 2014 Aug 5 96:127-34. [Content Brief]
Last Update	2025-04-01 14:45:47

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