发明名称 Flavonoid compounds
摘要 The present invention relates to compounds, compositions, and methods for treatment of conditions related to mitochondrial function. In various aspects, the present invention comprises administering one or more epicatechin derivatives in an amount effective to stimulate mitochondrial function in cells. The compounds, compositions, and methods described herein provide for reducing infarct size in the heart following permanent ischemia or ischemia/reperfusion event or method for delaying, attenuating or preventing adverse cardiac remodeling, and can assist in prevention of impaired mitochondria biogenesis and thus prevention of the consequences of impaired mitochondrial biogenesis in various diseases and conditions, as well as provide for the active therapy of mitochondrial depletion that may have already occurred.
申请公布号 US9187448(B2) 申请公布日期 2015.11.17
申请号 US201214237167 申请日期 2012.08.06
申请人 CARDERO THERAPEUTICS, INC. 发明人 Becker Cyrus K.;Schreiner George F.;Dugar Sundeep;Mahajan Dinesh
分类号 C07D311/62;C07D405/10;A61K31/353;A61K31/496 主分类号 C07D311/62
代理机构 Foley & Lardner LLP 代理人 Foley & Lardner LLP
主权项 1. A compound selected from the group consisting of: i. 2-(4-Hydroxy-3-propoxy-phenyl)-chroman-3,5,7-triol; ii. 2-(3-Hydroxy-4-propoxy-phenyl)-chroman-3,5,7-triol; iii. 2-(3-ethoxy-4-Hydroxy-phenyl)-chroman-3,5,7-triol; iv. 2-(4-ethoxy-3-Hydroxy-phenyl)-chroman-3,5,7-triol; v. 2-(3,4-Dihydroxy-phenyl)-3-propoxy-chroman-5,7-diol; vi. methyl 4-((2R,3R)-3-hydroxy-5,7-dimethoxychroman-2-yl)-2-methoxybenzoate; vii. methyl 5-((2R,3R)-3-hydroxy-5,7-dimethoxychroman-2-yl)-2-methoxybenzoate; viii. (4-((2R,3R)-3-hydroxy-5,7-dimethoxychroman-2-yl)-2-methoxyphenyl)(4-methylpiperazin-1-yl)methanone; ix. ethyl 2-(4-((2R,3R)-3-hydroxy-5,7-dimethoxychroman-2-yl)-2-methoxyphenoxy)acetate; x. ethyl 2-(5-((2R,3R)-3-hydroxy-5,7-dimethoxychroman-2-yl)-2-methoxyphenoxy)acetate; xi. 2-(4-((2R,3R)-3-hydroxy-5,7-dimethoxychroman-2-yl)-2-methoxyphenoxy) acetic acid; xii. ethyl 2-(2-hydroxy-4-((2R,3R)-3,5,7-dimethoxychroman-2-yl)phenoxy)acetate; xiii. ethyl 2-(2-hydroxy-5-((2R,3R)-3,5,7-dimethoxychroman-2-yl)phenoxy)acetate; xiv. (2R,3R)-2-(3,4-dihydroxyphenyl)-3-methoxychroman-5,7-diol; xv. (2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychroman-3-yl acetate; xvi. 1-(((2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychroman-3-yl)oxy)ethyl isobutyrate; xvii. (((2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychroman-3-yl)oxy)methyl diisopropylcarbamate; xviii. tert-butyl ((((2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychroman-3-yl)oxy)methyl)carbonate; xix. 4-((2R,3R)-3,5,7-trihydroxychroman-2-yl)-1,2-phenylene dioctanoate; xx. (2R,3R)-2-(3,4-dihydroxyphenyl)-5,7-dihydroxychroman-3-yl octanoate; xxi. (2R,3R)-2-(3,4-diacetoxyphenyl)chroman-3,5,7-triyl triacetate; xxii. 4-((2R,3R)-3,5,7-trihydroxychroman-2-yl)-1 phenylene diacetate; xxiii. 4-((2R,3R)-3,5,7-trihydroxychroman-2-yl)-1,2-phenylene diacetate; xxiv. (2R,3R)-2-(3,4-dihydroxyphenyl)-3-methylchroman-3,5,7-triol; and xxv. a racemic mixture or a pharmaceutically acceptable salt thereof of any of (i) to (xxiv).
地址 Sunnyvale CA US