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公开(公告)号:US20050004086A1
公开(公告)日:2005-01-06
申请号:US10825084
申请日:2004-04-15
申请人: Jeffery Raymond , Kang Han , Yuanlin Zhou , Yuehua He , Bradley Noren , James Yee
发明人: Jeffery Raymond , Kang Han , Yuanlin Zhou , Yuehua He , Bradley Noren , James Yee
IPC分类号: C07C35/21 , C07C35/32 , C07C69/013 , C07C69/03 , C07C311/04 , C07D211/58 , C07D213/30 , C07D213/38 , C07D213/74 , C07D233/54 , C07D233/56 , C07D295/096 , C07D307/66 , C07D317/66 , A61K31/56 , A61K31/155 , A61K31/18 , A61K31/19 , A61K31/40 , A61K31/44
CPC分类号: C07C35/32 , C07C35/14 , C07C35/21 , C07C51/083 , C07C51/347 , C07C62/34 , C07C69/013 , C07C213/00 , C07C213/08 , C07C215/42 , C07C233/18 , C07C233/21 , C07C233/72 , C07C247/14 , C07C279/08 , C07C311/04 , C07C315/00 , C07C2601/14 , C07C2602/08 , C07C2602/24 , C07D207/335 , C07D211/58 , C07D213/30 , C07D213/38 , C07D213/74 , C07D233/54 , C07D233/64 , C07D295/096 , C07D307/66 , C07D317/66 , C07D317/70 , Y10S514/825 , Y10S514/826 , Y10S514/863
摘要: Compounds of formula (Ia): wherein R1, R2, R3, R4a, R4b, R5 and R6 are defined herein, as well as other indene derivatives are disclosed herein. Pharmaceutical compositions containing the compounds and methods of using the compounds are also disclosed.
摘要翻译: 式(Ia)化合物:其中R 1,R 2,R 3,R 4a,R 4b,R 5和R 6在本文中定义,以及其它 茚衍生物在本文中公开。 还公开了含有化合物的药物组合物和使用该化合物的方法。
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公开(公告)号:US20050215534A9
公开(公告)日:2005-09-29
申请号:US10624946
申请日:2003-07-21
申请人: Jeffery Raymond , Claudia Kasserra , Yaping Shen
发明人: Jeffery Raymond , Claudia Kasserra , Yaping Shen
IPC分类号: A61K31/56 , A61K31/566 , A61K31/57 , A61K31/58 , A61P9/06 , A61P9/10 , A61P11/00 , A61P11/06 , A61P17/02 , A61P29/00 , A61P31/18 , A61P35/00 , A61P37/08 , A61P43/00 , C07J41/00 , C07J43/00 , C07J71/00
CPC分类号: C07J41/00 , C07J41/0005 , C07J41/0011 , C07J43/00 , C07J71/0047 , C07J71/0063 , Y02P20/55
摘要: A compound of the formula and pharmaceutically acceptable salts, solvates, stereoisomers and prodrugs thereof, in isolation or in mixture, wherein, independently at each occurrence: R1 and R2 are selected from hydrogen, oxygen so as to form nitro or oxime, amino, sulfate, and sulfonic acid, and organic groups having 1-30 carbons and optionally containing 1-6 heteroatoms selected from nitrogen, oxygen, phosphorous, silicon, and sulfur, where R1 and R2 may, together with the N to which they are both bonded, form a heterocyclic structure that may be part of an organic group having 1-30 carbons and optionally containing 1-6 heteroatoms selected from nitrogen, oxygen and silicon, and where R1 may be a 2, or 3 atom chain to numeral 2 so that —N—R1— forms part of a fused bicyclic structure to ring A; R3 and R4 are selected from direct bonds to 6 and 7 respectively so as to form carbonyl groups, hydrogen, or a protecting group such that R3 and/or R4 is part of hydroxyl or carbonyl protecting group; numerals 1 through 17 each represent a carbon having substitution as described. The compounds may be formulated into pharmaceutical compositions, and used in the treatment and/or prevention of various conditions, including inflammation, asthma, an allergic disease, chronic obstructive pulmonary disease, atopic dermatitis, solid tumors, AIDS, ischemia, and cardiac arrhythmias.
摘要翻译: R 1和R 2各自独立地是分别地或以混合物形式的式及其药学上可接受的盐,溶剂合物,立体异构体和前药的化合物,其中每次出现:R 1和 选自氢,氧,以形成硝基或肟,氨基,硫酸根和磺酸,以及具有1-30个碳原子并且任选地含有1-6个选自氮,氧,磷,硅和硫的杂原子的有机基团,其中 R 1和R 2可以与它们都键合的N一起形成可以是具有1-30个碳的有机基团的一部分的杂环结构,以及 任选地含有1-6个选自氮,氧和硅的杂原子,并且其中R 1可以是2或3个原子链至2,使得-NR 1 - 形成环A的稠合双环结构的一部分; R 3和R 4分别选自6和7的直接键,以便形成羰基,氢或保护基,使得R 3, 和/或R 4是羟基或羰基保护基的一部分; 数字1至17各自表示如上所述具有取代的碳。 化合物可以配制成药物组合物,并用于治疗和/或预防各种病症,包括炎症,哮喘,过敏性疾病,慢性阻塞性肺病,特应性皮炎,实体瘤,AIDS,局部缺血和心律失常。
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公开(公告)号:US20070060553A1
公开(公告)日:2007-03-15
申请号:US11496052
申请日:2006-07-28
申请人: Jeffery Raymond , Claudia Kasserra , Yaping Shen
发明人: Jeffery Raymond , Claudia Kasserra , Yaping Shen
CPC分类号: C07J41/00 , C07J41/0005 , C07J41/0011 , C07J43/00 , C07J71/0047 , C07J71/0063 , Y02P20/55
摘要: A compound of the formula and pharmaceutically acceptable salts, solvates, stereoisomers and prodrugs thereof, in isolation or in mixture, wherein, independently at each occurrence: R1 and R2 are selected from hydrogen, oxygen so as to form nitro or oxime, amino, sulfate, and sulfonic acid, and organic groups having 1-30 carbons and optionally containing 1-6 heteroatoms selected from nitrogen, oxygen, phosphorous, silicon, and sulfur, where R1 and R2 may, together with the N to which they are both bonded, form a heterocyclic structure that may be part of an organic group having 1-30 carbons and optionally containing 1-6 heteroatoms selected from nitrogen, oxygen and silicon, and where R1 may be a 2, or 3 atom chain to numeral 2 so that —N—R1— forms part of a fused bicyclic structure to ring A; R3 and R4 are selected from direct bonds to 6 and 7 respectively so as to form carbonyl groups, hydrogen, or a protecting group such that R3 and/or R4 is part of hydroxyl or carbonyl protecting group; numerals 1 through 17 each represent a carbon having substitution as described. The compounds may be formulated into pharmaceutical compositions, and used in the treatment and/or prevention of various conditions, including inflammation, asthma, an allergic disease, chronic obstructive pulmonary disease, atopic dermatitis, solid tumors, AIDS, ischemia, and cardiac arrhythmias.
摘要翻译: R 1和R 2各自独立地是分别地或以混合物形式的式及其药学上可接受的盐,溶剂合物,立体异构体和前药的化合物,其中每次出现:R 1和 选自氢,氧,以形成硝基或肟,氨基,硫酸根和磺酸,以及具有1-30个碳原子并且任选地含有1-6个选自氮,氧,磷,硅和硫的杂原子的有机基团,其中 R 1和R 2可以与它们都键合的N一起形成可以是具有1-30个碳的有机基团的一部分的杂环结构,以及 任选地含有1-6个选自氮,氧和硅的杂原子,并且其中R 1可以是2或3个原子链至2,使得-NR 1 - 形成环A的稠合双环结构的一部分; R 3和R 4分别选自6和7的直接键,以便形成羰基,氢或保护基,使得R 3, 和/或R 4是羟基或羰基保护基的一部分; 数字1至17各自表示如上所述具有取代的碳。 化合物可以配制成药物组合物,并用于治疗和/或预防各种病症,包括炎症,哮喘,过敏性疾病,慢性阻塞性肺病,特应性皮炎,实体瘤,AIDS,局部缺血和心律失常。
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