-
1.
公开(公告)号:US06627632B2
公开(公告)日:2003-09-30
申请号:US09919590
申请日:2001-07-30
申请人: Thomas P. Parks , Vivien Mak , Jung-Chung Lee , Charles Lee
发明人: Thomas P. Parks , Vivien Mak , Jung-Chung Lee , Charles Lee
IPC分类号: A61K3150
CPC分类号: A61K9/0031 , A61K31/198 , A61K31/21 , A61K31/505 , A61K31/513 , A61K31/519 , A61K31/52 , A61K31/522
摘要: Compositions and methods for the treatment of anorectal disorders are provided in which certain combinations of NO donors, PDE inhibitors, superoxide (O2−) scavengers, &bgr;-adrenergic agonists, cAMP-dependent protein kinase activators, &agr;1-adrenergic antagonists, L-type Ca2+ channel blockers, estrogens, ATP-sensitive K+ channel activators and smooth muscle relaxants are used.
摘要翻译: 提供了用于治疗肛门直肠疾病的组合物和方法,其中NO供体,PDE抑制剂,超氧化物(O 2 - )清除剂,β-肾上腺素能激动剂,cAMP依赖性蛋白激酶激活剂,α1-肾上腺素能拮抗剂, 类型的Ca 2+通道阻滞剂,雌激素,ATP敏感性K +通道激活剂和平滑肌松弛剂。
-
2.
公开(公告)号:US06395736B1
公开(公告)日:2002-05-28
申请号:US09460306
申请日:1999-12-13
申请人: Thomas P. Parks , Vivien Mak , Jung-Chung Lee , Charles Lee
发明人: Thomas P. Parks , Vivien Mak , Jung-Chung Lee , Charles Lee
IPC分类号: A61K3150
CPC分类号: A61K31/21 , A61K31/198 , A61K31/505 , A61K31/52
摘要: Compositions and methods for the treatment of anorectal disorders are provided in which certain combinations of NO donors, PDE inhibitors, superoxide (O2−) scavengers, &bgr;-adrenergic agonists, cAMP-dependent protein kinase activators, &agr;1-adrenergic antagonists, L-type Ca2+ channel blockers, estrogens, ATP-sensitive K+ channel activators and smooth muscle relaxants are used.
摘要翻译: 提供了治疗肛门直肠疾病的组合物和方法,其中NO供体,PDE抑制剂,超氧化物(O 2 - )清除剂,β-肾上腺素能激动剂,cAMP依赖性蛋白激酶激活剂,α1-肾上腺素能拮抗剂,L型Ca2 + 使用通道阻滞剂,雌激素,ATP敏感性K +通道激活剂和平滑肌松弛剂。
-
公开(公告)号:US06391869B1
公开(公告)日:2002-05-21
申请号:US09595390
申请日:2000-06-14
申请人: Thomas P. Parks , Vivien Mak , Jung-Chung Lee , Charles Lee
发明人: Thomas P. Parks , Vivien Mak , Jung-Chung Lee , Charles Lee
IPC分类号: A61K3155
CPC分类号: A61K31/00 , A61K9/0031 , A61K9/02 , A61K31/137 , A61K31/4015 , A61K31/444 , A61K31/519 , A61K31/52 , A61K31/522 , A61K31/554 , A61K45/06 , A61K47/06 , A61K47/10 , A61K2300/00
摘要: Compositions and methods for the treatment of anorectal disorders are provided in which certain combinations of NO donors, PDE inhibitors, superoxide (O2−) scavengers, &bgr;-adrenergic agonists, cAMP-dependent protein kinase activators, &agr;1-adrenergic antagonists, L-type Ca2+ channel blockers, estrogens, ATP-sensitive K+ channel activators and smooth muscle relaxants are used.
-
公开(公告)号:US06699886B2
公开(公告)日:2004-03-02
申请号:US10160977
申请日:2002-05-31
申请人: Thomas P. Parks , Don R. Baker
发明人: Thomas P. Parks , Don R. Baker
IPC分类号: A61K31405
CPC分类号: A61K31/00 , A61K31/366 , A61K31/403 , A61K31/405 , A61K31/435
摘要: The present invention provides store operated calcium influx inhibitor compounds, pharmaceutical compositions, and methods of use. The compounds are useful for treating an inflammatory disease or treating an inflammatory reaction. Preferably, compounds, compositions and methods of this invention are used for treatment of inflammatory skin, pulmonary, musculoskeletal, and gastrointestinal diseases, as well as autoimmune disorders, transplantation treatment, and osteoporosis.
-
公开(公告)号:US06869961B2
公开(公告)日:2005-03-22
申请号:US10670665
申请日:2003-09-24
申请人: Thomas P. Parks , Don R. Baker
发明人: Thomas P. Parks , Don R. Baker
IPC分类号: A61K31/00 , A61K31/366 , A61K31/403 , A61K31/405 , A61K31/435 , C07D221/02 , C07D401/02
CPC分类号: A61K31/00 , A61K31/366 , A61K31/403 , A61K31/405 , A61K31/435
摘要: The present invention provides store operated calcium influx inhibitor compounds, pharmaceutical compositions, and methods of use. The compounds are useful for treating an inflammatory disease or treating an inflammatory reaction. Preferably, compounds, compositions and methods of this invention are used for treatment of inflammatory skin, pulmonary, musculoskeletal, and gastrointestinal diseases, as well as autoimmune disorders, transplantation treatment, and osteoporosis.
摘要翻译: 本发明提供商店操作的钙流入抑制剂化合物,药物组合物和使用方法。 该化合物可用于治疗炎性疾病或治疗炎性反应。 优选地,本发明的化合物,组合物和方法用于治疗炎性皮肤,肺,肌肉骨骼和胃肠道疾病,以及自身免疫性疾病,移植治疗和骨质疏松症。
-
公开(公告)号:US6093723A
公开(公告)日:2000-07-25
申请号:US908211
申请日:1997-08-08
IPC分类号: C07D491/048 , A61K31/4355 , A61K31/4365 , A61K31/437 , A61K31/444 , A61P37/02 , C07D471/04 , C07D495/04 , A61K31/44 , A61K31/535
CPC分类号: C07D471/04 , A61K31/437 , A61K31/444
摘要: This invention relates to 4-substituted .beta.-carbolines and .beta.-carboline analogs that inhibit Ca.sup.+2 influx and interleukin-2 (IL-2) production. The 4-substituted .beta.-carbolines and .beta.-carboline analogs of this invention are represented by formula (I): ##STR1## wherein Q, n, R, R', R" and R.sub.1 -R.sub.4 are as defined herein. This invention also relates to methods for producing .beta.-carbolines. Because of their selective immunomodulating properties, the compounds and pharmaceutical compositions of this invention are particularly well suited for preventing and treating immune disorders, including autoimmune disease, inflammatory disease, organ transplant rejection and other disorders associated with IL-2 mediated immune response.
摘要翻译: 本发明涉及抑制Ca + 2流入和白细胞介素-2(IL-2)产生的4-取代的β-咔啉和β-咔啉类似物。 本发明的4-取代的β-咔啉和β-咔啉类似物由式(I)表示:其中Q,n,R,R',R“和R 1 -R 4如本文所定义。 本发明还涉及生产β-咔啉的方法。 由于其选择性免疫调节特性,本发明的化合物和药物组合物特别适用于预防和治疗包括自身免疫性疾病,炎性疾病,器官移植排斥和与IL-2介导的免疫应答相关的其它病症的免疫疾病。
-
-
-
-
-