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公开(公告)号:US5621123A
公开(公告)日:1997-04-15
申请号:US247169
申请日:1994-05-20
申请人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased , Vera M. Wallach, legal representative
发明人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased , Vera M. Wallach, legal representative
CPC分类号: C07J51/00 , C07D213/38 , C07F9/224 , C07F9/2458 , C07J41/0005 , C07J41/005 , C07J41/0072 , C07J43/003 , Y10S514/866
摘要: Provided are cyclic hydrocarbons of Formula I ##STR1## with an aminoalkyl sidechain that are useful for treating phospholipase A2 mediated conditions, diabetes, and obesity.
摘要翻译: 提供式I的环状烃与氨基烷基侧链可用于治疗磷脂酶A2介导的病症,糖尿病和肥胖症。
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公开(公告)号:US5373095A
公开(公告)日:1994-12-13
申请号:US126153
申请日:1993-09-23
申请人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased
发明人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased
CPC分类号: C07J51/00 , C07D213/38 , C07F9/224 , C07F9/2458 , C07J41/0005 , C07J41/005 , C07J41/0072 , C07J43/003
摘要: Provided are cyclic hydrocarbons of Formula I ##STR1## with an aminoalkyl sidechain that are useful for treating phospholipase A2 mediated conditions, diabetes, and obesity.
摘要翻译: 提供式I的环状烃与氨基烷基侧链可用于治疗磷脂酶A2介导的病症,糖尿病和肥胖症。
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公开(公告)号:US5187299A
公开(公告)日:1993-02-16
申请号:US793486
申请日:1991-11-13
申请人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased , Wallach, Legal Representative, by Vera M.
发明人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased , Wallach, Legal Representative, by Vera M.
CPC分类号: C07J51/00 , C07D213/38 , C07F9/224 , C07F9/2458 , C07J41/0005 , C07J41/005 , C07J41/0072 , C07J43/003
摘要: Provided are cyclic hydrocarbons of Formula I ##STR1## with an aminoalkyl sidechain.
摘要翻译: 提供式I的环状烃与氨基烷基侧链。
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公开(公告)号:US5001234A
公开(公告)日:1991-03-19
申请号:US435481
申请日:1989-10-16
CPC分类号: C07J41/0072 , C07J41/0005 , C07J41/0094 , C07J51/00
摘要: This invention provides novel cyclic hydrocarbons of the formula: ##STR1## wherein R is selected from the group consisting of CH.sub.2 .dbd.CH--CH.sub.2 --, HO--CH.sub.2 CH.sub.2 CH.sub.2 --, and CH.sub.3 ;wherein R.sub.1 is selected from the group consisting of m-trifluoromethylphenylmethyl, 2-thienylmethyl, and p-aminosulfonylphenylethyl;wherein R.sub.2 and R.sub.3 are methyl or hydrogen;wherein R.sub.4 is hydrogen or --OH;a compound of the formula ##STR2## wherein R is (CH.sub.3).sub.2 NCH.sub.2 CH.sub.2 CH.sub.2 -- or NH.sub.2 CH.sub.2 CH.sub.2 CH.sub.2 --;or a compound of the formula ##STR3## wherein the dashed line indicates that the 2-3 bond is saturated or unsaturated and, wherein R is hydrogen or methyl.These compounds are useful for inhibiting adverse physiological symptoms associated with phospholipase A.sub.2 and for treating hyperglycemia associated diseases such as diabetes and obesity.
摘要翻译: PCT No.PCT / US88 / 00978 Sec。 371日期:1989年10月16日 102(e)日期1989年10月16日PCT提交1988年4月1日PCT公布。 出版物WO88 / 08002 本发明提供了下式的新型环状烃:其中R选自CH 2 = CH-CH 2 - ,HO-CH 2 CH 2 CH 2 - 和CH 3; 其中R1选自间三氟甲基苯甲基,2-噻吩基甲基和对氨基磺酰基苯乙基; 其中R2和R3是甲基或氢; 其中R4是氢或-OH; 其中R为(CH 3)2 NHCH 2 CH 2 CH 2 - 或NH 2 CH 2 CH 2 CH 2 - 的式 或式“IMAGE”的化合物,其中虚线表示2-3键是饱和或不饱和的,其中R是氢或甲基。 这些化合物可用于抑制与磷脂酶A2相关的不良生理学症状和用于治疗高血糖症相关疾病如糖尿病和肥胖症。
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公开(公告)号:US5145874A
公开(公告)日:1992-09-08
申请号:US663037
申请日:1991-02-25
申请人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased , by Vera M. Wallach, legal representative
发明人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased , by Vera M. Wallach, legal representative
CPC分类号: C07J51/00 , C07D213/38 , C07F9/224 , C07F9/2458 , C07J41/0005 , C07J41/005 , C07J41/0072 , C07J43/003
摘要: Provided are cyclic hydrocarbons of Formula I ##STR1## with an aminoalkyl sidechain that are useful for treating phospholipase A2 mediated conditions, diabetes, and obesity.
摘要翻译: 提供式I的环状烃与氨基烷基侧链可用于治疗磷脂酶A2介导的病症,糖尿病和肥胖症。
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公开(公告)号:US5334712A
公开(公告)日:1994-08-02
申请号:US976751
申请日:1992-11-16
申请人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased
发明人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased
CPC分类号: C07J51/00 , C07D213/38 , C07F9/224 , C07F9/2458 , C07J41/0005 , C07J41/005 , C07J41/0072 , C07J43/003 , Y10S514/866
摘要: Provided are cyclic hydrocarbons of Formula I ##STR1## with an aminoalkyl sidechain that are useful for treating phospholipase A2 mediated conditions, diabetes, and obesity.
摘要翻译: 提供式I的环状烃与氨基烷基侧链可用于治疗磷脂酶A2介导的病症,糖尿病和肥胖症。
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公开(公告)号:US5196542A
公开(公告)日:1993-03-23
申请号:US657721
申请日:1991-02-20
申请人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased
发明人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased
CPC分类号: C07J51/00 , C07D213/38 , C07F9/224 , C07F9/2458 , C07J41/0005 , C07J41/005 , C07J41/0072 , C07J43/003
摘要: Provided are cyclic hydrocarbons of Formula I ##STR1## with an aminoalkyl sidechain that are useful for treating phospholipase A2 mediated conditions, diabetes, and obesity.
摘要翻译: 提供式I的环状烃与氨基烷基侧链可用于治疗磷脂酶A2介导的病症,糖尿病和肥胖症。
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公开(公告)号:US4917826A
公开(公告)日:1990-04-17
申请号:US117851
申请日:1987-06-16
申请人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased
发明人: Roy A. Johnson , Gordon L. Bundy , Gilbert A. Youngdale , Douglas R. Morton , Donald P. Wallach, deceased
CPC分类号: C07J51/00 , C07D213/38 , C07F9/224 , C07F9/2458 , C07J41/0005 , C07J41/005 , C07J41/0072 , C07J43/003 , Y10S514/866
摘要: Provided are cyclic hydrocarbons of Formula I ##STR1## with an aminoalkyl sidechain that are useful for treating phospholipase A2 mediated conditions, diabetes, and obesity.
摘要翻译: PCT No.PCT / US86 / 02116 Sec。 371日期1987年6月16日第 102(e)日期1987年6月16日PCT提交1986年10月7日PCT公布。 公开号WO87 / 02367 日本1987年4月23日。提供了具有氨基烷基侧链的式I的环状碳氢化合物,其可用于治疗磷脂酶A2介导的病症,糖尿病和肥胖症。
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公开(公告)号:US5852195A
公开(公告)日:1998-12-22
申请号:US809224
申请日:1996-11-04
申请人: Karen Rene Romines , Gordon L. Bundy , Theresa M. Schwartz , Ruben A. Tommasi , Joseph W. Strohbach , Steven Ronald Turner , Suvit Thaisrivongs , Paul Adrian Aristoff , Paul D. Johnson , Harvey Irving Skulnick , Louis L. Skaletzky , David John Anderson , Joel Morris , Ronald B. Gammill , George P. Luke
发明人: Karen Rene Romines , Gordon L. Bundy , Theresa M. Schwartz , Ruben A. Tommasi , Joseph W. Strohbach , Steven Ronald Turner , Suvit Thaisrivongs , Paul Adrian Aristoff , Paul D. Johnson , Harvey Irving Skulnick , Louis L. Skaletzky , David John Anderson , Joel Morris , Ronald B. Gammill , George P. Luke
IPC分类号: A61K31/365 , A61K31/366 , A61K31/415 , A61K31/425 , A61K31/44 , A61K31/4427 , A61K31/443 , A61K31/47 , A61K31/4709 , A61K31/505 , A61K31/506 , A61K31/54 , A61P31/12 , C07D20060101 , C07D309/32 , C07D309/38 , C07D309/40 , C07D311/02 , C07D311/08 , C07D311/74 , C07D311/94 , C07D401/12 , C07D403/12 , C07D405/00 , C07D405/12 , C07D405/14 , C07D407/00 , C07D409/00 , C07D417/00 , C07D417/12
CPC分类号: C07D405/12 , C07D309/32 , C07D309/38 , C07D311/02 , C07D311/74 , C07D405/14
摘要: The present invention relates to compounds of formulae (I) and (II) which are pyran-2-ones, 5,6-dihydro-pyran-2-ones, 4-hydroxy-benzopyran-2-ones, 4-hydroxy-cycloalkyl�b!pyran-2-ones, and derivatives thereof, useful for inhibiting a retrovirus in a mammalian cell infected with said retrovirus, wherein R.sub.10 and R.sub.20 taken together are formulae (III) and (IV). ##STR1##
摘要翻译: PCT No.PCT / US95 / 05219 Sec。 371日期:1996年11月4日 102(e)日期1996年11月4日PCT提交1995年5月4日PCT公布。 公开号WO95 / 30670 PCT 日期:1月16日,1995本发明涉及式(I)和(II)的化合物,其为吡喃-2-酮,5,6-二氢 - 吡喃-2-酮,4-羟基 - 苯并吡喃-2-酮, 可用于抑制感染所述逆转录病毒的哺乳动物细胞中的逆转录病毒的4-羟基 - 环烷基[b]吡喃-2-酮及其衍生物,其中R 10和R 20一起为式(III)和(IV)。 (一)图像(二)<图像>(三)<图像>(四)
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公开(公告)号:US5502187A
公开(公告)日:1996-03-26
申请号:US317934
申请日:1994-10-03
IPC分类号: C07D471/04 , C07D487/04 , C07H15/26 , C07D265/04
CPC分类号: C07D471/04 , C07D487/04 , C07H15/26
摘要: The pharmaceutically active bicyclic heterocyclic amines (XXX) ##STR1## where W.sub.1 is --N.dbd. or --CH.dbd.; W.sub.3 is --N.dbd. or --CH.dbd.; W.sub.5 is --N.dbd. or --CR.sub.5 -- with the proviso that W.sub.5 is --CR.sub.5 -- when both W.sub.1 and W.sub.3 are --N.dbd. which are useful as pharmaceuticals in treating mild and/or moderate to severe head injury, subarachnoid hemorrhage and subsequent ischemic stroke, asthma and reduction of mucous formation/secretion in the lung and other diseases and injuries.
摘要翻译: 其中W1是-N =或-CH =的药学活性双环杂环胺(XXX)(XXX) W3是-N =或-CH =; W5是-N =或-CR5-,条件是当W 1和W 3均为-N =时,W 5为-CR 5,其可用作治疗轻度和/或中度至重度头部损伤,蛛网膜下腔出血和随后缺血性中风的药物 ,哮喘和肺部粘液形成/分泌减少等疾病和损伤。
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