摘要:
The present invention provides compounds for treating or preventing an HIV infection, or treating AIDS or ARC comprising administering a compound according to formula I where Ar, R1—R5, R7a, R7b, R7c, R8—R10, X1, X2 m, n, o and p are as defined herein
摘要:
The present invention provides compounds for treating or preventing an HIV infection, or treating AIDS or ARC comprising administering a compound according to formula I where Ar, R1-R5, R11c and X1 are as defined herein.
摘要:
The present invention provides compositions for treating an HIV infection comprising administering a compound according to formula I where Ar, R1-R5, R11c and X1 are as defined herein with at least one carrier, excipient or diluent.
摘要:
The present invention provides compositions for treating an HIV infection comprising administering a compound according to formula I where Ar, R1-R5, R11c and X1 are as defined herein with at least one carrier, excipient or diluent.
摘要:
The present invention provides compounds of the formula: wherein R2 is substituted cycloalkyl, heterosubstituted cycloalkyl, heteroalkylsubstituted cycloalkyl, heterosubstituted cycloalkyl-alkyl, optionally substituted heterocyclyl, spiro-substituted cycloalkyl, aralkoxy, alkoxy, -alkylene-S(O)n-alkyl (wherein n is 1 or 2), or —SO2Ar2; and R1, R3, and Ar1 are those defined herein, and methods for preparation and uses thereof.
摘要翻译:本发明提供下式的化合物:其中R2是取代的环烷基,杂取代的环烷基,杂烷基取代的环烷基,杂取代的环烷基 - 烷基,任选取代的杂环基,螺取代的环烷基,芳烷氧基,烷氧基, - 亚烷基-S(O) 其中n为1或2)或-SO 2 Ar 2; 且R1,R3和Ar1是本文定义的那些,以及其制备方法和用途。
摘要:
The invention provides compounds represented by the formula: wherein R1, R2, R3, R4, and n are as defined in the Summary of the Invention; and individual isomers, racemic or non-racemic mixtures of isomers, and pharmaceutically acceptable salts thereof. The invention further relates to pharmaceutical compositions containing such compounds, methods for their use as therapeutic agents, and methods of preparation thereof.
摘要:
The present invention provides compounds of the Formula I and II: wherein R1, R3, W, Z, X1, X2, Ar1, R8 and R9 are as defined herein, and methods and intermediates for their preparation and uses thereof.
摘要:
Disorders mediated by p38 kinase inhibitors are treated with compounds of the formula: or salts thereof, wherein: R1 is hydrogen or alkyl; R2 is substituted cycloalkyl, heterosubstituted cycloalkyl, helcroalkylsubstituted cycloalkyl, heterosubstituted cycloalkyl-alkly, heterocyclyl, heterocyclyl spiro cycloalkyl, aralkoxy, alkoxy, -alkylene-S(O)n-alkyl (where is 1 or 2) or —SO2Ar2; R3 is hydrogen, amino, monoalkylamino, dialkylamino, acylamino, —NR8—C(═O)—Rb (where Ra is hydrogen or alkyl and Rh is heterocyclyl or heteroalkyl), alkyl, cycloalkyl, phthalimidoalkyl, aryl, aralkyl, haloalkyl, heteroalkyl, cyanoalkyl, -alkylene-C(O) R (where R is hydrogen, alkyl, hydroxy, alkoxy, amino, monoalkylamino or dialkylamino) or acyl; and each of Ar1 and Ar2 is independently aryl.
摘要翻译:由p38激酶抑制剂介导的疾病用下式化合物或其盐处理,其中:R 1是氢或烷基; R 2是取代的环烷基,杂取代的环烷基,环烷基取代的环烷基,杂取代的环烷基 - 烷基,杂环基, 杂环基螺环烷基,芳烷氧基,烷氧基, - 亚烷基-S(O)n-烷基(其中为1或2)或-SO 2 Ar 2; R 3为氢,氨基,单烷基氨基,二烷基氨基,酰氨基, (其中R 1为氢或烷基且R h为杂环基或杂烷基),烷基,环烷基,苯二甲酰亚氨基烷基,芳基,芳烷基,卤代烷基,杂烷基,氰基烷基, - 亚烷基-C(O)R(其中R是氢,烷基,羟基,烷氧基,氨基,单烷基氨基或二烷基氨基)或酰基; Ar 1和Ar 2的每一个独立地是芳基。
摘要:
The present invention provides compounds of the Formula I and II: wherein R1, R3, W, Z, X1, X2, Ar1, R8 and R9 are as defined herein, and methods and intermediates for their preparation and uses thereof.
摘要:
The present invention provides compounds of the Formula I and II: wherein R1, R3, W, Z, X1, X2, Ar1, R8 and R9 are as defined herein, and methods and intermediates for their preparation and uses thereof.