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OXAZOLINONE DERIVATIVE HAVING INTRACELLULAR PHOSPHOLIPASE A₂INHIBITOR ACTIVITY With Intracellular Phospholipase A 2 Inhibitory Activity
OXAZOLINONE DERIVATIVE HAVING INTRACELLULAR PHOSPHOLIPASE A₂INHIBITOR ACTIVITY With Intracellular Phospholipase A 2 Inhibitory Activity
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机译:恶唑啉酮衍生物具有细胞内磷脂酶A 2的抑制活性和细胞内磷脂酶A 2的抑制活性
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摘要
The present invention relates to a compound of the general formula and a pharmaceutical composition containing the same:;Wherein a and b are each carbon atoms; combination of a and b Represents a single bond or a double bond; X is a hydrogen atom, an optionally substituted aryl group, an optionally substituted heteroaryl group or an optionally substituted aralkyl group; Y is a hydrogen atom, an optionally substituted aryl group, an optionally substituted aralkyl group or a carboxyl group or a related functional group thereof; Z is a hydrogen atom, an optionally substituted alkyl group, an optionally substituted alkenyl group, an optionally substituted alkynyl group, an optionally substituted aralkyl group, an optionally substituted arylalkenyl group, an optionally substituted heteroarylalkyl, optionally substituted Heteroarylalkenyl groups, optionally substituted aryloxyalkyl groups, optionally substituted aralkyloxyalkyl groups, optionally substituted arylcarbonylalkyl groups, optionally substituted arylsulfonyl alkyl groups, optionally substituted heteroarylsulfonylalkyl groups , Optionally substituted aminoalkyl group, optionally substituted aralkyloxycarbonyl group, optionally substituted arylcarbonyl group, optionally substituted alkylsulfonyl group, optionally substituted arylsulfonyl group or optionally substituted heteroarylsulfonyl group Provided that X, Y and Z are not simultaneously hydrogen atoms.;The compound of the present invention has intracellular posipolipase A 2 inhibitory activity.
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机译:本发明涉及通式化合物和含有该化合物的药物组合物:其中a和b分别是碳原子; a和b的组合表示单键或双键; X是氢原子,任选取代的芳基,任选取代的杂芳基或任选取代的芳烷基; Y为氢原子,任选取代的芳基,任选取代的芳烷基或羧基或其相关官能团; Z是氢原子,任选取代的烷基,任选取代的烯基,任选取代的炔基,任选取代的芳烷基,任选取代的芳基烯基,任选取代的杂芳基烷基,任选取代的杂芳基烯基,任选取代的芳氧基烷基,任选取代的芳烷氧基烷基,任选取代的芳基羰基烷基,任选取代的芳基磺酰基烷基,任选取代的氨基烷基,任选取代的芳烷氧基羰基,任选取代的芳羰基,任选取代的烷基磺酰基,任选取代的芳基磺酰基或任选取代的杂芳磺酰基前提是X,Y和Z不是同时为氢原子。;本发明的化合物具有细胞内Popolipolipase A 2 Sub>抑制活性虚拟性。
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