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MORPHOLINE AND THIOMORPHOLINE TACHYKININ RECEPTOR ANTAGONISTS

机译:吗啉和硫代高磷激肽激肽受体拮抗剂

摘要

Substituted heterocycles of general structural formula (I) or apharmaceutically acceptable salt thereof, wherein: R1 is selected from thegroup consisting of: hydrogen; C1-6 alkyl, unsubstituted or substituted; C2-6alkenyl, unsubstituted or substituted; C2-6 alkynyl; phenyl, unsubstitued orsubstituted; X is selected from the group consisting of: -O-, -S-, -SO-, -SO2-; Y is selected from the group consisting of: a single bond, -O-, -S-, -CO-, -CH2, -CHR5- and -CR15R16; Z = C1-6 alkyl, are tachykinin receptor antagonistsuseful in the treatment of inflammatory diseases, pain or migraine, asthma andemesis, and calcium channel blockers useful in the treatment of cardiovascularconditions such as angina, hypertension or ischemia.
机译:通式(I)或a的取代杂环其药学上可接受的盐,其中:R1选自氢:未取代或取代的C 1-6烷基; C2-6未取代或取代的烯基; C2-6炔基;未取代的苯基或替代X选自:-O-,-S-,-SO-,-SO2-; Y选自:单键,-O-,-S-,-CO-,-CH2,-CHR5-和-CR15R16; Z = C1-6烷基,是速激肽受体拮抗剂可用于治疗炎性疾病,疼痛或偏头痛,哮喘和呕吐和钙通道阻滞剂可用于治疗心血管疾病诸如心绞痛,高血压或局部缺血。

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