首页> 外国专利> SIGMA LIGANDS FOR POTENTIATION OF ANALGETIC EFFECT OF OPIOIDS AND OPIATES IN POSTOPERATIVE PAIN AND TO REDUCE THE DEPENDENCE ON THEM

SIGMA LIGANDS FOR POTENTIATION OF ANALGETIC EFFECT OF OPIOIDS AND OPIATES IN POSTOPERATIVE PAIN AND TO REDUCE THE DEPENDENCE ON THEM

机译:SIGMA配药可增强术后疼痛中阿片类药物和阿片类药物的镇痛作用,并降低它们的依赖性

摘要

1. A combination for simultaneous, separate or sequential administration, comprising at least one sigma ligand of the formula (I), or a pharmaceutically acceptable salt, isomer, prodrug or solvate thereof, and at least one opioid or opiate intended for the prevention and / or treatment of pain resulting from surgery, where R is selected from the group consisting of hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkenyl, substituted substituted or unsubstituted aryl, substituted or unsubstituted arylalkyl, substituted or unsubstituted, aromatic or non-aromatic heterocyclyl, substituted or unsubstituted heterocyclylalkyl, -COR, -C (O) OR, -C (O) NRR, -CH = NR, -CN, - OR, —OC (O) R, —S (O) —R, —NRR, —NRC (O) R, —NO, —N = CRR or halogen; R is selected from the group consisting of hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted aryl, substituted or unsubstituted arylalkyl, substituted or unsubstituted, aroma heterocyclyl substituted or unsubstituted heterocyclylalkyl, -COR, -C (O) OR, -C (O) NRR, -CH = NR, -CN, -OR, -OC (O) R, -S (O) -R, -NRR, -NRC (O) R, -NO, -N = CRR or halogen; R and R are independently selected from the group consisting of hydrogen, substituted or unsubstituted alkyl, substituted or unsubstituted cycloalkyl, substituted or unsubstituted alkenyl, substituted or unsubstituted aryl substituted or unsubstituted arylalkyl, substituted or unsubstituted, aromatic or non-aromatic heterocyclyl, substituted or unsubstituted heterocyclylalkyl
机译:1.用于同时,分开或顺序给药的组合,其包含至少一种式(I)的σ配体或其药学上可接受的盐,异构体,前药或溶剂化物,以及至少一种用于预防和预防阿片类药物或阿片类药物。 /或手术引起的疼痛的治疗,其中R选自氢,取代或未取代的烷基,取代或未取代的环烷基,取代或未取代的烯基,取代的取代或未取代的芳基,取代或未取代的芳基烷基,取代或未取代的基团,芳族或非芳族杂环基,取代或未取代的杂环基烷基,-COR,-C(O)OR,-C(O)NRR,-CH = NR,-CN,-OR,-OC(O)R,-S( O)-R,-NRR,-NRC(O)R,-NO,-N = CRR或卤素; R选自氢,取代或未取代的烷基,取代或未取代的环烷基,取代或未取代的烯基,取代或未取代的芳基,取代或未取代的芳基烷基,取代或未取代的,芳族杂环基取代或未取代的杂环基烷基,-COR,- C(O)OR,-C(O)NRR,-CH = NR,-CN,-OR,-OC(O)R,-S(O)-R,-NRR,-NRC(O)R,- NO,-N = CRR或卤素; R 1和R 2独立地选自氢,取代或未取代的烷基,取代或未取代的环烷基,取代或未取代的烯基,取代或未取代的芳基取代或未取代的芳烷基,取代或未取代的,芳族或非芳族杂环基,取代的或未取代的杂环基烷基

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