where R1 is chosen from a group including hydrogen atom, (C1-C12)alkyl phenyl, naphthyl, (C5-C14)phenyl(C1-C12)alkyl, indolylalkyl which can contain up to 3 substitutes independently chosen from a group including halogen, -F, -CI, -Br, -I, -NO2, (C1-C12)alkyl, phenyl, naphthyl, -O-(C1-C12)alkyl; R2 is chosen from a group including (C1-C12)alkyl, phenyl, naphthyl, (C5-C14)phenyl (C1-C12)alkyl, indolylalkyl which can contain up to 3 substitutes independently chosen from a group including halogen, -F, -Cl, -Br, -I, -NO2, (C1-C12)alkyl, phenyl, naphthyl, -O-(C1-C12)alkyl; one of radicals R3 and R4 represents hydrogen atom, and other radical are chosen from a group including hydrogen atom, phenyl, naphthyl, indolylalkyl; R5 is chosen from a group including hydrogen atom, phenyl, naphthyl, -CO-(C3-C8)cycloalkyl, -CO-phenyl, -CO-(C5-C7)heteroaryl containing 1, 2 nitrogen atoms, -CO-(C3-C7)heteroaryl(C1-C4)alkyl containing 1, 2 nitrogen atoms, -CO-(C5-C6)heterocyclyl containing 1, 2 nitrogen or oxygen atoms, -CO-C*(R9R10)-NH2, -CO-CH2-C*(R9R10)-NH2, -CO-C*(R9R10)-CH2-NH2, phenylsulfonyl which can contain up to 3 substitutes independently chosen from a group including halogen, -F, -CI, -Br, -I, -N3, -CN, -NR7R8, -OH, -NO2, (C1-C4)alkyl; R6 represents hydrogen atom; R7 and R8 represent hydrogen atom; R9 and R10 are independently chosen from a group including hydrogen atom and (C1-C4)alkyl; m relates to 0, 1 or 2, and preferentially 0; and * means carbon atom in a R or S configurations, if it is chiralene.;EFFECT: invention refers to GHSS receptors antagonists and agonists which can be used for modulation of these receptors and are effective in treatment of said conditions, particularly growth impairment, cachexia, short-term, intermediate and/or long-term energy balance control; short-term, intermediate and/or long-term food intake control (stimulation and/or suppression); adipogenesis, adiposity and/or obesity; body weight growth and/or reduction in mammals.;22 cl, 6 tbl, 15 ex, 46 dwg"/> METHOD OF TREATMENT OR PREVENTION OF PHYSIOLOGICAL AND/OR PATHOPHYSIOLOGICAL CONDITIONS MEDIATED BY GROWTH HORMONE SECRETION STIMULATING RECEPTORS, TRIAZOLE AND BASED PHARMACEUTICAL COMPOSITION
首页> 外国专利> METHOD OF TREATMENT OR PREVENTION OF PHYSIOLOGICAL AND/OR PATHOPHYSIOLOGICAL CONDITIONS MEDIATED BY GROWTH HORMONE SECRETION STIMULATING RECEPTORS, TRIAZOLE AND BASED PHARMACEUTICAL COMPOSITION

METHOD OF TREATMENT OR PREVENTION OF PHYSIOLOGICAL AND/OR PATHOPHYSIOLOGICAL CONDITIONS MEDIATED BY GROWTH HORMONE SECRETION STIMULATING RECEPTORS, TRIAZOLE AND BASED PHARMACEUTICAL COMPOSITION

机译:治疗或预防生长激素分泌刺激受体,三唑和基础药物组合物介导的生理和/或生理条件的方法

摘要

FIELD: medicine, pharmaceutics.;SUBSTANCE: present invention refers to administration of formula (I) described new triazole derivatives as greline-like ligands of growth hormone secretion stimulating receptors (GHSS receptors) that can be effective in treatment or prevention of GHSS receptors mediated physiological and/or pathophysiological conditions in mammals, preferentially in humans. Formula (I): where R1 is chosen from a group including hydrogen atom, (C1-C12)alkyl phenyl, naphthyl, (C5-C14)phenyl(C1-C12)alkyl, indolylalkyl which can contain up to 3 substitutes independently chosen from a group including halogen, -F, -CI, -Br, -I, -NO2, (C1-C12)alkyl, phenyl, naphthyl, -O-(C1-C12)alkyl; R2 is chosen from a group including (C1-C12)alkyl, phenyl, naphthyl, (C5-C14)phenyl (C1-C12)alkyl, indolylalkyl which can contain up to 3 substitutes independently chosen from a group including halogen, -F, -Cl, -Br, -I, -NO2, (C1-C12)alkyl, phenyl, naphthyl, -O-(C1-C12)alkyl; one of radicals R3 and R4 represents hydrogen atom, and other radical are chosen from a group including hydrogen atom, phenyl, naphthyl, indolylalkyl; R5 is chosen from a group including hydrogen atom, phenyl, naphthyl, -CO-(C3-C8)cycloalkyl, -CO-phenyl, -CO-(C5-C7)heteroaryl containing 1, 2 nitrogen atoms, -CO-(C3-C7)heteroaryl(C1-C4)alkyl containing 1, 2 nitrogen atoms, -CO-(C5-C6)heterocyclyl containing 1, 2 nitrogen or oxygen atoms, -CO-C*(R9R10)-NH2, -CO-CH2-C*(R9R10)-NH2, -CO-C*(R9R10)-CH2-NH2, phenylsulfonyl which can contain up to 3 substitutes independently chosen from a group including halogen, -F, -CI, -Br, -I, -N3, -CN, -NR7R8, -OH, -NO2, (C1-C4)alkyl; R6 represents hydrogen atom; R7 and R8 represent hydrogen atom; R9 and R10 are independently chosen from a group including hydrogen atom and (C1-C4)alkyl; m relates to 0, 1 or 2, and preferentially 0; and * means carbon atom in a R or S configurations, if it is chiralene.;EFFECT: invention refers to GHSS receptors antagonists and agonists which can be used for modulation of these receptors and are effective in treatment of said conditions, particularly growth impairment, cachexia, short-term, intermediate and/or long-term energy balance control; short-term, intermediate and/or long-term food intake control (stimulation and/or suppression); adipogenesis, adiposity and/or obesity; body weight growth and/or reduction in mammals.;22 cl, 6 tbl, 15 ex, 46 dwg
机译:领域:药物:本发明涉及式(I)的施用,其描述了作为生长激素分泌刺激受体(GHSS受体)的greline样配体的新三唑衍生物,其可以有效治疗或预防介导的GHSS受体哺乳动物,尤其是人类的生理和/或病理生理状况。公式(I):其中R1选自氢原子,(C1- C 12)烷基苯基,萘基,(C 5 -C 14)苯基(C 1 -C 12)烷基,吲哚基烷基,其可包含多达3个独立地选自卤素,-F,-Cl,-Br,-I,-NO的取代基 2 ,(C1-C12)烷基,苯基,萘基,-O-(C1-C12)烷基; R 2 选自包括以下的组:(C 1 -C 12)烷基,苯基,萘基,(C 5 -C 14)苯基(C 1 -C 12)烷基,吲哚基烷基,其可以包含多达3个独立地选自的取代基。包括卤素,-F,-Cl,-Br,-I,-NO 2 ,(C1-C12)烷基,苯基,萘基,-O-(C1-C12)烷基的基团;基团R3和R4之一代表氢原子,其他基团选自氢原子,苯基,萘基,吲哚基烷基; R 5选自氢原子,苯基,萘基,-CO-(C 3 -C 8)环烷基,-CO-苯基,-CO-(C 5 -C 7)含1、2个氮原子的杂芳基,-CO-(C3含1、2个氮原子的-C7)杂芳基(C1-C4)烷基,含1、2个氮或氧原子的-CO-(C5-C6)杂环基,-CO-C *(R9R10)-NH 2 < / Sub>,-CO-CH 2 -C *(R9R10)-NH 2 ,-CO-C *(R9R10)-CH 2 -NH 2 ,苯磺酰基,最多可包含3个独立选自卤素,-F,-Cl,-Br,-I,-N 3 的取代基,-CN,-NR7R8,-OH,-NO 2 ,(C1-C4)烷基; R6代表氢原子; R7和R8代表氢原子; R9和R10独立地选自氢原子和(C1-C4)烷基; m与0、1或2有关,优选为0; *效果:本发明涉及GHSS受体拮抗剂和激动剂,其可用于调节这些受体并有效治疗所述病症,特别是生长障碍,恶病质,短期,中期和/或长期能量平衡控制;短期,中期和/或长期食物摄入控制(刺激和/或抑制);脂肪形成,肥胖和/或肥胖;体重增加和/或哺乳动物的减少。; 22 cl,6 tbl,15 ex,46 dwg

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