首页> 外国专利> Combination comprising an HMG-CoA reductase inhibitor and an insulin secretor enhancer or an insulin sensitizer

Combination comprising an HMG-CoA reductase inhibitor and an insulin secretor enhancer or an insulin sensitizer

机译:包含HMG-CoA还原酶抑制剂和胰岛素分泌增强剂或胰岛素敏化剂的组合

摘要

Claim 1: a combination of at least two components selected from the group consisting of: (i) an HMG CoA reductase inhibitor or a pharmaceutically acceptable Salt thereof, selected from the group consisting of atorvastatin, cerivastatin, fluvastatin, L Ovastatina, pitavastatin, pravastatin, rosuvastatin,And simvastatin; and (ii) a potentiating insulin secretion or a pharmaceutically acceptable Salt thereof; or (b) an insulin Sensitizing or a pharmaceutically acceptable Salt thereof.Claim 2: a combination of at least two components selected from the group consisting of: (i) an HMG CoA reductase inhibitor or a pharmaceutically acceptable Salt thereof; and (ii) a potentiating insulin secretion or a pharmaceutically acceptable Salt The Same,Selected from the group consisting of: tolbutamide chlorpropamide tolazamide acetohexamide,;;; glicopiramida; Glibenclamide; Gliclazide; 1 - butyl - 4 - metanilurea; carbutamide; glibonurida; glipizide; gliquidone; glisoxepide glybuthiazol glybuzole glyhexamide;;;; glimidina glypinamide; fenbutam; Ida; tolilciclamida, nateglinide, repaglinide, mitiglinide, glimepiride, dpp-iv Inhibitors, GLP1,GLP1, glp-1 (7 36); gln.sup.9-glp-1 (7 - 37); d-gln.sup.9-glp-1 (7 - 37); acetil-lys-sup.9-glp-1 (7 - 37); thr.sup.16-lys.sup.18-glp-1 (7 - 37); and lys.sup.18-glp-1 (7 - 37); or (b) an insulin Sensitizing or a pharmaceutically acceptable Salt thereof.A combination of claim 10: According to claim 1, wherein: (a) the Enhancer of insulin secretion or a pharmaceutically acceptable Salt thereof is nateglinide or a pharmaceutically acceptable Salt of the same; or (b) Sensitizing insulin secretion and S Metformin.
机译:权利要求1:选自以下的至少两种成分的组合:(i)HMG CoA还原酶抑制剂或其药学上可接受的盐,其选自阿托伐他汀,西立伐他汀,氟伐他汀,L Ovastatina,匹伐他汀,普伐他汀,瑞舒伐他汀和辛伐他汀; (ii)增强胰岛素分泌或其药学上可接受的盐;权利要求2:至少两种选自以下的组分的组合:(i)HMG CoA还原酶抑制剂或其药学上可接受的盐;或(b)胰岛素增敏剂或其药学上可接受的盐。 (ii)增强胰岛素的分泌或药学上可接受的盐Same,选自:甲苯磺丁酰胺,氯丙酰胺,甲苯磺酰胺乙酰己酰胺;和;和角膜纤毛虫格列本脲;格列齐特; 1-丁基-4-偏脲;卡布丁胺glibonurida;格列吡嗪格列酮格列索肽格列布丁唑格列唑乙己酰胺;;; glimidina glypinamide;芬布坦艾达托西卡米达,那格列奈,瑞格列奈,米格列奈,格列美脲,dpp-iv抑制剂,GLP1,GLP1,glp-1(7 36); gln.sup.9-glp-1(7-37); d-gln.sup.9-glp-1(7-37);乙腈-溶解-sup.9-glp-1(7-37); thr.sup.16-lys.sup.18-glp-1(7-37);和lys.sup.18-glp-1(7-37); 11.根据权利要求10所述的组合,其特征在于:(a)胰岛素分泌增强剂或其药学上可接受的盐是那格列奈或其药学上可接受的盐。相同;或(b)刺激胰岛素分泌和二甲双胍。

著录项

  • 公开/公告号AU2007201989A1

    专利类型

  • 公开/公告日2007-05-24

    原文格式PDF

  • 申请/专利权人 NOVARTIS AG;

    申请/专利号AU20070201989

  • 申请日2007-05-04

  • 分类号A61K45/00;A61K31/015;A61K31/155;A61K31/175;A61K31/198;A61K31/21;A61K31/22;A61K31/366;A61K31/40;A61K31/401;A61K31/4035;A61K31/404;A61K31/426;A61K31/433;A61K31/435;A61K31/4418;A61K31/4439;A61K31/4453;A61K31/47;A61K31/505;A61K31/5415;A61K31/64;A61P1/04;A61P1/16;A61P3/00;A61P3/04;A61P3/06;A61P3/10;A61P5/14;A61P5/24;A61P5/50;A61P9/00;A61P9/04;A61P9/10;A61P9/12;A61P13/12;A61P15/00;A61P15/10;A61P17/00;A61P19/04;A61P27/02;A61P27/12;A61P43/00;

  • 国家 AU

  • 入库时间 2022-08-21 20:52:47

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