长效二甲-4抑制剂的开发:结构演变和长效决定因素
Qing Li1, Xiaoyan Deng1, Yan-Jun Xu1
1College of Chemistry and Materials Science, Sichuan Normal University, Chengdu 610068, China.
Journal of medicinal chemistry
|August 30, 2023
概括
开发长期作用的二二酶-4 (DPP-4) 抑制剂旨在通过更少的剂量来改善患者的坚持. 这一观点回顾了这些关键糖尿病药物的历史发展和设计策略.
科学领域:
- 药理学 药理学是指药理学的学科.
- 药物开发 药物开发
- 药用化学 医学化学
背景情况:
- 双基化酶-4 (DPP-4) 抑制剂是关键的口服抗糖尿病药物.
- 改善患者的坚持是长效配方的主要目标.
- 长效DPP-4抑制剂的合理设计提出了重大挑战.
研究的目的:
- 综合总结了长期作用的DPP-4抑制剂在三十年中的发展.
- 检查影响这些药物的作用持续时间的决定因素.
- 讨论延长释放DPP-4抑制剂的合理设计的潜在方法.
主要方法:
- 历史化合物及其演变的回顾.
- 分析影响药物持续时间的因素:向性质,强度,结合动力学,晶体结构,选择性.
- 检查临床前和临床的药理动力学和药理动力学数据.
主要成果:
- 在近30年的时间里,DPP-4抑制剂化合物的演变已被记录下来.
- 已经确定了实现长时间行动的关键决定因素.
- 讨论了长效口服药物的各种设计策略.
结论:
- 了解长效的决定因素对于设计有效的DPP-4抑制剂至关重要.
- 本综述提供了洞察力,以促进开发更安全,更有效的长效DPP-4抑制剂.
- 讨论的原则也可能适用于其他口服药物开发工作.
相关概念视频
Dipeptidyl Peptidase 4 Inhibitors
211
Dipeptidyl peptidase 4 (DPP-4) is a serine protease widely distributed in the body. It's involved in the inactivation of GLP-1 and GIP hormones, which are crucial for insulin regulation. DPP-4 inhibitors, such as sitagliptin (Januvia), saxagliptin (Onglyza), linagliptin (Tradjenta), alogliptin (Nesina), and vildagliptin (Galvus), help increase the proportion of active GLP-1, enhancing insulin secretion. These inhibitors work by competitively binding to DPP-4. This binding causes a...
211
Glucagon-like Receptor Agonists
358
Incretins include glucagon-like peptide-1 (GLP-1) and glucose-dependent insulinotropic polypeptide (GIP), which stimulate insulin secretion post-meals. In type 2 diabetes, GIP's efficacy is reduced, making GLP-1 a viable drug target. GIP originates from preproGIP.
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
GLP-1, when administered in high doses intravenously, triggers insulin secretion, inhibits glucagon release, slows gastric emptying, reduces food intake, and restores normal insulin secretion. However, its rapid inactivation by...
358
Insulin Formulations: Types and Delivery
225
Insulin preparations are categorized by their duration of action into short-acting and long-acting types. Two strategies are used to modify insulin's absorption and pharmacokinetic profile: slowing the absorption post-subcutaneous injection, or altering human insulin's amino acid sequence or protein structure. These changes retain the insulin's ability to bind to the insulin receptor, but alter its behavior in solution or after injection.
Short-acting insulins are divided into...
Short-acting insulins are divided into...
225
Insulin: Biosynthesis, Chemistry, and Preparation
424
The endoplasmic reticulum (ER) of pancreatic β-cells synthesizes preproinsulin, which consists of a signal peptide, A and B chains, and a C-peptide. Preproinsulin is then cleaved and folded into proinsulin, which translocates to the Golgi apparatus for sorting and packaging into secretory granules. In these granules, enzymatic clipping generates insulin and C-peptide.
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment...
Damage or functional impairment of β-cells inhibits insulin production, leading to diabetes. Diabetes treatment...
424
Insulin: Dosing Regimen and Adverse Effects
205
Insulin-replacement therapy usually includes both long-acting insulin (basal) and short-acting insulin (to cater to postprandial needs). In a diverse group of type 1 diabetes patients, the average daily insulin dose is typically 0.5-0.7 units/kg body weight. However, obese patients and pubertal adolescents may need more due to insulin resistance.
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
The basal dose constitutes about 40%-50% of the total daily dose, with the rest as premeal insulin. The mealtime insulin dose should mirror...
205
Oral Hypoglycemic Agents: Glinides
184
Repaglinide (Prandin) and Nateglinide (Starlix), known as glinides, are oral insulin secretagogues that stimulate insulin release from pancreatic β cells by closing the ATP-sensitive potassium channels (KATP channel). Repaglinide controls insulin release from pancreatic β cells by managing potassium efflux. It shares two binding sites with sulfonylureas and also has a unique site, indicating overlapping mechanisms of action. With a rapid onset and a 4-7 hour duration, it effectively...
184


