Modern trends in diuretics development

被引:26
作者
Titko, Tetiana [1 ]
Perekhoda, Lina [1 ]
Drapak, Iryna [2 ]
Tsapko, Yevgen [3 ]
机构
[1] Natl Univ Pharm, Dept Med Chem, 53 Pushkinska Str, UA-61002 Kharkiv, Ukraine
[2] Danylo Halytsky Lviv Natl Med Univ, Dept Gen Bioinorgan Phys & Colloidal Chem, 69 Pekarska Str, UA-79010 Lvov, Ukraine
[3] Natl Univ Pharm, Dept Inorgan Chem, 53 Pushkinska Str, UA-61002 Kharkiv, Ukraine
关键词
Diuretics; Small molecular drugs; SGLT2 inhibitors (gliflozins); Urea transporter (UT); ROMK; Aquaporin (AQP); NATRIURETIC PEPTIDE RECEPTOR; WNK SIGNALING INHIBITORS; SMALL-MOLECULE INHIBITORS; ACUTE HEART-FAILURE; TRANSPORTER UT-B; NANOMOLAR-POTENCY; BLOOD-PRESSURE; NPR-A; VASOPRESSIN ANTAGONIST; ROMK INHIBITORS;
D O I
10.1016/j.ejmech.2020.112855
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Diuretics are the first-line therapy for widespread cardiovascular and non-cardiovascular diseases. Traditional diuretics are commonly prescribed for treatment in patients with hypertension, edema and heart failure, as well as with a number of kidney problems. They are diseases with high mortality, and the number of patients suffering from heart and kidney diseases is increasing year by year. The use of several classes of diuretics currently available for clinical use exhibits an overall favorable risk/benefit balance. However, they are not devoid of side effects. Hence, pharmaceutical researchers have been making efforts to develop new drugs with a better pharmacological profile. High-throughput screening, progress in protein structure analysis and modern methods of chemical modification have opened good possibilities for identification of new promising agents for preclinical and clinical testing. In this review, we provide an overview of the medicinal chemistry approaches toward the development of small molecule compounds showing diuretic activity that have been discovered over the past decade and are interesting drug candidates. We have discussed promising natriuretics/aquaretics/osmotic diuretics from such classes as: vasopressin receptor antagonists, SGLT2 inhibitors, urea transporters inhibitors, aquaporin antagonists, adenosine receptor antagonists, natriuretic peptide receptor agonists, ROMK inhibitors, WNK-SPAK inhibitors, and pendrin inhibitors. (C) 2020 Elsevier Masson SAS. All rights reserved.
引用
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页数:27
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