How to design a potent, specific, and stable angiotensin-converting enzyme inhibitor

Drug Discov Today. 2014 Nov;19(11):1731-1743. doi: 10.1016/j.drudis.2014.06.026. Epub 2014 Jul 3.

Abstract

Angiotensin-converting enzyme inhibitors (ACE-Is) are a valuable class of antihypertensive drugs used in the treatment of cardiovascular system-related diseases. Hence, constant research into, and the development of, such compounds remain within the priorities of modern medical sciences. In this respect, a thorough understanding of their chemistry and biology is an important aspect of drug design; therefore, we present here available data on the pharmaceutical properties of ACE-Is. We also review the structural and biochemical features of the molecular target of ACE-Is and demonstrate several known enzyme-inhibitor complexes. Finally, we attempt to create a mathematical model describing the relation between the potency and/or stability of ACE-Is and their structural characteristics using quantitative structure-activity relation (QSAR), and quantitative structure-property relation (QSPR) techniques.

Publication types

  • Review

MeSH terms

  • Angiotensin I / chemistry
  • Angiotensin I / metabolism
  • Angiotensin I / physiology
  • Angiotensin II / chemistry
  • Angiotensin II / metabolism
  • Angiotensin II / physiology
  • Angiotensin-Converting Enzyme Inhibitors* / chemistry
  • Angiotensin-Converting Enzyme Inhibitors* / pharmacology
  • Animals
  • Antihypertensive Agents* / chemistry
  • Antihypertensive Agents* / pharmacology
  • Drug Design
  • Humans
  • Peptidyl-Dipeptidase A / chemistry
  • Peptidyl-Dipeptidase A / metabolism
  • Quantitative Structure-Activity Relationship

Substances

  • Angiotensin-Converting Enzyme Inhibitors
  • Antihypertensive Agents
  • Angiotensin II
  • Angiotensin I
  • Peptidyl-Dipeptidase A