Peter A Meredith
Index: Curr. Med. Res. Opin. 23(7) , 1693-705, (2007)
Full Text: HTML
Therapeutic interventions that block the renin-angiotensin-aldosterone system (RAAS) have an important role in slowing the progression of cardiovascular risk actors to established cardiovascular diseases. In recent years, angiotensin receptor blockers (ARBs) have emerged as effective and well-tolerated alternatives to an angiotensin-converting enzyme inhibitor (ACEi) for RAAS blockade. The ARB candesartan was initially established as an effective once-daily antihypertensive treatment, providing 24-h blood pressure (BP) control with a trough:peak ratio close to 100%.A Medline literature search was undertaken to identify randomised, controlled trials that examined the efficacy and cardiovascular outcomes associated with candesartan cilexetil in hypertension and chronic heart failure (CHF).Compared with other ARBs, candesartan demonstrates the strongest binding affinity to the angiotensin II type 1 receptor. Clinical trials have demonstrated that candesartan is well tolerated in combination with diuretics or calcium channel blockers (CCBs), making it a suitable treatment option for patients whose hypertension is not adequately controlled by monotherapy. Subsequently, candesartan became the only ARB licensed in the UK to treat patients with CHF and left ventricular ejection fraction < or = 40% as add-on therapy to an ACEi or when an ACEi is not tolerated. Studies in patients with symptomatic HF have indicated that candesartan treatment was associated with significant relative risk reductions in cardiovascular mortality and hospitalisation due to CHF.There are clear indications that the clinical benefits of candesartan may extend beyond its proven antihypertensive effects to a wider range of complications across the cardiovascular continuum, including diabetes, left ventricular hypertrophy, atherosclerosis and stroke. Such results suggest that candesartan treatment may offer significant patient benefits as well as practical advantages over conventional treatment.
Structure | Name/CAS No. | Molecular Formula | Articles |
---|---|---|---|
![]() |
Candesartan cilexetil
CAS:145040-37-5 |
C33H34N6O6 |
Development and characterization of mixed niosomes for oral ...
2015-02-01 [AAPS PharmSciTech 16(1) , 108-17, (2015)] |
Use of compounded dispersing media for extemporaneous pediat...
2014-12-01 [Acta. Pharm. 64(4) , 463-74, (2014)] |
Hepatic, intestinal, renal, and plasma hydrolysis of prodrug...
2014-09-01 [Drug Metab. Dispos. 42(9) , 1522-31, (2014)] |
The application of solid-state NMR spectroscopy to study can...
2014-10-01 [Biochim. Biophys. Acta 1838(10) , 2439-50, (2014)] |
Dual blockade with candesartan cilexetil and lisinopril in h...
2003-06-01 [J. Renin Angiotensin Aldosterone Syst. 4(2) , 96-9, (2003)] |
Home | MSDS/SDS Database Search | Journals | Product Classification | Biologically Active Compounds | Selling Leads | About Us | Disclaimer
Copyright © 2024 ChemSrc All Rights Reserved