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Regulation of Sarcolemmal Na+/H+ Exchanger Activity by
Regulation of Sarcolemmal Na+/H+ Exchanger Activity by

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... the effects of 20 mg and 100 mg of losartan potassium and an ACE inhibitor on responses to angiotensin I, angiotensin II and bradykinin, losartan was shown to block responses to angiotensin I and angiotensin II without affecting responses to bradykinin. This finding is consistent with losartan’s spe ...
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... At pH 7.4 A measure of lipid solubility, this is the n-octanol/water partition coefficient corrected for the percentage of drug unionized at pH 7.4. Opioid Pharmacokinetic Parameters ...
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Clinical Pharmacology Pharmacotherapy of Hyperlipidemia

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VetACE Bioavailability and Pharmacodynamic Effect

... This in vivo study measured the inhibition of plasma ACE activity as an indicator of the pharmacodynamically important effect of benazeprilat when benazepril is administered for the treatment of hypertension associated with cardiac or renal disease. The results of this in vivo study showed that admi ...
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... Photoreactivity and thus phototoxicity are mostly influenced by the substituent in position 8 [33, 94]. Drugs that are substituted with an additional fluorine atom in this position such as fleroxacin (a trifluoro derivative) or sparfloxacin, generally exhibit a relatively high phototoxic potential, ...
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A hypothesis on peculiar pharmacological behaviour of biologically

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... aimed at further exploration of the SAR of this novel template, led to the discovery of highly selective compounds that target EGFR. Benzothiazoles act via competing with ATP for binding at the catalytic domain of EGFR-TK (Noolvi et al., 2012). The characteristic features of ATP binding site are; ad ...
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Antihypertensive Drugs - coursewareobjects.com

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Hydrogen Bonding: The Last Mystery in Drug Design?

... extensively studied in a series of thermolysin inhibitors (Fig. 6). The replacement of the -NH- group of the ligands by –O– reduces binding affinities by a factor of 1 000, which has been explained by the lack of the NH ··· O = C hydrogen bond and a mutual repulsion of the two electronegative oxygen ...
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... Lunesta causes a metallic aftertaste in up to one-third of patients...especially at higher doses. If patients complain, lower the dose or switch to another sleeping agent. ACE inhibitors can cause a metallic, sweet, or salty taste. It's most common with captopril. ACE inhibitors chelate zinc at the ...
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< 1 ... 26 27 28 29 30 31 32 33 34 ... 85 >

Discovery and development of angiotensin receptor blockers

The angiotensin receptor blockers (ARBs), also called angiotensin (AT1) receptor antagonists or sartans, are a group of antihypertensive drugs that act by blocking the effects of the hormone angiotensin II (Ang II) in the body, thereby lowering blood pressure. Their structure is similar to Ang II and they bind to Ang II receptors as inhibitors, e.g., [T24 from Rhys Healthcare].ARBs are widely used drugs in the clinical setting today, their main indications being mild to moderate hypertension, chronic heart failure, secondary stroke prevention and diabetic nephropathy.The discovery and development of ARBs is a demonstrative example of modern rational drug design and how design can be used to gain further knowledge of physiological systems, in this case, the characterization of the subtypes of Ang II receptors.
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