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No Slide Title
No Slide Title

Monday 23rd December: PSA2
Monday 23rd December: PSA2

mind altering… synthetic (designer) and naturally occuring
mind altering… synthetic (designer) and naturally occuring

Slide 1
Slide 1

- BioTek Instruments
- BioTek Instruments

12th Conference in Advanced Medicinal Chemistry
12th Conference in Advanced Medicinal Chemistry

... to update the material taught to the undergraduate students. It was then the first time students were taught about the role of physicochemical properties in drug action, subjects like structure/activity relationships, drug metabolism and the role of chemical bonds in the development of drug action, ...
Introduction
Introduction

Best Practice Management of CINV in Oncology Patients: I
Best Practice Management of CINV in Oncology Patients: I

Document
Document

Kinetic and Affinity Analysis using Biacore
Kinetic and Affinity Analysis using Biacore

On the Discovery and Development of Pimavanserin
On the Discovery and Development of Pimavanserin

`drug`.
`drug`.

... EC50 - The agonist concentration that causes 50% of the maximum response. pEC50 = - log10(EC50) Antagonists: Situation more complex. Antagonists displace the agonist dose-response curve rightwards – most accurate measure of potency (pA2) requires measurement of agonist binding at multiple concentrat ...
Cozaar
Cozaar

Drug Metabolism Phcy 172 - University of North Carolina at
Drug Metabolism Phcy 172 - University of North Carolina at

Aniracetam - Supplement Support Homepage
Aniracetam - Supplement Support Homepage

... that's enough." This results in a decrease of glutamanergic activity. This helps prevent exitotoxicity and may be where the anxiolytic effects of aniracetam arise from. N-anisoyl-GABA also indirectly increases levels of dopamine and serotonin in the prefrontal cortex. It seems to do this via interac ...
Molecular determinants of drug–receptor binding kinetics
Molecular determinants of drug–receptor binding kinetics

Anti-platelets
Anti-platelets

... • Dose: 0.25 mg/kg IV before PCI followed by 10 g/min for 12 hrs 2) Eptifibatide • Cyclic peptide inhibitor of the fibrinogen binding site on GpIIb/IIIa receptor • Short duration of action: 6-12 hrs • Given with aspirin and heparin • Use: – Acute coronary syndrome – Angioplastic coronary interventi ...
toxicology 3 - Calgary Emergency Medicine
toxicology 3 - Calgary Emergency Medicine

How should ankle oedema caused by calcium channel blockers be
How should ankle oedema caused by calcium channel blockers be

... The mechanisms by which ARBs reduce incidence of CCB induced ankle oedema remains unknown, but are likely to be similar to that involved when ACEIs are added to CCB therapy2 One open-label, blinded end point study found a significant reduction in the incidence of markers of ankle oedema (Ankle-foot ...
coagulation final 2
coagulation final 2

obeticholic acid
obeticholic acid

Opioid Analgesics and Antagonists
Opioid Analgesics and Antagonists

... Administration: Absorption of morphine from the gastrointestinal tract is slow and erratic, and the drug is usually not given orally. Codeine, by contrast, is well absorbed when given by mouth. Significant first pass metabolism of morphine occurs in the liver Distribution: Morphine rapidly enters al ...
lec.8-426
lec.8-426

Opioids
Opioids

G protein-coupled receptor dimers: Functional
G protein-coupled receptor dimers: Functional

< 1 ... 36 37 38 39 40 41 42 43 44 ... 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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