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Selective phosphodiesterase inhibitors for the treatment
Selective phosphodiesterase inhibitors for the treatment

Commissioning Support DPP-4 inhibitors (`Gliptins`)
Commissioning Support DPP-4 inhibitors (`Gliptins`)

exercise/weight/diet- how much/how little
exercise/weight/diet- how much/how little

Steroid Hormones
Steroid Hormones

... - Progesterone receptor antagonist of the uterus - Promotes shedding of endometrium, softening of the cervix, and uterine contractions leading to ...
Chemotherapy
Chemotherapy

lipids - UNT Chemistry
lipids - UNT Chemistry

... estimated that a 60 kg person has a total of about 175 g of cholesterol distributed throughout the body. Much of this cholesterol is bonded through ester links to fatty acids, but some is found as the free alcohol. Gallstones, for example, are nearly purecholesterol. • Cholesterol serves two importa ...
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L5 ADHD
L5 ADHD

Discovery of (2,4-Dihydroxy-5-isopropylphenyl)-[5
Discovery of (2,4-Dihydroxy-5-isopropylphenyl)-[5

... affinities for Hsp90 by ITC or to obtain protein ligand crystal structures presumably because they bind so weakly. There are two possible explanations for this drop in affinity. The first is the electronic impact that a fluorine atom has on the two phenolic groups and the carbonyl of the tertiary am ...
Drug-induced acute pancreatitis
Drug-induced acute pancreatitis

Macrocycles in new drug discovery
Macrocycles in new drug discovery

... -26.4 ± 1.59 kJmol-1). From ana­lysis of x-ray cocrystal structures of 1 and 2 , the authors found that the bound linear peptide 1 in fact formed an intramolecular hydrogen bond between the carbonyl oxygen of the phosphotyrosine residue and the NH of the valine residue, while the corresponding inter ...
Selective Serotonin Reuptake Inhibitors (SSRIs) with Dual
Selective Serotonin Reuptake Inhibitors (SSRIs) with Dual

... combining the pharmacophoric profiles of 5-HT reuptake inhibition with 5HT1B/1D antagonism in one molecule can be conducted via: I) Modification of already existed hybrid molecules previously made by other research groups or II) the tethering technique or fragment based drug discovery. Tethering tec ...
Phytosom e
Phytosom e

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Pharmacy_Lecture_08_..

Lecture 12, computers CORRECTED
Lecture 12, computers CORRECTED

... N-benzyl: decreased affinity and selectivity. ...
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2nd T. 5th L. Updated

HTN.SFGH.April_.2012..
HTN.SFGH.April_.2012..

... Very effective for systolic BP Do not increase sudden death Most effective in LVH regression Lipid effects are short lasting (1 y) Hyperglycemia only in high doses Still effective in early chronic kidney disease (to GFR 40-45) • Erectile dysfunction in 20% • More effective in Blacks and older ...
Tuberculosis - ichapps.com
Tuberculosis - ichapps.com

... mycobacterium, with a MIC against M. tuberculosis of 0.01 to 0.25 mcg/mL. Most nontuberculous mycobacterium such as M. avium is resistant to Isoniazid. Isoniazid is readily absorbed from the GI tract and from intramuscular injection sites. Isoniazid should be given on an empty stomach whenever poss ...
candicid forte - Ortho Molecular Products
candicid forte - Ortho Molecular Products

Slajd 1 - Zakład Farmakologii Klinicznej w Poznaniu
Slajd 1 - Zakład Farmakologii Klinicznej w Poznaniu

Drug Therapy for Hypertension
Drug Therapy for Hypertension

SYNTHESIS, DOCKING AND BIOLOGICAL STUDIES OF THE LINEAR TETRAPEPTIDE PWPV-A
SYNTHESIS, DOCKING AND BIOLOGICAL STUDIES OF THE LINEAR TETRAPEPTIDE PWPV-A

PARKINSON*S DISEASE
PARKINSON*S DISEASE

... • Typically late effect, and with higher doses • Narrowing of therapeutic window • Rare in LD-naive patients on DA monotherapy • Most common is “peak dose” dyskinesia – disappears with dose reduction • Choreiform, ballistic and dystonic movements • Most patients prefer some dyskinesias over the alte ...
Psychotropic Drugs
Psychotropic Drugs

Competitive advantage
Competitive advantage

< 1 ... 41 42 43 44 45 46 47 48 49 ... 70 >

Discovery and development of ACE inhibitors



The discovery of an orally inactive peptide from snake venom established the important role of angiotensin converting enzyme (ACE) inhibitors in regulating blood pressure. This led to the development of Captopril, the first ACE inhibitor. When the adverse effects of Captopril became apparent new derivates were designed. Then after the discovery of two active sites of ACE: N-domain and C-domain, the development of domain-specific ACE inhibitors began.
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