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Agents for VRE: Oxazolidinones, Stretogramins, Cyclic
Agents for VRE: Oxazolidinones, Stretogramins, Cyclic

... Catheter-Related Bacteremias- March, 2007 – The FDA issued an alert to healthcare professionals regarding an increased rate of death among patients treated with linezolid for catheter-related bacteremia and catheter-site infections. – Linezolid is not approved for the treatment of catheter-related b ...
Selective Inhibitors of Picornavirus Replication
Selective Inhibitors of Picornavirus Replication

... replication in vitro by preventing virion uncoating.55,56 In vivo, arildone prevented poliovirusinduced paralysis and death in mice.57 Further attempts to improve the activity of arildone, as well as the chemical and metabolic instability of the beta-diketone moiety, led to the development of WIN517 ...
Free PDF
Free PDF

... HAART. On the other hand, DDIs can be anticipated with alkylating agents, corticosteroids, epipodophyllotoxins, taxanes, tyrosine-kinase inhibitors and vinca alkaloids. Vinca alkaloids (Vinblastine, Vincristine, Vinorelbina): the vinca alkaloids remain an important class of AC traditionally associat ...
new-ff-Benzodiazepines-
new-ff-Benzodiazepines-

... greater the binding. They are also very effectively distributed to the brain. Compounds without 3-OH group have long half-lives and undergo conversion to the 3-hydroxyl compounds by hepatic oxidation. Compounds with 3-OH (oxazepam, lorazepam) are short-acting because they are rapidly conjugated and ...
Pharmacy_Lecture_08_..
Pharmacy_Lecture_08_..

... • The starting point for the development was chemistry-driven, I.e. to identify acidic, but not carboxylic acid-containing (salicylic acid) structurally novel compounds. • Measurement of a physical property (pKa) as well as serum half-life in dogs was the guide for the synthesis program. • Several g ...
THE 6 TH NATIONAL SCIENTIFIC CONFERENCE ON HIV/AIDS
THE 6 TH NATIONAL SCIENTIFIC CONFERENCE ON HIV/AIDS

... • Median CD4 and HIV RNA at 2nd-line ART initiation were 158 cells/mm3 and 4.1 log10 copies/mL, respectively • Boosted PI + 2 NRTIs, indicated by genotype results, was used as 2ndline regimen • At 6, 12, 24, and 36 months of 2nd-line ART, – 67%, 62%, 84%, and 90% achieved HIV RNA <50 copies/mL ...
Department of Pharmacology
Department of Pharmacology

...  Each student must be present with the group they have been assigned to.  Student’s attendance during the seminars is mandatory – only 1 unjustified absence during the whole course will be accepted.  The absence during the seminar must be justified by a duly authorised document (doctor’s note, Un ...
Product Information: Dolutegravir (as sodium)
Product Information: Dolutegravir (as sodium)

... against 2 non-nucleoside (NN)-RTI-resistant, 3 nucleoside (N)-RTI-resistant, and 2 PIresistant HIV-1 mutant clones (1 triple and 1 sextuple) compared to the wildtype strain. Cross Resistance: Integrase Inhibitor-Resistant HIV-1 Strains: Sixty integrase inhibitor-resistant mutant HIV-1 viruses (28 wi ...
UNIVERSITY OF PÉCS Thermodynamic studies on a few factors
UNIVERSITY OF PÉCS Thermodynamic studies on a few factors

... The fluorescence quenching effect of the emission intensity of a novel ‘deepened’ cavitand (6) by some transition metal ions has been investigated using steady-state fluorescence spectroscopy. The results show that amongst the used transition metal ions including Ag+, Cd2+, Cu2+, Fe3+,Cr3+, Hg2+, La ...
Class Update: Sodium-glucose Cotransporter 2 (SGLT2) Inhibitors
Class Update: Sodium-glucose Cotransporter 2 (SGLT2) Inhibitors

... unknown if the risk reduction would also be seen in T2DM patients without preexisting CV disease. A systematic review and meta‐analysis of dapagliflozin  and canagliflozin studies demonstrated inconclusive findings on the effect of SGLT2 inhibitors on CV outcomes (OR 0.89; 95% CI, 0.70 to 1.14).4 Re ...
9-Methyl-7-Bromoeudistomin D, a Caffeine Like
9-Methyl-7-Bromoeudistomin D, a Caffeine Like

... H-MBED binding to liver microsomes from rats treated with PB, a typical inducer of CYP2B subfamily enzymes, but α-NF, a typical inhibitor of CYP1A subfamily enzymes, had no effect on this binding (fig.5). These results suggest that in rat liver microsomes, 3H-MBED probably binds to CYP1A1 and CYP2B. ...
Aminoglycosides
Aminoglycosides

...  Prototype of this class [first one used] is Streptomycin. M.O.A: [inhibition of bacterial protein biosynthesis] Irreversibly binding the 30S ribosomal subunit of m.o. through specific receptor protein  inhibit initiation of protein synthesis  cause misreading of genetic code on recognition regio ...
MACROLIDES Macrolide antibiotics contain a many membered
MACROLIDES Macrolide antibiotics contain a many membered

... • Distorts the tRNA fmet binding site which overlaps both ribosomal subunits, preventing initiation complex formation . • Binding site is unique so cross-resistance doesn’t occur. ...
History and progress of antiviral drugs: From acyclovir to direct
History and progress of antiviral drugs: From acyclovir to direct

... against HCV infection was proven, it became the standard of care (SOC) for this disease, and despite its shortcomings (50% response rate and 50% relapse rate on patients infected with genotype 1b, and unwanted side effects), it remained as such for more than 15 years.27,28 During this time, using bl ...
Chemotherapy regimen: Hyper CVAD
Chemotherapy regimen: Hyper CVAD

... One study evaluated the use of hyper-CVAD for patients with HIV-associated Burkitt’s leukemia/lymphoma. A total of 6/7 (86%) patients receiving a PI based cART achieved complete response and remained alive (median 29 month follow-up). HIV viral load remained undetectable for all adherent patients wh ...
PocketQuery: protein–protein interaction inhibitor
PocketQuery: protein–protein interaction inhibitor

... virtual screening workflow. This functionality is provided under the Export tab of the molecular viewer panel. Export is available for two online virtual screening search engines: AnchorQuery (http://anchorquery.csb .pitt.edu) and ZINCPharmer (http://zincpharmer.csb .pitt.edu). Both AnchorQuery and Z ...
Outline
Outline

... A. Tissue Amebicides 1. Metronidazole (Flagyl) ...
platelet - WordPress.com
platelet - WordPress.com

... of recurrent myocardial infarction, and to decrease mortality in pre- and post-myocardial infarct patients. The recommended dose of aspirin ranges from 50 to 325 mg, with side effects determining the dose chosen. Formerly known as “baby aspirin,” 81-mg aspirin is most commonly used . ** Aspirin is f ...
Meeting Critical Radioisotope Needs in a World Concerned about
Meeting Critical Radioisotope Needs in a World Concerned about

... protein due to alterations in target protein structure or to altered levels of target protein expression resulting in resistance or sensitivity to drug effects represent pharmacodynamic attributes of drug action. Examples of genetic variants that alter either the pharmacokinetics or pharmacodynamics ...
Lack of Susceptibility of Bicyclic Nucleoside Analogs, Highly Potent
Lack of Susceptibility of Bicyclic Nucleoside Analogs, Highly Potent

... (Wassilew et al., 2001), BVDU is highly susceptible to the hydrolytic activity of human and bacterial thymidine phosphorylase (TPase), whereas BVaraU is resistant to human TPase but sensitive to the catabolic activity of bacterial TPase (Desgranges et al., 1983, 1984; Liermann and Herrmann, 1983). M ...
Adverse effects
Adverse effects

... • Viruses are more difficult ‘targets’ than bacteria: they are most vulnerable during reproduction, but all use host cell organelles and enzymes to do this, so that antiviral compounds are often as toxic to host cells as to virus. ...
VH B - IS MU
VH B - IS MU

... Rizzetto M. EASL 2009 ...
Antimycobacterial drugs
Antimycobacterial drugs

... There is no cross-resistance between streptomycin and amikacin, but kanamycin resistance often indicates resistance to amikacin as well. Amikacin must be used in combination with at least one and preferably two or three other drugs to which the isolate is susceptible for treatment of drug-resistant ...
Drug Interactions—Principles, Examples and Clinical Consequences
Drug Interactions—Principles, Examples and Clinical Consequences

... glomerular perfusion through a reduction of local prostaglandin E2 synthesis with corresponding reactive secretion of renin. In a controlled clinical study, the blood pressure of healthy volunteers treated with lisinopril rose by 7 to 9 mmHg when they were given piroxicam (e9). It was recently repor ...
Damaging effects of water-borne cadmium chloride on
Damaging effects of water-borne cadmium chloride on

... respiratory system is affected severely by the inhalation of cadmium-contaminated air. Shortness of breath, lung edema, and destruction of mucous membranes as part of cadmium-induced pneumonitis have been described (Seidal et al., 1993). Cadmium causes lung damage, pulmonary fibrosis, emphysema, and ...
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Discovery and development of integrase inhibitors

The first human immunodeficiency virus (HIV) case was reported in the United States in the early 1980s. Many drugs have been discovered to treat the disease but mutations in the virus and resistance to the drugs make development difficult. Integrase is a viral enzyme that integrates retroviral DNA into the host cell genome. Integrase inhibitors are a new class of drugs used in the treatment of HIV. The first integrase inhibitor, raltegravir, was approved in 2007 and other drugs were in clinical trials in 2011.
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