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Carbon Compounds
Carbon Compounds

... The Chemistry of Carbon Carbon atoms have four valence electrons, allowing them to form strong covalent bonds with many other elements, including hydrogen, oxygen, phosphorus, sulfur, and nitrogen. Living organisms are made up of molecules that consist of carbon and these other elements. ...
Cyclodextrins as Sustained
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... of luteinizing hormone–releasing hormones and is used for the treatment of endocrine-dependent metastatic prostate carcinoma. Because of its short biological half-life, frequent injections and nasal applications of the drug must be administered so that its therapeutic concentration is maintained (1 ...
COURSE TITLE - Metropolitan Community College
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... List the five (5) sources of drugs. Describe the two broad classes of drug names, giving advantages and/or disadvantages. Differentiate between prescription items and over-the-counter items. Describe the contents of the publications used in dental offices, such as a. USP c. ADT b. NF d. PDR 6. Descr ...
Brief Bioinform-2015-Siavelis-bib_bbv048
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... Magnitude and sign quantify the gene signatures’ correlation, and biological interpretations build on the signature reversion principle: if a drug treatment anti-correlates with a disease signature, then it opposes to a cell’s pathologic gene expression pattern, and by extension to the disease pheno ...
Ecstasy - University of Illinois at Chicago
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... transient experience that mimics a psychosis). This drug is a psychoactive hallucinogen that can cause dramatic and sometimes frightening mindstates. They include psychedelic-like changes in visual perception, mood and body sensations, emotional swings, and feelings of detachment ...
Strategies in Designing Clinicals for Fixed
Strategies in Designing Clinicals for Fixed

... – Studies designed to demonstrate efficacy for such vaccines could be based upon epidemiologic data regarding the disease incidence of each serotype in the target population. Thus, while the primary endpoint may be the aggregate of disease with all serotypes included in the vaccine, the study should ...
general pharmacology
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ANTI-INFLAMMATORY EFFECT OF THE SERRATIOPEPTIDASE
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PPT
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ХРОМАТОГРАММЫ
ХРОМАТОГРАММЫ

... applications), Grodno, 2000, 315 p. 3. Ledneva I.O., Velichko M.G., Nefyodov L.I. Effects of deryvativs of L- glutamin and Lphenilalanin in the tumorbraiding, Grodno, GSU, 2003, 108 p. 4. Amino Acids And Their Derivatives//Proc of Internat. Symp/Ed. V. Soldatov, L. Nefydov, 1996, Grodno, 125 p 5. Ne ...
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Pharmacokinetic and pharmacodynamic aspects
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... also makes it possible to obtain certain selectivity in the elicited pharmacological effect of drugs that activate different types of receptors at different concentrations. 1.2.3. Reduced counter-activity of the body In many cases, the pharmacological response which intervenes with the natural physi ...
6. NaF
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... molecule of chlorine trifluoride, ClF3 contains 1 atom of chlorine and 3 atoms of fluorine. Rule 1. The element with the lower group number is written first in the name; the element with the higher group number is written second in the name. Rule 2. If both elements are in the same group, the elemen ...
cost effective analysis of commonly used topical drugs in
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Biophysics 101 Genomics and Computational Biology
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Science 1206 Unit 3 Part 1
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... resistance was first documented and described in the early 1990s when the use of AZT as monotherapy was common.5-7 Drug resistance has since been described for all ARV drugs approved for HIV-1 treatment.8 Consequently, the Department of Health and Human Services recommends screening for drug resista ...
Chemical Genetics: Where Genetics and Pharmacology
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... (B) Inhibition of a drug-sensitized yeast cyclin-dependent kinase Cdc28 with a low dose of 1NM-PP1 (0.5 µM) induces cell-cycle arrest at G2/M, whereas a higher dose of 1NM-PP1 (5 µM) induces cell-cycle arrest in G1. Mutant yeast with temperature-sensitive Cdc28 alleles also arrest in G1. (C) An incr ...
ANTI MYCOBACTERIAL DRUGS
ANTI MYCOBACTERIAL DRUGS

... most antibiotics.  They grow slowly compared with other bacteria, antibiotics that are most active against growing cells are relatively ineffective. so, that’s why we use cobination of drugs.  Mycobacterial cells can also be dormant and thus completely resistant to many drugs or killed only very s ...
Design fabrication and characterization of controlled
Design fabrication and characterization of controlled

... Various types of oral controlled release formulation have been developed to improve the clinical efficacy of drugs having short half-lives as well as to increase patient compliance. [4] These formulations are designed to deliver drugs at a predetermined rate over a wide range of conditions and durat ...
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Drug discovery



In the fields of medicine, biotechnology and pharmacology, drug discovery is the process by which new candidate medications are discovered. Historically, drugs were discovered through identifying the active ingredient from traditional remedies or by serendipitous discovery. Later chemical libraries of synthetic small molecules, natural products or extracts were screened in intact cells or whole organisms to identify substances that have a desirable therapeutic effect in a process known as classical pharmacology. Since sequencing of the human genome which allowed rapid cloning and synthesis of large quantities of purified proteins, it has become common practice to use high throughput screening of large compounds libraries against isolated biological targets which are hypothesized to be disease modifying in a process known as reverse pharmacology. Hits from these screens are then tested in cells and then in animals for efficacy.Modern drug discovery involves the identification of screening hits, medicinal chemistry and optimization of those hits to increase the affinity, selectivity (to reduce the potential of side effects), efficacy/potency, metabolic stability (to increase the half-life), and oral bioavailability. Once a compound that fulfills all of these requirements has been identified, it will begin the process of drug development prior to clinical trials. One or more of these steps may, but not necessarily, involve computer-aided drug design. Modern drug discovery is thus usually a capital-intensive process that involves large investments by pharmaceutical industry corporations as well as national governments (who provide grants and loan guarantees). Despite advances in technology and understanding of biological systems, drug discovery is still a lengthy, ""expensive, difficult, and inefficient process"" with low rate of new therapeutic discovery. In 2010, the research and development cost of each new molecular entity (NME) was approximately US$1.8 billion. Drug discovery is done by pharmaceutical companies, with research assistance from universities. The ""final product"" of drug discovery is a patent on the potential drug. The drug requires very expensive Phase I, II and III clinical trials, and most of them fail. Small companies have a critical role, often then selling the rights to larger companies that have the resources to run the clinical trials.Discovering drugs that may be a commercial success, or a public health success, involves a complex interaction between investors, industry, academia, patent laws, regulatory exclusivity, marketing and the need to balance secrecy with communication. Meanwhile, for disorders whose rarity means that no large commercial success or public health effect can be expected, the orphan drug funding process ensures that people who experience those disorders can have some hope of pharmacotherapeutic advances.
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