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Balancing Chemical Equations – A Primer
Balancing Chemical Equations – A Primer

... You may observe that the suffix endings of the compound names end in either ITE or ATE. This occurs when there are two polyatomics with a different charge or bonding configuration of the “same” compound. For example, there is NO2 nitrite and NO3 nitrate. The lesser on is ITE and the larger one is AT ...
chapter one
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Drugs acting on the uterus
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... 1. Oxytocin: (nonapeptide=9 a.a peptide) - Contracts the myoepithelial cells of the breast → milk letdown; milk ejection Major stimuli, baby cry and suckling - Contracts the uterus → delivery The uterus is insensitive to oxytocin in early pregnancy but its sensitivity increases with advanced pregnan ...
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Sample Exercise 2.1 Illustrating the Size of an Atom
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... Magnesium has three isotopes, with mass numbers 24, 25, and 26. (a) Write the complete chemical symbol (superscript and subscript) for each of them. (b) How many neutrons are in an atom of each isotope? Solution (a) Magnesium has atomic number 12, so all atoms of magnesium contain 12 protons and 12 ...
Pharmacokinetic interaction of rifapentine and
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... days 1 –4 of Period 1; rifapentine (900 mg once weekly for 3 weeks) on days 1, 8 and 15 of Period 2 and raltegravir (400 mg every 12 h for 4 days) on days 12 –15 of Period 2; and rifapentine (600 mg once daily for 10 scheduled doses) on days 1, 4 –8 and 11 –14 of Period 3 and raltegravir (400 mg eve ...
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... Magnesium has three isotopes, with mass numbers 24, 25, and 26. (a) Write the complete chemical symbol (superscript and subscript) for each of them. (b) How many neutrons are in an atom of each isotope? Solution (a) Magnesium has atomic number 12, so all atoms of magnesium contain 12 protons and 12 ...
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...  The patient exhibits unacceptable behaviour (based on the pharmacist’s professional judgement), which may result in a ban  The patient presents in an intoxicated state and treatment is withheld  The pharmacist is concerned at the observed deterioration in the health of a patient  The pharmacist ...
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... Aspirin (acetylsalicylic acid), carbaspirin calcium, choline salicylate, magnesium salicylate, sodium salicylate, ibuprofen, naproxen sodium, and ketoprofen are all classified as NSAIDs. Drug category and indications for use NSAIDs may be used to reduce fever and provide temporary relief for minor a ...
IN­VITRO TARTRATE  Research Article   
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... Among  the  various  routes  of  drug  delivery,  oral  route  is  the  most  suitable  and  most  widely  accepted  one  by  the  patients  for  the  delivery  of  the  therapeutically  active  drugs.  But,  after  oral  drug  administration  many  drugs  are  subjected  to  presystemic  clearance  ...
Amphetamines: An Update on Forensic Issues
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Chemistry and Biochemistry - St. Mary`s University Academic Catalog
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... This course is designed to provide a general overview of these two specific areas of chemistry for non- majors. It will provide the general basics of organic chemistry including basic carbon chemistry, nomenclature, structures of organic compounds, chemical characteristics and function,reactions, an ...
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... between chemical substances determined in the laboratory. The table had two intended uses: to ‘discover or explain’ what went on in the mixtures of several bodies and to ‘predict’ what had to result from particular mixtures (5). In the early years of the 18th century, Newton tried to find a theoreti ...
Polyamine transporter selective compounds as anticancer agents
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... drugs which use the polyamine transporter system to gain access to cells (i.e. polyamine conjugates). Chinese hamster ovary cells which are chemically mutated to be polyamine transport-deficient will be referred to as the CHO-MG cell line. This cell type should have lower susceptibility to polyamine ...
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... the choice of chemical library directs the type of molecular processes that are disrupted, as well the approach of target pathway identification [16]. Traditionally, the discovery of new drugs has been achieved through the isolation of natural products from plants and microbes [17]. Screening a libr ...
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... • Defining criteria on how to apply the risk management process • Identification of circumstances, if any, when applying risk management principles is not feasible or appropriate • Defining what principles of risk management apply to industry, regulators or both across the life-cycle of the product ...
Biochemical Markers as Tools to Increase Efficiency in Drug
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... testing for their ability to reflect structural changes of articular cartilage.6 Assays validated for such abilities are expected to facilitate and accelerate the otherwise difficult, time-consuming and ultimately ...
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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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