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hit and lead generation: beyond high-throughput screening
hit and lead generation: beyond high-throughput screening

1. Naturally occurring boron consists of two isotopes, boron–10 and
1. Naturally occurring boron consists of two isotopes, boron–10 and

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... For each example, you need to determine the average atomic mass (amu) for each given atom. Remember… 1. Change each percentage to their decimal equivalent 2. Multiply that decimal percent by the mass of the isotope 3. Add all of the masses together at the end to determine the amu Iron, where…. 80.0% ...
Chemistry Academic v. 2016
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Notes -- Unit 5 -- Reactions and Stoichiometry

... reacts with an aqueous solution of potassium chloride. A precipitate is produced. 1. Determine the precipitate using Ksp. 2. Write the Molecular, Ionic, and Net Ionic equations for the above reaction ...
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... In the example seen above, 3O2 had to be added to the right side of the equation to balance it and show that the excess oxygen is not consumed during the reaction. In this example, methane is called the limiting reactant. Although we have discussed balancing equations in terms of numbers of atoms an ...
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... 1. The order of binding of substrates and release of product serves to define the reactants present at the active site during catalysis: it does not establish the kinetically preferred order of substrate addition and product release or allow conclusions pertaining to the events occurring between sub ...
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Process chemistry

Process chemistry is the arm of pharmaceutical chemistry concerned with the development and optimization of a synthetic scheme and pilot plant procedure to manufacture compounds for the drug development phase. Process chemistry is distinguished from medicinal chemistry, which is the arm of pharmaceutical chemistry tasked with designing and synthesizing molecules on small scale in the early drug discovery phase.Medicinal chemists are largely concerned with synthesizing a large number of compounds as quickly as possible from easily tunable chemical building blocks (usually for SAR studies). In general, the repertoire of reactions utilized in discovery chemistry is somewhat narrow (for example, the Buchwald-Hartwig amination, Suzuki coupling and reductive amination are commonplace reactions). In contrast, process chemists are tasked with identifying a chemical process that is safe, cost and labor efficient, “green,” and reproducible, among other considerations. Oftentimes, in searching for the shortest, most efficient synthetic route, process chemists must devise creative synthetic solutions that eliminate costly functional group manipulations and oxidation/reduction steps.This article will focus exclusively on the chemical and manufacturing processes associated with the production of small molecule drugs. Biological medical products (more commonly called “biologics”) represent a growing proportion of approved therapies, but the manufacturing processes of these products are beyond the scope of this article. Additionally, the many complex factors associated with chemical plant engineering (for example, heat transfer and reactor design) and drug formulation will be treated cursorily.
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