Advances in Amino Acid Mimetics and Peptidomimetics, Volume by A. Abell

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By A. Abell

Peptidomimetics have chanced on vast program as bioavailable, and infrequently powerful mimetics of average peptides. They shape the root of vital periods of enzyme inhibitors, they act as receptor agonists and antagonists, they usually have even been used to imitate DNA constitution. fresh advances within the use of solid-phase natural synthesis have cleared the path for the guidance of libraries of those constructions to permit the quick optimization of theri organic homes and for that reason healing power. we're additionally commencing to achieve a better realizing of the structural beneficial properties of this category of compounds that effect their skill to permeate membranes, and their expense of clearance and metabolism. This quantity brings jointly lots of those severe concerns by way of highlighting contemporary advances in a few center peptidomimetic-based study.

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Synthesis of HIV protease inhibitors. Combinatorial Synthesis of Peptidomimetics 27 Figure 5. Templates for symmetric and pseudo-symmetric HIV protease inhibitors. by displacement of the tosylate with either a secondary amine to afford 100 or a primary amine. In the example of a primary amine, the resulting displacement product was treated with triphosgene, with subsequent addition of a second amine to yield urea 101. Reduction of azide moiety afforded the corresponding amine, which could then be further elaborated.

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