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L-756423 is a potent, selective, and competitive small molecule inhibitor of HIV protease (HIV-1 PR), developed by Merck & Co. It is chemically similar to indinavir but features a longer half-life in animal models. The compound was investigated as an antiviral agent for the treatment of HIV infections and reached phase II clinical trials before development was discontinued. Its mechanism involves direct inhibition of the HIV protease enzyme, thereby blocking viral replication[3][5][9].
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