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Non-Nucleoside HIV Integrase Inhibitors

Responsible for the quick construction of two subunits through Click Reaction  [Pg.52]

It is evident from the results that the click chemistry reaction methodology has been quite useful in the design of HIV-integrase inhibitors producing a promising new starting point for further elaboration and optimization [Pg.53]

17 Miscellaneous Therapeutic Segments 1,2,3-Triazole-Linked Dopamine D3 Receptor (D3R)-Setect/Ve Therapeutic Agents [Pg.53]

D3 receptor (D3R)-selective ligands may be used to treat a variety of neuropsychiatric disorders associated with aberrant dopamine signaling including schizophrenia [118], Parkinson s disease and associated dyskinesias [106,107,119,120], and drug addiction [121-123]. [Pg.53]

In the present series, indolyl-triazole 93 has the best overall profile in terms of D3R affinity, selectivity, lipophilicity, and metabolic stability. [Pg.53]


Figure 2.26 Improved variants of L-708906 as non-nucleoside HIV integrase inhibitors. Figure 2.26 Improved variants of L-708906 as non-nucleoside HIV integrase inhibitors.

See other pages where Non-Nucleoside HIV Integrase Inhibitors is mentioned: [Pg.50]   


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HIV inhibitors

HIV integrase inhibitor

HIV-1 integrase

Integrase inhibitors

Integrases

Non-nucleosides

Nucleoside inhibitors

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