期刊
JOURNAL OF MEDICINAL CHEMISTRY
卷 44, 期 21, 页码 3343-3346出版社
AMER CHEMICAL SOC
DOI: 10.1021/jm0155401
关键词
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Truncation of the original piperidino-2(S)-methyl piperazine lead structure 2, from a family of muscarinic antagonists, gave compound 8 which has improved selectivity for the HIV-1 co-receptor CCR5 over muscarinic receptors. Further optimization for pharmacokinetic properties afforded Sch-350634 (1), a prototypical piperazine-based CCR5 antagonist, which is a potent inhibitor of HIV-1 entry and replication in PBMCs. The title compound (1) has excellent oral bioavailability in rat, dog, and monkey.
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