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Structure-Based Design, Synthesis and Structure-Activity Relationship Studies of HIV-1 Protease Inhibitors Incorporating Phenyloxazolidinones

A series of new HIV-1 protease inhibitors with the hydroxyethylamine core and different phenyloxazolidinone P2 ligands were designed and synthesized. Variation of phenyl substitutions at the P2 and P2′ moieties significantly affected the inhibitors’ binding affinity and antiviral potency. In general...

Πλήρης περιγραφή

Αποθηκεύτηκε σε:
Λεπτομέρειες βιβλιογραφικής εγγραφής
Κύριοι συγγραφείς: Ali, Akbar, Kiran Kumar Reddy, G. S., Nalam, Madhavi N. L., Anjum, Saima Ghafoor, Cao, Hong, Schiffer, Celia A., Rana, Tariq M.
Μορφή: Artigo
Γλώσσα:Inglês
Έκδοση: 2010
Θέματα:
Διαθέσιμο Online:https://ncbi.nlm.nih.gov/pmc/articles/PMC2996262/
https://ncbi.nlm.nih.gov/pubmed/20958050
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1021/jm1008743
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