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2011 | 1 |
2013 | 1 |
2014 | 1 |
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Design of cell-permeable stapled peptides as HIV-1 integrase inhibitors.
J Med Chem. 2013 Jul 11;56(13):5601-12. doi: 10.1021/jm4006516. Epub 2013 Jun 24.
J Med Chem. 2013.
PMID: 23758584
Free PMC article.
Design and discovery of flavonoid-based HIV-1 integrase inhibitors targeting both the active site and the interaction with LEDGF/p75.
Li BW, Zhang FH, Serrao E, Chen H, Sanchez TW, Yang LM, Neamati N, Zheng YT, Wang H, Long YQ.
Li BW, et al.
Bioorg Med Chem. 2014 Jun 15;22(12):3146-58. doi: 10.1016/j.bmc.2014.04.016. Epub 2014 Apr 19.
Bioorg Med Chem. 2014.
PMID: 24794743
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Design of HIV-1 integrase inhibitors targeting the catalytic domain as well as its interaction with LEDGF/p75: a scaffold hopping approach using salicylate and catechol groups.
Fan X, Zhang FH, Al-Safi RI, Zeng LF, Shabaik Y, Debnath B, Sanchez TW, Odde S, Neamati N, Long YQ.
Fan X, et al.
Bioorg Med Chem. 2011 Aug 15;19(16):4935-52. doi: 10.1016/j.bmc.2011.06.058. Epub 2011 Jun 26.
Bioorg Med Chem. 2011.
PMID: 21778063
Free PMC article.
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