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Target-induced formation of neuraminidase inhibitors from in vitro virtual combinatorial libraries.
Proc Natl Acad Sci U S A. 2002 Mar 19;99(6):3382-7. doi: 10.1073/pnas.052703799. Epub 2002 Mar 12.
3
Influenza neuraminidase inhibitors: structure-based design of a novel inhibitor series.
Biochemistry. 2003 Jan 28;42(3):718-27. doi: 10.1021/bi0205449.
5
Design and synthesis of 6-oxo-1,4,5,6-tetrahydropyrimidine-5-carboxylate derivatives as neuraminidase inhibitors.
Eur J Med Chem. 2014 Aug 18;83:466-73. doi: 10.1016/j.ejmech.2014.06.059. Epub 2014 Jun 26.
7
Drug screening for influenza neuraminidase inhibitors.
Sci China C Life Sci. 2005 Feb;48(1):1-5. doi: 10.1360/062004-69.
8
QSAR analyses on avian influenza virus neuraminidase inhibitors using CoMFA, CoMSIA, and HQSAR.
J Comput Aided Mol Des. 2006 Sep;20(9):549-66. doi: 10.1007/s10822-006-9080-0. Epub 2006 Nov 11.

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Auto In Silico Ligand Directing Evolution to Facilitate the Rapid and Efficient Discovery of Drug Lead.
iScience. 2020 Jun 26;23(6):101179. doi: 10.1016/j.isci.2020.101179. Epub 2020 May 18.
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Proteintemplat-gesteuerte Fragmentligationen - von der molekularen Erkennung zur Wirkstofffindung.
Angew Chem Weinheim Bergstr Ger. 2017 Jun 19;129(26):7464-7485. doi: 10.1002/ange.201610372. Epub 2017 May 31.
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Guest Binding Drives Host Redistribution in Libraries of Co L Cages.
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Optimized Inhibitors of MDM2 via an Attempted Protein-Templated Reductive Amination.
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Source of oseltamivir resistance due to single E119D and double E119D/H274Y mutations in pdm09H1N1 influenza neuraminidase.
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Tailored therapeutics based on 1,2,3-1-triazoles: a mini review.
Medchemcomm. 2019 May 14;10(8):1302-1328. doi: 10.1039/c9md00218a. eCollection 2019 Aug 1.
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Discovery of potent inhibitors of human β-tryptase from pre-equilibrated dynamic combinatorial libraries.
Chem Sci. 2015 Mar 1;6(3):1792-1800. doi: 10.1039/c4sc02943g. Epub 2014 Dec 8.
8
Protein-Templated Fragment Ligations-From Molecular Recognition to Drug Discovery.
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Dynamic thiol exchange with β-sulfido-α,β-unsaturated carbonyl compounds and dithianes.
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Dynamic combinatorial chemistry.
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A novel approach to antiviral therapy for influenza.
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Molecular evolution: dynamic combinatorial libraries, autocatalytic networks and the quest for molecular function.
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Target-oriented and diversity-oriented organic synthesis in drug discovery.
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Neuraminidase inhibitors as anti-influenza virus agents.
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Dynamic combinatorial chemistry: evolutionary formation and screening of molecular libraries.
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