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  1. 1.   N-terminal alpha-amino group modification of antibodies using a site-selective click chemistry method
  2. Li, De-zhi; Han, Bing-nan; Wei, Rui; Yao, Gui-Yang; Chen, Zhizhen; Liu, Jie; Poon, Terence C. W.; Su, Wu; Zhu, Zhongyu; Dimitrov, Dimiter S.; Zhao, Qi
  3. MABS. 2018, Jul; 10(5): 712-719.
  1. 2.   Oxime-based linker libraries as a general approach for the rapid generation and screening of multidentate inhibitors
  2. Bahta, M.; Liu, F.; Kim, S. E.; Stephen, A. G.; Fisher, R. J.; Burke, T. R.
  3. Nature Protocols. 2012, Apr; 7(4): 686-702.
  1. 3.   Design and synthesis of a new, conformationally constrained, macrocyclic small-molecule inhibitor of STAT3 via 'click chemistry'
  2. Chen, J. Y.; Nikolovska-Coleska, Z.; Yang, C. Y.; Gomez, C.; Gao, W.; Krajewski, K.; Jiang, S.; Roller, P.; Wang, S. M.
  3. Bioorganic & Medicinal Chemistry Letters. 2007, Jul; 17(14): 3939-3942.
  1. 4.   Application of azide-alkyne cycloaddition 'click chemistry' for the synthesis of Grb2 SH2 domain-binding macrocycles
  2. Choi, W. J.; Shi, Z. D.; Worthy, K. M.; Bindu, L.; Karki, R. G.; Nicklaus, M. C.; Fisher, R. J.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry Letters. 2006, Oct; 16(20): 5265-5269.
  1. 5.   Bioorthogonal oncometabolite ligation
  2. Briney, Chloe A; Najera, Susana; Meier,Jordan
  3. Methods in enzymology. 2019 622: 431-448.
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