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  1. 1.   Repurposing the Pummerer Rearrangement: Determination of Methionine Sulfoxides in Peptides
  2. Woodroofe, Carolyn C.; Ivanic,Joseph; Monti, Sarah; Levine, Rodney L.; Swenson, Rolf E.
  3. CHEMBIOCHEM. 2019, OCT 25;
  1. 2.   Development of tricyclic hydroxy-1H-pyrrolopyridine-trione containing HIV-1 integrase inhibitors
  2. Zhao, X. Z.; Maddali, K.; Metifiot, M.; Smith, S. J.; Vu, B. C.; March, C.; Hughes, S. H.; Pommier, Y.; Burke, T. R.
  3. Bioorganic & Medicinal Chemistry Letters. 2011, May; 21(10): 2986-2990.
  1. 3.   A diaryl sulfide, sulfoxide, and sulfone bearing structural similarities to combretastatin A-4
  2. Barbosa, E. G.; Bega, L.; Beatriz, A.; Sarkar, T.; Hamel, E.; do Amaral, M. S.; de Lima, D. P.
  3. European Journal of Medicinal Chemistry. 2009 44(6): 2685-2688.
  1. 4.   Overcoming Problems of Compound Storage in DMSO: Solvent and Process Alternatives
  2. Waybright, T. J.; Britt, J. R.; McCloud, T. G.
  3. Journal of Biomolecular Screening. 2009 14(6): 708-715.
  1. 5.   An armed-disarmed approach for blocking aglycon transfer of thioglycosides
  2. Li, Z. T.; Gildersleeve, J. C.
  3. Tetrahedron Letters. 2007, Jan; 48(4): 559-562.
  1. 6.   Mechanistic studies and methods to prevent aglycon transfer of thioglycosides
  2. Li, Z. T.; Gildersleeve, J. C.
  3. Journal of the American Chemical Society. 2006, Sep; 128(35): 11612-11619.
  1. 7.   Isolation and characterization of novel cyclotides from Viola hederaceae - Solution structure and anti-HIV activity of vhl-1, a leaf-specific expressed cyclotide
  2. Chen, B.; Colgrave, M. L.; Daly, N. L.; Rosengren, K. J.; Gustafson, K. R.; Craik, D. J.
  3. Journal of Biological Chemistry. 2005, JUN 10; 280(23): 22395-22405.
  1. 8.   Binding affinity difference induced by the stereochemistry of the sulfoxide bridge of the cyclic peptide inhibitors of Grb2-SH2 domain: NMR studies for the structural origin
  2. Shi, Y. H.; Song, Y. L.; Lin, D. H.; Tan, J. Z.; Roller, P. P.; Li, Q.; Long, Y. Q.; Song, G. Q.
  3. Biochemical and Biophysical Research Communications. 2005, MAY 20; 330(4): 1254-1261.
  1. 9.   Development of L-3-aminotyrosine suitably protected for the synthesis of a novel nonphosphorylated hexapeptide with low-nanomolar Grb2-SH2 domain-binding affinity
  2. Song, Y. L.; Roller, P. P.; Long, Y. Q.
  3. Bioorganic & Medicinal Chemistry Letters. 2004 14(12): 3205-3208.
  1. 10.   Potentiating effect of distant sites in non-phosphorylated cyclic peptide antagonists of the Grb2-SH2 domain
  2. Long, Y. Q.; Guo, R. B.; Luo, J. H.; Yang, D. J.; Roller, P. P.
  3. Biochemical and Biophysical Research Communications. 2003 310(2): 334-340.
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