Huiyuan Li, Ph.D.

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Li H, Rahimi F, Bitan G. (2016) Modulation of amyloid β-protein (Aβ) assembly by homologous C-terminal fragments as a strategy for inhibiting Aβ toxicity. Acs Chemical Neuroscience
Bailey LD, Kalyana Sundaram RV, Li H, et al. (2015) Disulfide sensitivity in the Env protein underlies lytic inactivation of HIV-1 by peptide triazole thiols. Acs Chemical Biology
Zheng X, Wu C, Liu D, et al. (2015) Mechanism of C-Terminal Fragments of Amyloid β-Protein as Aβ Inhibitors: Do C-Terminal Interactions Play a Key Role in Their Inhibitory Activity? The Journal of Physical Chemistry. B
Li H, Aneja R, Chaiken I. (2013) Click chemistry in peptide-based drug design. Molecules (Basel, Switzerland). 18: 9797-817
Long YQ, Huang SX, Zawahir Z, et al. (2013) Design of cell-permeable stapled peptides as HIV-1 integrase inhibitors. Journal of Medicinal Chemistry. 56: 5601-12
Solomonov I, Korkotian E, Born B, et al. (2012) Zn2+-AÎ²40 complexes form metastable quasi-spherical oligomers that are cytotoxic to cultured hippocampal neurons. The Journal of Biological Chemistry. 287: 20555-64
Li H, Zemel R, Lopes DH, et al. (2012) A two-step strategy for structure-activity relationship studies of N-methylated aÎ²42 C-terminal fragments as aÎ²42 toxicity inhibitors. Chemmedchem. 7: 515-22
Gessel MM, Wu C, Li H, et al. (2012) AÎ²(39-42) modulates AÎ² oligomerization but not fibril formation. Biochemistry. 51: 108-17
Li H, Du Z, Lopes DH, et al. (2011) C-terminal tetrapeptides inhibit AÎ²42-induced neurotoxicity primarily through specific interaction at the N-terminus of AÎ²42. Journal of Medicinal Chemistry. 54: 8451-60
Li H, Monien BH, Lomakin A, et al. (2010) Mechanistic investigation of the inhibition of Abeta42 assembly and neurotoxicity by Abeta42 C-terminal fragments. Biochemistry. 49: 6358-64