H-Glu-Thr-OH, a dipeptide, formed by the connection of two amino acids-glutamic acid and threonine through a peptide bond, is usually found as a building block or fragment [1]. H-Glu-Thr-OH can be used for the study of the structure-activity relationship and can be analyzed to show a preference for structures in aqueous solutions[2].
References:
[1] Merlino F, Yousif A M, Billard É, et al. Urotensin II (4–11) azasulfuryl peptides: synthesis and biological activity[J]. Journal of Medicinal Chemistry, 2016, 59(10): 4740-4752.
[2] Grieco P, Carotenuto A, Patacchini R, et al. Design, synthesis, conformational analysis, and biological studies of urotensin-II lactam analogues[J]. Bioorganic & medicinal chemistry, 2002, 10(12): 3731-3739.
H-Glu-Thr-OH是由谷氨酸与苏氨酸通过肽键连接形成的二肽，通常作为结构单元或片段存在[1]。H-Glu-Thr-OH可用于构效关系研究，并且可以通过分析来显示在水溶液中对特定结构的偏好[2]。