Journal
TETRAHEDRON LETTERS
Volume 50, Issue 20, Pages 2377-2380Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2009.02.213
Keywords
Ester linkage; Marinostatin (MST); Protease inhibitor; Regioselective esterification
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Funding
- Program for Promotion of Fundamental Studies in Health Science of National Institute of Biomedical Innovation (NIBL)
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Marinostatin (MST) (1) isolated from a marine organism is a serine protease inhibitor consisting of 12 amino acids with two internal ester linkages that are formed between the P-hydroxyl and [I-carboxyl groups, Thr-(3)-Asp(9) and Ser(8)-Asp(11). We synthesized MST by a regioselective esterification procedure employing two sets of orthogonally removable protecting groups at the side-chains of Asp and Ser/Thr. We optimized the esterification conditions to preferentially form the intramolecular ester linkages without any significant aspartimide (Asi) formation at Asp(9) and Asp(11). The inhibitory potency of the synthetic MST against subtilisin (Ki, 0.6 nM) was comparable with a reported value for native MST (1.5 nM). (C) 2009 Elsevier Ltd. All rights reserved.
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