4.4 Article

Total synthesis of marinostatin, a serine protease inhibitor isolated from the marine bacterium Pseudoallteromonas sagamiensis

Journal

TETRAHEDRON LETTERS
Volume 50, Issue 20, Pages 2377-2380

Publisher

PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetlet.2009.02.213

Keywords

Ester linkage; Marinostatin (MST); Protease inhibitor; Regioselective esterification

Funding

  1. 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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