A solid-phase synthesis for β-turn mimetics of sialyl Lewis X

Kiriko Kurokawa; Hiroshi Kumihara; Hirosato Kondo

doi:10.1016/S0960-894X(00)00358-9

A solid-phase synthesis for β-turn mimetics of sialyl Lewis X

Kiriko Kurokawa, Hiroshi Kumihara, Hirosato Kondo

Research output: Contribution to journal › Article › peer-review

7 Citations (Scopus)

Abstract

A solid-phase synthesis of heterocyclic β-turn mimetics of sialyl Lewis X, which is a natural carbohydrate ligand of selectins, was established. This synthetic method could be very useful for drug discovery of selectin antagonists using combinatorial chemistry techniques. (C) 2000 Elsevier Science Ltd. All rights reserved.

Original language	English
Pages (from-to)	1827-1830
Number of pages	4
Journal	Bioorganic and Medicinal Chemistry Letters
Volume	10
Issue number	16
DOIs	https://doi.org/10.1016/S0960-894X(00)00358-9
Publication status	Published - Aug 21 2000
Externally published	Yes

All Science Journal Classification (ASJC) codes

Biochemistry
Molecular Medicine
Molecular Biology
Pharmaceutical Science
Drug Discovery
Clinical Biochemistry
Organic Chemistry

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10.1016/S0960-894X(00)00358-9

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abstract = "A solid-phase synthesis of heterocyclic β-turn mimetics of sialyl Lewis X, which is a natural carbohydrate ligand of selectins, was established. This synthetic method could be very useful for drug discovery of selectin antagonists using combinatorial chemistry techniques. (C) 2000 Elsevier Science Ltd. All rights reserved.",

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AU - Kumihara, Hiroshi

AU - Kondo, Hirosato

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AB - A solid-phase synthesis of heterocyclic β-turn mimetics of sialyl Lewis X, which is a natural carbohydrate ligand of selectins, was established. This synthetic method could be very useful for drug discovery of selectin antagonists using combinatorial chemistry techniques. (C) 2000 Elsevier Science Ltd. All rights reserved.

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ER -

A solid-phase synthesis for β-turn mimetics of sialyl Lewis X

Abstract

All Science Journal Classification (ASJC) codes

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