synthesis of new lipophilic phosphonate and phosphonamidate analogues of n-acetylmuramyl-l-alanyl-d-isoglutamine related to lk 423的新合成亲脂性的膦酸酯和n-acetylmuramyl-l-alanyl-d-isoglutamine phosphonamidate类似物与路423.pdfVIP
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synthesis of new lipophilic phosphonate and phosphonamidate analogues of n-acetylmuramyl-l-alanyl-d-isoglutamine related to lk 423的新合成亲脂性的膦酸酯和n-acetylmuramyl-l-alanyl-d-isoglutamine phosphonamidate类似物与路423
Molecules 2002, 7, 394-404
molecules
ISSN 1420-3049
Synthesis of New Lipophilic Phosphonate and Phosphonamidate
Analogues of N-Acetylmuramyl-L-alanyl-D-isoglutamine
Related to LK 423
1 1,2
Stanislav Gobec*, and Uroš Urleb
1 University of Ljubljana, Faculty of Pharmacy, Aökerčeva 7, 1000 Ljubljana, Slovenia.
2 Lek d.d., Verovökova 57, 1000 Ljubljana, Slovenia.
* Author to whom correspondence should be addressed; E-mail: gobecs@ffa.uni-lj.si
Received: 9 January 2002; in revised form: 2 May 2002 / Accepted: 2 May 2002/ Published: 2 May
2002
Abstract: A syntheses of three new muramyl dipeptide (MDP) analogues related to LK 423
as potential immunomodulators are presented. The dipeptide part of the lead compound was
modified by introducing a phosphonamide isostere instead of the amide bond between L-
alanine and D-glutamic acid (or D-isoglutamine), yielding new MDP analogues 5 and 9.
Furthermore, the amide bond between L-Ala and D-Glu was replaced by a phosphonate
isostere, giving peptidyl phosphonate 14. The scope and limitations of the synthetic
strategies employed are discussed.
Keywords: Muramyl dipeptide, analogues, phosphonamidates, phosphonates,
immunomodulators.
Introduction
Bacterial cell wall components like proteoglycans, lipopolysaccharides and lipoproteins possess
strong immunostimulating activities. Since 1974 N-acetylmuramyl-L-alanyl-D-isoglutamine (muramyl
dipeptide, MDP, Figure 1) has been known as the smallest immunol
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