Diketopiperazines in peptide and combinatorial chemistry

被引:177
作者
Fischer, PM [1 ]
机构
[1] Cyclacel Ltd, Dundee DD1 5JJ, Scotland
关键词
diketopiperazine; DKP; piperazine-2,5-dione; combinatorial chemistry; SPPS; SPOC; side reaction; peptide cyclization;
D O I
10.1002/psc.446
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Diketopiperazines (DKPs), the smallest cyclic peptides, represent an important class of biologically active natural products and their research has been fundamental to many aspects of peptide chemistry. The advent of combinatorial chemistry has revived interest in DKPs for two reasons: firstly, they are simple heterocyclic scaffolds in which diversity can be introduced and stereochemically controlled at up to four positions; secondly, they can be prepared from readily available alpha-amino acids using very robust chemistry. Here synthetic methods, conformation, as well as applications of DKPs are summarized and discussed critically. Copyright (C) 2003 European Peptide Society and John Wiley Sons, Ltd.
引用
收藏
页码:9 / 35
页数:27
相关论文
共 220 条
[1]   Studies on the effect of the formation of amino acid ester concerned alcohol group on the formation rate of 2.5-dioxo-iperazine and the origin of guanidine compounds and the effect of guanidine on various amino acid esters. [J].
Abderhalden, E ;
Suzuki, S .
HOPPE-SEYLERS ZEITSCHRIFT FUR PHYSIOLOGISCHE CHEMIE, 1928, 176 (1/2) :101-108
[2]  
ABENIUS PW, 1888, CHEM BER, V21, P1662
[3]   Solid-phase synthesis of substituted imidazoline-tethered 2,3-diketopiperazines, cyclic ureas, and cyclic thioureas [J].
Acharya, AN ;
Ostresh, JM ;
Houghten, RA .
JOURNAL OF COMBINATORIAL CHEMISTRY, 2001, 3 (06) :612-623
[4]   13 The anhydrides of basic amino-acids [J].
Adamson, DW .
JOURNAL OF THE CHEMICAL SOCIETY, 1943, :39-40
[5]   UV PHOTOELECTRON-SPECTRA OF PEPTIDE UNIT MODEL COMPOUNDS - METHIONYL-CONTAINING CYCLIC DIPEPTIDES [J].
AJO, D ;
GRANOZZI, G ;
GUANTIERI, V ;
TAMBURRO, AM .
JOURNAL OF MOLECULAR STRUCTURE, 1983, 96 (3-4) :369-372
[6]   FMOC-BASED SOLID-PHASE PEPTIDE-SYNTHESIS USING A NEW TERT-ALCOHOL TYPE 4-(1',1'-DIMETHYL-1'-HYDROXYPROPYL)PHENOXYACETYL HANDLE (DHPP) RESIN (FMOC = FLUOREN-9-YLMETHOXYCARBONYL) [J].
AKAJI, K ;
KISO, Y ;
CARPINO, LA .
JOURNAL OF THE CHEMICAL SOCIETY-CHEMICAL COMMUNICATIONS, 1990, (07) :584-586
[7]  
ALBERICIO F, 1985, INT J PEPT PROT RES, V26, P92
[8]   ACID-CATALYZED DECARBOBENZOXYLATION [J].
ALBERTSON, NF ;
MCKAY, FC .
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, 1953, 75 (21) :5323-5326
[9]   BICYCLIC AND TRICYCLIC PRODUCTS FROM TETRA-PEPTIDES AND PENTA-PEPTIDES OF ALPHA-METHYLALANINE [J].
ALI, MY ;
DALE, J ;
TITLESTAD, K .
ACTA CHEMICA SCANDINAVICA, 1973, 27 (05) :1509-1518
[10]   Use of N-tritylamino acids and PyAOP(1) for the suppression of diketopiperazine formation in Fmoc/(t)Bu solid-phase peptide synthesis using alkoxybenzyl ester anchoring linkages [J].
Alsina, J ;
Giralt, E ;
Albericio, F .
TETRAHEDRON LETTERS, 1996, 37 (24) :4195-4198