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1.
Bioorg Khim ; 20(7): 740-50, 1994 Jul.
Artigo em Russo | MEDLINE | ID: mdl-7993378

RESUMO

Four new analogues of beta-cazomorphine-5 modified at the C-end with ethylenediamine- and glycine-containing derivatives were synthesized by the standard method of peptide chemistry (mixed anhydrides, carbodiimide, activated esters): H-Tyr-Pro-Phe-Pro-Gly-EtDA-Gly-II (I) H-Tyr-Pro-Phe-Pro-Gly-EtDA-Gly-Gly-II (II) H-Tyr-Pro-Phe-Pro-Gly-EtDA-Gly-Gly-CO-CH3 (III) H-Tyr-Pro-Phe-Pro-Gly-EtDA-Gly-Gly-CO-CH2-CH2-COOH (IV) The level of affinity and the degree of selectivity of the peptides towards the mu- and delta-opioid receptors of the rat brain lyophilized membranes were studied by the radioreceptor method. All the new peptides displayed analgetic activity, largely depending upon their structure.


Assuntos
Analgésicos/síntese química , Caseínas/química , Endorfinas/síntese química , Fragmentos de Peptídeos/síntese química , Sequência de Aminoácidos , Analgésicos/farmacologia , Animais , Encéfalo/efeitos dos fármacos , Encéfalo/metabolismo , Endorfinas/farmacologia , Camundongos , Camundongos Endogâmicos , Dados de Sequência Molecular , Fragmentos de Peptídeos/farmacologia , Ensaio Radioligante , Receptores Opioides delta/efeitos dos fármacos
2.
Bioorg Khim ; 13(10): 1313-20, 1987 Oct.
Artigo em Russo | MEDLINE | ID: mdl-3435555

RESUMO

Synthesis and study of catalytic properties of a series of regular polypeptide which contain residues of polyfunctional amino acids forming the active centre of esterases are described viz. (Ala-Tyr-Glu)n, (His-Ser-Glu)n, (Glu-His-Glu)n, (His-Glu)n, (Ser-His-Glu)n, His-(Tyr-Glu)n. Possibility of constructing catalytically active model polypeptides which can substitute some hydrolytic enzymes is assessed. Monomers for polycondensation were been synthesized by carbodiimide method in solution, and polypeptides were obtained via 2,4,5-trichlorphenylates. Gel-filtration was used for fractionation of and molecular mass-determination of polypeptides. Catalytic properties of the synthetic polypeptides were studied in hydrolysis of p-NFA, Z-L-Ala-ONp, and Z-D-Ala-ONp. It was revealed that polypeptides (Ala-Tyr-Glu)n and (His-Ser-Glu)n possess, in hydrolysis of Z-L-Ala-ONp- and Z-D-Ala-ONp some enantioselectivity with the value of KD/KL 1.3 and 1.17, resp. The upper and lower limits of enantioselectivity as dependent of the molecular mass of the corresponding polypeptides have been determined.


Assuntos
Aminoácidos , Esterases/metabolismo , Peptídeos/síntese química , Sítios de Ligação , Catálise , Hidrólise , Cinética , Peptídeos/metabolismo , Conformação Proteica , Especificidade por Substrato
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