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Wyświetlanie 1-2 z 2
Tytuł:
New bradykinin analogues acylated on the N-terminus: effect on rat uterus and blood pressure
Autorzy:
Labudda, Olga
Wierzba, Tomasz
Sobolewski, Dariusz
Śleszyńska, Małgorzata
Gawiński, Łukasz
Plackova, Marketa
Slaninová, Jiřina
Prahl, Adam
Powiązania:
https://bibliotekanauki.pl/articles/1041137.pdf
Data publikacji:
2007
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
rat blood pressure assay
bradykinin
rat uterotonic test in vitro
B2 antagonists
Opis:
Our previous studies suggested that acylation of the N-terminus of several known B2 antagonists with various kinds of bulky acyl groups consistently improved their antagonistic potency in rat blood pressure assay. On the other hand, our earlier observations also seemed to suggest that the effects of acylation on the contractility of isolated rat uterus depended substantially on the chemical character of the acyl group, as we observed that this modification might either change the range of antagonism or even transform it into agonism. Bearing all this in mind, we decided to synthesize seven new analogues of bradykinin by N-terminal acylation with various acyl groups of a moderately potent B2 antagonist, previously synthesized by Stewart's group, D-Arg-Arg-Pro-Hyp-Gly-Thr-Ser-D-Phe-Thi-Arg. The analogues were tested in vitro for their blood pressure-lowering and uterotonic activities. The modifications either preserved or increased the antagonistic potency in the rat blood pressure test. On the other hand, all seven substituents negatively influenced the interaction with the rat uterine receptors. Our results may be helpful for designing new B2 agonists and antagonists.
Źródło:
Acta Biochimica Polonica; 2007, 54, 1; 193-198
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
Tytuł:
New bradykinin B2 receptor antagonists - influence of C-terminal segment modifications on their pharmacological properties
Autorzy:
Śleszyńska, Małgorzata
Kwiatkowska, Anna
Sobolewski, Dariusz
Wierzba, Tomasz
Katarzyńska, Joanna
Zabrocki, Janusz
Borovickova, Lenka
Slaninová, Jiřina
Prahl, Adam
Powiązania:
https://bibliotekanauki.pl/articles/1040479.pdf
Data publikacji:
2009
Wydawca:
Polskie Towarzystwo Biochemiczne
Tematy:
bradykinin
B2antagonists
rat blood pressure test
in vitro rat uterotonic test
sterically restricted residue
Opis:
In the present study we describe the synthesis and some pharmacological properties of eight new analogues of bradykinin (BK). Two peptides were designed by substitution of position 7 or 8 of the known [d-Arg0,Hyp3,Thi5,8,d-Phe7]BK antagonist (Stewart's antagonist) with l-pipecolic acid (l-Pip). The next two analogues were obtained by replacement of the d-Phe residue in position 7 of the Stewart's peptide with l-β2-isoproline (l-β2-iPro) or l-β3-homoproline (l-β3-hPro). The four analogues mentioned above were also prepared in N-acylated form with 1-adamantaneacetic acid (Aaa). Biological activity of the compounds was assessed by isolated rat uterus and rat blood pressure tests. Our results showed that l-Pip in position 7 slightly increased antagonistic potency in the blood pressure test, but it turned the analogue into an agonist in the rat uterus test. Replacement of Thi by l-Pip in position 8 also enhanced antagonism in the rat pressure test but preserved the antagonism in the rat uterus test. l-β2-iPro or l-β3-hPro in position 7 decreased the potencies in both tests. We also demonstrated that acylation of the N-terminus did not increase, as was claimed previously, the antagonistic potencies of the resulting peptides. The results thus support the hypothesis about the existence of different types of BK receptors in the rat uterus and blood vessels. Our studies provide new information about the structure-activity relationship of BK antagonists which may help in designing more potent BK receptor blockers.
Źródło:
Acta Biochimica Polonica; 2009, 56, 4; 641-648
0001-527X
Pojawia się w:
Acta Biochimica Polonica
Dostawca treści:
Biblioteka Nauki
Artykuł
    Wyświetlanie 1-2 z 2

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