Zobrazeno 1 - 10
of 10
pro vyhledávání: '"N V, Myshliakova"'
Publikováno v:
Bioorganicheskaia khimiia. 21(5)
In order to study the physiological functions of 11-deoxyprostaglandin E1-alpha, a series of its amide derivatives with amino acids and some amines were synthesized using mixed anhydride technique. The myotropic properties of newly synthesized compou
Publikováno v:
Biulleten' eksperimental'noi biologii i meditsiny. 113(4)
Kinin-like properties of two new peptides NRP-11 and P7 which have structural similarity with neurotensin (NT) and kallidin (K) were investigated. It was found that, unlike NT and K, the new peptides possess reduced myotropic and hypotensive activity
Publikováno v:
Biulleten' eksperimental'noi biologii i meditsiny. 113(2)
Biological properties of a novel vasopressin analogue were investigated. It was found that this analogue has no vasopressor and oxytocic activities but it exhibits a selective antidiuretic effect which is weaker than that of adiuretin (DDAVP). Novel
Autor:
F K, Mutulis, I E, Mutule, G Kh, Maurops, Iu, Bergmann, N V, Myshliakova, G M, Strazda, E E, Liepin'sh, Iu B, Saulitis, V D, Grigor'eva, Iu Iu, Balodis
Publikováno v:
Bioorganicheskaia khimiia. 17(10)
Cyclic analogues of substance P of the formula cyclo-[Glu-Phe-Phe-Gly-Leu-Met-NH(CH2)nNH-], where n = 3-10, 12, and open-chain analogues (XVIIIa, b) H-Glu.(NHR)-Phe-Phe-Gly-Leu-Met-NHR, where R = -CH3, -CH2CH2CH3, were synthesized. By NMR spectroscop
Autor:
I E, Mutule, F K, Mutulis, N V, Myshliakova, M M, Veveris, V V, Golubeva, E A, Porunkevich, M P, Ratkevich, G M, Strazda, V E, Klusha, Iu, Bergmann
Publikováno v:
Bioorganicheskaia khimiia. 16(11)
1 alpha-beta-carboxypropionyl-cyclo(9----1 epsilon)-[Lys1, Gly6]bradykinin (Suc-c[Lys1, Gly6]B), 1 alpha-beta-carboxypropionyl-cyclo(10----1 epsilon)kallidin (Suc-cK), cyclo(10 gamma----1 epsilon)-[Glu10]kallidin (c[Glu10]K) and cyclo(11 gamma----1 e
Publikováno v:
Bioorganicheskaia khimiia. 16(3)
Five angiotensin cycloanalogues have been synthesised by classical methods of peptide chemistry, cyclisation being carried out via pentafluorophenyl esters. Cycloanalogues (I-IV) with a fixed potential turn in the C-terminal part of the angiotensin m
Publikováno v:
Bioorganicheskaia khimiia. 13(12)
Two solution syntheses of cyclo(11----5 epsilon)-[Lys5]substance P-(5-11) (CLP) were carried out. The first synthesis involved the stepwise elongation of the peptide chain starting from glycine tert-butyl ester. At the stage of hexapeptide deprotecti
Publikováno v:
Problemy endokrinologii. 22(3)
The authors studied comparatively the properties of two angiotensin II analogues, a new compound (1-hydantoin acid, 5-valine, 8-alanine)-angiotensin II (compound III) and (1-asparagine, 5-valine, 8-alanine)-angiotensin II (compound II), as of the myo
Publikováno v:
Biulleten' eksperimental'noi biologii i meditsiny. 96(11)
Cyclic analogs of bradykinin (CBK) and kallidin (CK) have a weak myotropic activity and a marked and prolonged hypotensive effect unlike linear bradykinin (BK) and kallidin (K) which produce a short-term hypotension and considerable contraction of ra
Publikováno v:
Bioorganicheskaia khimiia. 11(12)
New cyclic analogues of neurotensin (NT): [cyclo (13----8), Gly8]NT-(8-13), [cyclo (13----7), Gly7]NT-(7-13), [cyclo (13----5 epsilon), Lys5]NT-(5-13), [cyclo (13----4 epsilon), Lys4]NT-(4-13), and their linear precursors have been synthesized. The l