Zobrazeno 1 - 10
of 18
pro vyhledávání: '"F. K. Mutulis"'
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:
Biokhimiia (Moscow, Russia). 55(6)
The histamine-releasing activity of some linear and cyclic analogues of bradykinin (BK) and kallidin (K) was studied on rat peritoneal mast cells and compared with that of angiotensin (AT) cycloanalogues assayed earlier. Peptide cyclization, irrespec
Autor:
N. V. Myshlyakova, R. O. Vitolinya, V. V. Golubeva, G. A. Afanas'eva, V. E. Klusha, F. K. Mutulis, I. �. Mutule, G. I. Chipens
Publikováno v:
Bulletin of Experimental Biology and Medicine. 96:1574-1577
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
Autor:
I. L. Kuranova, V. L. Dyudmirova, Filonova Eb, F. K. Mutulis, S. I. Churkina, Grigor'eva Vd, I. P. Sekatsis, F. M. Ibatullin
Publikováno v:
Chemistry of Natural Compounds. 25:475-484
With the aim of structural-functional studies in the bombesin series, a number of bombesin fragments and analogues have been synthesized. The synthesis was performed by the carbodiimide method and by the activated-ester method. Fragments with the seq
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:
Chemischer Informationsdienst. 9
Publikováno v:
Bioorganicheskaia khimiia. 12(4)
The role of charged groups of the nonapeptide bradykinin in stabilization of its spatial structure in dimethyl sulfoxide solution was investigated. The signal assignment in the 1H-NMR spectra was achieved by means of two dimensional correlated spectr
Publikováno v:
ChemInform. 20
Publikováno v:
Bioorganicheskaia khimiia. 14(3)
Cyclo-epsilon-(L-lysine1, glycine6-bradykinin) (CLGB) and cyclo-epsilon-kallidin have been synthesised in solution. To prepare linear precursors, fragment condensation (3 + 3 or 4) + 3 was used. Peptide bond formation, including cyclization, was carr