Zobrazeno 1 - 10
of 98
pro vyhledávání: '"Bruzgo I"'
Publikováno v:
In Advances in Medical Sciences 1 December 2011 56(2):323-326
Autor:
Paulina Uścinowicz, Ilona Zaręba, Urszula Tałałaj, Bruzgo I, Agnieszka Markowska, Arkadiusz Surażyński
Publikováno v:
Molecules
Volume 24
Issue 20
Molecules, Vol 24, Iss 20, p 3698 (2019)
Volume 24
Issue 20
Molecules, Vol 24, Iss 20, p 3698 (2019)
KTTKS is a matrikine that originates from the proteolytic hydrolysis of collagen. This peptide stimulates ECM production and types I and III collagen expression in vitro. A more stable form of KTTKS is pal-KTTKS, known as Matrixyl®
or palmito
or palmito
Publikováno v:
Advances in Medical Sciences (De Gruyter Open). 2009, Vol. 54 Issue 1, p47-50. 4p. 2 Charts.
Autor:
Bruzgo I, Urszula Jaworowska, Arkadiusz Surażyński, Agnieszka Markowska, Krystyna Midura-Nowaczek, Maciej Purwin, Tomasz Rusak
Publikováno v:
International Journal of Peptide Research and Therapeutics
Fifteen new peptide derivatives of ɛ-aminocaproic acid (EACA) containing the known fragment –Ala–Phe–Lys– with an affinity for plasmin were synthesised in the present study. The synthesis was carried out a solid phase. The following compound
Publikováno v:
Journal of Enzyme Inhibition and Medicinal Chemistry. 25:629-634
The biological evaluation of carbocyclic minor groove binders 1-6 is described. The cytotoxicity of the obtained compounds was tested on MDA-MB-231 breast cancer cells. The mechanism of action of compounds 1-6 was studied employing the topoisomerase
Publikováno v:
International Journal of Peptide Research and Therapeutics. 14:215-218
Eight peptides of the general formula X-d-Ser-AA-Arg-Y where X = H, Ac; AA = Ala, Gly and Y = OH, NH2 were obtained and tested for their effect on the amidolytic activities of urokinase, thrombin, plasmin, and trypsin.
Publikováno v:
Acta Biochimica Polonica. 51:73-80
epsilon-Aminocaproic acid (EACA) is a synthetic low molecular drug with antifibrinolytic activity. However, treatment with this drug can be incidentally associated with an increased thrombotic tendency. The aim of the present work was to test synthet
Publikováno v:
Advances in medical sciences. 56(2)
Purpose The aim of this work was to study the effect of the synthetic antifibrinolytics: e-aminocaproic acid (EACA), tranexamic acid (AMCHA) and e-aminocaproyl-S-benzyl-L-cysteine (H-EACA-S-Bzl-L-Cys-OH) on the fibrinolytic activity of saliva in orde
Publikováno v:
Protein and peptide letters. 17(10)
Twelve peptides of the general X-SO(2)-D-Ser-Ala-Arg-OH formula (where X = methyl, phenyl, α-tolyl, p-tolyl, 4-methylbenzyl, 1-naphtyl, 2-naphtyl, 4-chlorophenyl, 4-bromophenyl, 2-mesityl, 2,4,6-triisopropylphenyl, 4-acetamidophenyl) were obtained a
Publikováno v:
Journal of enzyme inhibition and medicinal chemistry. 25(1)
Eleven peptides of the general formula H-d-Ser-Ala-Arg-NH-X, where X = (CH2)n-NH2, n = 2-9, (CH2)m-OH, m = 2-4, were obtained and tested for their effect on the amidolytic activities of urokinase, thrombin, trypsin, plasmin, t-PA, and kallikrein. H-D