Zobrazeno 1 - 9
of 9
pro vyhledávání: '"and Arie van der Bent"'
Autor:
Lieselot Vercruysse, Maté Ongenaert, Guy Smagghe, Aart van Amerongen, John Van Camp, Arie van der Bent
Publikováno v:
Peptides, 30(3, Special Issue), 575-582
Peptides 30 (2009) 3, Special Issue
Peptides 30 (2009) 3, Special Issue
A bioinformatics analysis to screen for high-potential sources of angiotensin converting enzyme (ACE) inhibitory peptides was conducted in the area of insect muscle proteins. Vertebrate muscle proteins are reported as good sources of ACE inhibitory p
Publikováno v:
Biochimica et Biophysica Acta. Biomembranes 1615 (2003) 1-2
Biochimica et Biophysica Acta. Biomembranes, 1615(1-2), 84-92
Biochimica et Biophysica Acta. Biomembranes, 1615(1-2), 84-92
Clavanin A is a special antimicrobial peptide that acts at the level of the membrane via a pH-dependent mechanism. At neutral pH, clavanin disrupts biological and model membranes in a nonspecific manner, causing efflux of large molecules. At mildly a
Autor:
Piet J. Boender, Hans J. W. de Haard, Bert Kazemier, Jan-Willem Arends, Bob van Gemen, P. Oudshoorn, Arie van der Bent
Publikováno v:
Immunotechnology 4 (1999) 3-4
Immunotechnology, 4(3-4), 203-215
Immunotechnology, 4(3-4), 203-215
Background: During the conversion of murine monoclonal antibodies directed against the human chorionic gonadotropin (hCG) into bacterially expressed single chain fragments (scFv), we found a major reduction of binding activity upon introduction of a
Synthesis and biological evaluation of lorglumide-like hybrid cholecystokinin-A receptor antagonists
Autor:
Ineke Van Wijngaarden, Willem Soudijn, Ingrid van den Brink, Arie van der Bent, Adriaan P. IJzerman
Publikováno v:
Drug Development Research. 31:197-205
The evaluation of gross structural homologies between the competitive cholecystokinin-A (CCK-A) receptor antagonists lorglumide and devazepide formerly enabled the development of compact hybrid analogues [Van der Bent et al. (1992): J Med Chem 35:104
Publikováno v:
Recueil des Travaux Chimiques des Pays-Bas. 109:160-167
(13–2H) 13-Demethylretinal, (11,12,13-2H,) 13-demethylretinal, (9-2H)9-demethylretinal and (9,10-2H2)9-demethylretinal were prepared in all-E, 9Z, 11Z and 13Z isomeric form with high deuterium incorporation. In the synthesis of (9,10-2H2)9-demethyl
Publikováno v:
Biochimie 86 (2004) 3.
Biochimie, 86(3.), 231-239
Biochimie, 86(3.), 231-239
Angiotensin I converting enzyme (ACE) inhibitory peptides can induce antihypertensive effects after oral administration. By means of an ACE inhibitory peptide database, containing about 500 reported sequences and their IC50 values, the different prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9b8e9ad22cf72b06741dce09e60a673
https://research.wur.nl/en/publications/a-quantitative-in-silico-analysis-calculates-the-angiotensin-i-co
https://research.wur.nl/en/publications/a-quantitative-in-silico-analysis-calculates-the-angiotensin-i-co
Publikováno v:
Plant Physiology, 130(4), 1764-1769
Plant Physiology 130 (2002) 4
Plant Physiology 130 (2002) 4
Programmed cell death (PCD) is a functional concept that refers to cell death that is part of the normal life of a multicellular organism; it involves controlled disassembly of the cell. In animal systems PCD is synonymous with apoptosis, a cell deat
Publikováno v:
Biochemistry 41 (2002) 24
Biochemistry, 41(24), 7529-7539
Biochemistry, 41(24), 7529-7539
The pH dependence of the antimicrobial and membrane activity of clavanin A, a peptide antibiotic that is rich in histidines and glycines, was analyzed in growth and membrane leakage experiments. Clavanin A more effectively inhibited the growth of the
Publikováno v:
European journal of pharmacology. 226(4)
The C 3 -substituted benzodiazepines derived from asperlicin, e.g. devazepide (L-364,718, MK-329), constitute the most potent class of cholecystokinin A-type (CCK A ) receptor antagonists. In order to gain insight into the prerequisites for binding,