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pro vyhledávání: '"J, Slaninová"'
Autor:
J. Slaninová, I. Derdowska, B. Hartrodt, A. Prahl, Klaus Neubert, W. Kowalczyk, Bernard Lammek, O. Dawidowska
Publikováno v:
Journal of Peptide Research. 63:420-425
Four new analogues of arginine vasopressin (AVP) substituted in positions 2 and 3 with all possible combinations of enantiomers of N-methylphenylalanine were synthesized and studied to assess the influence of N-methylation of the peptide bonds betwee
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::023c1dd0f4a28a4dd304994642a73052
https://doi.org/10.1111/j.1399-3011.2004.00140.x
https://doi.org/10.1111/j.1399-3011.2004.00140.x
Akademický článek
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A convenient and facile synthesis, in silico docking studies and in vitro biological evaluation of N-substituted 5-butylimidazole derivatives as potent Angiotensin II (ANG II) receptor type 1 (AT1) blockers (ARBs) has been reported in the current stu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______2127::d845412b1ba15e1660e466fa06ba3f77
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2956946
https://pergamos.lib.uoa.gr/uoa/dl/object/uoadl:2956946
Publikováno v:
The journal of peptide research : official journal of the American Peptide Society. 62(2)
In this study we describe the synthesis and some pharmacological properties of seven new analogues of arginine vasopressin (AVP) substituted in position 2 or 3 with 1-aminocyclohexane-1-carboxylic acid (Acc). All peptides were tested for the pressor,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::62e89a04c2a6f645bd97599533cb080b
https://pubmed.ncbi.nlm.nih.gov/12823619
https://pubmed.ncbi.nlm.nih.gov/12823619
Publikováno v:
The journal of peptide research : official journal of the American Peptide Society. 58(3)
Six [Pen(6)]oxytocin analogs were synthesized by substituting penicillamine for cysteine in oxytocin, [Mpa(1)]oxytocin, [dPen(1)]oxytocin, [5-t-BuPro(7)]oxytocin, [Mpa(1), 5-t-BuPro(7)]oxytocin and [dPen(1), 5-t-BuPro(7)]oxytocin. When tested in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::d25c9a8566beb797baa71274c1c3797a
https://pubmed.ncbi.nlm.nih.gov/11576333
https://pubmed.ncbi.nlm.nih.gov/11576333
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 7(8)
For the purpose of evaluating substitution effects in the ortho, meta or para positions of the aromatic ring of tyrosine or phenylalanine in position 2 of oxytocin on uterotonic activity in vitro in the presence and absence of magnesium ions, six new
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::60b687ab4a61e66b8f90a68b6cca6719
https://pubmed.ncbi.nlm.nih.gov/11548057
https://pubmed.ncbi.nlm.nih.gov/11548057
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 6(3)
Two cyclic disulfides of structure Cys-Tyr-Arg-Arg-Tyr-Cys-NH2 (1) and Cys-Tyr(Me)-Arg-Arg-Tyr(Me)-Cys-NH2 (2), two nonapeptide derivatives of 1 extended at the C-terminal with Pro-Arg-Gly-NH2 (3) or Pro-D-Arg-Gly-NH2 (4) and derivatives of 3 and 4 h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::bbe00677322a1bce08911e814c37132e
https://pubmed.ncbi.nlm.nih.gov/10759210
https://pubmed.ncbi.nlm.nih.gov/10759210
Publikováno v:
Peptide research. 9(3)
New methods have been developed for the synthesis of disulfide-bridged homo and hetero peptide dimers (both parallel and antiparallel), as exemplified in the oxytocin and deamino-oxytocin families. The linear sequences were assembled by 9-fluorenyl-m
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f6c905e77d6f4bf7ae6099083e359bc3
https://pubmed.ncbi.nlm.nih.gov/8875590
https://pubmed.ncbi.nlm.nih.gov/8875590
Autor:
Z. Procházka, J. Slaninová
Publikováno v:
Peptides 1994 ISBN: 9789072199218
Peptides 1994
Peptides 1994
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1fb3fdba40a20615be201a1f45322f23
https://doi.org/10.1007/978-94-011-1468-4_149
https://doi.org/10.1007/978-94-011-1468-4_149
Publikováno v:
Peptides ISBN: 9789401042956
Peptides
Peptides
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::240ce1b5a7519c1b8a6ca91451e7784b
https://doi.org/10.1007/978-94-011-0683-2_34
https://doi.org/10.1007/978-94-011-0683-2_34