Zobrazeno 1 - 10
of 62
pro vyhledávání: '"C. Wynants"'
Autor:
J.‐P. Bouillon, J. Feneau-Dupont, C. Wynants, Bernard Tinant, Jean-Paul Declercq, Zdenek Janousek, Hg. Viehe
Publikováno v:
Bulletin des Sociétés Chimiques Belges. 103:243-255
Heterocyclizations of 1,4-bis-nucleophiles with the new 3-trifluoroacetyl-lactams 1a-c differ from 1,2- or 1,3-bisnucleophiles since they proceed without opening of the lactam structure to give benzoxazolidines 4-6, benzothiazolidines 7-9 and benzimi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9e62a4a3c3ffa24cbc34fdcf7b14495b
https://doi.org/10.1002/bscb.19941030511
https://doi.org/10.1002/bscb.19941030511
Publikováno v:
International Journal of Peptide and Protein Research. 25:615-621
The possible conformations of SMS 201-995, an active analogue of somastostatin, have been studied in dimethylsulfoxide solution by 500 MHz proton n.m.r. spectroscopy. The assignments have been made by use of 2D-correlated methods to detect long-range
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::75eab968cc250f6e2ef33f623a845d3f
https://doi.org/10.1111/j.1399-3011.1985.tb02218.x
https://doi.org/10.1111/j.1399-3011.1985.tb02218.x
Publikováno v:
International Journal of Peptide and Protein Research. 25:608-614
The conformations of a cyclic analogue of somatostatin, SMS 201-995, have been studied by n.m.r. spectroscopy at 500 MHz in aqueous solution. Assignments were made by use of 2D-correlated methods, especially by detecting long-range connectivities in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f89b9691d61df273ffb88f3cbd601933
https://doi.org/10.1111/j.1399-3011.1985.tb02217.x
https://doi.org/10.1111/j.1399-3011.1985.tb02217.x
Publikováno v:
International Journal of Peptide and Protein Research. 30:541-547
The cyclic analogue of somatostatin (SRIF), D-Phe-Cys-Tyr-D-Trp-Lys-Thr-Cys-Thr-NH2 (CTC), exhibits good affinity for both opioid and SRIF receptor systems. Its conformational properties were examined in water by high-field proton n.m.r. spectroscopy
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::daf29a19d074d7af7e7e165890572e90
https://doi.org/10.1111/j.1399-3011.1987.tb03363.x
https://doi.org/10.1111/j.1399-3011.1987.tb03363.x
Publikováno v:
International Journal of Peptide and Protein Research. 25:622-627
The conformational properties of the somatostatin analogue 201-456 (1) have been studied by high field n.m.r. in DMSO. This analogue is the base structure of nine derivates synthesized by Bauer et al. and shows a very low biological activity, althoug
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f7677996eeaabc2710ded394108b5930
https://doi.org/10.1111/j.1399-3011.1985.tb02219.x
https://doi.org/10.1111/j.1399-3011.1985.tb02219.x
Publikováno v:
International Journal of Peptide and Protein Research. 26:561-567
A somatostatin octapeptide analogue has been synthesized and its conformational properties have been studied by high field n.m.r. in water. All the proton signals of the individual amino acids have been assigned except for the aromatic protons, by us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::96908dc68d3803818b00111cfa228a8d
https://doi.org/10.1111/j.1399-3011.1985.tb03212.x
https://doi.org/10.1111/j.1399-3011.1985.tb03212.x
Publikováno v:
International Journal of Peptide and Protein Research. 29:331-346
Two cyclic somatostatin analogues containing the active sequence Phe7-D-Trp8-Lys9-Thr10 and a meta- or para-(aminomethyl) phenylacetic acid (AMPA) spacer unit, have been synthesized. A conformational study using 2D n.m.r. techniques (COSY, NOESY) rev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2643564f418c2eaa68154a6548fb0ec0
https://doi.org/10.1111/j.1399-3011.1987.tb02260.x
https://doi.org/10.1111/j.1399-3011.1987.tb02260.x
Publikováno v:
International Journal of Peptide and Protein Research. 29:90-98
A series of nine closely related somatostatin analogues, containing the hexapeptide H-Cys2 -Phe3 -D-Trp4-Lys5 -Thr6 -Cys7-NH2 sequence have been synthesized by Bauer et al. The conformational properties of two of them, showing intermediate activities
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1eb62695aced8e462aa639ad00161f72
https://doi.org/10.1111/j.1399-3011.1987.tb02234.x
https://doi.org/10.1111/j.1399-3011.1987.tb02234.x
Autor:
C. Wynants
As the telecommunication industry introduces new sophisticated technologies, the nature of services and the volume of demands have changed. Indeed, a broad range of new services for users appear, combining voice, data, graphics, video, etc. This impl
Publikováno v:
Journal f�r Praktische Chemie/Chemiker-Zeitung. 338:538-543
3-Trifluoroacetyl- and other 3-acyl-1-methyl-lactams (1-5) undergo the Robinson annelation with alpha,beta-unsaturated ketones to produce spirocyclic cyclohexenones (6), their precursors hydroxycyclohexanones (7) or 3-acyl-3-oxobutyl-lactams (8) depe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d86bdfd3a1cf167bf43f23d09544f6a7
https://doi.org/10.1002/prac.199633801101
https://doi.org/10.1002/prac.199633801101