Zobrazeno 1 - 10
of 283
pro vyhledávání: '"H, Stammer"'
Autor:
O. Holubovska, P. Babich, A. Mironenko, J. Milde, Y. Lebed, H. Stammer, L. Mueller, A.J.W. te Velthuis, V. Margitich, A. Goy
SUMMARYBackgroundEnisamium (trade name Amizon® MAX) is an orally available therapeutic that inhibits influenza A virus and SARS-CoV-2 replication and improves influenza patient recovery. We aimed to evaluate the clinical efficacy of enisamium treatm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee32ea44daa5b0f8c077bcbc97b51754
https://doi.org/10.1101/2022.08.21.22279036
https://doi.org/10.1101/2022.08.21.22279036
Akademický článek
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Akademický článek
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Autor:
R. Jund, M. Mondigler, H. Steindl, H. Stammer, P. Stierna, C. Bachert, null ARhiSi II study group
Publikováno v:
Rhinology journal. 50:417-426
Objective: A herbal drug combination (Dry Extract BNO 1016) has been assessed for efficacy and tolerability in patients with acute viral rhinosinusitis. Methodology: In this randomised, controlled trial patients with symptom duration of up to 3 days,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::78c7663108fb305d6c867d254f929e50
https://doi.org/10.4193/rhino.12.015
https://doi.org/10.4193/rhino.12.015
Publikováno v:
International Journal of Peptide and Protein Research. 30:498-510
A series of esters of L-aspartyl-1-aminocyclopropane carboxylic acid has been prepared and their sweet tastes determined. The sweetest ester prepared was about 300 times sweeter than sucrose. An attempt to use basic conditions during preparation of t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce6d915ab0e644be2364f7d2f96cc5ed
https://doi.org/10.1111/j.1399-3011.1987.tb03358.x
https://doi.org/10.1111/j.1399-3011.1987.tb03358.x
Autor:
C. H. Stammer, S. Konno
Publikováno v:
International Journal of Peptide and Protein Research. 12:222-231
The direct oxidation of a dipeptide azlactone (1) by DDG affords an optically active unsaturated dipeptide azlactone (2). It was shown that the double bond had the Z-configuration and that no racemization of the proline moiety occurred during the oxi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6188463e93ed69df3af7db30561c097
https://doi.org/10.1111/j.1399-3011.1978.tb02890.x
https://doi.org/10.1111/j.1399-3011.1978.tb02890.x
Publikováno v:
International Journal of Peptide and Protein Research. 21:202-208
Two kinds of dehydropeptide analogs of enkephalin containing a delta Tyr unit at the N-terminus have been synthesized by coupling Boc-delta Tyr-(Cl2 Bzl)-OH with amino acid amides and tetrapeptide esters using the water soluble carbodiimide-HOBt meth
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::da23cbd2abf82142d57f68a5ae605390
https://doi.org/10.1111/j.1399-3011.1983.tb03094.x
https://doi.org/10.1111/j.1399-3011.1983.tb03094.x
Publikováno v:
International Journal of Peptide and Protein Research. 20:199-206
The Gly3 residue in Gly2- and D-Ala2-enkephalins has been replaced by delta Ala3 and Ser3 in order to examine the effect on binding to the delta and mu opiate receptors. [D-Ala2, delta Ala3, Leu5]-enkephalin maintains most of its receptor binding aff
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8869a2b738bf8f4aad4d668ef42da824
https://doi.org/10.1111/j.1399-3011.1982.tb03050.x
https://doi.org/10.1111/j.1399-3011.1982.tb03050.x
Publikováno v:
International Journal of Peptide and Protein Research. 27:522-529
The dehydrophenylalanine4-enkephalin having the E-configuration (delta EPhe; phenyl and C = 0, cis) was prepared by photoisomerization of the Z-isomer with 3100 A light, followed by reversed-phase HPLC separation of the resulting mixture of the Z- an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9170a9206ecd70d8f3965b575b5924fa
https://doi.org/10.1111/j.1399-3011.1986.tb01051.x
https://doi.org/10.1111/j.1399-3011.1986.tb01051.x
Publikováno v:
International Journal of Peptide and Protein Research. 22:489-494
The delta Phe4-enkephalins have been synthesized and examined in an in vitro receptor binding assay and an in vivo tail flick analgesia test. The delta Phe4 residue was derived from Boc-Gly-Phe(beta-OH)-OH by spontaneous dehydration and azlactonizati
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91828d04acb4fb3bf977c72b2f6ee1d8
https://doi.org/10.1111/j.1399-3011.1983.tb02119.x
https://doi.org/10.1111/j.1399-3011.1983.tb02119.x