Zobrazeno 1 - 10 of 363 pro vyhledávání: '"R. Tomatis"'
1
STUDIES ON TRYPSIN INHIBITORS
Autor: A, Guggi, R, Tomatis, S, Salvadori, R, Rocchi
Publikováno v: International Journal of Peptide and Protein Research. 8:115-124
Synthesis is described of the partially protected nonapeptide tert-butyloxycarbonyl-valylleucylisoleucylglutaminyl-N-trifluoroacetyllsylserylglycylprolyl-S-acetamido-methylcysteine corresponding to positions 44-52 of the amino acid sequence of porcin
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5e2e0300806edc9eee414720fadf06da
https://doi.org/10.1111/j.1399-3011.1976.tb02487.x
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2
STUDIES ON TRYPSIN INHIBITORS
Autor: R, Tomatis, A, Guggi, R, Ferroni, R, Rocchi
Publikováno v: International Journal of Peptide and Protein Research. 8:87-95
The synthesis of the amino-protected decapeptide tert-butyloxycarbonylhydrazide corresponding to positions 15-24 of the amino acid sequence of porcine pancreatic secretory trypsin inhibitor II (Kazal inhibitor) is described. The tripeptide free base
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::dd05e8c219cc2056ea9ed244f8268829
https://doi.org/10.1111/j.1399-3011.1976.tb02484.x
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3
Synthesis, conformation and biological activity of dermorphin and delthorphin 1 peptide-peptoid hybrids
Autor: L. Biondi, E. Giannini, F. Filira, M. Gobbo, M. Marastoni, L. Negri, B. Scolaro, R. Tomatis, R. Rocchi
Publikováno v: 18th American Peptide Symposium, Boston (MA) USA, 2003
info:cnr-pdr/source/autori:L. Biondi, E. Giannini, F. Filira, M. Gobbo, M. Marastoni, L. Negri, B. Scolaro, R. Tomatis, R. Rocchi/congresso_nome:18th American Peptide Symposium/congresso_luogo:Boston (MA) USA/congresso_data:2003/anno:2003/pagina_da:/pagina_a:/intervallo_pagine
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=cnr_________::6e31618c8054d7f6e65d880b2bef3bde
http://www.cnr.it/prodotto/i/104143
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4
Synthesis and biological activity of chelator-peptide T conjugates
Autor: M, Marastoni, S, Spisani, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 48(10)
The solid phase procedure was used to prepare two peptide T derivatives in which the 4-[(1,4,8,11-tetraazacyclotetradec-1-yl)methyl]benzoyl unit is linked to their N-terminus. In a human monocyte chemotaxis assay, both chelator-peptide conjugates sho
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::a5765a97310d62c73993b0f24b7cfec3
https://pubmed.ncbi.nlm.nih.gov/9825124
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5
Structure-activity relationships of HIV-1 protease inhibitors containing gem-diaminoserine core unit
Autor: M, Marastoni, F, Bortolotti, S, Salvadori, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 48(6)
Two series of peptidomimetics containing 1,1-diamino-2-hydroxyethane (gSer) core structure were prepared, from amino acid starting materials, and evaluated as inhibitors of HIV-1 protease (HIV-1 Pr). Asymmetrical pseudodipeptides, Y-Xaa-gSer-Y (Y = Z
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::e486692d44d2c26d662ebf9f777267a5
https://pubmed.ncbi.nlm.nih.gov/9689433
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6
Symmetry-based HIV protease inhibitors containing (S,S) or (R,R) tartaric acid core structure
Autor: M, Marastoni, M, Bergonzoni, F, Bortolotti, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 47(7)
Two series of symmetry-based HIV protease inhibitors containing (S,S) or (R,R) tartaric acid core structure were prepared and tested for inhibitory property against the enzyme. All compounds showed weak antiprotease activity.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::7ddb546b90225b59ac12eeac8994a51d
https://pubmed.ncbi.nlm.nih.gov/9272250
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7
Effects of peptide T derivatives on the proliferation of cultured human keratinocytes
Autor: M, Marastoni, V, Scaranari, F, Fantini, C, Sevignani, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 45(8)
[D-Ala1]peptideT-amide, the linear hexapeptide H-Thr-Hse-Asn-Tyr-Thr-Asp-OH (LPT) and its cyclic analog, cyclo(-Thr-Hse-Asn-Tyr-Thr-Asp-) (CPT), were tested for their effects on the proliferation of cultured normal human keratinocytes (KTs) in compar
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::ca43807661414746be4523fc061d22d6
https://pubmed.ncbi.nlm.nih.gov/7575755
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9
Synthesis and biological activity of D-glucopyranosyl peptide T derivatives
Autor: M, Marastoni, S, Spisani, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 44(8)
The solid phase procedure, based on the Fmoc (9-fluorenylmethyloxycarbonyl) chemistry, was used to prepare some peptide T analogues in which D-glucopyranosyl units are beta-O-glycosidically linked to Thr4 and/or Thr5 side chains. All glycopeptides sh
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::4ad8db6d13e5dd286a8201c1918040d9
https://pubmed.ncbi.nlm.nih.gov/7945547
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10
Studies on the anti-phospholipase A2 and anti-inflammatory activities of a uteroglobin fragment and related peptides
Autor: M, Marastoni, V, Scaranari, P, Romualdi, A, Donatini, S, Ferri, R, Tomatis
Publikováno v: Arzneimittel-Forschung. 43(9)
The nonapeptide antiflammin P1 (H-Met-Gln-Met-Lys-Lys-Val-Leu-Asp-Ser-OH), its isoAsp8 analogue and the corresponding aminosuccinyl peptide were prepared, characterized and tested for inhibition of phospholipase A2 (PLA2) in vitro and for anti-inflam
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::52d7f80d0eb42312baba54507a4dc7e3
https://pubmed.ncbi.nlm.nih.gov/8240467
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