Zobrazeno 1 - 10
of 354
pro vyhledávání: '"G. Mastropietro"'
Autor:
J. Moya, Daniel G. Mastropietro
Publikováno v:
Computational Materials Science. 188:110230
The development of bulk metallic glasses (BMGs) is a topic of current interest due to the unique set of properties that distinguish them from their crystalline counterpart and make them attractive in industrial applications as both structural and fun
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dcc82edfc2e7f1dc9a63bdda238a8cc4
https://doi.org/10.1016/j.commatsci.2020.110230
https://doi.org/10.1016/j.commatsci.2020.110230
Autor:
Marco Gambera, L. Degli Esposti, Adriano Vercellone, E. Nava, Vittorio Perrone, Stefania Saragoni, D. Alessandrini, T.A. Calamia, G. Mastropietro
Publikováno v:
Value in Health. 22:S539
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1620f906711d807bb1255a0034998e1a
https://doi.org/10.1016/j.jval.2019.09.712
https://doi.org/10.1016/j.jval.2019.09.712
Autor:
Gino Lucente, Susanna Spisani, M. Paglialunga Paradisi, G. Pagani Zecchini, G. Mastropietro, Ines Torrini
Publikováno v:
The Journal of Peptide Research. 55:102-109
In order to obtain chemotactic peptides with selective bioactivity, a new type of structural modification was introduced at the N-terminal position of HCO-Nle-Leu-Phe-OMe. Two groups of analogs have been synthesized both containing a N-terminal resid
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68bd0e20a2248bfeab0c5f1d9af1689e
https://doi.org/10.1034/j.1399-3011.2000.00159.x
https://doi.org/10.1034/j.1399-3011.2000.00159.x
Autor:
G. Mastropietro, Mario Paglialunga Paradisi, Ines Torrini, Fernando Mazza, Gino Lucente, Giampiero Pagani Zecchini, Enrico Gavuzzo
Publikováno v:
Tetrahedron. 55:2077-2090
The new pseudodipeptide Boc-azaTic-Leu-OMe (1), incorporating the conformationally and topographically constrained 3,4-dihydro-2(1H)-phthalazinecarboxylic acid (azaTic) residue, has been synthesized together with the three related models Boc-azaTic-N
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::06be76252b635785620b85f60459ad88
https://doi.org/10.1016/s0040-4020(98)01219-8
https://doi.org/10.1016/s0040-4020(98)01219-8
Autor:
I. Torriai, M. Paghalunga Paradisi, G. Mastropietro, Susanna Spisani, Gino Lucente, G. Pagani Zecchini
Publikováno v:
Amino Acids. 14:301-309
The synthesis and the biological activity of a pseudopeptide analogue of the chemotactic N-formyltripeptide fMLP-OMe, containing the azaTic (3,4-dihydro-2(1H)-phthalazinecarboxylic acid) residue replacing the native phenylalanine, is described. Where
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b45751d16c59ec66c378cfaa296f0f5b
https://doi.org/10.1007/bf01318849
https://doi.org/10.1007/bf01318849
Autor:
Gino Lucente, Mario Paglialunga Paradisi, Ines Torrini, Fernando Mazza, Giorgio Pochetti, G. Mastropietro, Giampiero Pagani Zecchini, Enrico Gavuzzo
Publikováno v:
Tetrahedron. 54:165-178
3,4-Dihydro-2(1 H )-phthalazinecarboxylic acid (azaTic) is a new conformationally restricted analogue of phenylalanine which, due to its α-aza-nature, should allow, in addition to the topographical control typical of the Tic residue, a definite loca
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f17a6a4534370c619a3989eb7e565994
https://doi.org/10.1016/s0040-4020(97)10267-8
https://doi.org/10.1016/s0040-4020(97)10267-8
Autor:
Gino Lucente, Mario Paglialunga Paradisi, Susanna Spisani, Giampiero Pagani Zecchini, Ines Torrini, Maurizio Paci, G. Mastropietro
Publikováno v:
Archiv der Pharmazie. 329:517-523
The role exercised by the central residue of the chemotactic N-formyltripeptide HCO-Met-Leu-Phe-OMe (fMLP-OMe) in controlling both the backbone conformation and the biochemical activity is the subject of recent interest. Here, two new centrally const
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bdce2b96a810a8b173fc005c8efcaaab
https://doi.org/10.1002/ardp.19963291202
https://doi.org/10.1002/ardp.19963291202
Publikováno v:
Tetrahedron Letters. 34:3763-3766
The reaction of 2-triflyloxyacetophenone derivatives 1 with carbon monoxide in the presence of a palladium catalyst affords 3-ylidenephthalides 2 in good yields and under mild conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d7cf4fb473bec515724be1b52b7fa227
https://doi.org/10.1016/s0040-4039(00)79222-7
https://doi.org/10.1016/s0040-4039(00)79222-7
Publikováno v:
ChemInform. 24
The reaction of 2-triflyloxyacetophenone derivatives 1 with carbon monoxide in the presence of a palladium catalyst affords 3-ylidenephthalides 2 in good yields and under mild conditions.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::031dead4f0fe03195d5e268bfb511f88
https://doi.org/10.1002/chin.199343120
https://doi.org/10.1002/chin.199343120
Autor:
Susanna Spisani, Mario Paglialunga Paradisi, G. Mastropietro, Maurizio Paci, Giampiero Pagani Zecchini, Gino Lucente, Ines Torrini
Publikováno v:
ChemInform. 28
The role exercised by the central residue of the chemotactic N-formyltripeptide HCO-Met-Leu-Phe-OMe (fMLP-OMe) in controlling both the backbone conformation and the biochemical activity is the subject of recent interest. Here, two new centrally const
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7e44484480828b5ff878c1dccd473b7a
https://doi.org/10.1002/chin.199725188
https://doi.org/10.1002/chin.199725188