Zobrazeno 1 - 10
of 73
pro vyhledávání: '"Enrico Gavuzzo"'
Publikováno v:
International Journal of Peptide and Protein Research. 31:447-453
The 10-membered cyclotripeptide cyclo(-MeβAla-Phe-Pro) 3 and its diastereoisomer cyclo(-MeβAla-Phe-dPro-) 4 have been synthesized under mild cyclization conditions starting from linear precursors containing C-terminal proline. The crystal and molec
Autor:
Giancarlo Zanotti, Silvio Cerrini, Gino Lucente, Fernando Mazza, Enrico Gavuzzo, Francesco Pinnen
Publikováno v:
International Journal of Peptide and Protein Research. 22:410-421
In order to investigate the relative formation tendency of different tautomeric ring systems (cyclols, cyclodepsipeptides and corresponding N-acyl-diketopiperazines), two linear peptide precursors containing proline as C-terminal residue, have been s
Publikováno v:
International Journal of Peptide and Protein Research. 34:409-415
The tripeptide N-formyl-L-Met-L-Leu-L-Phe-OMe (FMLP-OMe) crystallizes in the orthorhombic system, space group P 2(1)2(1)2(1), with the following unit-cell parameters: a = 21.727, b = 21.836, c = 5.133 A, Z = 4. The structure has been solved and refin
Publikováno v:
Crystal Growth & Design. 8:3700-3705
The solid-state self-assembly properties of distal dimethoxy-p-H-calix[4]dihydroquinone, 3, are described. Three different crystalline forms were obtained under different crystallization conditions. The cone conformation is maintained in all three cr
Publikováno v:
Organic Letters. 10:1393-1396
The epoxidation of quinone rings of calixquinones represents a valid route for the introduction of oxygenated functionalities into the de-tert-butylated calixarene walls originating cis-diepoxy-p-dione moieties. Carbonyl reduction of these systems le
Autor:
Massimiliano Aschi, Alessio Bocedi, Gianluca Bianchini, Fernando Mazza, Enrico Gavuzzo, Paolo Ascenzi
Publikováno v:
Proteins: Structure, Function, and Bioinformatics. 64:385-390
One of the molecular factors contributing to Leishmania sp. virulence and pathogenesis is the major surface metalloprotease GP63, alternatively called leishmanolysin, MSP, and PSP (EC 3.4.24.36). Here, the molecular dynamics simulation of Leishmania
Autor:
Giovanni Maga, Enrico Gavuzzo, Roberto Di Santo, Ettore Novellino, Reynel Cancio, Roberto Cirilli, Antonio Lavecchia, Roberta Costi, Marino Artico, Rino Ragno, Francesco La Torre
Publikováno v:
ChemMedChem
1 (2006): 82–95.
info:cnr-pdr/source/autori:Di Santo R, Costi R, Artico M, Ragno R, Lavecchia A, Novellino E, Gavuzzo E, La Torre F, Cirilli R, Cancio R, Maga G./titolo:Design, synthesis, biological evaluation, and molecular modeling studies of TIBO-like cyclic sulfones as non-nucleoside HIV-1 reverse transcriptase inhibitors./doi:/rivista:ChemMedChem (Print)/anno:2006/pagina_da:82/pagina_a:95/intervallo_pagine:82–95/volume:1
1 (2006): 82–95.
info:cnr-pdr/source/autori:Di Santo R, Costi R, Artico M, Ragno R, Lavecchia A, Novellino E, Gavuzzo E, La Torre F, Cirilli R, Cancio R, Maga G./titolo:Design, synthesis, biological evaluation, and molecular modeling studies of TIBO-like cyclic sulfones as non-nucleoside HIV-1 reverse transcriptase inhibitors./doi:/rivista:ChemMedChem (Print)/anno:2006/pagina_da:82/pagina_a:95/intervallo_pagine:82–95/volume:1
TIBO- and TBO-like sulfone derivatives 1 and 2 were designed, synthesized, and tested for their ability to block the replication cycle of HIV-1 in infected cells. The anti-HIV-1 activities of sulfones 3, which were intermediates in the syntheses of 1
Publikováno v:
Organic Letters. 4:2649-2652
[structure: see text] The first example of two discrete calix[8]arene conformational isomers, 2 and 2a, has been obtained by exhaustive benzylation of 1,5-tetramethylene-bridged calix[8]arene 1. It is demonstrated, with the aid of X-ray crystallograp
Autor:
Harald Tschesche, Carlo Gallina, Alfredo Di Nola, Enrico Gavuzzo, Massimiliano Aschi, Danilo Roccatano, Giorgio Pochetti, Michael Pieper, Fernando Mazza
Publikováno v:
Journal of Computer-Aided Molecular Design. 16:213-225
Human neutrophil collagenase (HNC, MMP-8) is one of the target enzymes for drug treatment of pathologic extracellular matrix degradation. Peptidomimetic inhibitors bind in the S'-side of the enzyme active site occupying the S-1(') primary specificity
Autor:
Enrico Gavuzzo, Massimo Pomponi
Publikováno v:
Journal of Biochemical and Molecular Toxicology. 16:64-69
The effect of a series of physostigmine analogs on acetylcholinesterase activity was investigated. The second-order rate constant kon of the enzyme–inhibitor complex correlates with the conformational positioning of aromatic residues, especially Tr