Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Francesco Cuda"'
Autor:
Abigail L. Male, Fedor Forafonov, Francesco Cuda, Gong Zhang, Siqi Zheng, Petra C. F. Oyston, Peng R. Chen, E. Diane Williamson, Ali Tavassoli
Publikováno v:
Scientific Reports, Vol 7, Iss 1, Pp 1-9 (2017)
Abstract The protein-protein interaction between the human CMG2 receptor and the Bacillus anthracis protective antigen (PA) is essential for the transport of anthrax lethal and edema toxins into human cells. We used a genetically encoded high through
Externí odkaz:
https://doaj.org/article/e4170e0bad4d42f1b4715b788d8d0feb
Autor:
Hoda Soleymani Abyaneh, Amir Hassan Soleimani, Mohammad Reza Vakili, Rania Soudy, Kamaljit Kaur, Francesco Cuda, Ali Tavassoli, Afsaneh Lavasanifar
Publikováno v:
Pharmaceutics, Vol 10, Iss 4, p 196 (2018)
Hypoxia can induce chemoresistance, which is a significant clinical obstacle in cancer therapy. Here, we assessed development of hypoxia-induced chemoresistance (HICR) against free versus polymeric cisplatin micelles in a triple negative breast cance
Externí odkaz:
https://doaj.org/article/e9afad8d0ea84580a99590b31667717d
Autor:
Cristina Nativi, Antonio Guidi, Francesco Cuda, Stefania Meini, Stefano Menichetti, Franco Pasqui, Giuseppe Balacco, Maria Altamura, Annalisa Guerri
Publikováno v:
Tetrahedron. 62:6754-6761
An original way to manage both stereochemistry and conformational constraints in ligand candidates for bioassays is presented with reference to a group of model N,N′-tetrasubstituted o-phthalamides and thioamides. The study shows that a scale of th
Autor:
Paolo Dapporto, Annalisa Guerri, Francesco Cuda, Cristina Nativi, Patrizia Rossi, Maria Altamura, Antonio Guidi, Giacomo Coppini, Paola Paoli
Publikováno v:
Journal of Molecular Structure. 749:20-30
The aim of the paper was to estimate the degrees of freedom, i.e. the flexibility, of four compounds (1‐4) belonging to the tertiary aromatic o-substituted oxo(thio) amide family in the perspective to exploit them as scaffolds for generating chemic
Publikováno v:
Journal of organic chemistry 69 (2004): 3654–3661. doi:10.1021/jo049899j
info:cnr-pdr/source/autori:Paolo Sarri; Francesca Venturi; Francesco Cuda; Stefano Roelens/titolo:Binding of Acetylcholine and Tetramethylammonium to Flexible Cyclophane Receptors. Improving on Binding Ability by Optimizing Host's Geometry/doi:10.1021%2Fjo049899j/rivista:Journal of organic chemistry/anno:2004/pagina_da:3654/pagina_a:3661/intervallo_pagine:3654–3661/volume:69
info:cnr-pdr/source/autori:Paolo Sarri; Francesca Venturi; Francesco Cuda; Stefano Roelens/titolo:Binding of Acetylcholine and Tetramethylammonium to Flexible Cyclophane Receptors. Improving on Binding Ability by Optimizing Host's Geometry/doi:10.1021%2Fjo049899j/rivista:Journal of organic chemistry/anno:2004/pagina_da:3654/pagina_a:3661/intervallo_pagine:3654–3661/volume:69
The structure of a cyclophanic tetraester (1), previously employed for investigations on the cation-pi interaction, has been optimized to better accommodate acetylcholine (ACh) and tetramethylammonium (TMA) guests. Following indications from molecula
Autor:
Francesco Cuda, Paolo Dapporto, Cristina Nativi, M. Altamura, Antonio Guidi, Patrizia Rossi, Annalisa Guerri
Publikováno v:
Acta Crystallographica Section A Foundations of Crystallography. 60:s269-s269