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pro vyhledávání: '"Anna L. Adams"'
Autor:
Anna L Adams, Kiernan Trevett
Publikováno v:
Therapeutic Advances in Drug Safety, Vol 10 (2019)
Externí odkaz:
https://doaj.org/article/40f838ae6f39403db238c5abc5632123
Autor:
Kiernan Trevett, Anna L. Adams
Publikováno v:
Therapeutic Advances in Drug Safety, Vol 10 (2019)
Autor:
Fabio De Gregorio, Arduino A. Mangoni, Giovanni Furlan, Terenzio Ignoni, Marco Tuccori, Hervé Le Louet, Bert van Leeuwen, Nicola Gian Castiglione, Manuela Camisa, Marco Sardella, Anna L. Adams, Paolo Porcelli, Doris Irene Stenver, Glyn Belcher, Elena Prokofyeva, Valentina Mancini, Brian Edwards, Ilaria Grisoni, Mircea Ciuca, Mario Bertazzoli Grabinski Broglio, Margherita D'Antuono, David Chonzi, Laura Boga, Calin Lungu, Christian Rausch, Paola Kruger, Sarah Hall
Publikováno v:
Therapeutic Advances in Drug Safety, Vol 12 (2021)
Therapeutic Advances in Drug Safety
Therapeutic Advances in Drug Safety
The collection and assessment of individual case safety reports (ICSRs) is important to detect unknown adverse drug reactions particularly in the first decade after approval of new chemical entities. However, regulations require that these activities
Publikováno v:
Journal of Chemical Education. 96:1143-1151
Student-built photometers are recognized as being useful tools in teaching laboratories that help students understand the concepts behind experimental measurements, and several devices have been reported that employ photoresistors as the detector of
Autor:
Rachel E. Morgan, Ben Cowper, Derek Macmillan, Bhavesh Premdjee, Stephen Caddick, Anna L. Adams
Publikováno v:
Angewandte Chemie (International Ed. in English)
Tagging the terminus: N→S acyl transfer in native peptides and proteins can be reliably intercepted with hydrazine. The method allows selective labeling and ligation, without recourse to the use of protein-splicing elements. NCL=native chemical lig
Autor:
Anna L. Adams, Derek Macmillan
Publikováno v:
Journal of Peptide Science. 19:65-73
Native chemical ligation is widely used for the convergent synthesis of proteins. The peptide thioesters required for this process can be challenging to produce, particularly when using Fmoc-based solid-phase peptide synthesis. We have previously rep
Publikováno v:
Israel Journal of Chemistry
Peptide thioester synthesis by N→S acyl transfer is being intensively explored by many research groups the world over. Reasons for this likely include the often straightforward method of precursor assembly using Fmoc-based chemistry and the fundame
Autor:
Anna L, Adams, Derek, Macmillan
Publikováno v:
Journal of peptide science : an official publication of the European Peptide Society. 19(2)
Native chemical ligation is widely used for the convergent synthesis of proteins. The peptide thioesters required for this process can be challenging to produce, particularly when using Fmoc-based solid-phase peptide synthesis. We have previously rep
Publikováno v:
ChemInform. 43
Publikováno v:
Bioorganic & Medicinal Chemistry Letters
Graphical abstract We describe experiments that give us a sense of the impact of native chemical ligation, on N-glycopeptide thioester synthesis via N→S acyl transfer.
Peptide thioesters are important tools for the total synthesis of proteins
Peptide thioesters are important tools for the total synthesis of proteins