Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Fabio Begnini"'
Autor:
Naziia Kurmasheva, Aida Said, Boaz Wong, Priscilla Kinderman, Xiaoying Han, Anna H. F. Rahimic, Alena Kress, Madalina E. Carter-Timofte, Emilia Holm, Demi van der Horst, Christoph F. Kollmann, Zhenlong Liu, Chen Wang, Huy-Dung Hoang, Elina Kovalenko, Maria Chrysopoulou, Krishna Sundar Twayana, Rasmus N. Ottosen, Esben B. Svenningsen, Fabio Begnini, Anders E. Kiib, Florian E. H. Kromm, Hauke J. Weiss, Daniele Di Carlo, Michela Muscolini, Maureen Higgins, Mirte van der Heijden, Angelina Bardoul, Tong Tong, Attila Ozsvar, Wen-Hsien Hou, Vivien R. Schack, Christian K. Holm, Yunan Zheng, Melanie Ruzek, Joanna Kalucka, Laureano de la Vega, Walid A. M. Elgaher, Anders R. Korshoej, Rongtuan Lin, John Hiscott, Thomas B. Poulsen, Luke A. O’Neill, Dominic G. Roy, Markus M. Rinschen, Nadine van Montfoort, Jean-Simon Diallo, Henner F. Farin, Tommy Alain, David Olagnier
Publikováno v:
Nature Communications, Vol 15, Iss 1, Pp 1-28 (2024)
Abstract The presence of heterogeneity in responses to oncolytic virotherapy poses a barrier to clinical effectiveness, as resistance to this treatment can occur through the inhibition of viral spread within the tumor, potentially leading to treatmen
Externí odkaz:
https://doaj.org/article/cf343351f5cf4766ad351ee93729ee99
Autor:
Peter Sjö, Vasanthanathan Poongavanam, Stefan Geschwindner, Fabio Begnini, Björn Over, Stefan Schiesser, Jan Kihlberg, Patrik Johansson, Lisa Wissler, Mohit Tyagi, Christian Tyrchan, Marie Castaldo
Publikováno v:
Journal of Medicinal Chemistry
'Journal of Medicinal Chemistry ', vol: 64, pages: 1054-1072 (2021)
'Journal of Medicinal Chemistry ', vol: 64, pages: 1054-1072 (2021)
Lead generation for difficult-to-drug targets that have large, featureless, and highly lipophilic or highly polar and/or flexible binding sites is highly challenging. Here, we describe how cores of macrocyclic natural products can serve as a high-qua
Autor:
Fabio Begnini, Stefan Geschwindner, Patrik Johansson, Lisa Wissler, Richard J. Lewis, Emma Danelius, Andreas Luttens, Pierre Matricon, Jens Carlsson, Stijn Lenders, Beate König, Anna Friedel, Peter Sjö, Stefan Schiesser, Jan Kihlberg
Upregulation of the transcription factor Nrf2 by inhibition of the interaction with its negative regulator Keap1 constitutes an opportunity for the treatment of disease caused by oxidative stress. We report a structurally unique series of nanomolar K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2356a884998258f24d9f2fdfe2f58424
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-477522
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-477522
Autor:
Fabio Begnini, Stefan Geschwindner, Patrik Johansson, Lisa Wissler, Richard J. Lewis, Emma Danelius, Andreas Luttens, Pierre Matricon, Jens Carlsson, Stijn Lenders, Beate König, Anna Friedel, Peter Sjö, Stefan Schiesser, Jan Kihlberg
Publikováno v:
Journal of Medicinal Chemistry. 66:2204-2204
Autor:
Yoseph Atilaw, Stefan Schiesser, Vasanthanathan Poongavanam, Fabio Begnini, Jan Kihlberg, Máté Erdélyi
Publikováno v:
ACS Medicinal Chemistry Letters
Conformation-dependent 3D descriptors have been shown to provide better predictions of the physicochemical properties of macrocycles than 2D descriptors. However, the computational identification of relevant conformations for macrocycles is nontrivia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2e5303ce42c9bde21d3977a5b3d3070a
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-448939
http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-448939
Publikováno v:
Chemistry – A European Journal. 26
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 26(1)
Drugs in the chemical space beyond the rule of 5 (bRo5) can modulate targets with difficult binding sites while retaining cell permeability and oral absorption. Reviewing the syntheses of bRo5 drugs approved since 1990 highlights synthetic chemistry'
Publikováno v:
Synlett. 27:2831-2835
A one-pot, three-component reaction has been developed and successfully employed for the synthesis of biologically relevant, highly functionalized spirooxindole-fused 3-thiazoline derivatives. Starting from ammonia, three mercapto carbonyl components
Autor:
Alessandra Silvani, Mariska De Munnik, Giulia Rainoldi, Fabio Begnini, Eelco Ruijter, Romano V. A. Orru, Leonardo Lo Presti, Giordano Lesma, Christophe M. L. Vande Velde
Publikováno v:
Rainoldi, G, Begnini, F, De Munnik, M, Lo Presti, L, Vande Velde, C M L, Orru, R, Lesma, G, Ruijter, E & Silvani, A 2018, ' Sequential Multicomponent Strategy for the Diastereoselective Synthesis of Densely Functionalized Spirooxindole-Fused Thiazolidines ', ACS Combinatorial Science, vol. 20, no. 2, pp. 98-105 . https://doi.org/10.1021/acscombsci.7b00179
ACS combinatorial science
ACS Combinatorial Science, 20(2), 98-105. American Chemical Society
ACS combinatorial science
ACS Combinatorial Science, 20(2), 98-105. American Chemical Society
We developed two Ugi-type three-component reactions of spirooxindole-fused 3-thiazolines, isocyanides, and either carboxylic acids or trimethylsilyl azide, to give highly functionalized spirooxindole-fused thiazolidines. Two diverse libraries were ge
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1540f0a341547c3a4c6a7efe3aaf8f15
https://research.vu.nl/en/publications/044abadd-7ca8-4850-95b7-466d91819aed
https://research.vu.nl/en/publications/044abadd-7ca8-4850-95b7-466d91819aed