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Szabolcs Sipos

Showing results (1-10 of 6) with videos related to

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Carbohydrate Research|May 18, 2011
Preparation of 1-C-glycosyl aldehydes by reductive hydrolysisSzabolcs Sipos, István Jablonkai
Carbohydrate Research|November 16, 2011
Preparation of 2-amino-2-C-glycosyl-acetonitriles from C-glycosyl aldehydes by Strecker reactionSzabolcs Sipos, István Jablonkai, Orsolya Egyed, et al.
Chemmedchem|February 3, 2025
Structure-Atropisomer Stability Relationship in Selective MCL-1 InhibitorsSzabolcs Sipos, Barbara Balazs, Tamas Gati, et al.
ACS Omega|September 9, 2021
The Effect of Core Replacement on S64315, a Selective MCL-1 Inhibitor, and Its AnaloguesSzabolcs Sipos, Balázs Bálint, Zoltán B Szabó, et al.
Journal of Medicinal Chemistry|November 4, 2020
Discovery of S64315, a Potent and Selective Mcl-1 InhibitorZoltan Szlavik, Marton Csekei, Attila Paczal, et al.
Nature|October 28, 2016
The MCL1 inhibitor S63845 is tolerable and effective in diverse cancer modelsAndrás Kotschy, Zoltán Szlavik, James Murray, et al.
Pageof 1

Showing results (1-10 of 6) with videos related to

Sort By:
Pageof 1
Carbohydrate Research|May 18, 2011
Preparation of 1-C-glycosyl aldehydes by reductive hydrolysisSzabolcs Sipos, István Jablonkai
Carbohydrate Research|November 16, 2011
Preparation of 2-amino-2-C-glycosyl-acetonitriles from C-glycosyl aldehydes by Strecker reactionSzabolcs Sipos, István Jablonkai, Orsolya Egyed, et al.
Chemmedchem|February 3, 2025
Structure-Atropisomer Stability Relationship in Selective MCL-1 InhibitorsSzabolcs Sipos, Barbara Balazs, Tamas Gati, et al.
ACS Omega|September 9, 2021
The Effect of Core Replacement on S64315, a Selective MCL-1 Inhibitor, and Its AnaloguesSzabolcs Sipos, Balázs Bálint, Zoltán B Szabó, et al.
Journal of Medicinal Chemistry|November 4, 2020
Discovery of S64315, a Potent and Selective Mcl-1 InhibitorZoltan Szlavik, Marton Csekei, Attila Paczal, et al.
Nature|October 28, 2016
The MCL1 inhibitor S63845 is tolerable and effective in diverse cancer modelsAndrás Kotschy, Zoltán Szlavik, James Murray, et al.
Pageof 1