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Chemistry (Weinheim an Der Bergstrasse, Germany)|August 7, 2021
Phosphate-Based Self-Immolative Linkers for Tuneable Double Cargo ReleasePetr Šimon, Markéta Tichotová, María García Gallardo, et al.Chemistry (Weinheim an Der Bergstrasse, Germany)|May 31, 2021
Phosphate-Based Self-Immolative Linkers for Tuneable Double Cargo ReleasePetr Šimon, Markéta Tichotová, María García Gallardo, et al.Bioorganic & Medicinal Chemistry Letters|December 3, 2014
Inhibition of microbial β-N-acetylhexosaminidases by 4-deoxy- and galacto-analogues of NAG-thiazolineJana Krejzová, Lubica Kalachova, Petr Šimon, et al.Dalton Transactions (Cambridge, England : 2003)|March 24, 2012
Monomeric organoantimony(III) sulphide and selenide with terminal Sb-E bond (E = S, Se). Synthesis, structure and theoretical considerationPetr Šimon, Roman Jambor, Aleš Růžička, et al.Chemical Communications (Cambridge, England)|December 10, 2020
Phosphate linkers with traceable cyclic intermediates for self-immolation detection and monitoringEliška Procházková, Petr Šimon, Michal Straka, et al.European Journal of Medicinal Chemistry|July 3, 2016
Novel (2,6-difluorophenyl)(2-(phenylamino)pyrimidin-4-yl)methanones with restricted conformation as potent non-nucleoside reverse transcriptase inhibitors against HIV-1Petr Šimon, Ondřej Baszczyňski, David Šaman, et al.ACS Chemical Biology|November 30, 2018
Identification of Protein Targets of Bioactive Small Molecules Using Randomly Photomodified ProbesPetr Šimon, Tomáš Knedlík, Kristýna Blažková, et al.Antiviral Chemistry & Chemotherapy|February 22, 2019
Synthesis and anti-human immunodeficiency virus activity of substituted ( o,o-difluorophenyl)-linked-pyrimidines as potent non-nucleoside reverse transcriptase inhibitorsLucie Čechová, Milan Dejmek, Ondřej Baszczyňski, et al.Plos Biology|September 17, 2019
MCC950/CRID3 potently targets the NACHT domain of wild-type NLRP3 but not disease-associated mutants for inflammasome inhibitionLieselotte Vande Walle, Irma B Stowe, Pavel Šácha, et al.Plos Biology|October 17, 2019
Correction: MCC950/CRID3 potently targets the NACHT domain of wild-type NLRP3 but not disease-associated mutants for inflammasome inhibitionLieselotte Vande Walle, Irma B Stowe, Pavel Šácha, et al.Pageof 1