Petr Simon

Prague, PR 12843, Czech Republic

Last Updated: 09/26/2026

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Found 13 publications

Phosphate-Based Self-Immolative Linkers for Tuneable Double Cargo Release.

Phosphate-Based Self-Immolative Linkers for Tuneable Double Cargo Release.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: August 07, 2021

Phosphate-Based Self-Immolative Linkers for Tuneable Double Cargo Release.

Phosphate-Based Self-Immolative Linkers for Tuneable Double Cargo Release.

Journal: Chemistry (Weinheim an der Bergstrasse, Germany)

Published: May 21, 2021

Phosphate linkers with traceable cyclic intermediates for self-immolation detection and monitoring.

Phosphate linkers with traceable cyclic intermediates for self-immolation detection and monitoring.

Journal: Chemical communications (Cambridge, England)

Published: December 10, 2020

Correction: MCC950/CRID3 potently targets the NACHT domain of wild-type NLRP3 but not disease-associated mutants for inflammasome inhibition.

Correction: MCC950/CRID3 potently targets the NACHT domain of wild-type NLRP3 but not disease-associated mutants for inflammasome inhibition.

Journal: PLoS biology

Published: October 17, 2019

MCC950/CRID3 potently targets the NACHT domain of wild-type NLRP3 but not disease-associated mutants for inflammasome inhibition.

MCC950/CRID3 potently targets the NACHT domain of wild-type NLRP3 but not disease-associated mutants for inflammasome inhibition.

Journal: PLoS biology

Published: May 20, 2019

Synthesis and anti-human immunodeficiency virus activity of substituted ( o,o-difluorophenyl)-linked-pyrimidines as potent non-nucleoside reverse transcriptase inhibitors.

Synthesis and anti-human immunodeficiency virus activity of substituted ( o,o-difluorophenyl)-linked-pyrimidines as potent non-nucleoside reverse transcriptase inhibitors.

Journal: Antiviral chemistry & chemotherapy

Published: February 22, 2019

Identification of Protein Targets of Bioactive Small Molecules Using Randomly Photomodified Probes.

Identification of Protein Targets of Bioactive Small Molecules Using Randomly Photomodified Probes.

Journal: ACS chemical biology

Published: November 30, 2018

Inhibitor-GCPII Interaction: Selective and Robust System for Targeting Cancer Cells with Structurally Diverse Nanoparticles.

Inhibitor-GCPII Interaction: Selective and Robust System for Targeting Cancer Cells with Structurally Diverse Nanoparticles.

Journal: Molecular pharmaceutics

Published: February 02, 2018

Novel (2,6-difluorophenyl)(2-(phenylamino)pyrimidin-4-yl)methanones with restricted conformation as potent non-nucleoside reverse transcriptase inhibitors against HIV-1.

Novel (2,6-difluorophenyl)(2-(phenylamino)pyrimidin-4-yl)methanones with restricted conformation as potent non-nucleoside reverse transcriptase inhibitors against HIV-1.

Journal: European journal of medicinal chemistry

Published: April 15, 2016

Inhibition of microbial β-N-acetylhexosaminidases by 4-deoxy- and galacto-analogues of NAG-thiazoline.

Inhibition of microbial β-N-acetylhexosaminidases by 4-deoxy- and galacto-analogues of NAG-thiazoline.

Journal: Bioorganic & medicinal chemistry letters

Published: August 11, 2014

Inhibition of GlcNAc-processing glycosidases by C-6-azido-NAG-thiazoline and its derivatives.

Inhibition of GlcNAc-processing glycosidases by C-6-azido-NAG-thiazoline and its derivatives.

Journal: Molecules (Basel, Switzerland)

Published: February 04, 2014

Monomeric organoantimony(III) sulphide and selenide with terminal Sb-E bond (E = S, Se). Synthesis, structure and theoretical consideration.

Monomeric organoantimony(III) sulphide and selenide with terminal Sb-E bond (E = S, Se). Synthesis, structure and theoretical consideration.

Journal: Dalton transactions (Cambridge, England : 2003)

Published: March 24, 2012

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Last Updated: 09/26/2026