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M

Maria Bretner

Polish Academy of Sciences

H指数:27

被引数:2,222

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A competition between hydrophobic and electrostatic interactions in protein-ligand systems. Binding of heterogeneously halogenated benzotriazoles by the catalytic subunit of human protein kinase CK2

IF3.2

2020-03-124

OAAI

Formylation of a metathesis-derived ansa[4]-ferrocene: a simple route to anticancer organometallics

DALTON TRANSACTIONS

IF3.3

2020-01-0116

PREAI

Diacritic Binding of an Indenoindole Inhibitor by CK2α Paralogs Explored by a Reliable Path to Atomic Resolution CK2α′ Structures

IF4.3

2019-03-1919

OAAI

Synthesis of novel proxyphylline derivatives with dual Anti-Candida albicans and anticancer activity

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2018-04-0121

PREAI

Synthesis of novel polybrominated benzimidazole derivatives-potential CK2 inhibitors with anticancer and proapoptotic activity

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2016-02-0140

PRE

Synthesis of novel chiral TBBt derivatives with hydroxyl moiety. Studies on inhibition of human protein kinase CK2α and cytotoxicity properties

EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY

IF5.9

2014-09-0120

PREAI

Unbiased Functional Proteomics Strategy for Protein Kinase Inhibitor Validation and Identification of bona fide Protein Kinase Substrates: Application to Identification of EEF1D as a Substrate for CK2

JOURNAL OF PROTEOME RESEARCH

IF3.6

2011-10-1340

OAAI

Design and synthesis of CK2 inhibitors

MOLECULAR AND CELLULAR BIOCHEMISTRY

IF3.7

2011-07-1315

PRE

Enzymatic activity with an incomplete catalytic spine: insights from a comparative structural analysis of human CK2α and its paralogous isoform CK2α'

MOLECULAR AND CELLULAR BIOCHEMISTRY

IF3.7

2011-07-0820

PRE

Casein kinase II-mediated phosphorylation of general repressor Maf1 triggers RNA polymerase III activation

酪蛋白激酶II介导的一般阻遏物Maf1的磷酸化触发RNA聚合酶III的激活

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

IF9.1

2011-03-0756

OAAI

Treatment of cultured human astrocytes and vascular endothelial cells with protein kinase CK2 inhibitors induces early changes in cell shape and cytoskeleton

MOLECULAR AND CELLULAR BIOCHEMISTRY

IF3.7

2010-12-0229

OA

Studies on the anti-hepatitis C virus activity of newly synthesized tropolone derivatives: Identification of NS3 helicase inhibitors that specifically inhibit subgenomic HCV replication

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2010-07-0126

PRE

Synthesis of new analogs of benzotriazole, benzimidazole and phthalimide-potential inhibitors of human protein kinase CK2

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2009-02-0145

PRE

Inhibition of protein kinase CK2 suppresses angiogenesis and hematopoietic stem cell recruitment to retinal neovascularization sites

MOLECULAR AND CELLULAR BIOCHEMISTRY

IF3.7

2008-07-0958

OA

New inhibitors of protein kinase CK2, analogues of benzimidazole and benzotriazole

MOLECULAR AND CELLULAR BIOCHEMISTRY

IF3.7

2008-06-1227

PRE

An unbiased evaluation of CK2 inhibitors by chemoproteomics

MOLECULAR & CELLULAR PROTEOMICS

IF5.5

2008-06-0193

OAAI

Nuclear export of S6K1II is regulated by protein kinase CK2 phosphorylation at Ser-17

JOURNAL OF BIOLOGICAL CHEMISTRY

IF3.9

2006-08-0844

PREAI

Synthesis and activity of 1H-benzimidazole and 1H-benzotriazole derivatives as inhibitors of Acanthamoeba castellanii

BIOORGANIC & MEDICINAL CHEMISTRY

IF3

2004-05-01120

PREAI

Ring-expanded (fat) nucleoside and nucleotide analogues exhibit potent in vitro activity against Flaviviridae NTPases/helicases, including those of the West Nile virus, hepatitis C virus, and Japanese encephalitis virus

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2003-08-1397

PREAI

2-THIO DERIVATIVES OF DURD AND 5-FLUORO-DURD AND THEIR 5'-MONOPHOSPHATES - SYNTHESIS, INTERACTION WITH TUMOR THYMIDYLATE SYNTHASE, AND IN-VITRO ANTITUMOR-ACTIVITY

JOURNAL OF MEDICINAL CHEMISTRY

IF6.8

2002-05-0163

PREAI