日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Nanoscale Direct-to-Biology Optimization and Structural Insights into Selective S. aureus TrmD Inhibitors

纳米尺度直接生物优化及选择性金黄色葡萄球菌TrmD抑制剂的结构解析

Hübner, Ariane F; Weldert, Annabelle C; Marciniak, Tessa; Hof, Florian; Beck, Vivien S; Carien, Samuel; Mulartschyk, Sophie N; Wolf, Eva; Ziebuhr, Wilma; Barthels, Fabian

A microscale thermophoresis-based enzymatic RNA methyltransferase assay enables the discovery of DNMT2 inhibitors

基于微尺度热泳的酶促RNA甲基转移酶检测方法能够发现DNMT2抑制剂

Nidoieva, Zarina; Sabin, Mark O; Dewald, Tristan; Weldert, Annabelle C; Hoba, Sabrina N; Helm, Mark; Barthels, Fabian

Surface Density of Mono- and Trivalent High-Mannan-Derived Targeting Structures with Different Affinities Impacts Cellular Uptake of Human Serum Albumin-Derived Nanocarriers

具有不同亲和力的单价和三价高甘露聚糖衍生靶向结构的表面密度影响人血清白蛋白衍生纳米载体的细胞摄取

Forster, Robert; Lantzberg, Bellinda; Weldert, Annabelle; Rosenberger, Laura; Zeyn, Yanira; Kowalczyk, Danuta; Kuan, Seah Ling; Kersten, Christian; Bros, Matthias; Weil, Tanja; Schirmeister, Tanja; Opatz, Till

DNA-encoded library screening uncovers potent DNMT2 inhibitors targeting a cryptic allosteric binding site.

DNA编码文库筛选发现了靶向隐蔽变构结合位点的强效DNMT2抑制剂

Frey Ariane F, Schwan Merlin, Weldert Annabelle C, Kadenbach Valerie, Kopp Jürgen, Nidoieva Zarina, Zimmermann Robert A, Gleue Lukas, Zimmer Collin, Jörg Marko, Friedland Kristina, Helm Mark, Sinning Irmgard, Barthels Fabian

Parallel synthesis of 5'-amino-5'-deoxy-adenosine derivatives for focused chemical space exploration and their application as methyltransferase inhibitors

5'-氨基-5'-脱氧腺苷衍生物的平行合成及其在聚焦化学空间探索中的应用及其作为甲基转移酶抑制剂的应用

Hoba, Sabrina N; Schwickert, Marvin; Kammerer, Luis; Sabin, Mark; Weldert, Annabelle C; Nidoieva, Zarina; Meidner, J Laurenz; Barthels, Fabian; Schirmeister, Tanja; Kersten, Christian

Support Vector Machine Identification of Small Molecule Binders to an Understudied Allosteric Site of SARS-CoV-2 Mpro for Next-Generation PROTAC-Based Therapeutics

利用支持向量机识别SARS-CoV-2 Mpro蛋白一个研究不足的变构位点的小分子结合剂,用于下一代基于PROTAC的疗法

Fassi, Enrico Mario Alessandro; Mekni, Nedra; Albani, Marco; Maehrlein, Sabine; Weldert, Annabelle Carolin; Schirmeister, Tanja; Langer, Thierry; Razioso, Giovannf

Structure-guided design of a methyltransferase-like 3 (METTL3) proteolysis targeting chimera (PROTAC) incorporating an indole-nicotinamide chemotype.

结构导向设计甲基转移酶样 3 (METTL3) 蛋白水解靶向嵌合体 (PROTAC),其中包含吲哚-烟酰胺化学类型

Weldert Annabelle C, Frey Ariane F, Krone Mackenzie W, Krähe Franziska, Kuhn Hannah, Kersten Christian, Barthels Fabian

Peptidyl nitroalkene inhibitors of main protease rationalized by computational and crystallographic investigations as antivirals against SARS-CoV-2

通过计算和晶体学研究,我们发现肽基硝基烯烃类主蛋白酶抑制剂可作为抗SARS-CoV-2病毒药物。

Medrano, Francisco J; de la Hoz-Rodríguez, Sergio; Martí, Sergio; Arafet, Kemel; Schirmeister, Tanja; Hammerschmidt, Stefan J; Müller, Christin; González-Martínez, Águeda; Santillana, Elena; Ziebuhr, John; Romero, Antonio; Zimmer, Collin; Weldert, Annabelle; Zimmermann, Robert; Lodola, Alessio; Świderek, Katarzyna; Moliner, Vicent; González, Florenci V

Improving binding entropy by higher ligand symmetry? - A case study with human matriptase

通过更高的配体对称性来提高结合熵?- 人类蛋白裂解酶的案例研究

Stefan J Hammerschmidt, Hannah Maus, Annabelle C Weldert, Michael Gütschow, Christian Kersten