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Matteo Santucci

Università di Modena e Reggio Emilia
H指数:15
被引数:730

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The discovery of aryl-2-nitroethyl triamino pyrimidines as anti-Trypanosoma brucei agents

aryl-2-nitroethyl三氨基嘧啶作为抗布氏锥虫剂的发现

2024-01-013
PRE
High-Throughput Phenotypic Screening and Machine Learning Methods Enabled the Selection of Broad-Spectrum Low-Toxicity Antitrypanosomatidic Agents
2023-11-033
OAAI
Destabilizers of the thymidylate synthase homodimer accelerate its proteasomal degradation and inhibit cancer growth

胸苷酸合酶同型二聚体的去稳定剂加速其蛋白酶体降解并抑制癌症生长

2022-12-076
OAAI
Multitarget, Selective Compound Design Yields Potent Inhibitors of a Kinetoplastid Pteridine Reductase 1

多目标,选择性化合物设计可产生动质体蝶啶还原酶1的有效抑制剂

2022-06-0813
OAAI
Folic Acid-Peptide Conjugates Combine Selective Cancer Cell Internalization with Thymidylate Synthase Dimer Interface Targeting
2021-03-1217
OAAI
Identification of a 2,4-diaminopyrimidine scaffold targeting Trypanosoma brucei pteridine reductase 1 from the LIBRA compound library screening campaign
2020-03-0110
OAAI
Conformational Propensity and Biological Studies of Proline Mutated LR Peptides Inhibiting Human Thymidylate Synthase and Ovarian Cancer Cell Growth
2018-07-237
OAAI
Computational and biological profile of boronic acids for the detection of bacterial serine- and metallo-β-lactamases

用于检测细菌丝氨酸和金属 β-内酰胺酶的硼酸的计算和生物学特征

2017-12-1829
OAAI
Chroman-4-One Derivatives Targeting Pteridine Reductase 1 and Showing Anti-Parasitic Activity

靶向蝶啶还原酶1并显示抗寄生虫活性的Chroman-4-One衍生物

2017-03-0846
OAAI