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Rosaria Luciani

University of Modena and Reggio Emilia
H指数:20
被引数:1,165

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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
Discovery of a benzothiophene-flavonol halting miltefosine and antimonial drug resistance in Leishmania parasites through the application of medicinal chemistry, screening and genomics

通过药物化学,筛选和基因组学的应用,在利什曼原虫中发现苯并噻吩-黄酮醇可阻止米替福新和锑耐药性

2019-12-0121
PREAI
Enhancement of Benzothiazoles as Pteridine Reductase-1 Inhibitors for the Treatment of Trypanosomatidic Infections

增强苯并噻唑作为蝶啶还原酶-1抑制剂治疗锥虫感染

2019-03-2528
OAAI
SAR Studies and Biological Characterization of a Chromen-4-one Derivative as an Anti-Trypanosoma brucei Agent

作为抗布氏锥虫剂的Chromen-4-one衍生物的SAR研究和生物学特性

2019-01-297
OAAI
Conformational Propensity and Biological Studies of Proline Mutated LR Peptides Inhibiting Human Thymidylate Synthase and Ovarian Cancer Cell Growth
2018-07-237
OAAI
Aryl thiosemicarbazones for the treatment of trypanosomatidic infections

用于治疗锥虫感染的芳基硫代氨基脲

2018-02-0132
OAAI
Exploiting the 2-Amino-1,3,4-thiadiazole Scaffold To Inhibit Trypanosoma brucei Pteridine Reductase in Support of Early-Stage Drug Discovery

利用2-氨基-1,3,4-噻二唑支架抑制布氏锥虫蝶啶还原酶以支持早期药物发现

2017-09-1129
OAAI
Profiling of Flavonol Derivatives for the Development of Antitrypanosomatidic Drugs

用于开发抗锥虫病药物的黄酮醇衍生物的分析

2016-08-0542
OAAI