arrow
J

Jaime Mella

universidad de valparaiso
H指数:18
被引数:813

个人简介

暂无内容

教育背景

暂无内容

工作经历

暂无内容

荣誉奖项

暂无内容

Evolution of Multitarget Strategies for Alzheimer’s Disease: From Cholinergic Inhibition to Network-Oriented Therapeutic Design (2006–2025)

阿尔茨海默病多靶点策略的演变:从胆碱能抑制到网络导向的药物治疗设计(2006—2025)

2026-08-140
OA
Integrated computational modeling of chalcone-based inhibitors targeting carbonic anhydrase I and II: 3D-QSAR, molecular docking, and dynamics simulations

基于查尔酮类抑制剂的碳酸酐酶I和II靶向的整合计算建模:3D-QSAR、分子对接和动力学模拟

2026-05-140
PRE
Structure-Guided Discovery of Benzoic-Acid-Based TRPC6 Ligands: An Integrated Docking, MD, and MM-GBSA SAR Study: Potential Therapeutic Molecules for Autism Spectrum Disorder

结构导向的苯甲酸基TRPC6配体发现:综合对接、分子动力学和MM-GBSA构效关系研究:自闭症谱系障碍的潜在治疗分子

2026-03-030
OAAI
Design of Hybrid Quinoline–Chalcone Compounds Against Leishmania amazonensis Based on Computational Techniques: 2D- and 3D-QSAR with Experimental Validation

基于计算技术的针对利什曼原虫(Leishmania amazonensis)的杂合喹啉-查尔酮化合物设计:2D-和3D-QSAR与实验验证

2025-10-170
OAAI
Benzo[d]imidazole–Naphthalen-Arylmethanone Regioisomers as CB1 Ligands: Evaluation of Agonism via an Indirect Cytotoxicity-Based Approach

苯并[d]咪唑-萘基芳基甲酮同分异构体作为CB1配体:通过间接细胞毒性为基础的方法评估激动剂活性

2025-10-140
OAAI
New Dimethoxyaryl-Sesquiterpene Derivatives with Cytotoxic Activity Against MCF-7 Breast Cancer Cells: From Synthesis to Topoisomerase I/II Inhibition and Cell Death Mechanism Studies

新型双甲氧基芳基-倍半萜衍生物及其对MCF-7乳腺癌细胞的细胞毒性活性:从合成到拓扑异构酶I/II抑制及细胞死亡机制研究

2025-05-090
OA
Synthesis, Docking, 3-D-Qsar, and Biological Assays of Novel Indole Derivatives Targeting Serotonin Transporter, Dopamine D2 Receptor, and Mao-A Enzyme: In the Pursuit for Potential Multitarget Directed Ligands
2020-10-107
OAAI
Synthesis, in vitro evaluation and molecular docking of a new class of indolylpropyl benzamidopiperazines as dual AChE and SERT ligands for Alzheimer's disease
2020-07-0119
PREAI