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Molecular Diversity|November 6, 2025
Exploration of new azole derivatives containing ethanolamine moiety as anti-UC agents by inhibiting NF-κB/MAPK pathwaysMing-Qian Ju, Zheng-Xiao Huang, Qing-Yan Mo, et al.
Molecular Diversity|November 18, 2025
Rational in silico design of PPARγ agonists for type 2 diabetes: an integrated study using pharmacophore modeling, 3D-QSAR, molecular docking, MD simulations, DFT, and toxicity predictionTathagata Pradhan, Ojasvi Gupta, Gita Chawla
Molecular Diversity|October 5, 2025
Thiadiazole based β-carboline derivatives as potential α-glucosidase inhibitors: design, synthesis, and bioactivity evaluationHuan Zhou, Yaxin Wen, Shao-Hua Wang, et al.
Molecular Diversity|October 6, 2025
Design and development of N-Heterocyclic protease inhibitors for flaviviral infections: a synthetic and SAR-based reviewRajarshi Nath, Md Jawaid Akhtar, Sudin Sundar Pradhan, et al.
Molecular Diversity|October 6, 2025
Novel carbazole-triazole-thioether conjugates as multifunctional antimicrobial agents against phytopathogenAwei Zhang, Huiyan Quan, Danqing Wang, et al.
Molecular Diversity|September 23, 2025
Targeting p53-MDM2 pathway with novel triazole-oxazole hybrids: a fragment-based drug discovery approach for next-generation cancer therapiesApurva Prajapati, Hitesh Patel
Molecular Diversity|January 2, 2021
Monophosphoramide derivatives: synthesis and crystal structure, theoretical and experimental studies of their biological effectsKhodayar Gholivand, Zahra Roshanian, Maryam Rahimzadeh Dashtaki, et al.
Molecular Diversity|December 25, 2019
Novel amide derivatives of 3-phenylglutaric acid as potent soluble epoxide hydrolase inhibitorsElham Rezaee, Somayeh Minaei Amrolah, Maryam Nazari, et al.
Molecular Diversity|November 23, 2022
Synthesis, biological assessment, and computational investigations of nifedipine and monastrol analogues as anti-leishmanial major and anti-microbial agentsMahdieh Khalilzadeh, Sedigheh Saberi, Ghazal Noori, et al.
Molecular Diversity|April 7, 2020
N-Benzylation of 6-aminoflavone by reductive amination and efficient access to some novel anticancer agents via topoisomerase II inhibitionNitin M Thorat, Aniket P Sarkate, Deepak K Lokwani, et al.
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