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For: Kumar RR, Sahu B, Pathania S, Singh PK, Akhtar MJ, Kumar B. Piperazine, a Key Substructure for Antidepressants: Its Role in Developments and Structure-Activity Relationships. ChemMedChem 2021;16:1878-901. [PMID: 33751807 DOI: 10.1002/cmdc.202100045] [Cited by in Crossref: 12] [Cited by in F6Publishing: 14] [Article Influence: 12.0] [Reference Citation Analysis]
Number Citing Articles
1 Nandi NK, Bhatia R, Saini S, Rawat R, Sharma S, Raj K, Rangra N, Kumar B. Design, Synthesis, Pharmacological and In Silico Screening of Disubstituted-Piperazine Derivatives as Selective and Reversible MAO-A Inhibitors for Treatment of Depression. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.134671] [Reference Citation Analysis]
2 Sparaco R, Kędzierska E, Kaczor AA, Bielenica A, Magli E, Severino B, Corvino A, Gibuła-Tarłowska E, Kotlińska JH, Andreozzi G, Luciano P, Perissutti E, Frecentese F, Casertano M, Leśniak A, Bujalska-Zadrożny M, Oziębło M, Capasso R, Santagada V, Caliendo G, Fiorino F. Synthesis, Docking Studies and Pharmacological Evaluation of Serotoninergic Ligands Containing a 5-Norbornene-2-Carboxamide Nucleus. Molecules 2022;27:6492. [PMID: 36235029 DOI: 10.3390/molecules27196492] [Reference Citation Analysis]
3 Li T, Huang X, Sun J, Geng C, Zhang X, Chen J. Synthesis and biological evaluation of (+)-paeoveitol derivatives as novel antidepressants. Med Chem Res. [DOI: 10.1007/s00044-022-02973-0] [Reference Citation Analysis]
4 Romanelli MN, Manetti D, Braconi L, Dei S, Gabellini A, Teodori E. The piperazine scaffold for novel drug discovery efforts: the evidence to date. Expert Opin Drug Discov 2022. [PMID: 35848922 DOI: 10.1080/17460441.2022.2103535] [Reference Citation Analysis]
5 Zhang H, Wang Y, Wang Y, Li X, Wang S, Wang Z. Recent advance on carbamate-based cholinesterase inhibitors as potential multifunctional agents against Alzheimer's disease. Eur J Med Chem 2022;240:114606. [PMID: 35858523 DOI: 10.1016/j.ejmech.2022.114606] [Cited by in Crossref: 3] [Cited by in F6Publishing: 1] [Article Influence: 3.0] [Reference Citation Analysis]
6 Meanwell NA, Loiseleur O. Applications of Isosteres of Piperazine in the Design of Biologically Active Compounds: Part 1. J Agric Food Chem . [DOI: 10.1021/acs.jafc.2c00726] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Pal R, Jawaid Akhtar M, Raj K, Singh S, Sharma P, Kalra S, Chawla PA, Kumar B. Design, synthesis and evaluation of piperazine clubbed 1,2,4-triazine derivatives as potent anticonvulsant agents. Journal of Molecular Structure 2022;1257:132587. [DOI: 10.1016/j.molstruc.2022.132587] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
8 Lu Y, Feng Y, Li Z, Li J, Zhang H, Hu X, Jiang W, Shi T, Wang Z. Novel piperazine based benzamide derivatives as potential anti-glioblastoma agents inhibiting cell proliferation and cell cycle progression. Eur J Med Chem 2022;227:113908. [PMID: 34656900 DOI: 10.1016/j.ejmech.2021.113908] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
9 Lesnikov VK, Nelyubina YV, Sukhorukov AY. Piperazine-1,4-diol (PipzDiol): synthesis, stereodynamics and assembly of supramolecular hydrogen-bonded 2D networks. New J Chem 2022;46:20386-20394. [DOI: 10.1039/d2nj03012h] [Reference Citation Analysis]
10 Al-ghorbani M, Gouda MA, Baashen M, Ranganatha V. L. Pyrimidine-Piperazine Hybrids; Recent Synthesis and Biological Activities. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2021.1998144] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]