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For: Rani A, Anand A, Kumar K, Kumar V. Recent developments in biological aspects of chalcones: the odyssey continues. Expert Opinion on Drug Discovery 2019;14:249-88. [DOI: 10.1080/17460441.2019.1573812] [Cited by in Crossref: 29] [Cited by in F6Publishing: 18] [Article Influence: 9.7] [Reference Citation Analysis]
Number Citing Articles
1 Mara Silva de Pádua G, Maria De Souza J, Celia Moura Sales M, Gomes de Vasconcelos L, Luiz Dall'Oglio E, Faraggi TM, Moreira Sampaio O, Campos Curcino Vieira L. Evaluation of Chalcone Derivatives as Photosynthesis and Plant Growth Inhibitors. Chem Biodivers 2021;18:e2100226. [PMID: 33998137 DOI: 10.1002/cbdv.202100226] [Reference Citation Analysis]
2 Matthee C, Terre'Blanche G, Legoabe LJ, Janse van Rensburg HD. Exploration of chalcones and related heterocycle compounds as ligands of adenosine receptors: therapeutics development. Mol Divers 2021. [PMID: 34176057 DOI: 10.1007/s11030-021-10257-9] [Reference Citation Analysis]
3 Abdelgawad MA, Oh JM, Parambi DG, Kumar S, Musa A, Ghoneim MM, Nayl A, El-ghorab AH, Ahmad I, Patel H, Kim H, Mathew B. Development of bromo- and fluoro-based α, β-unsaturated ketones as highly potent MAO-B inhibitors for the treatment of Parkinson's disease. Journal of Molecular Structure 2022;1266:133545. [DOI: 10.1016/j.molstruc.2022.133545] [Reference Citation Analysis]
4 Burmaoglu S, Gobek A, Aydin BO, Yurtoglu E, Aydin BN, Ozkat GY, Hepokur C, Ozek NS, Aysin F, Altundas R, Algul O. Design, synthesis and biological evaluation of novel bischalcone derivatives as potential anticancer agents. Bioorg Chem 2021;111:104882. [PMID: 33839582 DOI: 10.1016/j.bioorg.2021.104882] [Reference Citation Analysis]
5 Rani A, Singh A, Kaur J, Singh G, Bhatti R, Gumede N, Kisten P, Singh P, Sumanjit, Kumar V. 1H-1,2,3-triazole grafted tacrine-chalcone conjugates as potential cholinesterase inhibitors with the evaluation of their behavioral tests and oxidative stress in mice brain cells. Bioorg Chem 2021;114:105053. [PMID: 34120027 DOI: 10.1016/j.bioorg.2021.105053] [Reference Citation Analysis]
6 Kaushal R, Kaur M. Bio-medical potential of chalcone derivatives and their metal complexes as antidiabetic agents: a review. Journal of Coordination Chemistry 2021;74:725-42. [DOI: 10.1080/00958972.2021.1875450] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
7 Silva PTD, Freitas TSD, Sena DM, Bandeira PN, Julião MSDS, Marinho ES, Alcanfor AAC, Marinho EM, Lima-neto PD, Nogueira CES, Coutinho HDM, Leal ALAB, Barreto HM, Martins N, Rodrigues Teixeira AM, Santos HSD. Structural, Vibrational and Electrochemical Analysis and Antibacterial Potential of Isomeric Chalcones Derived from Natural Acetophenone. Applied Sciences 2020;10:4713. [DOI: 10.3390/app10144713] [Cited by in Crossref: 6] [Cited by in F6Publishing: 4] [Article Influence: 3.0] [Reference Citation Analysis]
8 da Silva P, da Cunha Xavier J, Freitas T, Oliveira M, Coutinho H, Leal A, Barreto H, Bandeira P, Nogueira C, Sena D, Almeida-neto F, Marinho E, Santos H, Teixeira A. Synthesis, spectroscopic characterization and antibacterial evaluation by chalcones derived of acetophenone isolated from Croton anisodontus Müll.Arg. Journal of Molecular Structure 2021;1226:129403. [DOI: 10.1016/j.molstruc.2020.129403] [Cited by in Crossref: 7] [Cited by in F6Publishing: 3] [Article Influence: 7.0] [Reference Citation Analysis]
9 Elkhalifa D, Al-Hashimi I, Al Moustafa AE, Khalil A. A comprehensive review on the antiviral activities of chalcones. J Drug Target 2021;29:403-19. [PMID: 33232192 DOI: 10.1080/1061186X.2020.1853759] [Cited by in Crossref: 4] [Cited by in F6Publishing: 1] [Article Influence: 2.0] [Reference Citation Analysis]
10 Targanski SK, Sousa JR, Pádua GM, Sousa JM, Vieira LC, Soares MA. Larvicidal activity of substituted chalcones against Aedes aegypti (Diptera: Culicidae) and non‐target organisms. Pest Manag Sci 2021;77:325-34. [DOI: 10.1002/ps.6021] [Cited by in Crossref: 4] [Cited by in F6Publishing: 3] [Article Influence: 2.0] [Reference Citation Analysis]
11 Roy T, Boateng ST, Banang-Mbeumi S, Singh PK, Basnet P, Chamcheu RN, Ladu F, Chauvin I, Spiegelman VS, Hill RA, Kousoulas KG, Nagalo BM, Walker AL, Fotie J, Murru S, Sechi M, Chamcheu JC. Synthesis, inverse docking-assisted identification and in vitro biological characterization of Flavonol-based analogs of fisetin as c-Kit, CDK2 and mTOR inhibitors against melanoma and non-melanoma skin cancers. Bioorg Chem 2021;107:104595. [PMID: 33450548 DOI: 10.1016/j.bioorg.2020.104595] [Cited by in Crossref: 1] [Cited by in F6Publishing: 2] [Article Influence: 0.5] [Reference Citation Analysis]
12 Sooknual P, Pingaew R, Phopin K, Ruankham W, Prachayasittikul S, Ruchirawat S, Prachayasittikul V. Synthesis and neuroprotective effects of novel chalcone-triazole hybrids. Bioorganic Chemistry 2020;105:104384. [DOI: 10.1016/j.bioorg.2020.104384] [Cited by in Crossref: 2] [Cited by in F6Publishing: 3] [Article Influence: 1.0] [Reference Citation Analysis]
13 Rohit S. Shinde. Synthesis, Characterization and Theoretical Insights into Molecular Properties of 2-(4-fluorophenyl)-4H-chromen-4-one. J Adv Chem Sci 2021;7:721-4. [DOI: 10.30799/jacs.235.21070201] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
14 Aguiar LO, Silva EDO, David JM. Biotransformation of chalcones and flavanones: An update on their bio-based derivatizations. Biocatalysis and Biotransformation. [DOI: 10.1080/10242422.2022.2073226] [Reference Citation Analysis]
15 Matthee C, Terre'Blanche G, Janse van Rensburg HD, Aucamp J, Legoabe LJ. Chalcone-inspired rA1 /A2A adenosine receptor ligands: Ring closure as an alternative to a reactive substructure. Chem Biol Drug Des 2021. [PMID: 34878728 DOI: 10.1111/cbdd.13999] [Reference Citation Analysis]
16 Roy T, Boateng ST, Banang-Mbeumi S, Singh PK, Basnet P, Chamcheu RN, Ladu F, Chauvin I, Spiegelman VS, Hill RA, Kousoulas KG, Nagalo BM, Walker AL, Fotie J, Murru S, Sechi M, Chamcheu JC. Identification of new fisetin analogs as kinase inhibitors: Data on synthesis and anti-skin cancer activities evaluation. Data Brief 2021;35:106858. [PMID: 33665254 DOI: 10.1016/j.dib.2021.106858] [Reference Citation Analysis]
17 Akhtar MS, Rehman AU, Arshad H, Malik A, Fatima M, Tabassum T, Raza AR, Bukhsh M, Murtaza MA, Mehmood MH, Sultan A, Rasool G, Riaz M. In Vitro Antioxidant Activities and the Therapeutic Potential of Some Newly Synthesized Chalcones Against 4-Acetaminophenol Induced Hepatotoxicity in Rats. Dose Response 2021;19:1559325821996955. [PMID: 33795997 DOI: 10.1177/1559325821996955] [Reference Citation Analysis]
18 Luo B, Song X. A comprehensive overview of β-carbolines and its derivatives as anticancer agents. Eur J Med Chem 2021;224:113688. [PMID: 34332400 DOI: 10.1016/j.ejmech.2021.113688] [Cited by in Crossref: 1] [Article Influence: 1.0] [Reference Citation Analysis]
19 Gomes LR, Low JN, Turner AB, Wardell JL, Pinheiro AC. Crystal structures, Hirshfeld surface analysis and PIXEL calculations of four (E)-1-(2-hydroxyphenyl)-3-phenylprop-2-en-1-one derivatives, containing methoxy substituents. The importance of π interactions. Journal of Molecular Structure 2020;1221:128652. [DOI: 10.1016/j.molstruc.2020.128652] [Cited by in Crossref: 2] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
20 de Souza PS, Bibá GCC, Melo EDDN, Muzitano MF. Chalcones against the hallmarks of cancer: a mini-review. Nat Prod Res 2021;:1-18. [PMID: 34865580 DOI: 10.1080/14786419.2021.2000980] [Reference Citation Analysis]
21 Minsat L, Peyrot C, Brunissen F, Renault JH, Allais F. Synthesis of Biobased Phloretin Analogues: An Access to Antioxidant and Anti-Tyrosinase Compounds for Cosmetic Applications. Antioxidants (Basel) 2021;10:512. [PMID: 33806117 DOI: 10.3390/antiox10040512] [Reference Citation Analysis]
22 Alotibi MF, Abdel-wahab BF, Yousif E, Hegazy AS, Kariuki BM, El-hiti GA. Crystal structure of ( E )-3-(3-(5-methyl-1-phenyl-1 H -1,2,3-triazol-4-yl)-1-phenyl-1 H -pyrazol-4-yl)-1-phenylprop-2-en-1-one, C 27 H 21 N 5 O. Zeitschrift für Kristallographie - New Crystal Structures 2020;235:479-81. [DOI: 10.1515/ncrs-2019-0779] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 0.7] [Reference Citation Analysis]
23 Oh JM, Kang MG, Hong A, Park JE, Kim SH, Lee JP, Baek SC, Park D, Nam SJ, Cho ML, Kim H. Potent and selective inhibition of human monoamine oxidase-B by 4-dimethylaminochalcone and selected chalcone derivatives. Int J Biol Macromol 2019;137:426-32. [PMID: 31271801 DOI: 10.1016/j.ijbiomac.2019.06.167] [Cited by in Crossref: 9] [Cited by in F6Publishing: 6] [Article Influence: 3.0] [Reference Citation Analysis]
24 Serdyuk OV, Hampel F, Abaev VT. Synthesis of Isoxazolylvinyl Ketones from Substituted Furans. Chem Heterocycl Comp 2020;56:1477-84. [DOI: 10.1007/s10593-020-02841-y] [Cited by in Crossref: 1] [Article Influence: 0.5] [Reference Citation Analysis]
25 Omar S, Shkir M, Ajmal Khan M, Ahmad Z, Alfaify S. A comprehensive study on molecular geometry, optical, HOMO-LUMO, and nonlinear properties of 1,3-diphenyl-2-propen-1-ones chalcone and its derivatives for optoelectronic applications: A computational approach. Optik 2020;204:164172. [DOI: 10.1016/j.ijleo.2020.164172] [Cited by in Crossref: 12] [Cited by in F6Publishing: 1] [Article Influence: 6.0] [Reference Citation Analysis]
26 Romeu MC, Freire PT, Ayala AP, Barreto AC, Oliveira LS, Bandeira PN, dos Santos HS, Teixeira AM, Vasconcelos DL. Synthesis, crystal structure, ATR-FTIR, FT-Raman and UV spectra, structural and spectroscopic analysis of (3E)‐4‐[4‐(dimethylamine)phenyl]but‐3‐en‐2‐one. Journal of Molecular Structure 2022;1264:133222. [DOI: 10.1016/j.molstruc.2022.133222] [Reference Citation Analysis]
27 Sharma B, Gu L, Pillay RP, Cele N, Awolade P, Singh P, Kaur M, Kumar V. Design, synthesis, and anti-proliferative evaluation of 1 H -1,2,3-triazole grafted tetrahydro-β-carboline-chalcone/ferrocenylchalcone conjugates in estrogen responsive and triple negative breast cancer cells. New J Chem 2020;44:11137-47. [DOI: 10.1039/d0nj00879f] [Cited by in Crossref: 11] [Cited by in F6Publishing: 4] [Article Influence: 5.5] [Reference Citation Analysis]
28 Panda P, Chakroborty S. Navigating the Synthesis of Quinoline Hybrid Molecules as Promising Anticancer Agents. ChemistrySelect 2020;5:10187-99. [DOI: 10.1002/slct.202002790] [Cited by in Crossref: 5] [Cited by in F6Publishing: 1] [Article Influence: 2.5] [Reference Citation Analysis]
29 Selvaraj B, Nguyen UTT, Huh G, Nguyen DH, Mok IK, Lee H, Kang K, Bae AN, Kim DW, Lee JW. Synthesis and biological evaluation of chalcone derivatives as neuroprotective agents against glutamate-induced HT22 mouse hippocampal neuronal cell death. Bioorg Med Chem Lett 2020;30:127597. [PMID: 33022369 DOI: 10.1016/j.bmcl.2020.127597] [Reference Citation Analysis]
30 Dadou S, Altay A, Koudad M, Türkmenoğlu B, Yeniçeri E, Çağlar S, Allali M, Oussaid A, Benchat N, Karrouchi K. Design, synthesis, anticancer evaluation and molecular docking studies of new imidazo [2, 1-b] thiazole -based chalcones. Med Chem Res. [DOI: 10.1007/s00044-022-02916-9] [Reference Citation Analysis]
31 Park H, Jin UH, Karki K, Allred C, Davidson LA, Chapkin RS, Orr AA, Nowshad F, Jayaraman A, Tamamis P, Safe S. Hydroxylated Chalcones as Aryl Hydrocarbon Receptor Agonists: Structure-Activity Effects. Toxicol Sci 2021;180:148-59. [PMID: 33263770 DOI: 10.1093/toxsci/kfaa179] [Reference Citation Analysis]