BPG is committed to discovery and dissemination of knowledge
Cited by in F6Publishing
For: Ouyang Y, Li J, Chen X, Fu X, Sun S, Wu Q. Chalcone Derivatives: Role in Anticancer Therapy. Biomolecules 2021;11:894. [PMID: 34208562 DOI: 10.3390/biom11060894] [Cited by in Crossref: 27] [Cited by in F6Publishing: 33] [Article Influence: 13.5] [Reference Citation Analysis]
Number Citing Articles
1 Russell AE, Gines BR. Chalcones: Potential Chemotherapeutic Compounds and Educational Tools for Closing the Loop in STEM. Acc Chem Res 2023. [PMID: 36696370 DOI: 10.1021/acs.accounts.2c00583] [Reference Citation Analysis]
2 Omidkhah N, Hadizadeh F, Zarghi A, Ghodsi R. Synthesis, cytotoxicity, Pan-HDAC inhibitory activity and docking study of new N-(2-aminophenyl)-2-methylquinoline-4-carboxamide and (E)-N-(2-aminophenyl)-2-styrylquinoline-4-carboxamide derivatives as anticancer agents. Med Chem Res 2023. [DOI: 10.1007/s00044-023-03018-w] [Reference Citation Analysis]
3 Padmaja V, Sumakanth M, Shashikala P. Synthesis, Characterization and Molecular Docking Studies of Novel Mannich Bases of Indole Analogs as Potent Antibacterial and Anticancer Agents. Asian J Chem 2023;35:217-233. [DOI: 10.14233/ajchem.2023.24004] [Reference Citation Analysis]
4 Sharma A, Sharma L, Nandy SK, Payal N, Yadav S, Vargas-De-La-Cruz C, Anwer MK, Khan H, Behl T, Bungau SG. Molecular Aspects and Therapeutic Implications of Herbal Compounds Targeting Different Types of Cancer. Molecules 2023;28. [PMID: 36677808 DOI: 10.3390/molecules28020750] [Reference Citation Analysis]
5 Blanco-acuña EF, Vázquez-lópez LA, Gasque L, García-ortega H. AIEgens-NLOphores coumarin-triphenylamine chalcone derivatives: Synthesis, photophysical properties and DFT computational study. Journal of Molecular Structure 2023;1271:134009. [DOI: 10.1016/j.molstruc.2022.134009] [Reference Citation Analysis]
6 Vera DR, Mantilla JP, Palma A, Díaz Costa I, Cobo J, Glidewell C. A three-step pathway from (2-aminophenyl)chalcones to novel styrylquinoline-chalcone hybrids: synthesis and spectroscopic and structural characterization of three examples. Acta Crystallogr C Struct Chem 2023;79:3-11. [PMID: 36602015 DOI: 10.1107/S2053229622011263] [Reference Citation Analysis]
7 Ye Y, Ma Y, Kong M, Wang Z, Sun K, Li F. Effects of Dietary Phytochemicals on DNA Damage in Cancer Cells. Nutr Cancer 2022;:1-15. [PMID: 36562548 DOI: 10.1080/01635581.2022.2157024] [Reference Citation Analysis]
8 Abou‐zied HA, Beshr EAM, Gomaa HAM, Mostafa YA, Youssif BGM, Hayallah AM, Abdel‐aziz M. Discovery of new cyanopyridine/chalcone hybrids as dual inhibitors of EGFR/BRAF V600E with promising antiproliferative properties. Archiv der Pharmazie 2022. [DOI: 10.1002/ardp.202200464] [Reference Citation Analysis]
9 Sinha S, Medhi B, Radotra BD, Batovska DI, Markova N, Bhalla A, Sehgal R. Antimalarial and immunomodulatory potential of chalcone derivatives in experimental model of malaria. BMC Complement Med Ther 2022;22:330. [PMID: 36510199 DOI: 10.1186/s12906-022-03777-w] [Reference Citation Analysis]
10 Hawash M. Recent Advances of Tubulin Inhibitors Targeting the Colchicine Binding Site for Cancer Therapy. Biomolecules 2022;12. [PMID: 36551271 DOI: 10.3390/biom12121843] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
11 Santarsiero A, Pappalardo I, Rosa GM, Pisano I, Superchi S, Convertini P, Todisco S, Scafato P, Infantino V. Mitochondrial Role in Intrinsic Apoptosis Induced by a New Synthesized Chalcone in Hepatocellular Carcinoma Cells. Biomedicines 2022;10. [PMID: 36551876 DOI: 10.3390/biomedicines10123120] [Reference Citation Analysis]
12 Altıntop MD, Özdemir A, Temel HE, Demir Cevizlidere B, Sever B, Kaplancıklı ZA, Akalın Çiftçi G. Design, synthesis and biological evaluation of a new series of arylidene indanones as small molecules for targeted therapy of non-small cell lung carcinoma and prostate cancer. European Journal of Medicinal Chemistry 2022;244:114851. [DOI: 10.1016/j.ejmech.2022.114851] [Reference Citation Analysis]
13 Wu Q, Gao Z, Yu X, Wang P. Dietary regulation in health and disease. Sig Transduct Target Ther 2022;7. [DOI: 10.1038/s41392-022-01104-w] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
14 Kuttithodi AM, Nikhitha D, Jacob J, Narayanankutty A, Mathews M, Olatunji OJ, Rajagopal R, Alfarhan A, Barcelo D. Antioxidant, Antimicrobial, Cytotoxicity, and Larvicidal Activities of Selected Synthetic Bis-Chalcones. Molecules 2022;27. [PMID: 36500302 DOI: 10.3390/molecules27238209] [Reference Citation Analysis]
15 Dong G, Jiang Y, Zhang F, Zhu F, Liu J, Xu Z. Recent updates on 1,2,3‐, 1,2,4‐, and 1,3,5‐triazine hybrids (2017–present): The anticancer activity, structure–activity relationships, and mechanisms of action. Archiv der Pharmazie 2022. [DOI: 10.1002/ardp.202200479] [Reference Citation Analysis]
16 da Silva APP, Rodrigues VC, Felippe WQ, Goulart CM, Echevarria A. Chalcone-thiosemicarbazone Hybrids as Inhibitors of Human Hepatocellular Carcinoma HepG2 Cells Viability and Oxygen Consumption. CBC 2022;18. [DOI: 10.2174/1573407218666220111104011] [Reference Citation Analysis]
17 Jin L, Gao Y, Sun Z, Jia Y, Shen B, Li X, Geng Q, Mu X. Study on the Interaction between Chalcone and DNA with Spectroscopy and Molecular Docking Technique. Polycyclic Aromatic Compounds. [DOI: 10.1080/10406638.2022.2133946] [Reference Citation Analysis]
18 Dhaliwal JS, Moshawih S, Goh KW, Loy MJ, Hossain MS, Hermansyah A, Kotra V, Kifli N, Goh HP, Dhaliwal SKS, Yassin H, Ming LC. Pharmacotherapeutics Applications and Chemistry of Chalcone Derivatives. Molecules 2022;27:7062. [DOI: 10.3390/molecules27207062] [Reference Citation Analysis]
19 Tang W, Gao Y, Tong H, Xu X, Zhu Z, Liu B, Liu B. Green synthesis of ferrocenyl chalcones against triple negative breast cancer.. [DOI: 10.21203/rs.3.rs-2145219/v1] [Reference Citation Analysis]
20 Gazdova M, Michalkova R, Kello M, Vilkova M, Kudlickova Z, Baloghova J, Mirossay L, Mojzis J. Chalcone-Acridine Hybrid Suppresses Melanoma Cell Progression via G2/M Cell Cycle Arrest, DNA Damage, Apoptosis, and Modulation of MAP Kinases Activity. Int J Mol Sci 2022;23:12266. [PMID: 36293123 DOI: 10.3390/ijms232012266] [Reference Citation Analysis]
21 Ganguli K, Mandal A, Kundu S. Well-Defined Bis(NHC)Mn(I) Complex Catalyzed Tandem Transformation of α,β-Unsaturated Ketones to α-Methylated Ketones Using Methanol. ACS Catal . [DOI: 10.1021/acscatal.2c04131] [Reference Citation Analysis]
22 Moreira J, Saraiva L, Pinto MM, Cidade H. Bioactive Diarylpentanoids: Insights into the Biological Effects beyond Antitumor Activity and Structure–Activity Relationships. Molecules 2022;27:6340. [DOI: 10.3390/molecules27196340] [Reference Citation Analysis]
23 Marotta L, Rossi S, Ibba R, Brogi S, Calderone V, Butini S, Campiani G, Gemma S. The green chemistry of chalcones: Valuable sources of privileged core structures for drug discovery. Front Chem 2022;10:988376. [DOI: 10.3389/fchem.2022.988376] [Reference Citation Analysis]
24 Kumara K, Jyothi M, Kouser S, Kumar AHU, Warad I, Khanum SA, Lokanath NK. Structural investigations and theoretical insights of a polymethoxy chalcone derivative: Synthesis, crystal structure, 3D energy frameworks and SARS CoV-2 docking studies. Journal of Molecular Structure 2022. [DOI: 10.1016/j.molstruc.2022.134226] [Reference Citation Analysis]
25 Konečná K, Diepoltová A, Holmanová P, Jand’ourek O, Vejsová M, Voxová B, Bárta P, Maixnerová J, Trejtnar F, Kučerová-chlupáčová M. Comprehensive insight into anti-staphylococcal and anti-enterococcal action of brominated and chlorinated pyrazine-based chalcones. Front Microbiol 2022;13:912467. [DOI: 10.3389/fmicb.2022.912467] [Reference Citation Analysis]
26 Elkanzi NAA, Hrichi H, Alolayan RA, Derafa W, Zahou FM, Bakr RB. Synthesis of Chalcones Derivatives and Their Biological Activities: A Review. ACS Omega. [DOI: 10.1021/acsomega.2c01779] [Cited by in Crossref: 4] [Cited by in F6Publishing: 7] [Article Influence: 4.0] [Reference Citation Analysis]
27 Shen N, Wang T, Gan Q, Liu S, Wang L, Jin B. Plant flavonoids: Classification, distribution, biosynthesis, and antioxidant activity. Food Chem 2022;383:132531. [PMID: 35413752 DOI: 10.1016/j.foodchem.2022.132531] [Cited by in Crossref: 65] [Cited by in F6Publishing: 72] [Article Influence: 65.0] [Reference Citation Analysis]
28 Noser AA, Shehadi IA, Abdelmonsef AH, Salem MM. Newly Synthesized Pyrazolinone Chalcones as Anticancer Agents via Inhibiting the PI3K/Akt/ERK1/2 Signaling Pathway. ACS Omega 2022;7:25265-77. [DOI: 10.1021/acsomega.2c02181] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
29 Patel S, Challagundla N, Rajput RA, Mishra S. Design, synthesis, characterization and anticancer activity evaluation of deoxycholic acid-chalcone conjugates. Bioorg Chem 2022;127:106036. [PMID: 35878450 DOI: 10.1016/j.bioorg.2022.106036] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
30 Królicka E, Kieć-Kononowicz K, Łażewska D. Chalcones as Potential Ligands for the Treatment of Parkinson's Disease. Pharmaceuticals (Basel) 2022;15:847. [PMID: 35890146 DOI: 10.3390/ph15070847] [Cited by in Crossref: 3] [Cited by in F6Publishing: 2] [Article Influence: 3.0] [Reference Citation Analysis]
31 Jin X, Mei Y, Shen Z, Zhu J, Xing S, Yang H, Liang G, Zheng X. A chalcone-syringaldehyde hybrid inhibits triple-negative breast cancer cell proliferation and migration by inhibiting CKAP2-mediated FAK and STAT3 phosphorylation. Phytomedicine 2022;101:154087. [DOI: 10.1016/j.phymed.2022.154087] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
32 Kumar S, Saroha B, Kumar G, Lathwal E, Kumar S, Parshad B, Kumari M, Kumar N, Mphahlele-makgwane MM, Makgwane PR. Recent Developments in Nanocatalyzed Green Synthetic Protocols of Biologically Potent Diverse O-Heterocycles—A Review. Catalysts 2022;12:657. [DOI: 10.3390/catal12060657] [Reference Citation Analysis]
33 Li L, Yu J, Cheng S, Peng Z, Ben-David Y, Luo H. Transcription factor Fli-1 as a new target for antitumor drug development. Int J Biol Macromol 2022;209:1155-68. [PMID: 35447268 DOI: 10.1016/j.ijbiomac.2022.04.076] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 1.0] [Reference Citation Analysis]
34 Maciejewska N, Olszewski M, Jurasz J, Serocki M, Dzierzynska M, Cekala K, Wieczerzak E, Baginski M. Novel chalcone-derived pyrazoles as potential therapeutic agents for the treatment of non-small cell lung cancer. Sci Rep 2022;12:3703. [PMID: 35260633 DOI: 10.1038/s41598-022-07691-6] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
35 Möller G, Temml V, Cala Peralta A, Gruet O, Richomme P, Séraphin D, Viault G, Kraus L, Huber-cantonati P, Schopfhauser E, Pachmayr J, Tokarz J, Schuster D, Helesbeux J, Dyar KA. Analogues of Natural Chalcones as Efficient Inhibitors of AKR1C3. Metabolites 2022;12:99. [DOI: 10.3390/metabo12020099] [Cited by in Crossref: 2] [Cited by in F6Publishing: 2] [Article Influence: 2.0] [Reference Citation Analysis]
36 Pozzetti L, Ibba R, Rossi S, Taglialatela-Scafati O, Taramelli D, Basilico N, D'Alessandro S, Parapini S, Butini S, Campiani G, Gemma S. Total Synthesis of the Natural Chalcone Lophirone E, Synthetic Studies toward Benzofuran and Indole-Based Analogues, and Investigation of Anti-Leishmanial Activity. Molecules 2022;27:463. [PMID: 35056779 DOI: 10.3390/molecules27020463] [Cited by in Crossref: 4] [Cited by in F6Publishing: 4] [Article Influence: 4.0] [Reference Citation Analysis]
37 Rudrapal M, Khan J, Dukhyil AAB, Alarousy RMII, Attah EI, Sharma T, Khairnar SJ, Bendale AR. Chalcone Scaffolds, Bioprecursors of Flavonoids: Chemistry, Bioactivities, and Pharmacokinetics. Molecules 2021;26:7177. [PMID: 34885754 DOI: 10.3390/molecules26237177] [Cited by in Crossref: 9] [Cited by in F6Publishing: 14] [Article Influence: 4.5] [Reference Citation Analysis]
38 Cioce M, Sacconi A, Pass HI, Canino C, Strano S, Blandino G, Fazio VM. Insights into Intra-Tumoral Heterogeneity: Transcriptional Profiling of Chemoresistant MPM Cell Subpopulations Reveals Involvement of NFkB and DNA Repair Pathways and Contributes a Prognostic Signature. Int J Mol Sci 2021;22:12071. [PMID: 34769499 DOI: 10.3390/ijms222112071] [Cited by in F6Publishing: 1] [Reference Citation Analysis]
39 Constantinescu T, Lungu CN. Anticancer Activity of Natural and Synthetic Chalcones. Int J Mol Sci 2021;22:11306. [PMID: 34768736 DOI: 10.3390/ijms222111306] [Cited by in Crossref: 4] [Cited by in F6Publishing: 11] [Article Influence: 2.0] [Reference Citation Analysis]
40 Yepes AF, Arias JD, Cardona-g W, Herrera-r A, Moreno G. New class of hybrids based on chalcone and melatonin: a promising therapeutic option for the treatment of colorectal cancer. Med Chem Res 2021;30:2240-55. [DOI: 10.1007/s00044-021-02805-7] [Cited by in Crossref: 1] [Cited by in F6Publishing: 1] [Article Influence: 0.5] [Reference Citation Analysis]