ArticleRSC advances2019
Novel chalcone derivatives containing a 1,2,4-triazine moiety: design, synthesis, antibacterial and antiviral activities.
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Article in RSC advances, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers.
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18citing papers in PubMed
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Who cites it
18 citing papers in PubMed.
- Design and Synthesis of Novel Spiropyridine Derivatives as Promising Anti-inflammatory and Gene-targeting Agents Against COVID-19.Current pharmaceutical design · 2026Article
- Design, synthesis and antiviral activity of indole derivatives containing quinoline moiety.Molecular diversity · 2025Article
- Antiviral activity evaluation and action mechanism of myricetin derivatives containing thioether quinoline moiety.Molecular diversity · 2024Article
- Synthesis, antifungal activity and mechanism of action of novel chalcone derivatives containing 1,2,4-triazolo-[3,4-b]-1,3,4-thiadiazole.Molecular diversity · 2024Article
- Molecular dynamics simulation approach of hybrid chalcone-thiazole complex derivatives for DNA gyrase B inhibition: lead generation.RSC advances · 2023Article
- Design, Synthesis, and Anti-PVY Biological Activity of 1,3,5-Triazine Derivatives Containing Piperazine Structure.International journal of molecular sciences · 2023Article
- Article
- Chalcone: A Promising Bioactive Scaffold in Medicinal Chemistry.Pharmaceuticals (Basel, Switzerland) · 2022Review
- Computational investigation of benzalacetophenone derivatives against SARS-CoV-2 as potential multi-target bioactive compounds.Computers in biology and medicine · 2022Article
- Synthesis of novel antibacterial and antifungal quinoxaline derivatives.RSC advances · 2022Article
- New chalcone derivatives as effective against SARS-CoV-2 agent.International journal of clinical practice · 2021Article
- Anticancer Activity of Natural and Synthetic Chalcones.International journal of molecular sciences · 2021Review
- Thiazole-Chalcone Hybrids as Prospective Antitubercular and Antiproliferative Agents: Design, Synthesis, Biological, Molecular Docking Studies and In Silico ADME Evaluation.Molecules (Basel, Switzerland) · 2021Article
- In silico pharmacokinetic and molecular docking studies of natural flavonoids and synthetic indole chalcones against essential proteins of SARS-CoV-2.European journal of pharmacology · 2020Article
- Article
- Design, Synthesis, and Antimicrobial Evaluation of New Annelated Pyrimido[2,1-Molecules (Basel, Switzerland) · 2020Article
- Fabrication of pH-Sensitive Tetramycin Releasing Gel and Its Antibacterial Bioactivity againstMolecules (Basel, Switzerland) · 2019Article
- Synthesis and antibacterial and antiviral activities of myricetin derivatives containing a 1,2,4-triazole Schiff base.RSC advances · 2019Article
Corrections and comments
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Authors and funding
10 authors.
Xu TangState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Shijun SuState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Mei ChenState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Jun HeState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Rongjiao XiaState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Tao GuoState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Ying ChenState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Cheng ZhangState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Jun WangState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.
Wei XueState Key Laboratory Breeding Base of Green Pesticide and Agricultural Bioengineering, Key Laboratory of Green Pesticide and Agricultural Bioengineering, Ministry of Education, Center for Research and Development of Fine Chemicals, Guizhou University Guiyang 550025 China wxue@gzu.edu.cn +86-851-88292090 +86-851-88292090.ORCID https://orcid.org/0000-0002-9096-2961
Funding
No grant is acknowledged in the PubMed record.
Abstract
A series of novel chalcone derivatives containing the 1,2,4-triazine moiety were synthesized and their structures were confirmed by
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.