scispace - formally typeset
Search or ask a question

What are significant applications of chalcones? 


Best insight from top research papers

Chalcones have significant applications in various fields including medicinal chemistry, synthetic and pharmaceutical chemistry, and coordination chemistry . They have been found to possess antimicrobial, anticancer, antimalarial, antioxidant, anti-inflammatory, and neuroprotective properties . Chalcone derivatives have shown potential as therapeutic agents for the treatment of a variety of disorders, including cancer . They can be synthesized easily and have been explored for their use in the development of new anti-infective agents . Chalcones also exhibit antibacterial activity against Staphylococcus aureus, a microorganism with increasing resistance to conventional drugs . The diverse biological activities and ease of synthesis make chalcones and their derivatives promising candidates for the design of novel molecules with enhanced medicinal properties . Further research is needed to fully explore the therapeutic potential of chalcones and their derivatives in various applications .

Answers from top 5 papers

More filters
Papers (5)Insight
The paper does not explicitly mention the significant applications of chalcones.
The significant applications of chalcones include antibacterial, antifungal, anti-inflammatory, and anticancer properties.
The significant applications of chalcones include their use as intermediates in the biosynthesis of flavonoids and as precursors for the synthesis of therapeutic compounds with a wide range of biological activities.
The significant applications of chalcones include antimicrobial, anticancer, antimalarial, antioxidant, anti-inflammatory, antitubercular, antidiabetic, antileishmanial, anti-vitiligo, and neuroprotective properties.
The paper mentions that chalcones have significant applications in medicinal research and development, but does not provide specific details about these applications.

Related Questions

What are chalcogen bonds?4 answersChalcogen bonds (ChBs) are noncovalent interactions between electrophilic chalcogen atoms (S, Se, Te) and nucleophilic regions, akin to hydrogen and halogen bonds in strength and directionality. These bonds play crucial roles in various applications, such as solid-state architectures, anion recognition, and organic synthesis. ChBs exhibit different geometries, with Type II structures being stable and engaging in stronger interactions as the chalcogen atom size increases (S < Se < Te). The electrophilicity of chalcogen atoms, particularly sulfur, is essential in initiating chemical reactions and influencing biopharmacological activities of compounds like benzisothiazolinones. Computational studies have highlighted the debate on the relative contributions of covalency, electrostatics, and dispersion in ChB interactions.
How have chalcones been utilized in the development of new drugs and therapies over the past 5 years?5 answersChalcones have been extensively utilized in the past 5 years for developing new drugs and therapies due to their versatile nature. These α,β-unsaturated ketones have been incorporated into various heterocyclic structures, enhancing their pharmacological potential. Chalcones have been synthesized using diverse methods like condensation, Claisen-Schmidt condensation, and rearrangement reactions, leading to the creation of novel chalcone derivatives with reactive functional groups. The resulting chalcone derivatives have shown promising biological activities such as antimicrobial, anticancer, antioxidant, and anti-inflammatory properties, making them valuable candidates for drug development. Additionally, chalcone-based Schiff bases have been highlighted for their significant role in treating various ailments and their applications in drug design and synthesis.
What is chalcone?5 answersChalcone is a group of naturally occurring compounds that have various biological effects, including anti-inflammatory, anti-cancer, and antibacterial properties. It is a fascinating and well-studied group of organic molecules that has immense therapeutic and excellent photophysical properties. Chalcones are 1,3-diaryl-2-propen-1-ones, which are the precursors for flavonoids and isoflavonoids. They are considered as one of the most useful, readily available intermediates in heterocyclic synthesis and can be utilized to make a variety of heterocyclic compounds. Chalcones and their derivatives exhibit promising biological activities against cancer hallmarks and have the potential to be used as anticancer agents. Chalcones are also of high medicinal significance due to their α,β-unsaturated ketone functionality, and numerous functional modifications have been reported. Chalcone scaffold has great potential for use in the design and development of inhibitors for severe acute respiratory syndrome coronavirus 2 (SARS‐CoV‐2).
How can chalcone be synthesized?5 answersChalcone can be synthesized through various methods. One method involves the Claisen-Schmidt condensation of 3,4-dimethoxybenzaldehyde and 2,4-dihydroxyacetophenone using KOH 40% as a catalyst. Another method is the green synthesis approach using grinding technique, which is eco-friendly and solvent-free. Additionally, chalcones can be synthesized using recyclable ionic liquids as catalysts under ultrasonification, resulting in high yields and environmentally friendly reactions. Microwave synthesis has also been used to synthesize chalcone compounds, providing better cytotoxic activity. The condensation of 2-acetyl pyridine with different aromatic aldehydes in 40% alkali is another method for chalcone synthesis. These methods offer different advantages such as mild reaction conditions, high yields, and environmentally benign procedures.
What are the therapeutic applications of naringenin chalcone?5 answersNaringenin chalcone has therapeutic applications in various areas. It has been found to have antioxidant, antitumor, antiviral, antibacterial, anti-inflammatory, antiadipogenic, and cardioprotective effects. In adipocytes, naringenin chalcone promotes the production of adiponectin, a hormone involved in metabolic processes, and enhances mitochondrial energy metabolism, leading to insulin-sensitizing effects. Additionally, naringenin chalcone has been shown to inhibit angiogenesis, making it a potential treatment for diseases involving abnormal blood vessel formation. Furthermore, naringenin chalcone derivatives have been investigated for their potential in treating viral disorders, including viral lesions caused by Herpes Simplex virus. Overall, naringenin chalcone and its derivatives show promise in various therapeutic applications, including antioxidant, metabolic, antiangiogenic, and antiviral treatments.
What are the different types of chalcone epoxides?5 answersChalcone epoxides are a type of compound that can be synthesized through various reactions. One method involves treating chalcone-epoxide 1 with lithium tetramethylpiperidide, resulting in the formation of two anions: enolate 3 and the remote anion 4. An addition reaction then occurs between anion 4 and the unreacted starting material 1, leading to the formation of diastereoisomeric products 5 and 6. Another approach involves the Claisen-Schmidt condensation reaction between selected aldehydes and ketones. This reaction yields a variety of chalcones, such as thiophen-2-aldehydeacetophenone (TAAP), furan-2-aldehydeacetophenone (FAAP), 2-hydroxynapthaldehyde acetophenone (HNAP), and cinnamaldehydeacetophenone (CAAP). These chalcones can then be further transformed into quinoxalines through treatment with bromine water, acetic acid, and tetramethylenediamine. Additionally, prenylated chalcones, such as 2,4-dihydroxy-3-C-prenylacetophenone and 2,4-dihydroxy-5-C-prenylacetophenone, can be synthesized by treating resacetophenone with 2-methylbut-3-en-2-ol in the presence of BF3.Et2O as the catalyst.

See what other people are reading

What are the steps to generate a pharmacophore in discovery studio visualizer?
5 answers
To generate a pharmacophore in Discovery Studio Visualizer, the process involves several key steps. Firstly, pharmacophore models are created by exploiting features of known compounds or active sites. Subsequently, the models are refined using tools like ELIXIR-A to filter points from multiple ligand conformations. Following refinement, the pharmacophore models are utilized to screen databases for potential lead compounds, which are then subjected to molecular docking to assess interactions with the target protein. Finally, selected compounds are further evaluated through biophysical techniques like NMR to confirm binding affinity and interactions with the protein of interest. This comprehensive approach aids in identifying potential inhibitors or ligands for specific targets, facilitating drug discovery processes.
Can manipulating the dynamical networks of PPARgamma protein lead to new treatments for metabolic disorders?
5 answers
Manipulating the dynamical networks of the PPARγ protein shows promise in developing novel treatments for metabolic disorders. Post-translational modifications (PTMs) of PPARγ have been proposed as a potential strategy to address metabolic disorders with fewer side effects than traditional drugs like thiazolidinediones (TZDs). Additionally, combining PPARγ agonists with GPR120 agonists has shown synergistic effects in improving glucose tolerance and insulin sensitivity, hinting at the potential of targeting multiple pathways for enhanced therapeutic outcomes. Novel PPARγ agonists identified through dynamic pharmacophore modeling have also been suggested as a way to combat type 2 diabetes and obesity by regulating glucose metabolism and fatty acid accumulation. Therefore, manipulating the dynamical networks of PPARγ could indeed pave the way for innovative treatments for metabolic disorders.
What are the resideus of akt ative binding site?
5 answers
The residues involved in the active binding site of Akt include Lys14, Arg25, Tyr38, Arg48, Arg86, Thr21, and Arg23. These residues play a crucial role in interacting with phospholipids generated by PI3-K, thereby regulating Akt activity and promoting cell survival. Additionally, the Akt PH domain consists of specific loops and pockets that accommodate the phospholipids through hydrogen-bonding interactions, with key residues like Lys14, Arg25, and Tyr38 forming the bottom of the binding pocket. Furthermore, the Akt pathway, where Akt is the central protein, is essential in diseases like Alzheimer's, Parkinson's, and Diabetes, with small molecules binding to the PH domain of Akt to facilitate its phosphorylation and upregulate the pathway.
Is Mannitol Egg Yolk a differential media?
4 answers
Yes, Mannitol Egg Yolk medium can be considered a type of selective and differential media. It is designed to support the growth of specific bacterial species while inhibiting others, making it selective. Additionally, the medium allows for the differentiation of bacteria based on their ability to ferment mannitol, leading to observable color changes around colonies. For example, in the case of Staphylococci, the formation of yellow zones indicates mannitol fermentation, aiding in distinguishing pathogenic strains from nonpathogenic ones. Moreover, the Mannitol Egg Yolk medium has been shown to promote rapid bacterial growth, reduce mutation rates, and facilitate easy observation and analysis, further supporting its utility as a differential medium.
What infections does staph aureus cause?
5 answers
Staphylococcus aureus (S. aureus) causes a variety of infections, including skin-and-soft-tissue infections (SSTIs), food poisoning, endocarditis, sepsis, and diseases like atopic dermatitis, psoriasis, pulmonary cystic fibrosis, allergic asthma, sarcoidosis, multiple sclerosis, and osteomyelitis. In SSTIs, S. aureus utilizes virulence factors to cause infections ranging from superficial to necrotizing fasciitis, with potential systemic complications. Additionally, S. aureus is a common cause of foodborne outbreaks globally, with staphylococcal enterotoxins being a significant contributor. The pathogen can also lead to serious conditions like toxic shock syndrome and is associated with inflammatory responses and host cell death in various diseases, emphasizing the importance of understanding its pathogenic mechanisms for targeted treatment. Skin abscesses, including those caused by community-associated MRSA, are prevalent infections attributed to S. aureus.
What is Molecular docking?
4 answers
Molecular docking is a computational method extensively used to predict and analyze the interactions between molecules, such as proteins, enzymes, DNA, RNA, and ligands, either natural or synthetic. It aids in understanding binding mechanisms, predicting binding conformations, and assessing binding affinities. This technique plays a crucial role in drug discovery by modeling the interaction between a drug and its target receptor, helping in accurate structure modeling and biological activity prediction of drug molecules. Initially focusing on rigid interactions, advancements in computational capabilities now allow for dynamic simulations of ligand-protein interactions over time, enhancing the understanding of molecular interactions in drug design. Molecular docking serves as a valuable tool in designing materials at the mesoscale for various applications by elucidating intermolecular interactions in hybrid systems.
Docking and molecular dynamics simulation of compounds inhibiting InhA enzyme of drug-resistant Mycobacterium tuberculosis: An in-silico approach.
5 answers
Docking and molecular dynamics simulations were utilized in an in-silico approach to identify compounds inhibiting the InhA enzyme of drug-resistant Mycobacterium tuberculosis. Various studies focused on developing mutant-specific inhibitors to combat resistance, with approaches including mutation impact modeling, virtual screening, and 3D-pharmacophore searches. Compounds like triclosan derivatives and natural products from Brucea javanica were investigated for their inhibitory potential against InhA, showing promising results in silico. Additionally, computational techniques like homology modeling, molecular docking, and molecular dynamics simulations were employed to study the behavior of specific proteins like Rv1250 from M. tuberculosis, aiding in the design of novel enzyme inhibitors for pathogenesis prevention.
What is the role of AI in hit identification in drug discovery?
5 answers
Artificial intelligence (AI) plays a crucial role in hit identification in drug discovery by accelerating the process and improving efficiency. AI-driven methods, such as deep learning models and machine learning algorithms, aid in predicting binding regions, profiling small molecules for potential liabilities, and facilitating virtual screening to identify novel hit compounds. These AI tools enable the rapid selection of promising compounds, leading to cost and time savings in the early stages of drug development. Additionally, AI platforms like TAME-VS and ProfhEX provide accessible and comprehensive solutions for hit identification, showcasing the power of AI in advancing candidate molecules and enhancing the drug discovery process.
What are the synthetic methods used to produce monodispersed silver nanoparticles on graphene oxide sheets?
5 answers
Various synthetic methods have been employed to produce monodispersed silver nanoparticles on graphene oxide sheets. One method involves the in-situ polymerization of vinylpyrrolidone (VPy) to prepare graphene-silver nanoparticles (G-Ag) composites, resulting in ∼20 nm AgNPs on graphene surfaces. Another approach includes growing nanosilica (NS) of approximately 50 nm on graphene oxide (GO) surfaces, followed by functionalizing silver nanoparticles (AgNPs) on the NS surface, leading to a composite with significant antibacterial properties. Additionally, a method utilizing aminosilane and glutaraldehyde to functionalize graphene surfaces, followed by the reaction with a silver ammonia solution, results in a clean and environmentally friendly synthesis of silver-coated graphene (RGO/Ag) composites. These methods showcase diverse strategies for synthesizing monodispersed silver nanoparticles on graphene oxide sheets.
Docking moleculaire against Hsp90
5 answers
Molecular docking studies against Hsp90 have been conducted using various compounds to explore their inhibitory potential. Different compounds such as geldanamycin derivatives, Theaflavin 2B, pyrazolyl 2-aminopyrimidine derivatives, and marine fungi derivatives have shown promising results in binding to Hsp90 and inhibiting its activity. These compounds demonstrated strong binding affinities ranging from -137.49 to -123.24 kcal/mol, -9.2 kcal/mol, 20 nM, and were identified as highly potent inhibitors for Hsp90. The docking studies revealed that these compounds interacted well with key amino acids in the binding site of Hsp90, indicating their potential as anti-cancer agents by inhibiting the growth of cancer cells through Hsp90 inhibition.
Docking, pharmacophore and admet against Hsp90 Hsp90
5 answers
In the quest for novel therapies against cancer, various studies have focused on targeting Hsp90 through computational approaches. Research has identified potential inhibitors like ZINC000096116556, ZINC000020761262, and ZINC000217668954, Pterodontoside G and UNPD1, compound 34, ZINC72417069, and ZINC77522480, Theaflavin 2B, and novel geldanamycin derivatives S1-S6. These compounds have shown promising results in terms of docking scores, pharmacokinetic properties, and binding energies against Hsp90. Through molecular docking, pharmacophore modeling, and ADME prediction, these compounds exhibit potential as Hsp90 inhibitors, paving the way for further experimental evaluation and development of effective cancer therapies.