The DOI matches its Crossref record; 58 of the 58 references it cites were found in a registry or an index.
Synthesis, antioxidant evaluation, and quantitative structure–activity relationship studies of chalcones
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“ّن چٌیي، اؾتفازُ اظ تطذی ضاّثطزّای ؾاظگاضاًِ تٌؾین ّیزاى ّوچَى اضظیاتی هزسز قٌاذتی زض هَارِْ تا اؾتطؼ، اضغطاب، افؿطزگی ٍ ًَؾاًات ذلمی زض تؿیاضی اظ هَالـ فلاٍُ تط واؾتي اظ ّیزاًات هٌفی، هیتَاًس ّیزاًات هخثت ضا افعایف زّس 43( ، )44 .”
From Effectiveness of Mindfulness Training in Emotion Regulation and Distress Tolerance among Breast Cancer Patients (2024) · cites this paper as [43]
Citations
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Handbook of Molecular Descriptors
Todeschini, R., & Consonni, V. (2000) · Methods and Principles in Medicinal Chemistry · doi:10.1002/9783527613106 · Cited by 4,107 · cited 1×
“Several papers deal with the explanation of these structural descriptors (Todeschini et al., 1994; Todeschini and Consonni, 2000; Karelson, 2000).”
BackgroundOu, B., Huang, D., Hampsch‐Woodill, M., Flanagan, J. A., & Deemer, E. K. (2002) · Journal of Agricultural and Food Chemistry · doi:10.1021/jf0116606 · Cited by 1,324
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Cited by
Sorted by citations
Items 101–145 of 145
Síntesis y actividad biológica de chalconas
Escobedo, M. E. R., Bermúdez, L. B., Berúmen, C. P., Galindo, A. S., & Silva‐Belmares, S. Y. (2012) · Revista mexicana de ciencias farmacéuticas · Cited by 6
DEPENDENCE OF BIOLOGICAL ACTIVITY OF CHALCONES ON THEIR STRUCTURE
Stepkina, N. N., & Великородов, А. В. (2015) · Фундаментальные исследования (Fundamental Research) · doi:10.17513/fr.39449 · Cited by 6
Lima, I. K. C., de Sousa, F. D., Bento, A. J. D. M., Cruz, B. G., da Silva, P. T., Bandeira, P. N., dos Santos, H. S., Saraiva, G. D., Barreto, A. C. H., Freire, P., et al. (2020) · Vibrational Spectroscopy · doi:10.1016/j.vibspec.2020.103118 · Cited by 6
Structure and interaction roles in the release profile of chalcone-loaded liposomes
Silva, N. O., da Silva, L. S., Sanches, M. P., dos Santos, T. R., Konzgen, M., Parize, A. L., Sanches, E. A., Darelli, G. J. S., & de Lima, V. R. (2022) · Biophysical Chemistry · doi:10.1016/j.bpc.2022.106930 · Cited by 6
Rokkam, S. K., Mas‐Rosario, J. A., Joshi, B. P., Joshi, M., Choudhury, A. R., Kar, S., Golakoti, N. R., & Farkas, M. E. (2023) · Chemistry & Biodiversity · doi:10.1002/cbdv.202300822 · Cited by 5
Ali, M., maigali, S., Tawfik, H. A., Soliman, F. M., Moharam, M. E., & Dondeti, M. F. (2020) · Egyptian Journal of Chemistry · doi:10.21608/ejchem.2020.27574.2580 · Cited by 5
“responsible for their chemical and biological activities [21-26].”
BackgroundMethodAfonin, A. V., & Rusińska‐Roszak, D. (2022) · Journal of Computational Chemistry · doi:10.1002/jcc.26827 · Cited by 5
Krawczyk, P., Czeleń, P., Jeliński, T., & Cysewski, P. (2018) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2018.08.003 · Cited by 5
Sadgir, N. V., Dhonnar, S. L., Jagdale, B. S., Waghmare, B., & Sadgir, C. (2020) · Material Science Research India · doi:10.13005/msri/170311 · Cited by 5
Joy, M. N., Коvalev, I. S., Shabunina, O. V., Santra, S., & Zyryanov, G. V. (2024) · Antioxidants · doi:10.3390/antiox13101198 · Cited by 5
Synthesis and in vitro Antimicrobial Evaluation of 5’-Acetamido-2'-Hydroxy Chalcone derivatives
Rao, A. S., Simon, L., Srinivasan, K., Moorkoth, S., Haleem, Z. A., Jadon, S. S., Matsa, R. M., & Sagiraju, R. (2014) · Cited by 4
Antioxidant studies on monosubstituted chalcone derivatives - understanding substituent effects
Prabhakar, V. (2016) · Pakistan Journal of Pharmaceutical Sciences · doi:10.36721/pjps/29/1/01.01.2016/3102/165-171 · Cited by 4
“Hydrogen peroxide scavenging activity The ability of the synthetic compounds to scavenge the hydrogen peroxide free radicals was measured using the method of Ruch (Ruch et al., 1989; Sivakumar et al., 2011).”
MethodZaalan, A. H., Al-Hazam, H. A., Abdulsahib, H. T., & Al‐aqbi, Z. T. (2025) · Chemical Papers · doi:10.1007/s11696-025-03960-6 · Cited by 3
“…anticancer agents (Karthikeyan, et al. 2015), anti-inflammatory agents (Liu et al. 2014), anti-HIV agents (Sharma et al. 2011), anti-oxidants (Sivakumar et al. 2011), antifungals (Boeck et al. 2005) and have also shown the potential to form complexes with various elements (Mahapatra et al.…”
Salian, V. V., Narayana, B., Sarojini, B. K., Mahesh, N., Byrappa, K., & Kumar, S. M. (2018) · Chemical Data Collections · doi:10.1016/j.cdc.2018.04.003 · Cited by 3
Sarmiento‐Sánchez, J. I., Terán, A. O., & Rivero, I. A. (2014) · The Scientific World JOURNAL · doi:10.1155/2014/264762 · Cited by 3
Synthesis A New Bis Oxazine and Thiazine Derivatives and Study Their Biological Activities
Ameen, D. S. M. (2023) · Al Mustansiriyah Journal of Pharmaceutical Sciences · doi:10.32947/ajps.v22i4.962 · Cited by 2
Xie, Z., Cheng, X., Mao, J., Zhu, Y., Li, L., & Mei, Z. (2024) · Frontiers in Chemistry · doi:10.3389/fchem.2024.1425318 · Cited by 2
“However, the therapeutic effect of Homobutein has not yet been effectively developed because of the poor aqueous solubility, rapid metabolism, and low focus enrichment (Sivakumar et al., 2011).”
BackgroundKawale, R. A., Shaikh, M. H., Akolkar, H. N., Khedkar, V. M., Raut, D., & Shelke, S. N. (2024) · Russian Journal of Organic Chemistry · doi:10.1134/s1070428024090161 · Cited by 2
RECENT DEVELOPMENTS IN SYNTHESIS AND APPLICATION OF MULTIFACETED CHALCONE COMPOUNDS
Nandedkar, N., Jagdale, D. M., Arote, Y., Patel, M. P., & Kadam, V. J. (2013) · Indo American Journal of Pharmaceutical Research · Cited by 2
Abdelsalam, E. A., Eldehna, W. M., Hammad, S. F., Masurier, N., Ibrahim, T. M., Amagase, K., Nasralla, S. N., Abdel‐Aziz, H. A., Bekhit, A. A., & El-Haggar, R. S. (2026) · RSC Medicinal Chemistry · doi:10.1039/d6md00382f · Cited by 1
Burmudžija, A., Muškinja, J., & Ratković, Z. (2017) · Kragujevac Journal of Science · doi:10.5937/kgjsci1739123b · Cited by 1
“…et al., 2006; TRIVEDI et al., 2008), antifungal (MOSTAHAR et al., 2007; LAHTCHEV et al., 2008; BAG et al., 2009), antioxidant (VOGEL et al., 2008; SIVAKUMAR et al., 2010; VASILʼEV et al., 2010), antiprotozoal (LUNARDI et al., 2003), antitrichomonal (OYEDAPO et al., 2004), antimalarial (MOTTA et…”
BackgroundAcharjee, B., Dhineshkumar, E., Bandyopadhyay, D., & Srinivasan, S. (2021) · Asian Journal of Chemistry · doi:10.14233/ajchem.2021.23087 · Cited by 1
Турдыбеков, К. М., Zhanymkhanova, P. Z., Mukusheva, G. K., & Gatilov, Y. V. (2023) · Eurasian Journal of Chemistry · doi:10.31489/2959-0663/2-23-2 · Cited by 1
Choi, J. Y., Kang, J.-S., Han, J. G., & Byun, J. C. (2016) · Journal of Korean Ophthalmic Optics Society · doi:10.14479/jkoos.2016.21.4.333 · Cited by 1
“이와 같은 칼콘은 그 자체와 유도체들은 약물학적 활성에 있어서 항산화제,([29,30]) 항암,([31]) 항원생동 <초청논문>”
A Laconic Review on Chalcones: Synthesis, Antimicrobial and Antioxidant activities
Kaundal, V., Singh, D., Vipasha, V., Devi, A., Jindal, S., Ankalgi, A. D., & Goyal, K. (2022) · Asian Journal of Research in Pharmaceutical Sciences · doi:10.52711/2231-5659.2022.00005 · Cited by 1
(2022) · Journal of Chemical Biological and Physical Sciences · doi:10.24214/jcbps.a.11.4.48698 · Cited by 1
Parsaee, S., Jahani, N., Salehiniya, H., & Raeison, M. (2024) · Journal of Breast Diseases · doi:10.61186/ijbd.17.1.84
Chemical and biotransformation studies of some bioactive phenolics and heterocyclic compounds
Sharma, N. (2011) · INFLIBNET
(2E)-3-(4-Methylphenyl)-1-(pyridin-3-yl)prop-2-en-1-one
Oliveiria, M. D. S., de Souza, W. C., Napolitano, H. B., & Oliver, A. G. (2012) · Acta Crystallographica Section E Structure Reports Online · doi:10.1107/s1600536812032746
“For biological and medicinal applications of chalcones, see: Bandgar et al. (2010); Juvale et al. (2012); Liu et al. (2003); Sivakumar et al. (2011); Trivedi et al. (2007); Viana et al. (2003).”
BackgroundPerundevi, T., Jonathan, D. R., & Kothai, S. (2014) · International Journal of Pharma and Bio Sciences
Đào, T. T., Son, T. T., Vi, N. T. C., Trí, L. M., & Minh, T. K. (2017) · Y HOC TP HO CHI MINH · doi:10.32895/ump.mpr.1.1.15/suffix · Cited by 1
Synthesis, Antioxidant activity and Structure-Activity Relationship of gallic hydrazones AnaloguesPreprint
Wu, Z., Peng, C., & Liu, Y.-Q. (2021) · Research Square · doi:10.21203/rs.3.rs-968882/v1
4.2.2.3. A Solvent-Free Approach for Chalcone Synthesis via an Aldol Reaction
Friães, S. F. P., Boto, R. E., Almeida, P., Silva, A. M., & Reis, L. V. D. (2016) · Royal Society of Chemistry eBooks · doi:10.1039/9781849739634-00339
Synthesis and Crystal Structure of 2-bromobutoxy-4-methoxy-6-hydroxychalcone
Турдыбеков, К. М., Zhanymkhanova, P. Z., Mukusheva, G. K., Turdybekova, Y., & Adekenov, S. M. (2023) · Chemistry of Natural Compounds · doi:10.1007/s10600-023-04104-6
Narwanti, I., & Hidayati, A. K. (2023) · ALCHEMY Jurnal Penelitian Kimia · doi:10.20961/alchemy.19.2.66542.130-139
“Dengan metode konvensional dalam suasana alkalis (KOH, NaOH), sintesis senyawa ini memerlukan waktu pengadukan 2 ‒ 3 jam dan menghasilkan rendemen sebesar 76% ‒ 80% (Murtaza et al. , 2019; Sivakumar et al. , 2011).”
BackgroundAli, A., de Almeida, I. M., Magalhães, E. P., Guedes, J. M., Cajazeiras, F. F. M., Marinho, M. M., Marinho, E. S., de Menezes, R. R. P. P. B., Sampaio, T. L., dos Santos, H. S., et al. (2024) · Biological Chemistry · doi:10.1515/hsz-2024-0068
Chalcones and their derivatives as antioxidants: Mechanism and Applications
Nazir, B., Bhat, H., & Tabassum, N. (2025) · Elsevier eBooks · doi:10.1016/b978-0-443-30122-3.00019-4
Bairagee, D., Gupta, M., & Panchawat, S. (2025) · Next research. · doi:10.1016/j.nexres.2025.101068
Bromination of C-butylcalix[4]resorcinarene: Synthesis and antioxidant activity evaluation
Yuanita, E., Tamara, C. C., Dharmayani, N. K. T., Septiyana, M., Ulfa, M., & Lestarini, I. A. (2025) · AIP conference proceedings · doi:10.1063/5.0305707
Efficiency of using potential antioxidants in fish feed when rearing rainbow trout
Polovinkina, M. A., Plyukhina, E. V., Osipova, V. P., Великородов, А. В., & Ponomareva, E. N. (2026) · Rybovodstvo i rybnoe hozjajstvo (Fish Breeding and Fisheries) · doi:10.33920/sel-09-2606-05
Wable, J. B., Labhade, H. S., Prabhu, P. J., Akolkar, H. N., Darekar, N. R., & Khedkar, V. M. (2026) · SSRN Electronic Journal · doi:10.2139/ssrn.7442845
Metadata
- Authors
- Sivakumar, P. M., Prabhakar, P. K., & Doble, M.
- Affiliations
- Indian Institute of Technology Madras (IN)
- Corresponding author
- Doble, M.
- Venue
- Medicinal Chemistry Research
- Published
- 2010-03-23
- Volume
- 20
- Issue
- 4
- Pages
- 482-492
- ISSN
- 1054-2523 (ISSN-L)
- 1554-8120
- OpenAlex
- W2092646120
- Cited by
- 144
- References
- 58
- Citations by year
- 2026: 4 · 2025: 6 · 2024: 7 · 2023: 11 · 2022: 11 · 2021: 5 · 2020: 14 · 2019: 12 · 2018: 13 · 2017: 14 · 2016: 15 · 2015: 9 · 2014: 9 · 2013: 5 · 2012: 5
- FWCI
- 2.22
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- Medicinal Chemistry Research (publishedVersion)
- Funders
- Indian Institute of Technology Madras
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Heterocyclic Compound Synthesis and Bioactivity
- Physical Sciences › Chemistry › Organic Chemistry › Free Radicals and Antioxidants
- Physical Sciences › Chemistry › Organic Chemistry › Synthesis of Organic Compounds
- Keywords
- chalcones, chalcone derivatives, antioxidant activity, QSAR, Claisen-Schmidt condensation, superoxide radical scavenging, hydrogen peroxide scavenging, DPPH radical scavenging, reducing power, substituent effects, lipophilicity, structure-activity relationship
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