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Relevant bibliographies by topics / Anticancer agents

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Academic literature on the topic 'Anticancer agents'

Author: Grafiati

Published: 4 June 2021

Last updated: 25 July 2025

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Journal articles on the topic "Anticancer agents"

1

Siddiq, A., and V. Dembitsky. "Acetylenic Anticancer Agents." Anti-Cancer Agents in Medicinal Chemistry 8, no. 2 (2008): 132–70. http://dx.doi.org/10.2174/187152008783497073.

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Mann, John. "Nature's anticancer agents." Nature 361, no. 6407 (1993): 21–22. http://dx.doi.org/10.1038/361021a0.

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Caruso, Francesco, Miriam Rossi, and Claudio Pettinari. "Anticancer titanium agents." Expert Opinion on Therapeutic Patents 11, no. 6 (2001): 969–79. http://dx.doi.org/10.1517/13543776.11.6.969.

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Takigawa, Nagio. "Cytotoxic Anticancer Agents." Annals of Oncology 30 (October 2019): vi57. http://dx.doi.org/10.1093/annonc/mdz333.

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K., Gandhi Mansi, and Dr Shashi V. Ranga. "Insights into Quinoline Schiff Bases as Anticancer Agents." International Journal of Research Publication and Reviews 5, no. 11 (2024): 526–38. http://dx.doi.org/10.55248/gengpi.5.1124.3116.

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Valery M. Dembitsky, Tatyana A. Gloriozova, and Vladimir V. Poroikov. "Natural Peroxy Anticancer Agents." Mini-Reviews in Medicinal Chemistry 7, no. 6 (2007): 571–89. http://dx.doi.org/10.2174/138955707780859396.

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Kopustinskiene, Dalia M., Valdas Jakstas, Arunas Savickas, and Jurga Bernatoniene. "Flavonoids as Anticancer Agents." Nutrients 12, no. 2 (2020): 457. http://dx.doi.org/10.3390/nu12020457.

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Flavonoids are polyphenolic compounds subdivided into 6 groups: isoflavonoids, flavanones, flavanols, flavonols, flavones and anthocyanidins found in a variety of plants. Fruits, vegetables, plant-derived beverages such as green tea, wine and cocoa-based products are the main dietary sources of flavonoids. Flavonoids have been shown to possess a wide variety of anticancer effects: they modulate reactive oxygen species (ROS)-scavenging enzyme activities, participate in arresting the cell cycle, induce apoptosis, autophagy, and suppress cancer cell proliferation and invasiveness. Flavonoids have

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Yadav, Pratibha, and Kamal Shah. "Pyridopyrimidines as Anticancer Agents." ECS Transactions 107, no. 1 (2022): 11577–86. http://dx.doi.org/10.1149/10701.11577ecst.

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The main purpose of this review is to provide an overview of the current knowledge for development of new molecules of pyridopyrimidines by using different multi-component reactions that lead to give effective anticancer agents. Thus, the developed compounds have been derived from pyridine and pyrimidines fusion or from possible isomeric forms of pyridopyrimidine derivatives. They are obtained from different approaches of multistep synthesis reaction such as Tandemaza-witting reaction, annulations, and Biginelli type reactions. Apart from the synthetic schemes, their biological applications wi

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Scotti, Luciana, and Marcus T. Scotti. "Recent Natural Anticancer Agents." Current Medicinal Chemistry 29, no. 2 (2022): 164–65. http://dx.doi.org/10.2174/092986732902220103145922.

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Hameed, Rabia. "Diarylheptanoids: Potent Anticancer Agents." Clinical Cancer Drugs 8, no. 1 (2021): 18–26. http://dx.doi.org/10.2174/2212697x08666210930185846.

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Abstract: Diarylheptanoids are widely distributed among species belonging to the family Betulaceae. Being highly polar in nature, they can either be isolated from plants by using sophisticated chromatographic techniques or can be synthesized in the laboratory. They are found to exhibit a wide range of activities, from very simple analgesics to anticancer agents. Recently, they have gained considerable attention due to inhibitory activity against NF-κB activation, NO and TNF-α production, reduction in NO and COX-2 levels in a dose-dependent manner, and suppression of Tcell activation. The curre

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Dissertations / Theses on the topic "Anticancer agents"

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Hudnott, Anna Ruth. "Bioreductive anticancer agents." Thesis, University of Exeter, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302640.

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Pettersson, Hanna Ilse. "Quinolinequinones as anticancer agents." Thesis, University of Exeter, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249038.

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Fryatt, Tara. "Quinolinequinones as bioreductive anticancer agents." Thesis, University of Exeter, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.302535.

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McKeown, Paul. "Synthesis of novel anticancer agents." Thesis, University of Glasgow, 1996. http://theses.gla.ac.uk/7016/.

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Magri, Neal Francis. "Modified taxols as anticancer agents." Diss., Virginia Polytechnic Institute and State University, 1985. http://hdl.handle.net/10919/53892.

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Modifications of the potent anticancer agent taxol were carried out in order to gain an understanding of the chemical reactivity of the drug and the factors which contribute to its biological activity. The C-2' and/or the C-7 hydroxyl groups of taxol were substituted with acetyl, ßalanyl, silyl, succinyl, trichloroethyloxycarbonyl or carbonate linked dibenzylidene protected glucosyl groups. The C-7 position was selectively epimerized under free radical conditions and a 2'-epiacetyltaxol was produced via base catalysed epimerization. The C-2' amide became nucleophilic in the presence of base an

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Vervoort, Hélène C. "Novel anticancer agents from Ascidiacea /." Diss., Connect to a 24 p. preview or request complete full text in PDF format. Access restricted to UC campuses, 1999. http://wwwlib.umi.com/cr/ucsd/fullcit?p3035904.

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Kuder, Craig Heath. "Schweinfurthins as novel anticancer agents." Diss., University of Iowa, 2009. https://ir.uiowa.edu/etd/840.

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Several members of the schweinfurthin family are potent and selective inhibitors of cancer cell growth in the NCI 60-cell cancer screen. The schweinfurthins display unique activity in this screen which suggests that these compounds have a previously unexploited target. This activity encourages development of the schweinfurthins as anti-cancer agents; however, the scarcity of the natural products has hindered biological evaluation. For this reason, a program was initiated to synthesize the natural products and analogues thereof. These efforts have made 5 natural product schweinfurthins and over

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Pan, Ende. "Searching for Anticancer Agents and Antimalarial Agents from Madagascar." Diss., Virginia Tech, 2010. http://hdl.handle.net/10919/77260.

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In our continuing search for biologically active natural products from Madagascar as part of an International Cooperative Biodiversity Group (ICBG) program, a total of four antiproliferative extracts were studied, leading to the isolation of twelve novel compounds with antiproliferative activity against the A2780 human ovarian cancer line, and one extract with antimalarial activities was studied, which led to the isolation of five new natural products with antimalarial activities against the Dd2 and HB3 malarial parasites. The plants and their metabolites are discussed in the following order:

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Gandin, Valentina. "Metal complexes as potential anticancer agents." Doctoral thesis, Università degli studi di Padova, 2009. http://hdl.handle.net/11577/3426115.

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Metal-based antitumor drugs play a relevant role in antiblastic chemotherapy. Cisplatin is regarded as one of the most effective drugs, even if severe toxicities and drug resistance phenomena limit its clinical use. Therefore, in recent years there has been a rapid expansion in research and development of novel metal-based anticancer drugs to improve clinical effectiveness, to reduce general toxicity and to broaden the spectrum of activity. The variety of metal ion functions in biology has stimulated the development of new metallodrugs other than Pt drugs with the aim to obtain compounds acti

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Mjos, Katja Dralle. "Coordination chemistry of antimicrobial and anticancer agents." Thesis, University of British Columbia, 2015. http://hdl.handle.net/2429/54682.

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The World Health Organization has named the resistance of microbes to known antimicrobial drugs as an increasingly serious threat to global public health. Isolates of the ESKAPE pathogens (E. faecium, S. aureus, K. pneumonia, A. baumanii, P. aeruginosa, and Enterobacter species) are responsible for many nosocomial infections each year that require complicated, and therefore expensive, medical treatment, often leading to death in immune-compromised patients. Over the past 50 years, (fluoro-)quinolone antimicrobial agents have been widely used in the clinic as broad-spectrum antibiotics, but lat

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Books on the topic "Anticancer agents"

1

Ojima, Iwao, Gregory D. Vite, and Karl-Heinz Altmann, eds. Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.

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Georg, Gunda I., Thomas T. Chen, Iwao Ojima, and Dolatrai M. Vyas, eds. Taxane Anticancer Agents. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1995-0583.

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Casini, Angela, Anne Vessières, and Samuel M. Meier-Menches, eds. Metal-based Anticancer Agents. Royal Society of Chemistry, 2019. http://dx.doi.org/10.1039/9781788016452.

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L, Cragg Gordon M., Kingston David, and Newman David J, eds. Anticancer agents from natural products. Taylor & Francis, 2005.

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Károly, Lapis, Eckhardt S, and International Union Against Cancer, eds. Anticancer drug research. Akadémiai Kiadó, 1987.

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6

1945-, Ojima Iwao, Vite Gregory D, Altmann Karl-Heinz, American Chemical Society. Division of Organic Chemistry, American Chemical Society. Division of Medicinal Chemistry, and American Chemical Society Meeting, eds. Anticancer agents: Frontiers in cancer chemotherapy. American Chemical Society, 2001.

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7

William, Lown J., ed. Anthracycline and anthracenedione-based anticancer agents. Elsevier, 1988.

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8

National Cancer Institute (U.S.), ed. Fact sheets on anticancer drugs. National Cancer Institute, 1994.

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Convention, United States Pharmacopeial. Fact sheets on anticancer drugs. National Cancer Institute [distributor], 1994.

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10

Stephen, Neidle, and Waring Michael J, eds. Molecular aspects of anticancer drug-DNA interactions. Macmillan, 1994.

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Book chapters on the topic "Anticancer agents"

1

Sausville, E. A., J. I. Johnson, G. M. Cragg, and S. Decker. "Cancer Drug Discovery and Development: New Paradigms for a New Millennium." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch001.

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Pettit, George R. "Evolutionary Biosynthesis of Anticancer Drugs." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch002.

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Kadow, John F., Thomas Alstadt, Shu-Hui Chen, et al. "Some Recent Developments in the Synthesis and Structure-Activity Relationship of Novel Taxanes." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch003.

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Ojima, Iwao, Scott D. Kuduk, Subrata Chakravarty, et al. "New Generation Taxoids and Hybrids of Microtuble-Stabilizing Anticancer Agents." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch004.

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Horwitz, Susan Band, Laura A. Martello, Chia-Ping H. Yang, Amos B. Smith, and Hayley M. McDaid. "Discodermolide and Taxol: A Synergistic Drug Combination in Human Carcinoma Cell Lines." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch005.

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Vite, Gregory D., Robert M. Borzilleri, Soong-Hoon Kim, Alicia Regueiro-Ren, W. Griffith Humphreys, and Francis Y. F. Lee. "Highly Efficient Semisynthesis of Biologically Active Epothilone Derivatives." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch006.

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Altmann, Karl-Heinz, Marcel J. J. Blommers, Giorgio Caravatti, et al. "Synthetic and Semisynthetic Analogs of Epothilones: Chemistry and Biological Activity." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch007.

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Klar, Ulrich, Werner Skuballa, Bernd Buchmann, et al. "Synthesis and Biological Activity of Epothilones." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch008.

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Winssinger, Nicolas, and K. C. Nicolaou. "Epothilones and Sarcodictyins: From Combinatorial Libraries to Designed Analogs." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch009.

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Shih, Chuan, Rima S. Al-Awar, Andrew H. Fray, et al. "Synthesis and Structure-Activity Relationship Studies of Cryptophycins: A Novel Class of Potent Antimitotic Antitumor Depsipeptides." In Anticancer Agents. American Chemical Society, 2001. http://dx.doi.org/10.1021/bk-2001-0796.ch010.

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Conference papers on the topic "Anticancer agents"

1

Satya, Kulsum Hashmi, Sakshi Gupta, Armeen Siddique, and Seema Joshi. "Vanadium Complexes as Potential Anticancer Agents." In ASEC 2023. MDPI, 2023. http://dx.doi.org/10.3390/asec2023-15263.

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Amaravadi, Ravi K. "Abstract SY01-04: Chloroquine derivatives as anticancer agents." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-sy01-04.

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Mihigo, Helene, and Isabel Rozas. "Guanidinium-like protein kinase inhibitors as anticancer agents." In 6th International Electronic Conference on Medicinal Chemistry. MDPI, 2020. http://dx.doi.org/10.3390/ecmc2020-07508.

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Chen, Thomas C., Axel H. Schonthal, and Florence H. Hofman. "Abstract B77: Perillyl alcohol derivatives as anticancer agents." In Abstracts: AACR International Conference held in cooperation with the Latin American Cooperative Oncology Group (LACOG) on Translational Cancer Medicine; May 4-6, 2017; São Paulo, Brazil. American Association for Cancer Research, 2018. http://dx.doi.org/10.1158/1557-3265.tcm17-b77.

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Garrido, María, Patricia Cosme, Jonathan Delgado-Adámez, et al. "Sweet cherry extracts as natural potential anticancer agents." In 7th International Electronic Conference on Medicinal Chemistry. MDPI, 2021. http://dx.doi.org/10.3390/ecmc2021-11484.

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Alkadour, Ahmad Amer, Daoud Al-Badriyeh, and Wafa Al-Marridi. "Pharmacoeconomic Evaluations of Oral Anticancer Agents. Thematic Systematic Review." In Qatar Foundation Annual Research Conference Proceedings. Hamad bin Khalifa University Press (HBKU Press), 2016. http://dx.doi.org/10.5339/qfarc.2016.hbsp3300.

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Salehi, P., F. Nemati, K. Babanezhad-Harikandei, N. Hadian, M. Bararjanian, and I. Bruno. "Novel noscapine derivatives as potent anticancer and antiprotozoal agents." In 67th International Congress and Annual Meeting of the Society for Medicinal Plant and Natural Product Research (GA) in cooperation with the French Society of Pharmacognosy AFERP. © Georg Thieme Verlag KG, 2019. http://dx.doi.org/10.1055/s-0039-3399682.

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SHAH, GOPITKUMAR R., Shane Wesener, and Yi-Qiang Cheng. "Abstract 4646: Toward engineering of novel anticancer bio-agents." In Proceedings: AACR 103rd Annual Meeting 2012‐‐ Mar 31‐Apr 4, 2012; Chicago, IL. American Association for Cancer Research, 2012. http://dx.doi.org/10.1158/1538-7445.am2012-4646.

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Redda, Kinfe Ken, Madhavi Gangapuram, Mohammad A. Ghaffari, Suresh Eyunni, Nelly Mateeva, and Bereket Mochona. "Abstract 2229: Synthesis of heterocyclic compounds as anticancer agents." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-2229.

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Želazková, Jana. "Total Synthesis of Arctigenin Derivatives as Potential Anticancer Agents." In The 15th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2011. http://dx.doi.org/10.3390/ecsoc-15-00598.

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Reports on the topic "Anticancer agents"

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Lee, Anthony J. Studies on the Novel Anticancer Agents Metabolically Formed form 17-Beta-Estradiol. Defense Technical Information Center, 2004. http://dx.doi.org/10.21236/ada430564.

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Lee, Anthony J. Studies on the Novel Anticancer Agents Metabolically Formed from 17-Beta-Estradiol. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada418901.

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Inoue, Takashi, and Mamoru Narukawa. Anti-tumor efficacy of anti-PD-1/PD-L1 antibodies in combination with other anticancer drugs in solid tumors: a systematic review and meta-analysis. INPLASY - International Platform of Registered Systematic Review and Meta-analysis Protocols, 2022. http://dx.doi.org/10.37766/inplasy2022.10.0004.

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Review question / Objective: The aim of this systematic review is to compare the combination of PD-1/PD-L1 inhibitors plus other anticancer drugs and monotherapies of PD-1/PD-L1 inhibitors in terms of antitumor efficacy in the solid tumors to better inform clinical practice. To this end, the proposed systematic review will address the following question: Which is the best choice to enhance response rate in subjects with solid tumors, PD-1/PD-L1 inhibitors plus cytotoxic agents or PD-1/PD-L1 inhibitors plus other targeted anticancer drugs? Condition being studied: Cancer is the leading cause of

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Seto, Christopher T. Anticancer Agents Based on a New Class of Transition- State Analog Inhibitors for Serine and Cysteine Proteases. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada377205.

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Seto, Christopher. Anticancer Agents Based on a New Class of Transition-State Analog Inhibitors for Serine and Cysteine Proteases. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada383963.

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Campbell, Colin R. Molecular Determinants of Cellular Sensitivity to Flavopiridol, an Anti-Cell Signaling Anticancer Agent. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada403376.

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Campbell, Colin R. Molecular Determinants of Cellular Sensitivity to Flavopiridol an Anti-Cell Signaling Anticancer Agent. Defense Technical Information Center, 2003. http://dx.doi.org/10.21236/ada422275.

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Campbell, Colin R. Molecular Determinants of Cellular Sensitivity to Flavopiridol, and Anti-Cell Signaling Anticancer Agent. Defense Technical Information Center, 2000. http://dx.doi.org/10.21236/ada392588.

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Dyakova, Lora, Tanya Zhivkova, Rossen Spasov, Reni Kalfin, and Radostina Alexandrova. Disulfiram as a New Potential Anticancer Agent – Influence on Viability and Proliferation of Virus-transformed Tumour Cells. "Prof. Marin Drinov" Publishing House of Bulgarian Academy of Sciences, 2019. http://dx.doi.org/10.7546/crabs.2019.11.14.

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Annunziato, Dominick. HPLC Sample Prep and Extraction SOP v1.3 for Fungi. MagicMyco, 2023. http://dx.doi.org/10.61073/sopv1.3.08.11.2023.

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medicine, industry, and biotechnology. Fungi produce a wide range of bioactive compounds, such as alkaloids, antibiotics, antifungals, immunomodulators, anticancer agents, enzymes, and vitamins. However, these compounds are often locked inside the fungal cell wall, which is composed of chitin, a tough substance that is dif�icult to digest by humans1. Therefore, it is essential to have a good extraction technique that can break down the chitin and release the valuable compounds from the fungi, this is especially essential in the laboratory for accurate lab assays and potency determination durin

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