Добірка наукової літератури з теми "Antiproliferative activities"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся зі списками актуальних статей, книг, дисертацій, тез та інших наукових джерел на тему "Antiproliferative activities".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Статті в журналах з теми "Antiproliferative activities"
Zhou, Lin, Xiaohui Lin, Arshad Mehmood Abbasi, and Bisheng Zheng. "Phytochemical Contents and Antioxidant and Antiproliferative Activities of Selected Black and White Sesame Seeds." BioMed Research International 2016 (2016): 1–9. http://dx.doi.org/10.1155/2016/8495630.
Повний текст джерелаLiu, Ming, Xin Qi Li, Courtney Weber, Chang Yong Lee, Janice Brown, and Rui Hai Liu. "Antioxidant and Antiproliferative Activities of Raspberries." Journal of Agricultural and Food Chemistry 50, no. 10 (May 2002): 2926–30. http://dx.doi.org/10.1021/jf0111209.
Повний текст джерелаXu, XiXi, Tristan Rawling, Ariane Roseblade, Roger Bishop, and Alison T. Ung. "Antiproliferative activities of alkaloid-like compounds." MedChemComm 8, no. 11 (2017): 2105–14. http://dx.doi.org/10.1039/c7md00435d.
Повний текст джерелаMeyers, Katherine J., Christopher B. Watkins, Marvin P. Pritts, and Rui Hai Liu. "Antioxidant and Antiproliferative Activities of Strawberries." Journal of Agricultural and Food Chemistry 51, no. 23 (November 2003): 6887–92. http://dx.doi.org/10.1021/jf034506n.
Повний текст джерелаHuang, Hung-Tse, Chia-Ching Liaw, Yu-Chi Lin, Geng-You Liao, Chih-Hua Chao, Chun-Tang Chiou, Yao-Haur Kuo, and Kung-Ta Lee. "New Diterpenoids from Mesona procumbens with Antiproliferative Activities Modulate Cell Cycle Arrest and Apoptosis in Human Leukemia Cancer Cells." Pharmaceuticals 14, no. 11 (October 29, 2021): 1108. http://dx.doi.org/10.3390/ph14111108.
Повний текст джерелаZhou, Mingming, Pei Chen, Yuan Lin, Shengzuo Fang, and Xulan Shang. "A Comprehensive Assessment of Bioactive Metabolites, Antioxidant and Antiproliferative Activities of Cyclocarya paliurus (Batal.) Iljinskaja Leaves." Forests 10, no. 8 (July 26, 2019): 625. http://dx.doi.org/10.3390/f10080625.
Повний текст джерелаChang, Tien-Ning, Guan-Jhong Huang, Yu-Lin Ho, Shyh-Shyun Huang, Heng-Yuan Chang, and Yuan-Shiun Chang. "Antioxidant and Antiproliferative Activities of Crossostephium chinensis (L.) Makino." American Journal of Chinese Medicine 37, no. 04 (January 2009): 797–814. http://dx.doi.org/10.1142/s0192415x09007259.
Повний текст джерелаVollár, Martin, András Gyovai, Péter Szűcs, István Zupkó, Marianna Marschall, Boglárka Csupor-Löffler, Péter Bérdi, et al. "Antiproliferative and Antimicrobial Activities of Selected Bryophytes." Molecules 23, no. 7 (June 23, 2018): 1520. http://dx.doi.org/10.3390/molecules23071520.
Повний текст джерелаNegi, Arvind Singh, Suaib Luqman, Suchita Srivastava, Vinay Krishna, Namita Gupta, and Mahendra Pandurang Darokar. "Antiproliferative and antioxidant activities ofJuglans regiafruit extracts." Pharmaceutical Biology 49, no. 6 (May 9, 2011): 669–73. http://dx.doi.org/10.3109/13880209.2010.537666.
Повний текст джерелаB. Ng, T., and J. H. Wong. "Fungal Proteins with Antiproliferative and Anticancer Activities." Protein & Peptide Letters 20, no. 4 (February 1, 2013): 433–38. http://dx.doi.org/10.2174/092986613805290363.
Повний текст джерелаДисертації з теми "Antiproliferative activities"
Oliveira, Marcelio. "Synthesis and Evaluation of N6,5'-Bis-Ureido-5'-Amino-5'-Deoxyadenosine Derivatives: Novel Nucleosides with Antiproliferative and Protein Kinase Binding Activities." Diss., CLICK HERE for online access, 2009. http://contentdm.lib.byu.edu/ETD/image/etd3231.pdf.
Повний текст джерелаSAAB, Antoine. "Phytochemical analysis, antiproliferative against k562 humam chronic myelogenus leukemia, antiviral and hypoglycaemic activities of cedrus species and medicinal plants native from Libanon." Doctoral thesis, Università degli studi di Ferrara, 2011. http://hdl.handle.net/11392/2388806.
Повний текст джерелаSoares, Sarah Aparecida. "Isolamento biomonitorado de substâncias ativas de Croton pallidulus var. pallidulus (Euphorbiaceae)." Universidade de São Paulo, 2013. http://www.teses.usp.br/teses/disponiveis/41/41132/tde-31032014-104241/.
Повний текст джерелаCroton (Euphorbiaceae), is a promising genre for investigation of bioactive compounds, both for the variety of compouds, as for the diversity of use in traditional medicine. Pharmacological studies have demonstrated antimicrobial, antiviral, anti-inflammatory, cytotoxic, and antioxidant activities. In this study, fractionated extracts of leaves and stems of C. pallidulus Baill var. pallidulus (Baill.) L.B. S.F. Smith & Smith were obtained throught Soxhlet (hexane, dichloromethane, ethyl acetate and methanol). The following activities of these extracts were tested: 1) antibacterial activity, through microbroth dilution assay using: Staphylococcus aureus - sensitive and vancomycin-resistant strains, Pseudomonas aeruginosa, Escherichia coli and Salmonella choleraesuis; 2) antioxidant activity (free radical DPPH scavenging) and Artemia salina toxicity evaluation. The most active fraction in the latter test was selected to evaluate the cytotoxic activity using human uterine sarcoma cells. The total phenols, and total flavonols and flavones were quantified by colorimetric methods. The fractionation of hexane and dichloromethane extracts was done through silica column chromatography, while PVPP column was used for the ethyl acetate and methanol extracts. The isolation of the active fractions major compounds in the antibacterial activity (S. aureus - sensitive) and A. saline toxicity assays were performed by semipreparative HPLC. The total phenolic content of C. pallidulus var. pallidulus was 1.95 g GAE/100g DM and total flavonols and flavones was 0.56 g QE/100g MS. All extracts showed activity against S. aureus (sensitive and resistant), with MBC of 2048 mg/L, except for the methanol extract, which showed activity only against S. aureus (sensitive). Extracts showed no activity against the other strains. Fractions FH-5A-hexane (MBC: 256mg/L) and FA-7-ethyl acetate (MBC: 1024mg/L) showed the highest antibacterial activity. The fraction FH-5A was separated on a silica column, and its subfractions showed smaller antibacterial activity than FH-5A. The seven major compounds isolated from the FA-7 fraction, showed no antibacterial activity. Six of them are flavonoids, three apigenin C-glycosides, one kaempferol O-glucoside, one isorhamnetin O-galactoside and one isorhamnetin O-rutinoside. Only the dichloromethane extract showed activity in the A. salina toxicity assay, LC50: 385mg/L. The fraction with the highest toxicity was the FD-4A, LC50: 101mg/L. The most abundant substances in this fraction were isolated and identified as 8,9 - secokauranes derived from kongensin F. As for the cytotoxic activity, the FD-4A activity was three times higher than the dichloromethane extract activity. The extracts of ethyl acetate and methanol showed the highest antioxidant activity: 12.11 and 11.77 gQE/100g, respectively. It was observed that flavonoids were the phenolic substances that most influenced the antioxidant activity of the fractions of the ethyl acetate and methanol extracts. With these results we suggest that C. pallidulus var. pallidulus has antibacterial activity, cytotoxic and antioxidant properties, being a potential source of new drugs for treatment of infectious diseases and cancer. We also isolated three 8,9-secokauranes derived from kongensin F, which apparently had not been described yet
Abi, Aad Elizabeth. "Impact de la Détente Instantanée Contrôlée (DIC) sur l’extraction des molécules bioactives de rhizomes de Rheum ribes L." Electronic Thesis or Diss., La Rochelle, 2023. http://www.theses.fr/2023LAROS008.
Повний текст джерелаRheum ribes L. (rhubarb) is one of the most important Mediterranean medicinal plants. Preparing its rhizomes’ aqueous decoctions has become common among patients suffering from various diseases. Instant Controlled Pressure Drop (DIC) is a High-Temperature Short-Time treatment (HTST) followed by an abrupt pressure drop towards the vacuum (approximately 5 kPa). This technology increases the expansion and reduces the tortuosity of the treated matrix to ensure better diffusivity of the extraction solvents and greater availability of the active molecules. On the one hand, our research aimed at the impact of DIC treatment on the rhizomes of a Lebanese species of R. ribes L. The evaluations were based on the contents of total phenolics (TPC) and flavonoids (TFC) as well as the antioxidant capacities of aqueous extracts of the treated rhizomes. The results showed a negative correlation between the saturated steam pressure applied and the values of TPC, TFC, and the antioxidant activities of the samples. However, DIC treatment time had no significant influence on the response variables. In addition to these two DIC operating factors (pressure and treatment time), the effect of the rhizomes water content (W) was also studied. The results showed that the increase of “W” does not lead to better yields of phenolic compounds. On the other hand, this study presents the impact of DIC treatment on the biological activities (antibacterial and antiproliferative effects) of rhizome extracts. The results revealed that the aqueous extracts of DIC-treated rhizomes show weak antibacterial powers on E. coli and S. aureus, with slightly superior results in inhibiting the growth of S. aureus. Regarding the viability test of melanoma cancer cells, the results showed that the DIC treatment positively impacts the antiproliferative power of the treated samples compared with the untreated point (aqueous MP). In particular, two samples among those tested recorded an antiproliferative power of 60%. The HPLC and UHPLC assays revealed the presence of three anthraquinones (emodin, chrysophanol, and physcion) in the rhizome extracts and about twenty compounds from the flavonoid family. However, the amounts of anthraquinones detected are not significantly higher in the extracts treated with DIC than in the untreated ones. Finally, it was found that the total phenolic content of an aqueous sample treated with the optimal DIC parameters is equal to that of an untreated hydroalcoholic sample. Further experiments will be necessary to validate this result
BASTIAS, VENEGAS JORGE EDUARDO ROMILIO. "Activites antiproliferative et antitumorale d'un dextrane fonctionalise (cmdbj) sur les cellules de melanome 1205 l-u." Paris 13, 1999. http://www.theses.fr/1999PA132034.
Повний текст джерелаTomasi, Sophie. "Synthèse en solution et sur support solide de dérivés de polyamines : évaluation de leur activité antiproliférative." Rennes 1, 1999. http://www.theses.fr/1999REN10100.
Повний текст джерелаBoisbrun, Michel. "Reactions selectives de l'acide de meldrum : application a la synthese de beta-carbolines et de pyrrolo(3'4':5,6)pyrido(3,4-b)indoles a activite antiproliferative (doctorat : sciences du medicament)." Reims, 2000. http://www.theses.fr/2000REIMP205.
Повний текст джерелаHadj, Salem Jamila. "Extraction, identification, caractérisation des activités biologiques de flavonoïdes de Nitraria retusa et synthèse de dérivés acylés de ces molécules par voie enzymatique." Thesis, Vandoeuvre-les-Nancy, INPL, 2009. http://www.theses.fr/2009INPL057N/document.
Повний текст джерелаThe present work firstly consisted in studying the extraction and the identification of major flavonoids contained in Nitraria retusa leaves and evaluating their biological activities. Four flavonoids were identified in extracts and fractions: isorhamnetin, isorhamnetin-3-O-glucoside and the two isomers isorhamnetin-3-O-rutinoside and isorhamnetin-3-O-robinobioside. The evaluation of the biological activities of extracts and fractions of N. retusa allowed to establish a linear relationship between their antioxidant and antiproliferative activities and their total flavonoids content, the most enriched exhibiting the highest activities. The nature of the flavonoids present in the extracts and fractions was shown to be important too. Thus, the strong xanthine oxidase inhibition activity and the high DPPH radical scavenging capacity observed for the chloroform fraction can be attributed to its high content in the aglycone flavonoid isorhamnetin, a structural analogue of quercetin which is well known for its antioxidant activities. In a second part, the enzymatic acylation of isoquercitrin as a model compound and isorhamnetin-3-O-glucoside was studied in order to improve their properties. The enzymatic acylation of isoquercitrin by fatty acid ethyl esters of different chain lengths, catalyzed by the lipase B of Candida antarctica, showed that the performance of the reaction is inversely proportional to the acyl donor chain length. Similar results were obtained when acylating the isorhamnetin-3-O-glucoside. The activities of isoquercitrin and isorhamnetin-3-O-glucoside esters were determined and compared to that of initial flavonoids. Esters exhibited higher antiproliferative towards Caco2 cells and xanthine oxidase inhibition activities than original compounds. Finally, this work led to a better understanding of the structure-activity relationship of flavonoids and their acylated derivatives
Filleur, Fabrice. "Etude phytochimique et structure de lignoides isolés du macis de myristica argentea warb. (myristicaceae)." Limoges, 2001. http://www.theses.fr/2001LIMO301A.
Повний текст джерела"Antioxidant and antiproliferative activities of flower tea extracts." 2007. http://library.cuhk.edu.hk/record=b5896541.
Повний текст джерелаThesis submitted in: November 2006.
Thesis (M.Phil.)--Chinese University of Hong Kong, 2007.
Includes bibliographical references (leaves 103-128).
Abstracts in English and Chinese.
Thesis Committee --- p.i
Acknowledgements --- p.ii
Abstract --- p.iii
摘要 --- p.iv
Table of Contents --- p.v
List of Tables --- p.ix
List of Figures --- p.x
Abbreviations --- p.xiii
Chapter 1. --- Introduction
Chapter 1.1 --- Flower herbal teas --- p.1
Chapter 1.2 --- R. rugosa --- p.3
Chapter 1.2.1 --- The phytochemistry of R. rugosa --- p.3
Chapter 1.3 --- Secondary metabolites --- p.4
Chapter 1.4 --- Classification of secondary metabolites --- p.6
Chapter 1.5 --- Phenolic compounds --- p.6
Chapter 1.5.1 --- Phenylpropanoid compounds --- p.6
Chapter 1.5.2 --- Lignins --- p.7
Chapter 1.5.3 --- Coumarins --- p.7
Chapter 1.5.4 --- Stilbenes --- p.8
Chapter 1.5.5 --- Tannins --- p.8
Chapter 1.5.6 --- Flavonoids --- p.9
Chapter 1.6 --- Oxidative Stress --- p.13
Chapter 1.6.1 --- Diseases related to ROS --- p.13
Chapter 1.6.2 --- Significant chemical or biochemical conversion of ROS --- p.14
Chapter 1.6.3 --- Sources of ROS --- p.15
Chapter 1.7 --- Natural dietary antioxidants --- p.15
Chapter 1.7.1 --- Vitamin C --- p.15
Chapter 1.7.2 --- Vitamin E --- p.16
Chapter 1.7.3 --- Carotenoids --- p.16
Chapter 1.7.4 --- Phenolic compounds --- p.16
Chapter 1.8 --- Cancinogenesis --- p.17
Chapter 1.9 --- Cell cycle --- p.18
Chapter 1.9.1 --- Cell cycle of eukaryotic cells --- p.18
Chapter 1.9.2 --- Checkpoints of cell cycle --- p.18
Chapter 1.10 --- Cancer cell lines --- p.19
Chapter 1.11 --- The growth phases of cancer cell lines --- p.20
Chapter 1.12 --- Antiproliferative effects of phenolic compounds --- p.21
Chapter 1.13 --- Genotoxicity of phenolic compounds --- p.22
Chapter 1.14 --- Objectives --- p.23
Chapter 2. --- Methods and Materials
Chapter 2.1 --- Extraction of active substances --- p.40
Chapter 2.2 --- Determination of antioxidant activities TEAC assay --- p.40
Chapter 2.3 --- Determination of hydroxy 1 radical scavenging activity by the deoxyribose assay --- p.41
Chapter 2.4 --- Determination of phenolic contents by Folin´ؤCiocalteu assay --- p.43
Chapter 2.5 --- Determination of total flavonoid by aluminum chloride colorimetric method --- p.43
Chapter 2.6 --- Determination of oxidative DNA damage by comet assay --- p.44
Chapter 2.7 --- Cell lines propagation --- p.49
Chapter 2.8 --- Determination of antiproliferative activities by MTT assay (colorimetric) --- p.50
Chapter 2.9 --- Determination of antiproliferative activities by BrdU labeling assay --- p.52
Chapter 2.10 --- Cell cycle analysis by flow cytometry --- p.55
Chapter 2.11 --- Determination of genotoxicity by SOS chromotest --- p.57
Chapter 3. --- Results
Chapter 3.1 --- Dermination of antioxidant activities by TEAC assay --- p.59
Chapter 3.1.1 --- Trolox Standard Reference --- p.59
Chapter 3.1.2 --- TEAC of the seven flower extracts --- p.59
Chapter 3.2 --- Hydroxyl radical scavenging activity by deoxyribose assay --- p.60
Chapter 3.3 --- Determination of phenolic contents by Folin´ؤCiocalteu assay --- p.60
Chapter 3.4 --- Determination of total flavonoids by colorimetirc aluminium chloride assay --- p.61
Chapter 3.5 --- "The Inter-correlation between the antioxidant activities, total phenolic and flavonoid contents of flower extraction powders" --- p.61
Chapter 3.6 --- Determination of oxidative DNA damage by comet assay --- p.62
Chapter 3.7 --- Determination of antiproliferative activities by MTT assay --- p.63
Chapter 3.7.1 --- Antiporoliferative activities on HepG2 --- p.63
Chapter 3.7.2 --- Antiproliferative activities on MCF7 --- p.63
Chapter 3.7.3 --- IC50 of R. rugosa extract on both HepG2 and MCF7 --- p.64
Chapter 3.8 --- "The Inter-correlation between antioxidant activities, total phenolic contents, flavonoid contents, and the antiproliferative activities of flower extraction Powders" --- p.64
Chapter 3.9 --- Determination of DNA synthesis by BrdU labeling analysis --- p.65
Chapter 3.10 --- Cell cycle analysis by flow cytometry --- p.65
Chapter 3.11 --- Determination of genotoxicity by SOS chromotest --- p.66
Chapter 4. --- Discussions
Chapter 4.1 --- Extraction method --- p.90
Chapter 4.2 --- Comparison of TEAC of the dry flowers with other foods --- p.90
Chapter 4.3 --- Correlation between ABTS+ and hydroxyl scavenging ability of flower extraction powder --- p.91
Chapter 4.4 --- Comparison of phenolic contents of the fry flowers with other foods --- p.92
Chapter 4.5 --- Correlation between total phenolic contents and flavonoid contents of flower Eextraction powders --- p.92
Chapter 4.6 --- "Correlation between total phenolic, flavonoid content and antioxidant activities of flower extraction powders" --- p.93
Chapter 4.7 --- Factors affecting the antioxidant power besides total phenolic contents --- p.94
Chapter 4.8 --- Synergistic effect of phenolic compounds --- p.94
Chapter 4.9 --- Toxicity of drinking flower herbal tea --- p.95
Chapter 4.10 --- Recommended dose of flower herbal teas --- p.96
Chapter 4.11 --- Antiproliferative activities of flower extracts by MTT assay --- p.97
Chapter 4.12 --- Antiproliferation activities of flower extraction Powders by Brdu labeling assay --- p.98
Chapter 4.13 --- Protective effects of flower extraction powder on oxidative DNA damage determined by comet assay --- p.99
Chapter 4.14 --- Cell cycle analysis --- p.100
Chapter 4.15 --- Further Studies --- p.101
Chapter 5. --- Conclusion --- p.102
Chapter 6. --- References --- p.103
Частини книг з теми "Antiproliferative activities"
Anesini, Claudia A., María Rosario Alonso, and Renzo F. Martino. "Antiproliferative and Cytotoxic Activities." In Sesquiterpene Lactones, 303–23. Cham: Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-78274-4_13.
Повний текст джерелаMumtaz, Peerzada Tajamul, Showkeen Muzamil Bashir, Muzafar Ahmad Rather, Khalid Bashir Dar, Qamar Taban, Saima Sajood, Aarif Ali, Zubair Ahmad Rather, Insha Amin, and Mashooq Ahmad Dar. "Antiproliferative and Apoptotic Activities of Natural Honey." In Therapeutic Applications of Honey and its Phytochemicals, 345–60. Singapore: Springer Singapore, 2020. http://dx.doi.org/10.1007/978-981-15-6799-5_18.
Повний текст джерелаFraněk, F., M. Strnad, L. Havlíček, and V. Siglerová. "Antiproliferative and Growth-Stimulating Activities of Synthetic Cytokinin Analogs." In Animal Cell Technology: Basic & Applied Aspects, 315–19. Dordrecht: Springer Netherlands, 2002. http://dx.doi.org/10.1007/978-94-017-0728-2_56.
Повний текст джерелаWong, Jack Ho, Tzi Bun Ng, Evandro Fei Fang, and He-Xiang Wang. "Defense Proteins with Antiproliferative and Antimicrobial Activities from Fungi and Bacteria." In Antitumor Potential and other Emerging Medicinal Properties of Natural Compounds, 359–73. Dordrecht: Springer Netherlands, 2013. http://dx.doi.org/10.1007/978-94-007-6214-5_24.
Повний текст джерелаNg, Tzi-Bun, Jack H. Wong, Randy C. F. Cheung, Patrick H. K. Ngai, He-Xiang Wang, Xiujuan Ye, Sze-Kwan Lam, Yau-Sang Chan, and Evandro F. Fang. "Antiproliferative Activities of Chinese Cabbage (Brassica parachinensis) Seeds." In Nuts and Seeds in Health and Disease Prevention, 317–23. Elsevier, 2011. http://dx.doi.org/10.1016/b978-0-12-375688-6.10038-6.
Повний текст джерелаCascaes, Márcia M., Giselle M. S. P. Guilhon, Lidiane D. Nascimento, Angelo A. B. de Moraes, Sebastião G. Silva, Jorddy Neves Cruz, Oberdan O. Ferreira, Mozaniel S. Oliveira, and Eloisa H. A. Andrade. "Volatile Terpenoids of Annonaceae: Occurrence and Reported Activities." In Terpenoids: Recent Advances in Extraction, Biochemistry and Biotechnology, 105–28. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9781681089645122010007.
Повний текст джерелаPeeri, Hadar, and Hinanit Koltai. "Phytocannabinoids have cytotoxic, antiproliferative, and antimigratory activities on cancer cells and cancer stem cells." In Cannabis Use, Neurobiology, Psychology, and Treatment, 555–64. Elsevier, 2023. http://dx.doi.org/10.1016/b978-0-323-89862-1.00030-1.
Повний текст джерелаlzotova, Lara, and Sidney Pestka. "Receptor binding studies." In Cytokine Molecular Biology, 89–104. Oxford University PressOxford, 2000. http://dx.doi.org/10.1093/oso/9780199638581.003.0005.
Повний текст джерелаAyembilla, Jacob Apibilla, Phyllis Naa Yarley Otu, Eunice A. Dotse, Abigail Aning, Emmanuel Kweku Ofori, Regina Appiah-Opong, and Henry Asare-Annane. "Antioxidant and Anticancer Potential of Natural Cocoa Extract." In Technological Innovation Driving Sustainable Entrepreneurial Growth in Developing Nations, 156–75. IGI Global, 2023. http://dx.doi.org/10.4018/978-1-6684-9843-9.ch007.
Повний текст джерелаBonardi, Alessandro, Claudiu T. Supuran, and Alessio Nocentini. "Phenols and Polyphenols as Carbonic Anhydrase Inhibitors." In Flavonoids and Phenolics, 330–83. BENTHAM SCIENCE PUBLISHERS, 2022. http://dx.doi.org/10.2174/9789815079098122010014.
Повний текст джерелаТези доповідей конференцій з теми "Antiproliferative activities"
Mottaghipisheh, Javad, Márta Nové, Gabriella Spengler, Norbert Kúsz, Judit Hohmann, and Dezső Csupor. "Antiproliferative and cytotoxic activities of furocoumarins of Ducrosia anethifolia." In Fiatal Gyógynövénykutatók Fóruma. Szeged: Magyar Gyógyszerésztudományi Társaság Gyógynövény Szakosztálya, 2018. http://dx.doi.org/10.14232/fgykf.2018.b1.
Повний текст джерелаGarbuz, Olga, Ion Toderas, Ianina Ulchina, Vasile Graur, Nadejda Railean, and Аurelian Gulea. "The Antiproliferative, Antioxidant Activities and Toxicity of Mixed-Ligand Amine-Containing Copper (II) Coordination Compounds with 2-(2-Hydroxybenzylidene)-N-(Prop-2-En-1-Yl) Hydrazinecarbothioamide." In Xth International Conference of Zoologists. Institute of Zoology, Republic of Moldova, 2021. http://dx.doi.org/10.53937/icz10.2021.20.
Повний текст джерелаTavares, Clint D. J., Jiney Jose, Ashwini K. Devkota, Jihyun Park, Tamer S. Kaoud, Eric V. Anslyn, and Kevin N. Dalby. "Abstract 5462: Antiproliferative and cytotoxic activities of 5-(nonyloxy)tryptamine derivatives in breast cancer cells." In Proceedings: AACR Annual Meeting 2014; April 5-9, 2014; San Diego, CA. American Association for Cancer Research, 2014. http://dx.doi.org/10.1158/1538-7445.am2014-5462.
Повний текст джерелаLarson, Mathew, Jennifer H. Carlson, Yuliang Sun, Tonia Bucholz, Casey Williams, Nandini Dey, Brian Leyland-Jones, and Pradip De. "Abstract 3506: Carfilzomib demonstrates antiproliferative and proapoptotic activities in preclinical triple-negative breast cancer models." In Proceedings: AACR 107th Annual Meeting 2016; April 16-20, 2016; New Orleans, LA. American Association for Cancer Research, 2016. http://dx.doi.org/10.1158/1538-7445.am2016-3506.
Повний текст джерелаSegun Peter, A., MD Ismail Fyaz, OO Ogbole, L. Nahar, AR Evans, and D. Sarker Satyajit. "Antiproliferative activities of Citrus aurantium against breast (MCF7), cervix (HeLa) and urinary bladder (EJ138) carcinoma cells." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608385.
Повний текст джерелаKhan, Jesmine, Wan Nor I’zzah Wan Mohamad Zain, Nurul Suhaili Amirah Mamat, Raja Nurfirzanah Syaza Raja Sharin, Noor Masyitah Jumahat, and Jamal Houssaini. "Vitamin C and E contents and antioxidant, antibacterial, and antiproliferative activities of Citrus suhuiensis peel." In 5th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06296.
Повний текст джерелаWan Mohamad Zain, Wan Nor I'zzah, Taufiq Yap, Fauziah Othman, and Asmah Rahmat. "Nutrient composition, antioxidant and antiproliferative activities of Clausena excavata and Murraya koenigii leaves." In 5th International Electronic Conference on Medicinal Chemistry. Basel, Switzerland: MDPI, 2019. http://dx.doi.org/10.3390/ecmc2019-06332.
Повний текст джерелаAhmed, Elham, Abdul Khan, Kirti S. Prabhu, Kodappully Siveen, Zafar Nawaz, Hatem Zayed, and Shahab Uddin. "Sanguinarine Mediated Anti-Tumor activity Via Targeting JAK/STAT3 Pathway in Thyroid Cancer." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2020. http://dx.doi.org/10.29117/quarfe.2020.0155.
Повний текст джерелаBlaja, Svetlana, Lidia Lungu, Kaleria Kuchkova, Alexandru Ciocarlan, and Aculina Aricu. "Synthesis of new molecular hybrids with phenothiazine fragment from norambreinolide." In Scientific seminar with international participation "New frontiers in natural product chemistry". Institute of Chemistry, Republic of Moldova, 2023. http://dx.doi.org/10.19261/nfnpc.2023.ab10.
Повний текст джерелаHussein, Ola, Feras Alali, Ala‐Eddin Al Mustafa, and Ashraf Khalil. "Development of Novel Chalcone Analogs as Potential Multi-Targeted Therapies for Castration-Resistant Prostate Cancer." In Qatar University Annual Research Forum & Exhibition. Qatar University Press, 2021. http://dx.doi.org/10.29117/quarfe.2021.0114.
Повний текст джерела