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Статті в журналах з теми "Bioactive Lactones"
Shen, Ya-Ching, Kuang-Liang Lo, Yao Haur Kuo, and Ashraf Taha Khalil. "Bioactive Sesquiterpene Lactones from Eupatorium Kiirunense." Natural Product Communications 1, no. 7 (July 2006): 1934578X0600100. http://dx.doi.org/10.1177/1934578x0600100703.
Повний текст джерелаBokić, Jelena, Jovana Kojić, Jelena Krulj, Lato Pezo, Vojislav Banjac, Vesna Tumbas Šaponjac, Vanja Travičić, Diego A. Moreno, and Marija Bodroža-Solarov. "Bioactive, Mineral and Antioxidative Properties of Gluten-Free Chicory Supplemented Snack: Impact of Processing Conditions." Foods 11, no. 22 (November 17, 2022): 3692. http://dx.doi.org/10.3390/foods11223692.
Повний текст джерелаMandal, Sudip Kumar, Utsab Debnath, Amresh Kumar, Sabu Thomas, Subhash Chandra Mandal, Manabendra Dutta Choudhury, and Partha Palit. "Natural Sesquiterpene Lactones in the Prevention and Treatment of Inflammatory Disorders and cancer: A Systematic Study of this Emerging Therapeutic Approach based on Chemical and Pharmacological Aspect." Letters in Drug Design & Discovery 17, no. 9 (September 11, 2020): 1102–16. http://dx.doi.org/10.2174/1570180817999200421144007.
Повний текст джерелаYang, Sien-Sing, Guei-Jane Wang, Kuo-Fang Cheng, Chu-Huang Chen, Yu-Ming Ju, Ya-Jing Tsau та Tzong-Huei Lee. "Bioactive γ-Lactones from the Fermented Broth ofNeosartoryasp." Planta Medica 76, № 15 (5 травня 2010): 1701–5. http://dx.doi.org/10.1055/s-0030-1249907.
Повний текст джерелаBai, Lu, Mi Jiang, Sen Guo, Qingchao Liu, Xinxin Zhang, Xiao Tian, Li Zhang, Chi-Tang Ho, and Naisheng Bai. "Simultaneous quantification of six sesquiterpene lactones and a flavonoid in the whole life stage of Inula salsoloides by high performance liquid chromatography." Analytical Methods 8, no. 17 (2016): 3587–91. http://dx.doi.org/10.1039/c6ay00257a.
Повний текст джерелаStojanović, Milica, Slađana Savić, Abigaël Delcourt, Jean-Louis Hilbert, Philippe Hance, Jelena Dragišić Maksimović, and Vuk Maksimović. "Phenolics and Sesquiterpene Lactones Profile of Red and Green Lettuce: Combined Effect of Cultivar, Microbiological Fertiliser, and Season." Plants 12, no. 14 (July 11, 2023): 2616. http://dx.doi.org/10.3390/plants12142616.
Повний текст джерелаMaksymiak, Magdalena, Tomasz Bałakier, Janusz Jurczak, Marek Kowalczuk, and Grazyna Adamus. "Bioactive (co)oligoesters with antioxidant properties – synthesis and structural characterization at the molecular level." RSC Advances 6, no. 62 (2016): 57751–61. http://dx.doi.org/10.1039/c6ra09870c.
Повний текст джерелаErasto, P., D. S. Grierson, and A. J. Afolayan. "Bioactive sesquiterpene lactones from the leaves of Vernonia amygdalina." Journal of Ethnopharmacology 106, no. 1 (June 2006): 117–20. http://dx.doi.org/10.1016/j.jep.2005.12.016.
Повний текст джерелаLu, X., G. Zhu, Z. Wang, S. Ma, J. Ji, and Z. Zhang. "Enyne cyclization methodology for the synthesis of bioactive lactones." Pure and Applied Chemistry 69, no. 3 (January 1, 1997): 553–58. http://dx.doi.org/10.1351/pac199769030553.
Повний текст джерелаRen, Qiao, Shaofa Sun, Jiayao Huang, Wenjun Li, Minghu Wu, Haibing Guo та Jian Wang. "An enantioselective cascade reaction between α,β-unsaturated aldehydes and malonic half-thioesters: a rapid access to chiral δ-lactones". Chem. Commun. 50, № 46 (2014): 6137–40. http://dx.doi.org/10.1039/c4cc01736f.
Повний текст джерелаДисертації з теми "Bioactive Lactones"
Filipa, P. da Cruz Ana. "C-branched carbohydrate lactones : Versatile intermediatesin the synthesis of branched bioactive." Thesis, University of Oxford, 2009. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.509913.
Повний текст джерелаParat, Sabrina. "Approche synthétique d’une delta-lactone alpha, beta-insaturée naturelle bioactive, la (–)-Callystatine A." Aix-Marseille 3, 2008. http://www.theses.fr/2008AIX30016.
Повний текст джерела(–)-Callystatin A is a bioactive marine natural product. Our interest in the total synthsis of Callystatin A was triggered by its inherent complexity and potent biological activities. This thesis starts with a bibliographic part devoted to the previously reported nine total syntheses of Callystatin A and an overview of the use of meso compounds desymmetrisation in total synthesis. Our convergent synthesis is based on the original synthesis of three main fragments. The Western one was obtained by an enantioselective desymmetrisation of a meso diol and a diastereoselective crotylation to form the polypropionate part. A [2+2] cycloaddition and a translactonization of a β-lactone led the δ-lactone unit of the Eastern moiety. The Central part was obtained in its racemic form. Our strategy was validated by the backbone synthesis precursors. A palladium-mediated coupling combined with an olefination reaction should afford the target
Rabiller, Christine. "Nouvelles voies de synthèse de lactones bioactives." Nancy 1, 1994. http://www.theses.fr/1994NAN10339.
Повний текст джерелаVlad-Cristea, Mirela Simona. "Production of bioactive lactobionic acid using a novel catalytic method." Thesis, Université Laval, 2007. http://www.theses.ulaval.ca/2007/24772/24772.pdf.
Повний текст джерелаTexte en anglais avec des résumés en anglais et en français. Bibliogr.: f. 93-94. Publié aussi en version électronique dans la Collection Mémoires et thèses électroniques.
Khay, Mom. "Molécules bioactives issues de la biodiversité cambodgienne : Vernonia cinerea Less. et Vernonia elliptica DC." Thesis, Aix-Marseille, 2015. http://www.theses.fr/2015AIXM5500.
Повний текст джерелаOur PhD work is in the process of valorization of the Cambodian plant biodiversity. The objectives focused on phytochemical and pharmacological studies of two Cambodian plants of the Vernonia genus: Vernonia cinerea and Vernonia elliptica.An analytical HPLC method was developed and validated to quantify the major compound 8α-tigloyloxyhirsutinolide 13-O-acetate (H1) of Vernonia cinerea. We found that the compound H1 content ranges from 0.08% to 0.17% in samples collected from cambodian regions. We thus evaluated the anti-proliferative activity in vitro of extracts of V. cinerea and H1 compound against two human cancer cell lines HT29 and HepG2. For HepG2 cell line, the compound H1 has a similar IC50 to the positive control 5FU, 4.3 ± 0.2 versus 5.4 ± 0.9 µM. The interesting results on V. cinerea encouraged us to study other species of Vernonia genus growing in Cambodia, Vernonia elliptica. The phytochemical study conducted on this plant led to isolate a lignan [(+)-syringaresinol] and two sesquiterpene lactones [(+)-8,13-diacetyl-piptocarphol and Glaucolide B]. These compounds were described in this plant for the first time. The in vitro study of the anti-proliferative activity of the extracts of V. elliptica shows that the dichloromethane extract obtained from aqueous extract is very active
Rasamiravaka, Tsiry. "Inhibition du mécanisme de quorum sensing et de la formation de biofilm chez Pseudomonas aerugionsa par des composés bioactifs de Dalbergia trichocarpa (Fabaceae)." Doctoral thesis, Universite Libre de Bruxelles, 2014. http://hdl.handle.net/2013/ULB-DIPOT:oai:dipot.ulb.ac.be:2013/209303.
Повний текст джерелаDoctorat en Sciences
info:eu-repo/semantics/nonPublished
Ho, Ching-Jen, and 何景仁. "Studies on the Bioactive Diterpene Lactones of Soft Coral Cespitularia taeniata." Thesis, 2006. http://ndltd.ncl.edu.tw/handle/53008000460280192972.
Повний текст джерела國立中山大學
海洋生物科技暨資源學系研究所
94
Four new diterpenoids, cespitulactones A-B (1-2), C4B1 (7) and E3A (8), were isolated from the soft coral Cespitularia taeniata collected in Taiwan, at a depth of 25 m, together with five known compounds, cespitularin F (3), 6-O-acetylcespitularin F (4), cespitularin D (5), flaccidoxide-13-acetate (6) and florlide A (9). Compound 1 possesses a novel structure with a bond cleavage between C-10 and C-11, and having a 14-membered lactone ring junction between C-10 and C-12. Compounds 2 and 8 have the verticillane skeleton, and compound 9 possesses the cespitularane skeleton. Their structures were elucidated on the basis of extensive spectroscopic analysis and chemical derivatization. The isolated compounds were also evaluated for cytotoxicity toward human cancer cell lines. Compound 1 exhibited significant cytotoxicity against human cervical epitheloid carcinoma (HeLa) and colon adenocarcinoma (DLD-1) cancer cells with IC50 of 3.69 and 9.98 μg/mL, respectively. Flaccidoxide-13-acetate (6) showed mild activity against human medulloblastoma (Daoy) and colon (WiDr) cancer cells at 16.9 and 13.8 μg/mL, respectively.
Jang, Jiun-yang, and 張俊揚. "Studies on Bioactive Sesquiterpene Lactones From Eupatorium hualienense, Ou, Chung & Peng." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/43852480410824303871.
Повний текст джерела國立中山大學
海洋資源學系研究所
92
Sesquiterpene lactones contain α,β-unsaturated-γ-lactone as a major structural feature, which in recent studies have been shown to be associ- ated with anti-tumor, cytotoxic, anti-microbial and phytotoxic activities. Previous researchers isolated sesquiterpene lactones from Eupatorium formosanum Hay. Thus, we studied Eupatorium hualienense, a unique speces in Taiwan that grows near the eastern coast. Five new sesquiter- pene lactones of the germacranolide type, eupahualins A-E (1-5) along with the known lactone, eupasimplicin B (6). Their structures were determined by 1D-NMR(1H-NMR,13C-NMR) and 2D-NMR(COSY、NOESY、HMQC、HMBC). Eupahualin A (1) exhibits an aldehyde at C-10 and an a,b-unsatura ted acyl group at C-8. Eupahualin B (2) also has an aldehyde at C-10. The Z-form of C-4, C-5 double bond in eupahualin B (2) is the main difference from the trans-form C-4, C-5 double bond in eupahualin A (1). The difference of eupahualin C (3) and eupahualin A (1) lies in structure of a ester group at C-8. The methyl at C-4'''' in eupahualin A (1) was changed into hydroxy methyl while the hydroxy methyl of eupahualin A (1) was changed to methyl in eupahualin C (3). Eupahualin D (4) shows exocyclic double bond at C-10, OH at C-1 and OAc at C-3. An carboxylic group (COOH) at C-10 in eupahualin E (5) is the only difference from which in eupahualin A (1).
Tseng, Pei-Yi, and 曾佩儀. "Studies on the Bioactive Constituents Hirsutinolide-type Sesquiterpene lactones and Flavonoids from Vernonia cinerea L." Thesis, 2012. http://ndltd.ncl.edu.tw/handle/68227782831849338527.
Повний текст джерела國立陽明大學
生命科學系暨基因體科學研究所
100
Vernonia cinerea Less. (Compositae) is an annual herb which is used medicinally for a variety of purposes, including reducing fever, and promoting digestion. Previous investigations have shown that crude extracts of V. cinerea possess analgesic, antipyretic, antimalarial, antimicrobial, and cytotoxic activities. By a series of chromatography and bioassay-directed fractionation, seventeen hirsutinolide-type sesquiterpene lactones containing six new compounds, vernolides-E~J (V1~V6), eleven known ones, 8α-(2-methylacryloyloxy)-1β,4β-epoxy-1α-methoxy-13-O-acetate- 10βH-germacra-5E,7(11)-dien-12,6-olide (V7), vernolide-B (V8) , hirsutinolide 13-O-acetate (V9), 8α-(2-methylacryloyloxy)-hirsutinolide-13-O- acetate (V10), 8α-tigloyloxyhirsutinolide-13-O-acetate (V11), vernolide-A (V12), 8β-(2-methylacryloloxy)-1-O-methyl-hirsutinolide (V13), 8α-(2-hydroxymethacryloyloxy)-hirsutinolide-13-O-acetate (V14), vernobockolide B (V15), vernolide-D (V16), and 8α-tiglogloxy-hirsutinolide (V17), together with six flavonoids, 6,7,8,4'-tetramethoxyflavone (V18), 5,6,7,4'-tetramethoxyflavone (V19), 6,7,8,3',4'-pentamethoxyflavone (V20), apigenin (V21) , luteolin-7-O-β-D-glucopyranoside (V22), and genkwanin (V23) were isolated from 95% EtOH extract of Taiwanese V. cinerea. Structural elucidation of these compounds were based on spectroscopic analyses (MS, UV, IR, and NMR techniques), as well as comparison with the reported data. Cytotoxic assay showed that compounds V3, V4, V7, V8, V11, and V16 possess cytotoxicity against four human tumor cell lines (HEp-2, WiDr, A549, Hep-G2, ED50: 17~39 μM). The inhibitory effects on nitric oxide (NO) produced by RAW264.7 macrophages in response to lipopolysaccharide (LPS) showed that V3, V4, V7, V8, and V11 (IC50: 0.2~1.9 μM) have potent anti-inflammatory activity. These results indicated that the bioactive isolates from V.cinerea could be served as lead compounds for the development of anti- inflammatory drug.
Carvalho, Maria João Menezes. "Caracterização e isolamento de compostos bioactivos do fungo Laurobasidium lauri (Madre de louro)." Master's thesis, 2010. http://hdl.handle.net/10400.13/626.
Повний текст джерелаUniversidade da Madeira
Книги з теми "Bioactive Lactones"
Doran, Robert. Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20544-1.
Повний текст джерелаDoran, Robert. Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones. Springer, 2015.
Знайти повний текст джерелаDoran, Robert. Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones. Springer, 2016.
Знайти повний текст джерелаAsymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of a Alpha-Aryl Ketones. Springer International Publishing AG, 2015.
Знайти повний текст джерелаЧастини книг з теми "Bioactive Lactones"
Ye, Xiang-Yang, and Pratik Devasthale. "Carboxylic Acids and Lactones as HMG-CoA Reductase Inhibitors." In Bioactive Carboxylic Compound Classes: Pharmaceuticals and Agrochemicals, 71–85. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2016. http://dx.doi.org/10.1002/9783527693931.ch6.
Повний текст джерелаChaturvedi, Devdutt, Parmesh Kumar Dwivedi, and Mamta Mishra. "Sesquiterpene Lactones: A Versatile Class of Structurally Diverse Natural Products and Their Semisynthetic Analogs as Potential Anticancer Agents." In Bioactive Natural Products, 321–48. Weinheim, Germany: Wiley-VCH Verlag GmbH & Co. KGaA, 2015. http://dx.doi.org/10.1002/9783527684403.ch11.
Повний текст джерелаDoran, Robert. "Introduction to the Total Synthesis of Lactone-Containing Natural Products Using ZrCl4". У Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones, 1–11. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20544-1_1.
Повний текст джерелаDoran, Robert. "Asymmetric Synthesis of Both Enantiomers of a δ-Lactone Analogue of Muricatacin". У Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones, 35–56. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20544-1_3.
Повний текст джерелаDoran, Robert. "Asymmetric Synthesis of the β-Methyl-Substituted Analogues of (+)-Tanikolide and (–)-Malyngolide". У Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones, 13–34. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20544-1_2.
Повний текст джерелаDoran, Robert. "Introduction to the Development of a Catalytic Asymmetric Synthesis of Tertiary α-Aryl Ketones". У Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones, 57–102. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20544-1_4.
Повний текст джерелаDoran, Robert. "A Stereoselective Switch: Enantiodivergent Approach to the Synthesis of Isoflavanones". У Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones, 103–25. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20544-1_5.
Повний текст джерелаDoran, Robert. "Asymmetric Synthesis of Tertiary α-Aryl Ketones by Decarboxylative Asymmetric Protonation". У Asymmetric Synthesis of Bioactive Lactones and the Development of a Catalytic Asymmetric Synthesis of α-Aryl Ketones, 127–75. Cham: Springer International Publishing, 2015. http://dx.doi.org/10.1007/978-3-319-20544-1_6.
Повний текст джерелаSülsen, Valeria P., Orlando G. Elso, Jimena Borgo, Laura C. Laurella, and Cesar A. N. Catalán. "Recent patents on sesquiterpene lactones with therapeutic application." In Bioactive Natural Products, 129–94. Elsevier, 2021. http://dx.doi.org/10.1016/b978-0-12-819487-4.00017-3.
Повний текст джерелаRajak, Naina, Kavita, Praveen Kumar, Shikha Singh, and Neha Garg. "Pharmacological, Therapeutic, and Immunomodulatory Role of Tinospora cordifolia." In Bioactive Phytochemicals from Himalayas: A Phytotherapeutic Approach, 89–104. BENTHAM SCIENCE PUBLISHERS, 2023. http://dx.doi.org/10.2174/9789815123289123010010.
Повний текст джерелаТези доповідей конференцій з теми "Bioactive Lactones"
Oliveira, Wanderley Pereira, Victor Oloruntoba Bankole, and Claudia Regina F. Souza. "Spray dried proliposomes of Rosmarinus officinalis polyphenols: a quality by design approach." In 21st International Drying Symposium. Valencia: Universitat Politècnica València, 2018. http://dx.doi.org/10.4995/ids2018.2018.7859.
Повний текст джерела