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Статті в журналах з теми "Triterpenoilds"
Wen, Cuiping, Zhong Zhang, Qianqian Shi, Xiaoshan Duan, Jiangtao Du, Cuiyun Wu, and Xingang Li. "Methyl Jasmonate- and Salicylic Acid-Induced Transcription Factor ZjWRKY18 Regulates Triterpenoid Accumulation and Salt Stress Tolerance in Jujube." International Journal of Molecular Sciences 24, no. 4 (February 15, 2023): 3899. http://dx.doi.org/10.3390/ijms24043899.
Повний текст джерелаSun, Caowen, Shengzuo Fang, and Xulan Shang. "Triterpenoids Biosynthesis Regulation for Leaf Coloring of Wheel Wingnut (Cyclocaryapaliurus)." Forests 12, no. 12 (December 9, 2021): 1733. http://dx.doi.org/10.3390/f12121733.
Повний текст джерелаKim, Jaecheol, Si Chang Yang, Ah Young Hwang, Hyunnho Cho, and Keum Taek Hwang. "Composition of Triterpenoids in Inonotus obliquus and Their Anti-Proliferative Activity on Cancer Cell Lines." Molecules 25, no. 18 (September 6, 2020): 4066. http://dx.doi.org/10.3390/molecules25184066.
Повний текст джерелаAliffia Dwi Rahma, Hanifah Ismayfatin, Yulianti Khasanah, Aditiya Rizky Putra Abimanyu, and Himyatul Hidayah. "Identification of Tannin, Triterpenoid, and Flavonoid Function Groups of Jamblang Plants (Syzygium cumini): A Systematic Literature Review." Eureka Herba Indonesia 5, no. 1 (December 15, 2023): 377–82. http://dx.doi.org/10.37275/ehi.v5i1.102.
Повний текст джерелаChang, Te-Sheng, Chien-Min Chiang, Tzi-Yuan Wang, Yu-Li Tsai, Yu-Wei Wu, Huei-Ju Ting, and Jiumn-Yih Wu. "One-Pot Bi-Enzymatic Cascade Synthesis of Novel Ganoderma Triterpenoid Saponins." Catalysts 11, no. 5 (April 30, 2021): 580. http://dx.doi.org/10.3390/catal11050580.
Повний текст джерелаLiu, Zengcai, Ruipeng Liu, Xinyu Tong, and Li Zou. "New Insights into Methyl Jasmonate Regulation of Triterpenoid Biosynthesis in Medicinal Fungal Species Sanghuangporusbaumii (Pilát) L.W. Zhou & Y.C. Dai." Journal of Fungi 8, no. 9 (August 23, 2022): 889. http://dx.doi.org/10.3390/jof8090889.
Повний текст джерелаNumonov, Sodik, Farukh Sharopov, Muhammad Nasimullah Qureshi, Latofat Gaforzoda, Isomiddin Gulmurodov, Qosimjon Khalilov, William N. Setzer, Maidina Habasi, and Haji Akber Aisa. "The Ursolic Acid-Rich Extract of Dracocephalum heterophyllum Benth. with Potent Antidiabetic and Cytotoxic Activities." Applied Sciences 10, no. 18 (September 18, 2020): 6505. http://dx.doi.org/10.3390/app10186505.
Повний текст джерелаSi, Longlong, Kun Meng, Zhenyu Tian, Jiaqi Sun, Huiqiang Li, Ziwei Zhang, Veronica Soloveva, et al. "Triterpenoids manipulate a broad range of virus-host fusion via wrapping the HR2 domain prevalent in viral envelopes." Science Advances 4, no. 11 (November 2018): eaau8408. http://dx.doi.org/10.1126/sciadv.aau8408.
Повний текст джерелаXu, Hou-Chao, Kun Hu, Xiao-Huo Shi, Jian-Wei Tang, Xiao-Nian Li, Han-Dong Sun, and Pema-Tenzin Puno. "Synergistic use of NMR computation and quantitative interproton distance analysis in the structural determination of neokadcoccitane A, a rearranged triterpenoid featuring an aromatic ring D from Kadsura coccinea." Organic Chemistry Frontiers 6, no. 10 (2019): 1619–26. http://dx.doi.org/10.1039/c9qo00281b.
Повний текст джерелаLiang, Xiaoqin, Peng Niu, Jun Li, Xinlan Guan, Yanjun Zhang, and Jian Li. "Discovery of Anti-Inflammatory Triterpenoid Glucosides from the Heritiera littoralis Dryand." Molecules 28, no. 4 (February 9, 2023): 1658. http://dx.doi.org/10.3390/molecules28041658.
Повний текст джерелаДисертації з теми "Triterpenoilds"
MacKinnon, Shawna. "Bioactive triterpenoids of the Rutales." Thesis, University of Ottawa (Canada), 1995. http://hdl.handle.net/10393/9678.
Повний текст джерелаChen, Ying. "Determination of triterpenoids in Psidium guajava." Thesis, University of Macau, 2012. http://umaclib3.umac.mo/record=b2590321.
Повний текст джерелаHayasida, Willian. "Investigação química das folhas e galhos de Guarea convergens (Meliaceae)." Universidade Federal do Amazonas, 2011. http://tede.ufam.edu.br/handle/tede/4417.
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The Meliaceae family comprises has about 50 genus and approximately 700 species, generally arboreus, occurring in regions Pantropical. The predominant metabolites in the family are triterpenoids with cycloartane, dammarane, tirucallane and apotirucallane skeleta, further degraded triterpenoids (limonoids and steroids). The genus Guarea possesses about 50 species however chemical studies are limited to ten species, whose reports are sesquiterpenes, diterpenes and triterpenes (cycloartane, tirucallane lanostane and apotirucallane), further limonoids. Although the occurrence of approximately 30 species of Guarea in Amazon have few relates on chemical studies, this acted as stimulus for our investigation about Guarea convergens T.D. occurrent in Amazon. Thus, leaves and branches collected in the Adolpho Ducke Forest Reserve were submitted to maceration to obtain the organic extracts. The chromatographic fractionning of the CH2Cl2 and MeOH leaves extracts led to the isolation of apotirucallane triterpenes: the 24R-acetoxy,25-hydroxy-3,7-dioxo-apotirucalla-14-en-21,23- olide (1) and the 7a,24R,25-trihydroxy-3-oxo-apotirucalla-14-en-21,23-olide (4), steroids: ergosta-5,24-diene-3 ,4 ,22S-triol (2) and ergosta-5,24-diene-3 ,7 -21-triol (3). The compounds 1, 3 and 4 are being reported for first time. The CH2Cl2 branches extract yielded a mixture of steroids (b-sitosterol and stigmasterol, 5) and the tirucallane triterpenes namely melianone (6) and melianodiol (7). This is the first chemical study effected with species G. convergens whose isolated and identified compound provide contributions to knowledge of the chemosystematic of the Rutales order.
A família Meliaceae possui cerca 50 gêneros e aproximadamente 700 espécies, geralmente arbóreas de ocorrência nas regiões Pantropicais. Os metabólitos predominantes na família são os triterpenos com esqueletos cicloartano, damarano, tirucalano e apotirucalano além dos triterpenos degradados (limonóides e esteróides). O gênero Guarea apresenta cerca de 50 espécies, no entanto os estudos químicos são limitados a dez espécies cujos relatos são de sesquiterpenos, diterpenos e triterpenos (cicloartano, tirucalano, lanostano e apotirucalano), além dos limonóides. Apesar da ocorrência de aproximadamente 30 espécies de Guarea no Amazonas, existem poucos relatos sobre os estudos químicos, o que nos estimulou a seleção de G. convergens ocorrente no Amazonas. Assim, folhas e galhos coletados na Reserva Florestal Adolfo Ducke foram submetidos à maceração para obtenção dos extratos orgânicos. O fracionamento cromatográfico dos extratos CH2Cl2 e MeOH de folhas resultou no isolamento dos triterpenos com esqueleto apotirucalano, 24R-acetoxi-25-hidroxi-3,7-oxoapotirucala- 14-en-21,23-olideo (1) e 7a,24R,25-trihidroxi-3-oxo-apotirucala-14-en-21,23- olideo (4) e dos esteróides do tipo ergostano, ergosta-5,24-dieno-3 ,4 ,22S-triol (2) e ergosta-5,24-dieno-3 ,7a,21-triol (3). As substâncias 1, 3 e 4 estão sendo relatadas pela primeira vez. Nos extratos dos galhos, além de -sitosterol (5) foram isolados os triterpenos do tipo tirucalano, melianona (6) e melianodiol (7). Esse é o primeiro estudo químico da espécie G. convergens cujos compostos isolados e identificados fornecem contribuições para o conhecimento da quimiossistemática da ordem Rutales.
Perkins, Gemma. "Studies on the preparation of pentacyclic triterpenoids." Thesis, University of Bristol, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294547.
Повний текст джерелаHarris, Katherine S. M. Massachusetts Institute of Technology. "Diversity of polycyclic triterpenoids in Rhodospirillum rubrum." Thesis, Massachusetts Institute of Technology, 2010. http://hdl.handle.net/1721.1/58195.
Повний текст джерелаCataloged from PDF version of thesis.
Includes bibliographical references (p. 22-24).
Sedimentary rocks of all ages abound with geostable lipids of microbial origin, but many biomarkers lack known organismal sources and clear environmental contexts. Here we used Rhodospirillum rubrum, a metabolically versatile, genetically tractable c-Proteobacterium, to explore the diversity of its non-polar terpenoids as a function of growth condition and growth phase. We analyzed the nonpolar fraction of lipids extracted from R. rubrum grown under aerobic, anaerobic, heterotrophic and phototrophic conditions and detected a variety of bicyclic, tricyclic, tetracyclic and pentacyclic triterpenoids, derived from the enzymatic cyclization of squalene and produced in amounts comparable to diploptene. Identified compounds included bicyclic polypodatetraenes, malabaricatriene, euphadiene, adianane, and fernene. Prior to this work, malabaricatriene was an "orphan" biomarker suspected to have a microbial origin, yet it lacked a proven source. We observed similar patterns of polycyclic terpenoids in other hopanoid-producing c-proteobacteria, including Zymomonas mobilis, Rhodopseudomonas palustris, and Rhodomicrobium vannielii. The presence and relative abundance of polycyclic triterpenoids in R. rubrum varied with the growth stage (exponential versus early stationary phase) and growth condition (photoheterotrophic versus photoautotrophic growth). Since R. rubrum's genome contains a single squalene-hopene cyclase gene, the array of triterpenoids produced by it and other c-proteobacteria likely evolves from this enzyme performing low-fidelity cyclization. The observed diversity of sedimentary triterpenoids might therefore result from a select few squalene-hopene cyclase enzymes operating with varying specificity under a range of physiological and environmental conditions, rather than reflecting a great diversity of squalene-hopene cyclases.
by Katherine Harris.
S.M.
Papineni, Sabitha. "New synthetic derivatives of triterpenoids in the treatment of cancer." [College Station, Tex. : Texas A&M University, 2008. http://hdl.handle.net/1969.1/ETD-TAMU-3252.
Повний текст джерелаSmith, Zena Elizabeth Florence. "Characterisation of A-ring contracted triterpenoids in oils and shales : evidence for an alternative transformation pathway in the diagenesis of higher plant triterpenoids." Thesis, University of Bristol, 1995. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.294960.
Повний текст джерелаClement, Jason Anderson. "Studies of Bioactive Natural Products and Mechanism-Based Bioassays." Diss., Virginia Tech, 2005. http://hdl.handle.net/10919/29879.
Повний текст джерелаPh. D.
Xie, Nan. "Extraction of triterpenoids saponins from Australian plant using supercritical fluids." Thesis, The University of Sydney, 2010. https://hdl.handle.net/2123/28852.
Повний текст джерелаReed, James. "Transient expression for engineering triterpenoid diversity in plants." Thesis, University of East Anglia, 2016. https://ueaeprints.uea.ac.uk/67059/.
Повний текст джерелаКниги з теми "Triterpenoilds"
Dev, Sukh. CRC handbook of terpenoids--Triterpenoids. Boca Raton, Fla: CRC Press, 1989.
Знайти повний текст джерела1923-, Dev Sukh, ed. CRC handbook of terpenoid. Triterpenoids. Boca Roton, Pl: CRC Press, 1989.
Знайти повний текст джерелаS, Levin V., and Stonik V. A, eds. Khimicheskai͡a︡ morfologii͡a︡: Triterpenovye glikozidy goloturiĭ (Holothurioidea, Echinodermata). Vladivostok: Dalʹnauka, 1994.
Знайти повний текст джерелаState University College at Buffalo. Dept. of Art Conservation. and MOLART (Project), eds. Molecular studies of fresh and aged triterpenoid varnishes. [Amsterdam: MOLART, 1999.
Знайти повний текст джерелаHuspa, Desi Harneti Putri. Triterpenoid yang bersifat antimalaria dari tumbuhan meliaceae Indonesia: Laporan akhir penelitian hibah penelitian strategi nasional. Bandung]: Departemen Pendidikan Nasional, Universitas Padjadjaran, Fakultas Matematika dan Ilmu Pengetahuan Alam, 2010.
Знайти повний текст джерелаDev, Sukh. Handbook of Terpenoids : Volume I: Triterpenoids. Taylor & Francis Group, 2018.
Знайти повний текст джерелаDev, Sukh. Handbook of Terpenoids : Volume I: Triterpenoids. Taylor & Francis Group, 2018.
Знайти повний текст джерелаQin, Hailin, and Dequan Yu. Diterpenoids, Triterpenoids, Sesterterpenoids, Tetraterpenoids, and Carotenoids. De Gruyter, 2021. http://dx.doi.org/10.1515/9783110634723.
Повний текст джерелаDev, Sukh. Handbook of Terpenoids : Volume I: Triterpenoids. Taylor & Francis Group, 2018.
Знайти повний текст джерелаYu, Dequan, Hailin Qin, and Chemical Industry Chemical Industry Press. Diterpenoids, Triterpenoids, Sesterterpenoids, Tetraterpenoids, and Carotenoids. de Gruyter GmbH, Walter, 2021.
Знайти повний текст джерелаЧастини книг з теми "Triterpenoilds"
Pengelly, Andrew. "Triterpenoids and saponins." In The constituents of medicinal plants, 95–111. 3rd ed. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0006.
Повний текст джерелаConnolly, J. D., and R. A. Hill. "Triterpenoids." In Dictionary of Terpenoids, 1119–415. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-4513-6_6.
Повний текст джерелаDwivedi, Ram Snehi. "Triterpenoids." In Alternative Sweet and Supersweet Principles, 323–88. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-33-6350-2_8.
Повний текст джерелаDeng, Jianjun, Jianbo Xiao, and Haixia Yang. "Dietary Triterpenoids." In Handbook of Dietary Phytochemicals, 1–53. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1745-3_15-1.
Повний текст джерелаDeng, Jianjun, Jianbo Xiao, and Haixia Yang. "Dietary Triterpenoids." In Handbook of Dietary Phytochemicals, 423–75. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-4148-3_15.
Повний текст джерелаMahato, S. B., and S. Garai. "Triterpenoid Saponins." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products, 1–196. Vienna: Springer Vienna, 1998. http://dx.doi.org/10.1007/978-3-7091-6496-9_1.
Повний текст джерелаGütz, P. G. "Triterpenoids in Epicuticular Waxes." In Biological Role of Plant Lipids, 325–28. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-1303-8_75.
Повний текст джерелаCheng, Yongxian, and Dapeng Qin. "Classification of Diverse Triterpenoids." In Novel Plant Natural Product Skeletons, 49–63. Singapore: Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-7329-3_5.
Повний текст джерелаSahoo, Biswa Mohan, Bimal Krishna Banik, and Abhishek Tiwari. "Synthesis and Medicinal Uses of Triterpenoids." In Terpenoids, 285–329. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003008682-9.
Повний текст джерелаSkrukrud, C. L., S. E. Taylor, D. R. Hawkins, and M. Calvin. "Triterpenoid Biosynthesis in Euphorbia Lathyris." In The Metabolism, Structure, and Function of Plant Lipids, 115–18. Boston, MA: Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4684-5263-1_18.
Повний текст джерелаТези доповідей конференцій з теми "Triterpenoilds"
Kinaci, Emre, John Chea, Kirti Yenkie, and Kylie Howard. "Converting Birch Bark Extracts into Bio-based Thermosets." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/wcih1760.
Повний текст джерелаFaraoni, María, María Castro, and Ana Murray. "Lupane Triterpenoids, Selective Butyrylcholinesterase Inhibitors." In The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-b035.
Повний текст джерелаLuchnikova, N. A., K. M. Ivanova, E. V. Tarasova, V. V. Grishko, and I. B. Ivshina. "ACTINOBACTERIAL TRANSFORMATION OF OLEANANE TRITERPENOIDS." In Фундаментальные и прикладные аспекты биоинформатики, биотехнологии и недропользования. Пермский государственный национальный исследовательский университет, 2021. http://dx.doi.org/10.17072/fpabbn-2021-5-7.
Повний текст джерелаValdes, Alberto, Alejandro Cifuentes, Jose David Sanchez-Martinez, Miguel Herrero, Rocio Gallego, and Zully Suarez-Montenegro. "Foodomics study of the neuroprotective potential of natural products." In 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/bdyo8801.
Повний текст джерелаGao, Jie, Kenza Mamouni, Georgios Kallifatidis, Siva Panda, Muthusamy Thangaraju, and Bal L. Lokeshwar. "Abstract 5069: Breast cancer prevention by triterpenoids from allspice." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.sabcs18-5069.
Повний текст джерелаGao, Jie, Kenza Mamouni, Georgios Kallifatidis, Siva Panda, Muthusamy Thangaraju, and Bal L. Lokeshwar. "Abstract 5069: Breast cancer prevention by triterpenoids from allspice." In Proceedings: AACR Annual Meeting 2019; March 29-April 3, 2019; Atlanta, GA. American Association for Cancer Research, 2019. http://dx.doi.org/10.1158/1538-7445.am2019-5069.
Повний текст джерелаKazakova, O. B., and I. E. Smirnova. "Antiviral activity of lupane and oleanane A-seco-triterpenoids." In ACTUAL PROBLEMS OF ORGANIC CHEMISTRY AND BIOTECHNOLOGY (OCBT2020): Proceedings of the International Scientific Conference. AIP Publishing, 2022. http://dx.doi.org/10.1063/5.0069236.
Повний текст джерелаKonysheva, Anastasia V., and Victoria V. Grishko. "SAR analysis and bioactive potential of C(3) alkylated triterpenoids." In PROCEEDINGS OF INTERNATIONAL CONFERENCE ON RECENT TRENDS IN MECHANICAL AND MATERIALS ENGINEERING: ICRTMME 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0018484.
Повний текст джерелаRodriguez-Lopez, Fidel, Edgar G. Rodríguez-García, Hugo A. García-Gutiérrez та Rocío Gámez-Montaño. "Plant-Derived Triterpenoid Functionalization: Synthesis of α-Acyloxycarboxamides". У ECSOC 2023. Basel Switzerland: MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16061.
Повний текст джерелаDzubak, Petr, Renata Burianova, Martina Michalova, Barbora Liskova, Milan Urban, Jan Sarek, Adela Galandakova, Jitka Ulrichova, and Marian Hajduch. "Abstract 2077: Carbonate prodrugs derived from triterpenoids with high cytotoxic activity." 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.am2016-2077.
Повний текст джерелаЗвіти організацій з теми "Triterpenoilds"
Sporn, Michael B. Triterpenoids and Prevention of Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, October 2001. http://dx.doi.org/10.21236/ada405249.
Повний текст джерелаSporn, Michael B. Triterpenoids and Prevention of Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, October 1999. http://dx.doi.org/10.21236/ada384364.
Повний текст джерелаHawkins, D. R. Triterpenoid biosynthesis in Euphorbia lathyris latex. Office of Scientific and Technical Information (OSTI), November 1987. http://dx.doi.org/10.2172/5625757.
Повний текст джерелаHyer, Marc L. Modulating TRAIL-Mediated Apoptosis in Prostate Cancer Using Synthetic Triterpenoids. Fort Belvoir, VA: Defense Technical Information Center, January 2005. http://dx.doi.org/10.21236/ada434105.
Повний текст джерелаSchaffer, Arthur A., and Jocelyn Rose. Understanding Cuticle Development in Tomato through the Study of Novel Germplasm with Malformed Cuticles. United States Department of Agriculture, June 2013. http://dx.doi.org/10.32747/2013.7593401.bard.
Повний текст джерела