Literatura académica sobre el tema "Triterpenoilds"
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Artículos de revistas sobre el tema "Triterpenoilds"
Wen, Cuiping, Zhong Zhang, Qianqian Shi, Xiaoshan Duan, Jiangtao Du, Cuiyun Wu y 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, n.º 4 (15 de febrero de 2023): 3899. http://dx.doi.org/10.3390/ijms24043899.
Texto completoSun, Caowen, Shengzuo Fang y Xulan Shang. "Triterpenoids Biosynthesis Regulation for Leaf Coloring of Wheel Wingnut (Cyclocaryapaliurus)". Forests 12, n.º 12 (9 de diciembre de 2021): 1733. http://dx.doi.org/10.3390/f12121733.
Texto completoKim, Jaecheol, Si Chang Yang, Ah Young Hwang, Hyunnho Cho y Keum Taek Hwang. "Composition of Triterpenoids in Inonotus obliquus and Their Anti-Proliferative Activity on Cancer Cell Lines". Molecules 25, n.º 18 (6 de septiembre de 2020): 4066. http://dx.doi.org/10.3390/molecules25184066.
Texto completoAliffia Dwi Rahma, Hanifah Ismayfatin, Yulianti Khasanah, Aditiya Rizky Putra Abimanyu y Himyatul Hidayah. "Identification of Tannin, Triterpenoid, and Flavonoid Function Groups of Jamblang Plants (Syzygium cumini): A Systematic Literature Review". Eureka Herba Indonesia 5, n.º 1 (15 de diciembre de 2023): 377–82. http://dx.doi.org/10.37275/ehi.v5i1.102.
Texto completoChang, Te-Sheng, Chien-Min Chiang, Tzi-Yuan Wang, Yu-Li Tsai, Yu-Wei Wu, Huei-Ju Ting y Jiumn-Yih Wu. "One-Pot Bi-Enzymatic Cascade Synthesis of Novel Ganoderma Triterpenoid Saponins". Catalysts 11, n.º 5 (30 de abril de 2021): 580. http://dx.doi.org/10.3390/catal11050580.
Texto completoLiu, Zengcai, Ruipeng Liu, Xinyu Tong y 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, n.º 9 (23 de agosto de 2022): 889. http://dx.doi.org/10.3390/jof8090889.
Texto completoNumonov, Sodik, Farukh Sharopov, Muhammad Nasimullah Qureshi, Latofat Gaforzoda, Isomiddin Gulmurodov, Qosimjon Khalilov, William N. Setzer, Maidina Habasi y Haji Akber Aisa. "The Ursolic Acid-Rich Extract of Dracocephalum heterophyllum Benth. with Potent Antidiabetic and Cytotoxic Activities". Applied Sciences 10, n.º 18 (18 de septiembre de 2020): 6505. http://dx.doi.org/10.3390/app10186505.
Texto completoSi, 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, n.º 11 (noviembre de 2018): eaau8408. http://dx.doi.org/10.1126/sciadv.aau8408.
Texto completoXu, Hou-Chao, Kun Hu, Xiao-Huo Shi, Jian-Wei Tang, Xiao-Nian Li, Han-Dong Sun y 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, n.º 10 (2019): 1619–26. http://dx.doi.org/10.1039/c9qo00281b.
Texto completoLiang, Xiaoqin, Peng Niu, Jun Li, Xinlan Guan, Yanjun Zhang y Jian Li. "Discovery of Anti-Inflammatory Triterpenoid Glucosides from the Heritiera littoralis Dryand". Molecules 28, n.º 4 (9 de febrero de 2023): 1658. http://dx.doi.org/10.3390/molecules28041658.
Texto completoTesis sobre el tema "Triterpenoilds"
MacKinnon, Shawna. "Bioactive triterpenoids of the Rutales". Thesis, University of Ottawa (Canada), 1995. http://hdl.handle.net/10393/9678.
Texto completoChen, Ying. "Determination of triterpenoids in Psidium guajava". Thesis, University of Macau, 2012. http://umaclib3.umac.mo/record=b2590321.
Texto completoHayasida, 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.
Texto completoHarris, 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.
Texto completoCataloged 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.
Texto completoSmith, 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.
Texto completoClement, Jason Anderson. "Studies of Bioactive Natural Products and Mechanism-Based Bioassays". Diss., Virginia Tech, 2005. http://hdl.handle.net/10919/29879.
Texto completoPh. 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.
Texto completoReed, James. "Transient expression for engineering triterpenoid diversity in plants". Thesis, University of East Anglia, 2016. https://ueaeprints.uea.ac.uk/67059/.
Texto completoLibros sobre el tema "Triterpenoilds"
Dev, Sukh. CRC handbook of terpenoids--Triterpenoids. Boca Raton, Fla: CRC Press, 1989.
Buscar texto completo1923-, Dev Sukh, ed. CRC handbook of terpenoid. Triterpenoids. Boca Roton, Pl: CRC Press, 1989.
Buscar texto completoS, Levin V. y Stonik V. A, eds. Khimicheskai͡a︡ morfologii͡a︡: Triterpenovye glikozidy goloturiĭ (Holothurioidea, Echinodermata). Vladivostok: Dalʹnauka, 1994.
Buscar texto completoState University College at Buffalo. Dept. of Art Conservation. y MOLART (Project), eds. Molecular studies of fresh and aged triterpenoid varnishes. [Amsterdam: MOLART, 1999.
Buscar texto completoHuspa, 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.
Buscar texto completoDev, Sukh. Handbook of Terpenoids : Volume I: Triterpenoids. Taylor & Francis Group, 2018.
Buscar texto completoDev, Sukh. Handbook of Terpenoids : Volume I: Triterpenoids. Taylor & Francis Group, 2018.
Buscar texto completoQin, Hailin y Dequan Yu. Diterpenoids, Triterpenoids, Sesterterpenoids, Tetraterpenoids, and Carotenoids. De Gruyter, 2021. http://dx.doi.org/10.1515/9783110634723.
Texto completoDev, Sukh. Handbook of Terpenoids : Volume I: Triterpenoids. Taylor & Francis Group, 2018.
Buscar texto completoYu, Dequan, Hailin Qin y Chemical Industry Chemical Industry Press. Diterpenoids, Triterpenoids, Sesterterpenoids, Tetraterpenoids, and Carotenoids. de Gruyter GmbH, Walter, 2021.
Buscar texto completoCapítulos de libros sobre el tema "Triterpenoilds"
Pengelly, Andrew. "Triterpenoids and saponins." En The constituents of medicinal plants, 95–111. 3a ed. Wallingford: CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0006.
Texto completoConnolly, J. D. y R. A. Hill. "Triterpenoids". En Dictionary of Terpenoids, 1119–415. Boston, MA: Springer US, 1991. http://dx.doi.org/10.1007/978-1-4899-4513-6_6.
Texto completoDwivedi, Ram Snehi. "Triterpenoids". En Alternative Sweet and Supersweet Principles, 323–88. Singapore: Springer Nature Singapore, 2022. http://dx.doi.org/10.1007/978-981-33-6350-2_8.
Texto completoDeng, Jianjun, Jianbo Xiao y Haixia Yang. "Dietary Triterpenoids". En Handbook of Dietary Phytochemicals, 1–53. Singapore: Springer Singapore, 2019. http://dx.doi.org/10.1007/978-981-13-1745-3_15-1.
Texto completoDeng, Jianjun, Jianbo Xiao y Haixia Yang. "Dietary Triterpenoids". En Handbook of Dietary Phytochemicals, 423–75. Singapore: Springer Singapore, 2021. http://dx.doi.org/10.1007/978-981-15-4148-3_15.
Texto completoMahato, S. B. y S. Garai. "Triterpenoid Saponins". En 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.
Texto completoGütz, P. G. "Triterpenoids in Epicuticular Waxes". En Biological Role of Plant Lipids, 325–28. Boston, MA: Springer US, 1989. http://dx.doi.org/10.1007/978-1-4684-1303-8_75.
Texto completoCheng, Yongxian y Dapeng Qin. "Classification of Diverse Triterpenoids". En Novel Plant Natural Product Skeletons, 49–63. Singapore: Springer Nature Singapore, 2024. http://dx.doi.org/10.1007/978-981-99-7329-3_5.
Texto completoSahoo, Biswa Mohan, Bimal Krishna Banik y Abhishek Tiwari. "Synthesis and Medicinal Uses of Triterpenoids". En Terpenoids, 285–329. Boca Raton: CRC Press, 2022. http://dx.doi.org/10.1201/9781003008682-9.
Texto completoSkrukrud, C. L., S. E. Taylor, D. R. Hawkins y M. Calvin. "Triterpenoid Biosynthesis in Euphorbia Lathyris". En 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.
Texto completoActas de conferencias sobre el tema "Triterpenoilds"
Kinaci, Emre, John Chea, Kirti Yenkie y Kylie Howard. "Converting Birch Bark Extracts into Bio-based Thermosets". En 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/wcih1760.
Texto completoFaraoni, María, María Castro y Ana Murray. "Lupane Triterpenoids, Selective Butyrylcholinesterase Inhibitors". En The 18th International Electronic Conference on Synthetic Organic Chemistry. Basel, Switzerland: MDPI, 2014. http://dx.doi.org/10.3390/ecsoc-18-b035.
Texto completoLuchnikova, N. A., K. M. Ivanova, E. V. Tarasova, V. V. Grishko y I. B. Ivshina. "ACTINOBACTERIAL TRANSFORMATION OF OLEANANE TRITERPENOIDS". En Фундаментальные и прикладные аспекты биоинформатики, биотехнологии и недропользования. Пермский государственный национальный исследовательский университет, 2021. http://dx.doi.org/10.17072/fpabbn-2021-5-7.
Texto completoValdes, Alberto, Alejandro Cifuentes, Jose David Sanchez-Martinez, Miguel Herrero, Rocio Gallego y Zully Suarez-Montenegro. "Foodomics study of the neuroprotective potential of natural products". En 2022 AOCS Annual Meeting & Expo. American Oil Chemists' Society (AOCS), 2022. http://dx.doi.org/10.21748/bdyo8801.
Texto completoGao, Jie, Kenza Mamouni, Georgios Kallifatidis, Siva Panda, Muthusamy Thangaraju y Bal L. Lokeshwar. "Abstract 5069: Breast cancer prevention by triterpenoids from allspice". En 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.
Texto completoGao, Jie, Kenza Mamouni, Georgios Kallifatidis, Siva Panda, Muthusamy Thangaraju y Bal L. Lokeshwar. "Abstract 5069: Breast cancer prevention by triterpenoids from allspice". En 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.
Texto completoKazakova, O. B. y I. E. Smirnova. "Antiviral activity of lupane and oleanane A-seco-triterpenoids". En 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.
Texto completoKonysheva, Anastasia V. y Victoria V. Grishko. "SAR analysis and bioactive potential of C(3) alkylated triterpenoids". En 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.
Texto completoRodriguez-Lopez, Fidel, Edgar G. Rodríguez-García, Hugo A. García-Gutiérrez y Rocío Gámez-Montaño. "Plant-Derived Triterpenoid Functionalization: Synthesis of α-Acyloxycarboxamides". En ECSOC 2023. Basel Switzerland: MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16061.
Texto completoDzubak, Petr, Renata Burianova, Martina Michalova, Barbora Liskova, Milan Urban, Jan Sarek, Adela Galandakova, Jitka Ulrichova y Marian Hajduch. "Abstract 2077: Carbonate prodrugs derived from triterpenoids with high cytotoxic activity". En 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.
Texto completoInformes sobre el tema "Triterpenoilds"
Sporn, Michael B. Triterpenoids and Prevention of Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, octubre de 2001. http://dx.doi.org/10.21236/ada405249.
Texto completoSporn, Michael B. Triterpenoids and Prevention of Prostate Cancer. Fort Belvoir, VA: Defense Technical Information Center, octubre de 1999. http://dx.doi.org/10.21236/ada384364.
Texto completoHawkins, D. R. Triterpenoid biosynthesis in Euphorbia lathyris latex. Office of Scientific and Technical Information (OSTI), noviembre de 1987. http://dx.doi.org/10.2172/5625757.
Texto completoHyer, Marc L. Modulating TRAIL-Mediated Apoptosis in Prostate Cancer Using Synthetic Triterpenoids. Fort Belvoir, VA: Defense Technical Information Center, enero de 2005. http://dx.doi.org/10.21236/ada434105.
Texto completoSchaffer, Arthur A. y Jocelyn Rose. Understanding Cuticle Development in Tomato through the Study of Novel Germplasm with Malformed Cuticles. United States Department of Agriculture, junio de 2013. http://dx.doi.org/10.32747/2013.7593401.bard.
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