Relevant bibliographies by topics / Triterpenoid

Contents

  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Triterpenoid'

Author: Grafiati
Published: 4 June 2021
Last updated: 26 July 2025

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Journal articles on the topic "Triterpenoid"

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Song, Lijun, Li Zhang, Long Xu, et al. "Optimized Extraction of Total Triterpenoids from Jujube (Ziziphus jujuba Mill.) and Comprehensive Analysis of Triterpenic Acids in Different Cultivars." Plants 9, no. 4 (2020): 412. http://dx.doi.org/10.3390/plants9040412.

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Triterpenoid compounds are one of the main functional components in jujube fruit. In this study, the optimal process for ultrasound-assisted extraction (UAE) of total triterpenoids from jujube fruit was determined using response surface methodology (RSM). The optimal conditions were as follows: temperature of 55.14 °C, ethanol concentration of 86.57%, time of 34.41 min, and liquid-to-solid ratio of 39.33 mL/g. The triterpenoid yield was 19.21 ± 0.25 mg/g under optimal conditions. The triterpenoid profiles and antioxidant activity were further analyzed. Betulinic acid, alphitolic acid, maslinic
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Numonov, Sodik, Farukh Sharopov, Muhammad Nasimullah Qureshi, et al. "The Ursolic Acid-Rich Extract of Dracocephalum heterophyllum Benth. with Potent Antidiabetic and Cytotoxic Activities." Applied Sciences 10, no. 18 (2020): 6505. http://dx.doi.org/10.3390/app10186505.

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Pentacyclic triterpenoids are one of the main functional components in Dracocephalum heterophyllum. In this study the optimal process, the fairly simple and accessible extraction and purification of triterpenoids of D. heterophyllum, was developed by a remaceration method. Remaceration is characterized by minimal loss of biologically active compounds on diffusion, which contributes to the largest depletion of raw materials. The triterpenoid yield was 2.4% under optimal conditions which was enhanced to 98.03% after purification. The triterpenoid profiles and their anticancer and antidiabetic ac
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Wen, Cuiping, Zhong Zhang, Qianqian Shi, et al. "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 (2023): 3899. http://dx.doi.org/10.3390/ijms24043899.

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Triterpenoids are important, pharmacologically active substances in jujube (Ziziphus jujuba Mill.), and play an important role in the plant’s resistance to abiotic stress. However, regulation of their biosynthesis, and the underlying mechanism of their balance with stress resistance, remain poorly understood. In this study, we screened and functionally characterized the ZjWRKY18 transcription factor, which is associated with triterpenoid accumulation. The transcription factor is induced by methyl jasmonate and salicylic acid, and its activity was observed by gene overexpression and silencing e
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Fang, Zhu-Jun, Sheng-Nan Shen, Jia-Min Wang, et al. "Triterpenoids from Cyclocarya paliurus that Enhance Glucose Uptake in 3T3-L1 Adipocytes." Molecules 24, no. 1 (2019): 187. http://dx.doi.org/10.3390/molecules24010187.

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Four previously undescribed compounds, including three rarely occurring seco-dammarane triterpenoid glycosides and a pentacyclic triterpenic acid, were isolated from a 70% ethanol extract of the leaves of Cyclocarya paliurus (Juglandaceae), along with eleven known triterpenoids. Their structures were determined by spectroscopic techniques, including 2D NMR and HRESIMS, as well as chemical methods. Among them, several triterpenoids enhanced insulin stimulated glucose uptake in both 3T3-L1 adipocytes and C2C12 myotubes. Furthermore, compound 1 dose-dependently increased glucose uptake through ac
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Chang, Te-Sheng, Chien-Min Chiang, Tzi-Yuan Wang, et al. "One-Pot Bi-Enzymatic Cascade Synthesis of Novel Ganoderma Triterpenoid Saponins." Catalysts 11, no. 5 (2021): 580. http://dx.doi.org/10.3390/catal11050580.

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Ganoderma lucidum is a medicinal fungus whose numerous triterpenoids are its main bioactive constituents. Although hundreds of Ganoderma triterpenoids have been identified, Ganoderma triterpenoid glycosides, also named triterpenoid saponins, have been rarely found. Ganoderic acid A (GAA), a major Ganoderma triterpenoid, was synthetically cascaded to form GAA-15-O-β-glucopyranoside (GAA-15-G) by glycosyltransferase (BtGT_16345) from Bacillus thuringiensis GA A07 and subsequently biotransformed into a series of GAA glucosides by cyclodextrin glucanotransferase (Toruzyme® 3.0 L) from Thermoanaero
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Liu, 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 (2022): 889. http://dx.doi.org/10.3390/jof8090889.

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Triterpenoids are secondary metabolites produced by the fungus Sanghuangporus baumii that have important pharmacological activities. However, the yield of triterpenoids is low and cannot meet market demand. Here, we treated S. baumii with several concentrations of MeJA (methyl jasmonate) and found that the total triterpenoid content was highest (23.31 mg/g) when the MeJA concentration was 250 μmol/L. qRT-PCR was used to quantify the transcription of five key genes involved in triterpenoid biosynthesis. The results showed that the relative transcription of most genes increased with increasing M
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Supratman, Unang, Fajar Fauzi Abdullah, Kindi Farabi, Nurlelasari Nurlelasari, Khalijah Awang, and Mohamad Azlan Nafiah. "Triterpenoids From Swietenia mahagoni L Jacq. and Their Cytotoxic Activity against MCF-7 Breast Cancer and CV-1 Normal Kidney Cell Lines." Molekul 19, no. 2 (2024): 227. http://dx.doi.org/10.20884/1.jm.2024.19.2.9358.

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ABSTRACT. Triterpenoid is a group of natural products with various remarkable activities, including cytotoxic. One of the sources for this type of compounds is Swietenia genus belong to Meliaceae family. This genus known to contains various secondary metabolites including limonoids, flavonoids, and triterpenoids. Especially for triterpenoid, there is limited report on isolation as well as biological activity from Swietenia genus, such as Swietenia mahagoni. In this research, three triterpenoid compounds have been successively isolated and identified from n-hexane extract, namely, (-)-leucophyl
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Woźniak, Łukasz, Anna Szakiel, Agnieszka Głowacka, Elżbieta Rozpara, Krystian Marszałek, and Sylwia Skąpska. "Triterpenoids of Three Apple Cultivars—Biosynthesis, Antioxidative and Anti-Inflammatory Properties, and Fate during Processing." Molecules 28, no. 6 (2023): 2584. http://dx.doi.org/10.3390/molecules28062584.

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Triterpenoids are a group of secondary plant metabolites, with a remarkable pharmacological potential, occurring in the cuticular waxes of the aerial parts of plants. The aim of this study was to analyze triterpenoid variability in the fruits and leaves of three apple cultivars during the growing season and gain new insights into their health-promoting properties and fate during juice and purée production. The identification and quantification of the compounds of interest were conducted using gas chromatography coupled with mass spectrometry. The waxes of both matrices contained similar analyt
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Sun, Caowen, Shengzuo Fang, and Xulan Shang. "Triterpenoids Biosynthesis Regulation for Leaf Coloring of Wheel Wingnut (Cyclocaryapaliurus)." Forests 12, no. 12 (2021): 1733. http://dx.doi.org/10.3390/f12121733.

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Cyclocaryapaliurus leaves are rich in triterpenoids with positive results in the treatment of diabetes, antioxidation, and scavenging free radicals. C. paliurus red leaves have been found to contain higher flavonoids including anthocyanin, however, the triterpenoids accumulation pattern is still unclear. For the purpose of researching the triterpenoid accumulating mechanism during red new leaf development, transcriptome and metabolome analysis was conducted during C. paliurus the red leaf development process. The results uncovered that most triterpenoid ingredients were found to accumulate dur
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Kim, 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 (2020): 4066. http://dx.doi.org/10.3390/molecules25184066.

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The objective of this study was to determine the composition of triterpenoids in the extracts from the inner and outer parts of Inonotus obliquus and to evaluate their anti-proliferative activity against cancer cell lines (HT-29, AGS, MCF-7, and PC3). Inner and outer parts of I. obliquus were extracted with 80% methanol for 24 h. The extract was fractionated by Diaion HP-20 resin to obtain the triterpenoid fraction. Composition of triterpenoids in the fraction was analyzed by HPLC and LC-ESI-MS. Anti-proliferative activity was evaluated by MTT assay against cancer cell lines. Inotodiol and tra
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Dissertations / Theses on the topic "Triterpenoid"

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Roy, Animesh. "Studies on the oxidative reactions of triterpenoid." Thesis, University of North Bengal, 1991. http://hdl.handle.net/123456789/815.

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Reed, James. "Transient expression for engineering triterpenoid diversity in plants." Thesis, University of East Anglia, 2016. https://ueaeprints.uea.ac.uk/67059/.

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The triterpenes are one of the largest and most structurally diverse classes of plant specialised metabolites, with important commercial, agronomical and medical potential. However the structural complexity and low abundance of these compounds in nature presents significant challenges for exploiting this diversity. In recent years, advances in our understanding of triterpene biosynthesis in various plant species have greatly facilitated the ability to produce these compounds in other hosts. Plant-based host systems hold great promise because they may provide substrates, cofactors and subcellul
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Cheng, Zhengqi. "Screening triterpenoid compounds with potential to treat retinal diseases." Thesis, University of Sydney, 2020. https://hdl.handle.net/2123/22971.

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Retinal degeneration is a leading cause of impaired vision or even blindness all around the world, unfortunately, most retinal diseases are irreversible, and there is no ideal treatment to cure the diseases, therefore it is important to protect retina from disease progression. In the recent years, natural compounds have shown great pharmacological potentials. Pentacyclic triterpenoids (PTs) are a group of compounds widely existing in nature, they have shown diverse pharmacological effects in vitro and in vivo. In this thesis, we evaluated the antioxidative effect of betulin, betulinic acid and
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Arabzadeh, Seyedali M. "Investigation of the antiviral activity of triterpenoid compounds against retroviruses." Thesis, University of Glasgow, 1996. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.296982.

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Yu, Marcia Mei Lin. "In situ analysis of lateral triterpenoid distribution in plant cuticular waxes using Raman microspectroscopy and non-linear optical imaging." Thesis, University of British Columbia, 2008. http://hdl.handle.net/2429/2657.

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The above-ground organs of plants are covered by a protective cuticle, an extracellular membrane performing important physiological and ecological functions, that consists of cuticular wax and the fatty acid-derived polymer cutin. Until the past decade, the cuticular wax was thought to be a homogenous mixture. Hence, previous interpretations relating the chemical composition and biological functions of the cuticular wax were based on the total wax composition, an average taken over the entire area and depth of the cuticle. However, recent selective sampling experiments showed a heterogeneity o
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Li, Diana L. F. "The evaluation of 4-methylcamphor as an intermediate in Triterpenoid synthesis." Thesis, University of British Columbia, 1989. http://hdl.handle.net/2429/27577.

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A new synthetic route to (-)-4-methylcamphor 43 is described which involved initial conversion of (+)-camphor 1 to (-)-2-methylenebornane 41. Acid-catalyzed rearrangement of 41 provided ( +)-4-methylisobornyl acetate 40 which was reduced to (+)-4-methylisoborneol 42. Finally, oxidation of 42. produced (-)-4-methylcamphor 43. The optical purity of compounds 40 and 43 was determined by a chiral lanthanide shift reagent, [Eu[hfc)₃] 45 while the optical purity of 42 was determined by the Anderson-Shapiro reagent 48. Based on a mechanistic rationale, a different approach to the synthesis of optica
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Xu, Yang. "Proteomic and biochemical characterization of the anti-cancer mechanism of tubeimoside-1 extracted from the Chinese herbal medicine "Tu bei mu"." Click to view the E-thesis via HKUTO, 2010. http://sunzi.lib.hku.hk/hkuto/record/B44135968.

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Reynolds, Derrick James. "Genetic Dissection of Triterpenoid Saponin Production in Chenopodium quinoa Using Microarray Analysis." Diss., CLICK HERE for online access, 2009. http://contentdm.lib.byu.edu/ETD/image/etd3309.pdf.

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Barker, Emily Clegg. "The Isolation and Biological Evaluation of Anti-inflammatory and Chemopreventive Triterpenoid Natural Products." Case Western Reserve University School of Graduate Studies / OhioLINK, 2015. http://rave.ohiolink.edu/etdc/view?acc_num=case1428065668.

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Xu, Yang, and 徐阳. "Proteomic and biochemical characterization of the anti-cancer mechanism of tubeimoside-1 extracted from the Chinese herbalmedicine "Tu bei mu"." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 2010. http://hub.hku.hk/bib/B44135968.

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Books on the topic "Triterpenoid"

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State University College at Buffalo. Dept. of Art Conservation. and MOLART (Project), eds. Molecular studies of fresh and aged triterpenoid varnishes. MOLART, 1999.

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S, Levin V., and Stonik V. A, eds. Khimicheskai͡a︡ morfologii͡a︡: Triterpenovye glikozidy goloturiĭ (Holothurioidea, Echinodermata). Dalʹnauka, 1994.

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Huspa, Desi Harneti Putri. Triterpenoid yang bersifat antimalaria dari tumbuhan meliaceae Indonesia: Laporan akhir penelitian hibah penelitian strategi nasional. Departemen Pendidikan Nasional, Universitas Padjadjaran, Fakultas Matematika dan Ilmu Pengetahuan Alam, 2010.

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Dev, Sukh. CRC handbook of terpenoids--Triterpenoids. CRC Press, 1989.

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1923-, Dev Sukh, ed. CRC handbook of terpenoid. Triterpenoids. CRC Press, 1989.

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Banupriya, R. Triterpenoid Treatment for Hepatocellular Carcinoma. Quadry, Fatima, 2023.

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Spectroscopic Data of Saponins: The Triterpenoid Glycosides. CRC Press LLC, 2000.

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Spectroscopic Data of Saponins: The Triterpenoid Glycosides. CRC Press LLC, 2000.

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Spectroscopic Data of Saponins: The Triterpenoid Glycosides. CRC Press LLC, 2000.

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Ahmad, Viqar Uddin, and Anwer Basha. Spectroscopic Data of Saponins: The Triterpenoid Glycosides, 3-Volume Set. Taylor & Francis Group, 2000.

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Book chapters on the topic "Triterpenoid"

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Pengelly, Andrew. "Triterpenoids and saponins." In The constituents of medicinal plants, 3rd ed. CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0006.

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Abstract This chapter focuses on the various classes of triterpenoids (free triterpenes, triterpenoid saponins, steroidal saponins, cardiac glycosides, phytosterols, phytoecdysteroids, curcurbitacins and quassinoids), which occur in the free state within plants or as aglycones of glycosides. Information on the chemical structures and pharmacological actions of these triterpenoids and saponins are also presented.
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Mahato, S. B., and S. Garai. "Triterpenoid Saponins." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 1998. http://dx.doi.org/10.1007/978-3-7091-6496-9_1.

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Skrukrud, 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. Springer New York, 1987. http://dx.doi.org/10.1007/978-1-4684-5263-1_18.

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Gunatilaka, A. A. Leslie. "Triterpenoid Quinonemethides and Related Compounds (Celastroloids)." In Fortschritte der Chemie organischer Naturstoffe / Progress in the Chemistry of Organic Natural Products. Springer Vienna, 1996. http://dx.doi.org/10.1007/978-3-7091-9406-5_1.

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Haralampidis, Kosmas, Miranda Trojanowska, and Anne E. Osbourn. "Biosynthesis of Triterpenoid Saponins in Plants." In History and Trends in Bioprocessing and Biotransformation. Springer Berlin Heidelberg, 2002. http://dx.doi.org/10.1007/3-540-44604-4_2.

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Lacaille-Dubois, Marie-Aleth, Clément Delaude, and Anne-Claire Mitaine-Offer. "Triterpenoid Saponins: A Focus on Polygalaceae." In Natural Products. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_138.

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Zhang, Jinlan, and Feng Qu. "Methods for Analysis of Triterpenoid Saponins." In Natural Products. Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-22144-6_180.

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Lin-er, Luo, and L. M. Schoonhoven. "Sensory responses to the triterpenoid antifeedant toosendanin." In Proceedings of the 8th International Symposium on Insect-Plant Relationships. Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-1654-1_50.

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Minale, L., M. Iorizzi, E. Palagiano, and R. Riccio. "Steroid and Triterpenoid Oligoglycosides of Marine Origin." In Advances in Experimental Medicine and Biology. Springer US, 1996. http://dx.doi.org/10.1007/978-1-4899-1367-8_28.

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Wang, Zhi Yuan. "Anticarcinogenesis of Licorice and Its Major Triterpenoid Constituents." In ACS Symposium Series. American Chemical Society, 1994. http://dx.doi.org/10.1021/bk-1994-0547.ch033.

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Conference papers on the topic "Triterpenoid"

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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.

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Birch tree barks are regarded as waste in the pulp and papermaking industry and used as fuel. However, this material presents a source that contains many bio-based chemicals suitable for applications ranging from pharmaceuticals, plastics and composites, coatings, and antifeedants. Among the mixture of bio-derived chemicals in birch barks, triterpenoids, such as betulin, betulinic acid, and lupeol, can be present up to 30% weight of dry bark mass. They are highly valued for their anti-tumor, HIV, and inflammatory responses. In our presented work, triterpenoid mixtures were extracted through a
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Rodriguez-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. MDPI, 2023. http://dx.doi.org/10.3390/ecsoc-27-16061.

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Hu, Angela, Huabo Wang, Kelsey Pendleton, and Edward V. Prochownik. "Abstract 4760: Inhibition of c-myc by the triterpenoid celastrol." 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.am2012-4760.

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Kulkarni, Ajit A., Keith C. Olsen, R. M. Kottmann, et al. "Novel Triterpenoid CDDO-Me: An Emerging Therapy For Pulmonary Fibrosis." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a1942.

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Weng, JR. "A triterpenoid from wild bitter gourd inhibits prostate cancer cells." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608122.

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Khan, Noor, Ashutosh Srivastava, and Chetna Dubey. "A Triterpenoid Saponin from the Seeds of Ricinus communis." In The 14th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2010. http://dx.doi.org/10.3390/ecsoc-14-00478.

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Basyuni, Mohammad, Shigeyuki Baba, Hirosuke Oku, et al. "Difference Triterpenoid and Phytosterol Profile between Kandelia candel and K. obovata." In International Conference on Natural Resources and Technology. SCITEPRESS - Science and Technology Publications, 2019. http://dx.doi.org/10.5220/0008505400510054.

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Strigunov, Vsevolod S., Vladimir I. Grishkovets, and Nicolay N. Arnautov. "NEW AND KNOWN MINOR MONODESMOSIDE TRITERPENOID GLYCOSIDES FROM TETRAPANAX PAPYRIFERUM STEMS BARK." In XXIst International Carbohydrate Symposium 2002. TheScientificWorld Ltd, 2002. http://dx.doi.org/10.1100/tsw.2002.798.

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Scott, Latanya M., Liwei Chen, Kenyon G. Daniel, et al. "Abstract 3239: Shp2 inhibitor activity of estramustine phosphate and its triterpenoid analogues." In Proceedings: AACR 102nd Annual Meeting 2011‐‐ Apr 2‐6, 2011; Orlando, FL. American Association for Cancer Research, 2011. http://dx.doi.org/10.1158/1538-7445.am2011-3239.

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Arslan, Idris. "Success stories of triterpenoid-based hybrid molecules as new promising anticancer agents." In ICBRA 2022: 2022 9th International Conference on Bioinformatics Research and Applications. ACM, 2022. http://dx.doi.org/10.1145/3569192.3569217.

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Reports on the topic "Triterpenoid"

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Hawkins, D. R. Triterpenoid biosynthesis in Euphorbia lathyris latex. Office of Scientific and Technical Information (OSTI), 1987. http://dx.doi.org/10.2172/5625757.

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สุวรรณบริรักษ์, คณิต, та สุรัตนา อำนวยผล. การศึกษาทางพฤกษเคมีของต้นข้าวหลาม : รายงานผลการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 1996. https://doi.org/10.58837/chula.res.1996.14.

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ได้ทำการสกัดแยกสารจากเปลือกต้นข้าวหลาม Goniothalamus marcanii Craib โดยใช้วิธีทางโครมาโทกราฟีควบคู่ไปกับผลการทดสอบฤทธิ์ทางชีวภาพ ทำให้สามารถแยกสารได้ 4 กลุ่ม โดยการวิเคราะห์ข้อมูลจากสเปกโทรสโกปีเพื่อพิสูจน์สูตรโครงสร้างทางเคมีของสารที่แยกได้ ทำให้ทราบว่าสารทั้ง 4 กลุ่มคือ 1-azaanthraquinones, flavanoids, triterpenoids และ mono-THF annonaceous acetogenins โดยที่สารกลุ่ม 1-azaanthraquinoes ที่แยกได้เป็นสารชนิดใหม่ 1 ชนิด คือ marcanine C ร่วมกับสารที่ทราบสูตรโครงสร้างแล้ว 2 ชนิด คือ marcanine A และ dielsiquinone ส่วนสารกลุ่ม flavanoids ที่แยกได้เป็นสารที่ทราบสูตรโครงสร้างแล้ว 1 ชนิด คือ pinocembr
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ชัยเจริญพงศ์, จรรยา, ทรงจันทร์ ภู่ทอง та อณุมาศ บัวเขียว. ความเป็นพิษต่อเซลล์มะเร็งของพืชสมุนไพรไทยจากอุทยานแห่งชาติปางสีดา : รายงานการวิจัย. จุฬาลงกรณ์มหาวิทยาลัย, 2011. https://doi.org/10.58837/chula.res.2011.118.

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จากการทดสอบความเป็นพิษต่อเซลล์มะเร็งของพืชสมุนไพรที่เก็บตัวอย่างมาจากอุทยานแห่งชาติปางสีดา จำนวน 40 ชนิด สามารถคัดกรองพืชสมุนไพรที่มีฤทธิ์ยับยั้งการเจริญเติบโตของเซลล์มะเร็งได้ จำนวน 13 ชนิด ได้แก่ อ้อยสามสวน (ใบ), คัดเค้าป่า (ใบ), มะก่อง (ทั้งใบและกิ่ง), มะก่องใหญ่ (ใบ), ข้าวหลาม (ใบ), ตาเสือ (ทั้งใบและกิ่ง), คนทีสอ (กิ่ง), รางโคน (ใบ), เขียวพุ่ม (ใบ), ตะโกป่า (ใบ), ขานาง (ผล), พันชาด (ใบ) และพลองขี้ควาย(ใบ) สารสกัดหยาบเอทานอลจากใบมะก่องขม aglaia elaeagnoidea (A. Juss.) Benth.) ให้ผลกายับยั้งการเจริญของเซลล์มะเร็งได้ดีที่สุดจึงถูกเลือกนำมาแยกและหาสารบริสุทธิ์เพื่อทดสอบความสามารถยับยั้งการเจริ
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Sporn, Michael B. Triterpenoids and Prevention of Prostate Cancer. Defense Technical Information Center, 2001. http://dx.doi.org/10.21236/ada405249.

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Sporn, Michael B. Triterpenoids and Prevention of Prostate Cancer. Defense Technical Information Center, 1999. http://dx.doi.org/10.21236/ada384364.

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Schaffer, Arthur A., and Jocelyn Rose. Understanding Cuticle Development in Tomato through the Study of Novel Germplasm with Malformed Cuticles. United States Department of Agriculture, 2013. http://dx.doi.org/10.32747/2013.7593401.bard.

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Plant cuticle development and metabolism are still poorly understood, partly due to the chemical complexity of the cuticular layer. The overall research objective was to broaden and deepen our understanding of tomato fruit cuticle development by analyzing novel germplasm with cuticular malformations and by studying the transcriptome and proteome of the fruit epidermal tissues, as strategies to overcome the challenges posed by the recalcitrance of the biological system. During the project we succeeded in identifying two genes with major impact on cuticle development. One of these encoded the fi
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Hyer, Marc L. Modulating TRAIL-Mediated Apoptosis in Prostate Cancer Using Synthetic Triterpenoids. Defense Technical Information Center, 2005. http://dx.doi.org/10.21236/ada434105.

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