Relevant bibliographies by topics / Alkaloids

Contents

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

Academic literature on the topic 'Alkaloids'

Author: Grafiati
Published: 4 June 2021
Last updated: 25 July 2025

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Journal articles on the topic "Alkaloids"

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Han, Sunkyu, Sangbin Jeon, and Joonoh Park. "Syntheses of Dimeric Securinega Alkaloids." Synlett 28, no. 18 (2017): 2353–59. http://dx.doi.org/10.1055/s-0036-1590864.

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The isolation of flueggenines A and B by Yue and co-workers in 2006 has triggered a burst of isolation reports of dimeric and oligomeric securinega alkaloid natural products. The compelling molecular structures of these compounds with various modes of connection between monomeric securinega units have posed intriguing challenges to the synthetic organic community. Herein, we have categorized high-order securinega alkaloids based on their biosynthetic mode of dimerization or oligomerization. We then have compiled all reported syntheses of dimeric securinega alkaloids based on our classification
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Věžník, František, Eva Táborská, Hana Bochořáková, František Tureček, Vladimír Hanuš, and Jiří Slavík. "Alkaloids of Papaver nudicaule SUBSP. xanthopetalum (TRAUTV.) FEDDE and P. nudicaule SUBSP. album (REGEL) FEDDE from the section Scapiflora REICHB." Collection of Czechoslovak Chemical Communications 52, no. 6 (1987): 1634–40. http://dx.doi.org/10.1135/cccc19871634.

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The alkaloidal composition in the two title taxa differs only quantitatively. Both contain amurine as the main alkaloid. P. nudicaule ssp. xanthopetalum contains muramine, protopine and alkaloid PN1 (probably identical with (±)-nudaurine (Ia)) as dominant alkaloids; further were isolated amurensine, epialpinine, cryptopine, mecambridine and alpinigenine. Allocryptopine, papaverrubines A, B, D and G, palmatine and coptisine were detected chromatographically. The quaternary alkaloid fraction afforded cis-N-methylstylopinium hydroxide (as the iodide II) which was isolated for the first time from
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El-Shazly, Assem. "Pyrrolizidine Alkaloid Profiles of Some Senecio Species from Egypt." Zeitschrift für Naturforschung C 57, no. 5-6 (2002): 429–33. http://dx.doi.org/10.1515/znc-2002-5-604.

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Alkaloid profiles of two Egyptian Senecio species (Senecio aegyptius var. discoideus and S. desfontainei) in addition to a cultivated species (S. cineraria) were studied using capillary GLC and GLC-mass spectrometry with respect to pyrrolizidine alkaloids (PAs). Four alkaloids were identified in S. aegyptius var. discoideus, 8 in S. desfontainei and 13 in S. cineraria. Some of these alkaloids have not been reported from these plants. The alkaloidal pattern of different plant organs (flowers, leaves, stem, root) were also investigated. Senecionine has been found to be a one of the major alkaloi
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El-Shazly, A., A. M. Ateya, L. Witte, and M. Wink. "Quinolizidine Alkaloid Profiles of Retama raetam, R. sphaerocarpa and R. monosperma." Zeitschrift für Naturforschung C 51, no. 5-6 (1996): 301–8. http://dx.doi.org/10.1515/znc-1996-5-607.

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Abstract About 28 quinolizidine alkaloids and the dipiperidine alkaloids am modendrine, dehydroammodendrine and N -formylammodendrine were identified in the alkaloidal extracts of Retama raetam, Retama sphaerocarpa and Retama monosperma by capillary GLC and GLCMS. Alkaloid profiles of the three Retama species with a Mediterranean distribution are more similar than alkaloid patterns of different organs of the same plant. Whereas sparteine and retamine are the major components of stems, lupanine, retam ine, N-methylcytisine and cytisine dominate in flowers and pods, and cytisine in seeds indicat
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Slavík, Jiří, and Leonora Slavíková. "Alkaloids of Meconopsis cambrica (L.) VIG. and M. robusta HOOK. f. et THOMS." Collection of Czechoslovak Chemical Communications 61, no. 12 (1996): 1815–22. http://dx.doi.org/10.1135/cccc19961815.

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Additional alkaloids (+)-roemerine (3b), (+)-corytuberine (3d), (-)-N-methylmecambridinium and alkaloid MC 2 (the last two as iodides) were isolated as minor alkaloidal components from Meconopsis cambrica (L.) VIG. (Papaveraceae) besides of the dominant known alkaloids (-)-mecambrine (1), (-)-mecambridine (2), (-)-flavinantine (4) and (+)-magnoflorine (5), and a small amount of (+)-mecambroline (3a). Minute quantities of protopine, allocryptopine, roemeroline, papaverrubine D and C, berberine, coptisine, corysamine and palmatine were identified by thin layer chromatography (TLC). From M. robus
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Zhou, Shuaizhen, Ruolin Geng, Changqiang Ke, et al. "Expanding the Chemical Diversity of Stemona parviflora: Isolation and Characterization of New Parvistemoline-Type Alkaloids." Chemistry 7, no. 1 (2025): 6. https://doi.org/10.3390/chemistry7010006.

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A comprehensive phytochemical investigation of the whole plant of Stemona parviflora led to the isolation of 13 alkaloidal constituents, including five new alkaloids, parvistemonines B–F (1–5). The structures of these compounds were elucidated through extensive analyses of 1D and 2D NMR spectra, DFT NMR calculation, and comparisons with data in the literature. Notably, compounds 1–4 represent new examples of the rare parvistemoline-type alkaloids, with compound 4 showcasing a unique rearranged skeleton. Additionally, parvistemonine F (5) was identified as a distinct alkaloid skeleton character
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Sreevidya, Narasimhan, and Shanta Mehrotra. "Spectrophotometric Method for Estimation of Alkaloids Precipitable with Dragendorff's Reagent in Plant Materials." Journal of AOAC INTERNATIONAL 86, no. 6 (2003): 1124–27. http://dx.doi.org/10.1093/jaoac/86.6.1124.

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Abstract A rapid, easy, and simple spectrophotometric method was developed for the estimation of total alkaloids precipitated by Dragendorff's reagent (DR) in plant materials. It is based on the formation of yellow bismuth complex in nitric acid medium with thiourea. The yellow-colored complex formed obeys Lambert-Beer's law in the concentration range of 0.06–50 μg/mL with λmax at 435 nm. Using this method, the alkaloidal percentage of certain alkaloids (ajamalicine, papaverine, cinchonine, piperine, berberine) and some plant materials containing alkaloids (Berberis aristata, Solanum nigrum, a
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Lim, Hyeonggeun, Sikwang Seong, and Sunkyu Han. "Syntheses of Post-Iboga Alkaloids." Synthesis 51, no. 14 (2019): 2737–58. http://dx.doi.org/10.1055/s-0037-1612061.

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Post-iboga alkaloids are secondary metabolites that are biosynthetically derived from iboga-type alkaloids via rearrangements of the indole and/or isoquinuclidine moieties. Herein, we categorize post-iboga alkaloids into five types based on the biosynthetic mode of transformation of the iboga scaffold. We then describe reported syntheses of post-iboga alkaloids, including our laboratory’s recent contributions, based on our own categorization.1 Introduction1.1 Iboga and Post-Iboga Alkaloids1.2 Classification of Post-Iboga Alkaloids1.2.1 Introduction to Type I Post-Iboga Alkaloids1.2.2 Introduct
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Dewan, S. Bhakuni. "Biosynthesis and synthesis of biologically active alkaloids of Indian medicinal plants." Journal of Indian Chemical Society Vol. 79, Mar 2002 (2002): 203–10. https://doi.org/10.5281/zenodo.5840849.

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Central Drug Research Institute, Lucknow-226 001, India <em>E-mail :</em>Root@cdrilk.Sirnetd.ernet.in&nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp; &nbsp;&nbsp;&nbsp;<em>Fax : </em>91-0522-223405/223938 The structure and stereochemistry of biologically active alkaloids isolated from <em>Croton sparsiflorus, Cocculus laurifolius, C. pendulus, Corydalis meifolia </em>and <em>Stephania glabra </em>were established. Biosynthetic studies were carried out on proaporphine and dihydroproaporphgne alkaloids, crotsparine and crotsparinine, and abnormal aporphine alkaloid sparsiflorine; abnor&shy;mal <em>Eryt
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Doncheva, Tsvetelina, Gabriela Yordanova, Vassil Vutov, Nadezhda Kostova, and Stefan Philipov. "Comparative Study of Alkaloid Pattern of Four Bulgarian Fumaria Species." Natural Product Communications 11, no. 2 (2016): 1934578X1601100. http://dx.doi.org/10.1177/1934578x1601100220.

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The alkaloid pattern of four Fumaria species ( Fumaria kralikii, Fumaria rostellata, Fumaria schleicherii, Fumaria thuretii) growing in Bulgaria was investigated by GC-MS and twenty isoquinoline alkaloids were determined. Phytochemical investigation of the alkaloid composition on Fumaria thuretii Boiss was made for the first time. The alkaloid profile of the species was compared at two levels, between different species and within two species from different habitats. Two chemotypical groups, based on the types of isoquinoline alkaloids were suggested. To group A belong species F. kralikii, F. r
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Dissertations / Theses on the topic "Alkaloids"

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Witt, Anette. "Synthetic development towards benzodiazepine alkaloids : total synthesis of circumdatin F and C /." Stockholm, 2002. http://diss.kib.ki.se/2002/91-7349-077-6/.

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Callaghan, Owen. "Synthetic and mechanistic studies in free radical." Thesis, University of Strathclyde, 1999. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.366957.

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Kalusa, Andrew. "Synthesis of marine alkaloids." Thesis, University of Oxford, 2003. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.275274.

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Goddard, Euan. "Asymmetric Synthesis of Alkaloids." Thesis, University of Oxford, 2008. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.489446.

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Smith, Catherine Janet. "Synthesis of histrionicotoxin alkaloids." Thesis, University of Cambridge, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.620245.

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Brock, Elizabeth Anne. "Alkaloids from transannular iodoaminations." Thesis, University of Oxford, 2012. http://ora.ox.ac.uk/objects/uuid:0feddc99-0fde-4dcd-b717-b0c6b0515615.

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This thesis is concerned with the development of transannular iodoamination methodology for the synthesis of pyrrolizidine, indolizidine and tropane alkaloids. Chapter 1 introduces the concept of a ‘transannular cyclisation’ and outlines the utility of such cyclisations in the synthesis of a range of [x.y.z]-azabicyclic alkaloids. Chapter 2 describes the development of a three step lithium amide conjugate addition, ring-closing metathesis and transannular iodoamination protocol for the preparation of the pyrrolizidine scaffold ([3.3.0]-azabicycle). Cyclisation of a hexahydroazocine occurs with
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Stanley, Paul. "Semisynthesis of jerantinine alkaloids." Thesis, University of Nottingham, 2017. http://eprints.nottingham.ac.uk/47504/.

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This thesis details the synthetic studies undertaken on natural products with anti-cancer activity. The general aim was to explore the synthesis and find an efficient and effective method to generate compounds, which would be used to further examine novel biological action. The first half of this thesis details the synthetic studies on the jerantinine family of natural products. The approach utilised the complex alkaloid (-)-tabersonine as a starting material, which was isolated from an abundant and sustainable source. Ultimately the first synthesis of (-)-jerantinine A and first enantioselect
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Choi, Joong-Kwon. "Synthesis of pyrrolizidine alkaloids /." The Ohio State University, 1985. http://rave.ohiolink.edu/etdc/view?acc_num=osu1487259125219504.

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Saensuk, Pilan. "Phytochemistry of norditerpenoid alkaloids." Thesis, University of Bath, 2007. https://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.485128.

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Norditerpenoid alkaloids have important biological activities. Many of them are potent ligands and therefore promising leads for novel selective antagonists and/or agonists of subtypes of nicotinic acetylcholine receptors (nAChR) and voltage-gated sodium channels. Aconitum, Consolida, and Delphinium are important sources of norditerpenoid alkaloids. This thesis is focussed on the chemistry of norditerpenoid alkaloids from these three genera, starting with a review of those recently isolated from Aconitum, Consolida, and Delphinium with brief aspects of taxonomy, biological activities, and mode
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Sedlock, Andrea B. "Ergot alkaloids and herbivory in model animals and variation in an ergot alkaloid biosynthesis gene." Morgantown, W. Va. : [West Virginia University Libraries], 2003. http://etd.wvu.edu/templates/showETD.cfm?recnum=3190.

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Thesis (M.S.)--West Virginia University, 2003.<br>Title from document title page. Document formatted into pages; contains viii, 62 p. : ill. (some col.) Vita. Includes abstract. Includes bibliographical reference.
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Books on the topic "Alkaloids"

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Roberts, Margaret F., and Michael Wink, eds. Alkaloids. Springer US, 1998. http://dx.doi.org/10.1007/978-1-4757-2905-4.

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Linskens, Hans Ferdinand, and John F. Jackson, eds. Alkaloids. Springer Berlin Heidelberg, 1994. http://dx.doi.org/10.1007/978-3-642-84226-9.

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Cordell, Geoffrey A. The Alkaloids, Volume 59 (The Alkaloids) (The Alkaloids). Academic Press, 2002.

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The Alkaloids, Volume 59 (The Alkaloids) (The Alkaloids). Academic Press, 2002.

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Knölker, Hans-Joachim. Alkaloids. Elsevier Science & Technology Books, 2017.

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Knolker, Hans-Joachim. Alkaloids. Elsevier Science & Technology Books, 2015.

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Cordell, Geoffrey A. Alkaloids. Elsevier Science & Technology Books, 2003.

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Qin, Hailin, and Dequan Yu. Alkaloids. De Gruyter, 2021. http://dx.doi.org/10.1515/9783110627299.

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Alkaloids. Elsevier, 2015. http://dx.doi.org/10.1016/c2011-0-04166-2.

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Alkaloids. Elsevier, 2015. http://dx.doi.org/10.1016/c2012-0-07416-9.

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Book chapters on the topic "Alkaloids"

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Pengelly, Andrew. "Alkaloids." In The constituents of medicinal plants, 3rd ed. CABI, 2021. http://dx.doi.org/10.1079/9781789243079.0010.

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Abstract Found in roots, rhizomes, leaves, bark, fruit or seeds of 15-30% of all flowering plants, alkaloids are particularly common in certain families, such as the Fabaceae, Rubiaceae, Ranunculaceae, Apocynaceae, Solanaceae and Papaveraceae. Over 20,000 different alkaloids have been isolated from over 300 plant families. Over 150 alkaloids are known to occur in one species, Catharanthus roseus (Apocynaceae). The most widely occurring plant alkaloids are caffeine and berberine. This paper discusses the properties, nomenclature, pharmacological actions and classification of alkaloids. Tabulate
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Makkar, Harinder P. S., P. Siddhuraju, and Klaus Becker. "Alkaloids." In Plant Secondary Metabolites. Humana Press, 2007. http://dx.doi.org/10.1007/978-1-59745-425-4_18.

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Böttger, Angelika, Ute Vothknecht, Cordelia Bolle, and Alexander Wolf. "Alkaloids." In Lessons on Caffeine, Cannabis & Co. Springer International Publishing, 2018. http://dx.doi.org/10.1007/978-3-319-99546-5_12.

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Leonard, J. "Alkaloids." In The Chemistry of Natural Products. Springer Netherlands, 1993. http://dx.doi.org/10.1007/978-94-011-2144-6_6.

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Fox, Malcolm A. "Alkaloids." In Glossary for the Worldwide Transportation of Dangerous Goods and Hazardous Materials. Springer Berlin Heidelberg, 1999. http://dx.doi.org/10.1007/978-3-662-11890-0_4.

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Herbert, R. B. "Alkaloids." In The Biosynthesis of Secondary Metabolites. Springer Netherlands, 1989. http://dx.doi.org/10.1007/978-94-010-9132-9_6.

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Buckingham, J., and R. A. Hill. "Alkaloids." In Atlas of Stereochemistry. Springer US, 1986. http://dx.doi.org/10.1007/978-1-4899-3420-8_4.

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Bhutani, S. P. "Alkaloids." In Chemistry of Biomolecules. CRC Press, 2019. http://dx.doi.org/10.1201/9780429266423-7.

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Ahluwalia, V. K. "Alkaloids." In Biomolecules. CRC Press, 2024. http://dx.doi.org/10.1201/9781003494553-11.

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Shtilman, M. I., and I. A. Agabekov. "Alkaloids." In Immobilization on Polymers. CRC Press, 2023. http://dx.doi.org/10.1201/9780429071010-7.

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Conference papers on the topic "Alkaloids"

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Salam, Rudi, Suprihatin, Nastiti Siswi Indrasti, et al. "Electrochemical Biosensor Utilizing Alkaloids and Tannins from Areca Nuts for Environmental Quality Application." In 2024 IEEE International Conference on Agrosystem Engineering, Technology & Applications (AGRETA). IEEE, 2024. https://doi.org/10.1109/agreta61912.2024.10948997.

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T.Devakumar, N.Pathmavathi, and S. Thalamuthu. "Detection and Quantification of Catharanthine Alkaloids in Catharanthus Roseus Leaves using Electrochemical and Optical Methods." In 2025 5th International Conference on Trends in Material Science and Inventive Materials (ICTMIM). IEEE, 2025. https://doi.org/10.1109/ictmim65579.2025.10988095.

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Subhashree, A., G. Puthilibai, and Elakiyadevi B. "Exploring the Biomedical Applications and Computational Docking of Indole Alkaloids: An Evaluation of Bioinformatics Approaches." In 2025 International Conference on Computing and Communication Technologies (ICCCT). IEEE, 2025. https://doi.org/10.1109/iccct63501.2025.11019864.

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Seijas, Julio, M. Vázquez-Tato, Javier Seijo-Muras, Pablo Ramil-Rego, and M. Buján. "Alkaloids from Narcissus bulbocodium L." In The 8th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01978.

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Yunusov, M. S., E. M. Tsyrlina, S. A. Kryzhanovsky, I. B. Tsorin, and S. G. Yunusova. "ANTIARRHYTHMICS BASED ON DITERPENOID ALKALOIDS." In MedChem-Russia 2021. 5-я Российская конференция по медицинской химии с международным участием «МедХим-Россия 2021». Издательство Волгоградского государственного медицинского университета, 2021. http://dx.doi.org/10.19163/medchemrussia2021-2021-133.

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Seijas, Julio, M. Vázquez-Tato, M. Linares, Pablo Ramil-Rego, and M. Buján. "Mesembrine Alkaloids from Narcissus triandrus L." In The 8th International Electronic Conference on Synthetic Organic Chemistry. MDPI, 2004. http://dx.doi.org/10.3390/ecsoc-8-01979.

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Trauner, Dirk, Johann Mulzer, Jan Bats, Stefanie Porth, and Till Opatz. "Total Synthesis of Morphine- and Hasubanane Alkaloids." In The 1st International Electronic Conference on Synthetic Organic Chemistry. MDPI, 1997. http://dx.doi.org/10.3390/ecsoc-1-02045.

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Wipf, Peter, and Filip Petronijevic. "New Approaches to Indoles and Indole Alkaloids." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0388-1.

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Cheng, YB, CJ Su, SR Chen, and CY Chen. "New Alkaloids from Taiwanese Zoanthid Palythoa tuberculosa." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608091.

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Kaya, Gİ, K. Uzun, S. Demir, B. Bozkurt, MA Onur, and N. Unver Somer. "Isolation of further alkaloids from Galanthus cilicicus." In GA 2017 – Book of Abstracts. Georg Thieme Verlag KG, 2017. http://dx.doi.org/10.1055/s-0037-1608244.

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Reports on the topic "Alkaloids"

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Pereboom, D. P. K. H., P. P. J. Mulder, M. Sopel, and J. Grzetic. Proficiency test for ergot alkaloids in cereals : EURLPT-MP08 (2022). Wageningen Food Safety Research, 2023. http://dx.doi.org/10.18174/636591.

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Pereboom, D. P. K. H., A. Veršilovskis, P. P. J. Mulder, M. de Nijs, and J. G. J. Mol. Proficiency test for ergot alkaloids in cereals : EURL-PT-MP03 (2019). Wageningen Food Safety Research, 2020. http://dx.doi.org/10.18174/526444.

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Pereboom, D. P. K. H., W. C. M. de Nijs, and P. P. J. Mulder. Proficiency test for tropane alkaloids in food and feed matrices : EURLPT-MP04 (2020). Wageningen Food Safety Research, 2021. http://dx.doi.org/10.18174/544466.

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Pereboom, D. P. K. H., M. de Nijs, J. G. J. Mol, and P. P. J. Mulder. Research study for pyrrolizidine alkaloids in alfalfa and herbal tea : EURLPT-MP02 (2019). Wageningen Food Safety Research, 2021. http://dx.doi.org/10.18174/545714.

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Pereboom, D. P. K. H., P. P. J. Mulder, M. Sopel, and J. Grzetic. Proficiency test for opium alkaloids in poppy seeds and bakery products : EURLPT-MP09 (2023). Wageningen Food Safety Research, 2023. http://dx.doi.org/10.18174/641239.

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Annunziato, Dominick. HPLC Sample Prep and Extraction SOP v1.3 for Fungi. MagicMyco, 2023. http://dx.doi.org/10.61073/sopv1.3.08.11.2023.

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medicine, industry, and biotechnology. Fungi produce a wide range of bioactive compounds, such as alkaloids, antibiotics, antifungals, immunomodulators, anticancer agents, enzymes, and vitamins. However, these compounds are often locked inside the fungal cell wall, which is composed of chitin, a tough substance that is dif�icult to digest by humans1. Therefore, it is essential to have a good extraction technique that can break down the chitin and release the valuable compounds from the fungi, this is especially essential in the laboratory for accurate lab assays and potency determination durin
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Committee on Toxicology. New Approach Methodologies (NAMs) In Regulatory Risk Assessment Workshop Report 2020- Exploring Dose Response. Food Standards Agency, 2024. http://dx.doi.org/10.46756/sci.fsa.cha679.

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The UK Food Standards Agency (FSA) and the Committee on Toxicity of Chemicals in Food, Consumer Products and the Environment (COT) held an “Exploring Dose Response” workshop in a multidisciplinary setting inviting regulatory agencies, government bodies, academia and industry. The workshop provided a platform from which to address and enable expert discussions on the latest in silico prediction models, new approach methodologies (NAMs), physiologically based pharmacokinetics (PBPK), future methodologies, integrated approaches to testing and assessment (IATA) as well as methodology validation. U
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Houck, Marilyn, Uri Gerson, and Robert Luck. Two Predator Model Systems for the Biological Control of Diaspidid Scale Insects. United States Department of Agriculture, 1994. http://dx.doi.org/10.32747/1994.7570554.bard.

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Hemisarcoptes (Acari: Hamisarcoptidae) is a parasite of scale insects (Diaspididae), tenacious pests of vascular plants. Hemisarcoptes also has a stenoxenic phoretic (dispersal) relationship with Chilocorus (Coleoptera: Coccinellidae). Chilocorus feeds on diaspidids, transports mites as they feed, and has been applied to the control of scales, with limited success. U.S.-Israeli cooperation focused on this mite-beetle interaction so that a two-component system could be applied to the control of scale insects effectively. Life history patterns of Hemisarcoptes were investigated in response to ho
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Paterek, J. Robert. L51963 Environmental Benign Mitigation of Microbiologically Influenced Corrosion (MIC). Pipeline Research Council International, Inc. (PRCI), 2002. http://dx.doi.org/10.55274/r0011299.

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The objective is to develop and evaluate environmental benign agents or products that are effective in the prevention, inhibition, and mitigation of microbially influenced corrosion (MIC) on the internal surfaces of metallic natural gas pipelines. The goal is one or more products that can be applied to maintain the structure and dependability of the natural gas infrastructure. The technical approach for this year has been to evaluate a number of methods to fractionate and concentrate the components found in the pepper extracts. The separation methods considered include size exclusion chromatog
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Ramnaraine, Daveena. Beyond Antibiotics: Exploring the Antibacterial Mechanisms and Efficacy of Medicinal Plants and Endophytic Fungi. Florida International University, 2025. https://doi.org/10.25148/fiuurj.3.1.14.

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Due to the overuse of antibiotics, antibiotic resistance has become a global health crisis, and has forced an exploration of alternative antibacterial agents. This review explores natural solutions through the antibacterial potential of medicinal plants and their symbiotic endophytic fungi. Medicinal plants have been utilized for centuries to treat infections because of their rich phytochemical content, including alkaloids, flavonoids, and saponins, which exhibit antibacterial properties. Their efficacy is measured through minimum inhibitory concentration (MIC) assays, which showcase their abi
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