Relevant bibliographies by topics / Pyranocoumarins

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Academic literature on the topic 'Pyranocoumarins'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Pyranocoumarins"

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Khandy, Maria T., Valeria P. Grigorchuk, Anastasia K. Sofronova, and Tatiana Y. Gorpenchenko. "The Different Composition of Coumarins and Antibacterial Activity of Phlojodicarpus sibiricus and Phlojodicarpus villosus Root Extracts." Plants 13, no. 5 (2024): 601. http://dx.doi.org/10.3390/plants13050601.

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Phlojodicarpus sibiricus, a valuable endangered medicinal plant, is a source of angular pyranocoumarins used in pharmacology. Due to limited resource availability, other pyranocoumarin sources are needed. In the present research, the chemical composition of a closely related species, Phlojodicarpus villosus, was studied, along with P. sibiricus. High-performance liquid chromatography and mass-spectrometric analyses, followed by antibacterial activity studies of root extracts from both species, were performed. P. sibiricus and P. villosus differed significantly in coumarin composition. Pyranoco
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Krasylov, Igor V., Viktoriia Moskvina, and Volodymyr P. Khilya. "Synthetic approach to spiropyranocoumarins and their oxime derivatives." Ukr. Bioorg. Acta 2023, Vol. 18, N1 18, no. 1 (2023): 42–51. http://dx.doi.org/10.15407/bioorganica2023.01.042.

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This study explores the synthesis of a diverse series of linear (spiro)pyranocoumarins and their corresponding oximes, compounds known for their promising biological activities. Building on previous work, the authors expand the array of target compounds, adding structural features such as dimethyl groups and various cycloaliphatic rings. The novel synthetic procedure applied herein couples o-hydroxyacetyl coumarins with respective ketones via Kabbe condensation, yielding 16 derivatives, including 12 new compounds. A further step engages these (spiro)pyranocoumarins with hydroxylamine hydrochlo
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Khandy, Maria T., Anastasia K. Sofronova, Tatiana Y. Gorpenchenko, and Nadezhda K. Chirikova. "Plant Pyranocoumarins: Description, Biosynthesis, Application." Plants 11, no. 22 (2022): 3135. http://dx.doi.org/10.3390/plants11223135.

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This overview article contains information about pyranocoumarins over the last 55 years. The article is based on the authors’ phytochemical and physiological studies in vivo and in vitro as well as search and analysis of data in literature available on Google Scholar, Web of Science, PubMed, and ScienceDirect before January 2022. Pyranocoumarins are synthesized in plants of the Apiaceae, Rutaceae families, and one species in each of the Cornaceae, Calophyllaceae, and Fabaceae families can synthesize this class of compounds. The physiological role of these compounds in plants is not clear. It h
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Alshibl, Hanan M., Ebtehal S. Al-Abdullah, Mogedda E. Haiba, et al. "Synthesis and Evaluation of New Coumarin Derivatives as Antioxidant, Antimicrobial, and Anti-Inflammatory Agents." Molecules 25, no. 14 (2020): 3251. http://dx.doi.org/10.3390/molecules25143251.

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New pyranocoumarin and coumarin-sulfonamide derivatives were prepared and evaluated for their antioxidant, antimicrobial, and/or anti-inflammatory activities. Coumarin-sulfonamide compounds 8a–d demonstrated significant antioxidant activity, while 7c,d, 8c,d, and 9c,d exhibited antimicrobial activity equal to or higher than the standard antimicrobials against at least one tested microorganism. Regarding the anti-inflammatory testing, pyranocoumarins 2b, 3a,b and 5c and coumarin-sulfonamide compound 9a showed more potent antiproteinase activity than aspirin in vitro; however, five compounds wer
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Delgado, Guillermo, and José Garduño. "Pyranocoumarins from arracacia nelsonii." Phytochemistry 26, no. 4 (1987): 1139–41. http://dx.doi.org/10.1016/s0031-9422(00)82365-1.

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Sarker, Satyajit D., James A. Armstrong, Alexander I. Gray, and Peter G. Waterman. "Pyranocoumarins from Eriostemon apiculatus." Biochemical Systematics and Ecology 22, no. 6 (1994): 641–44. http://dx.doi.org/10.1016/0305-1978(94)90077-9.

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Uy, Neil Patrick, Sang Yun Lee, Jang Hoon Kim, Young Ho Yoon, and Sanghyun Lee. "Simultaneous Quantification of Phenolic Compounds in the Leaves and Roots of Peucedanum japonicum Thunb. Using HPLC-PDA with Various Extraction Solvents." Horticulturae 11, no. 3 (2025): 334. https://doi.org/10.3390/horticulturae11030334.

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This study investigated the extraction and quantification of specific phenolic compounds, including chlorogenic acid and several pyranocoumarin derivatives, from the leaves and roots of Peucedanum japonicum. Using high-performance liquid chromatography, this study aimed to optimize extraction methodologies with different solvents to maximize the yield of bioactive compounds. The extraction process involved meticulous steps, including reflux extraction and solvent evaporation, and the total phenolic content was assessed using a spectrophotometric assay. The results demonstrated that ethanol and
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Vlachou, Evangelia-Eirini N., and Konstantinos E. Litinas. "An Overview on Pyranocoumarins: Synthesis and Biological Activities." Current Organic Chemistry 23, no. 24 (2020): 2679–721. http://dx.doi.org/10.2174/1385272823666191025151236.

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Pyrano- and dipyranocoumarins are classes of naturally occurring organic compounds with very interesting biological activities. This review focuses on the synthetic strategies for the synthesis of pyranocoumarins and dipyranocoumarins and the biological properties of those compounds. The synthesis involves the formation of the pyran ring, at first, from a coumarin or the formation of pyranone moiety from an existing pyran. Pyranocoumarins and dipyranocoumarins present anti-HIV, anti-cancer, neuroprotective, antidiabetic, antibacterial, antifungal, anti-inflammatory activities. Especially khell
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NISHITA, Yoshitaka, Koji UESUGI, Yasuyoshi SATOH, and Takashi HARAYAMA. "Convenient Synthesis of Angular Pyranocoumarins." YAKUGAKU ZASSHI 118, no. 12 (1998): 599–608. http://dx.doi.org/10.1248/yakushi1947.118.12_599.

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Krasylov, I. V., V. S. Moskvina, S. V. Shilin, and V. P. Khilya. "Amino-Acid Derivatives of Pyranocoumarins." Chemistry of Natural Compounds 56, no. 5 (2020): 832–36. http://dx.doi.org/10.1007/s10600-020-03163-3.

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Book chapters on the topic "Pyranocoumarins"

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"Isoglycycoumarin (Pyranocoumarin)." In Natural Compounds. Springer New York, 2013. http://dx.doi.org/10.1007/978-1-4614-0535-1_1004.

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Conference papers on the topic "Pyranocoumarins"

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Inyutina, A. K., R. F. Fatykhov, I. A. Khalymbadzha, A. D. Sharapov, M. V. Bobkina, and O. N. Chupakhin. "New approach to the synthesis of biologically active derivatives of pyranocoumarins." In PROCEEDINGS OF THE 3RD INTERNATIONAL CONFERENCE ON AUTOMOTIVE INNOVATION GREEN ENERGY VEHICLE: AIGEV 2018. Author(s), 2019. http://dx.doi.org/10.1063/1.5087351.

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Wu, Wei, Manohar Puppala, Suni Tang, et al. "Abstract 2826: Equimolar vs. pharmacokinetics-guided dosing in anti-cancer efficacy assessment of precursor-product pairs: Example with pyranocoumarins from Korean Angelica." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-2826.

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Tang, Suni, Yong Zhang, Peixin Jiang, et al. "Abstract LB-184: A paradigm of carcinogenesis lineage specificities of cancer chemoprevention: KoreanAngelicaextract and its pyranocoumarins in the transgenic adenocarcinoma of mouse prostate model." In Proceedings: AACR 104th Annual Meeting 2013; Apr 6-10, 2013; Washington, DC. American Association for Cancer Research, 2013. http://dx.doi.org/10.1158/1538-7445.am2013-lb-184.

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Tang, Su-Ni, Jinhui Zhang, Wei Wu, Chengguo Xing, Cheng Jiang, and Juxuan Lü. "Abstract 1907: Transcriptomic signatures associated with the efficacy of Angelica gigas (AGN) ethanol extract and its pyranocoumarins on two lineages of carcinogenesis in TRAMP mice." In Proceedings: AACR 106th Annual Meeting 2015; April 18-22, 2015; Philadelphia, PA. American Association for Cancer Research, 2015. http://dx.doi.org/10.1158/1538-7445.am2015-1907.

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Li, Li, Jinhui Zhang, Yong Zhang, et al. "Abstract 4622: Determination of pyranocoumarin compounds decursin, decursinol angelate and decursinol simultaneously in mouse plasma and tumor tissue by liquid-liquid extraction and HPLC." 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.am2011-4622.

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Journal articles
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