Academic literature on the topic 'Pimaranes'

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Journal articles on the topic "Pimaranes"

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Maslovskaya, Lidia A., Andrei I. Savchenko, Victoria A. Gordon, et al. "EBC-316, 325–327, and 345: New Pimarane Diterpenes from Croton insularis Found in the Australian Rainforest." Australian Journal of Chemistry 68, no. 4 (2015): 652. http://dx.doi.org/10.1071/ch14550.

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Five new pimarane and related-type diterpenes (i.e. EBC-316, 325–327, and 345 (10–15)), together with two known pimaranes (EBC-221 (8) and EBC-346 (9)), were isolated from the stems of Croton insularis, found in the Australian rainforest. All pimarane diterpenes disclosed herein are suggested to be biogenetically related to the same keto-Jacobs–Reynolds intermediate 2, via ring A and C oxidation. Anticancer activities of compounds 11–13 are reported.
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Ferreira, Sandra, Patrícia Rijo, João G. Costa, et al. "Evaluation of the Lysyl Oxidase-Like 2 (LOXL2) inhibitory activity of pimaranes and their glycosyl derivatives." Journal Biomedical and Biopharmaceutical Research 20, no. 1 (2023): 1–12. http://dx.doi.org/10.19277/bbr.20.1.305.

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Lysyl oxidase (LOX) and LOX-like 1-4 (LOXL 1-4) enzymes catalyze the cross-linking of elastin and collagen in the extracellular matrix, facilitating cell migration and invasion. The inhibition of these enzymes, particularly LOXL2, has been suggested as a therapeutic strategy to prevent breast cancer metastasis. In this work, new natural LOXL2 inhibitors were searched from Aeollanthus rydingianus, a medicinal plant rich in bioactive products. Five pimarane diterpenoids, two isolated from the plant and three derivatives, were tested. These compounds have been described for their bioactive proper
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Stawiński, Tomasz M., and Mario González De La Parra Y. "Mass spectra of some pimaranes." Organic Mass Spectrometry 20, no. 10 (1985): 646–47. http://dx.doi.org/10.1002/oms.1210201010.

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Guo, Brian, Ming Zhao, Zhenlong Wu, Monday M. Onakpa, Joanna E. Burdette, and Chun-Tao Che. "19-nor-pimaranes from Icacina trichantha." Fitoterapia 144 (July 2020): 104612. http://dx.doi.org/10.1016/j.fitote.2020.104612.

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Hanson, James R. "Diterpenoids of terrestrial origin." Natural Product Reports 33, no. 10 (2016): 1227–38. http://dx.doi.org/10.1039/c6np00059b.

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This review covers the isolation and chemistry of diterpenoids from terrestrial as opposed to marine sources and includes labdanes, clerodanes, pimaranes, abietanes, kauranes, cembranes and their cyclization products. The literature from January to December, 2015 is reviewed.
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Hanson, James R. "Diterpenoids of terrestrial origin." Natural Product Reports 34, no. 10 (2017): 1233–43. http://dx.doi.org/10.1039/c7np00040e.

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This review covers the isolation and chemistry of diterpenoids from terrestrial as opposed to marine sources and includes labdanes, clerodanes, abietanes, pimaranes, kauranes, cembranes and their cyclization products. The literature from January to December, 2016 is reviewed.
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Hanson, James R. "Diterpenoids of terrestrial origin." Natural Product Reports 32, no. 12 (2015): 1654–63. http://dx.doi.org/10.1039/c5np00087d.

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This review covers the isolation and chemistry of diterpenoids from terrestrial as opposed to marine sources and includes, labdanes, clerodanes, pimaranes, abietanes, kauranes, gibberellins, cembranes and their cyclization products. The literature from January to December, 2014 is reviewed.
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Hanson, James R. "Diterpenoids of terrestrial origin." Natural Product Reports 32, no. 1 (2015): 76–87. http://dx.doi.org/10.1039/c4np00108g.

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This review covers the isolation and chemistry of diterpenoids from terrestrial as opposed to marine sources and includes labdanes, clerodanes, pimaranes, abietanes, kauranes, gibberellins, cembranes and their cyclization products. The literature from January to December 2013 is reviewed.
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Sun, Meng, Brian Guo, Mingming Xu та ін. "(9βH)- and 17-Nor-Pimaranes from Icacina oliviformis". Journal of Natural Products 84, № 4 (2021): 949–55. http://dx.doi.org/10.1021/acs.jnatprod.9b01131.

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Guo, Brian, Monday M. Onakpa, Xiao-Jun Huang, et al. "Di-nor- and 17-nor-pimaranes from Icacina trichantha." Journal of Natural Products 79, no. 7 (2016): 1815–21. http://dx.doi.org/10.1021/acs.jnatprod.6b00289.

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Dissertations / Theses on the topic "Pimaranes"

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Techer, Sophie. "Criblage d’activités biologiques de plantes endémiques ou indigènes de La Réunion - Recherche de molécules antivirales ciblant le virus du chikungunya." Thesis, La Réunion, 2013. http://www.theses.fr/2013LARE0014/document.

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Ce travail de thèse s'attache à identifier des plantes et/ou molécules à activités cytotoxique, antioxydante, anti-inflammatoire et antivirale ciblant le virus du chikungunya (CHIKV) dans le but de trouver des alternatives thérapeutiques vis-à-vis du stress oxydatif et de l'inflammation, mécanismes impliqués dans les maladies chroniques non transmissibles (diabète, obésité…), et de la maladie du chikungunya, maladie vectorielle réémergente. La première partie de ces travaux présente les résultats obtenus lors d'un criblage d'activités biologiques réalisé sur une sélection de dix-huit plantes e
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Book chapters on the topic "Pimaranes"

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Atta-ur-Rahman and Viqar Uddin Ahmad. "Pimarane." In 13C-NMR of Natural Products. Springer US, 1992. http://dx.doi.org/10.1007/978-1-4615-3288-0_11.

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"10.5 Pimarane- and isopimarane-type diterpenoids." In Diterpenoids, Triterpenoids, Sesterterpenoids, Tetraterpenoids, and Carotenoids. De Gruyter, 2021. http://dx.doi.org/10.1515/9783110634723-018.

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Nguyen, Phi Hung, Dao Cuong To, and Manh Hung Tran. "Pimarane Diterpenes from Vietnamese Orthosiphon stamineus Benth. and Their Glucose Uptake Stimulatory and PTP1B Inhibitory Activities." In Current Advances in Chemistry and Biochemistry Vol. 1. Book Publisher International (a part of SCIENCEDOMAIN International), 2021. http://dx.doi.org/10.9734/bpi/cacb/v1/7264d.

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Conference papers on the topic "Pimaranes"

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Sass, Daiane Cristina, Vladimir C. G. Heleno, Aline Nazaré Silva, Simone Cavalcante Silva, and Mauricio Gomes Constantino. "Synthesis of Pimarane-type Diterpenes from Constituents of Copaiba Oil." In 14th Brazilian Meeting on Organic Synthesis. Editora Edgard Blücher, 2013. http://dx.doi.org/10.5151/chempro-14bmos-r0132-2.

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