Relevant bibliographies by topics / Cycloartane derivatives

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  1. Journal articles

Academic literature on the topic 'Cycloartane derivatives'

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

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Journal articles on the topic "Cycloartane derivatives"

1

Cabrera, Gabriela M., Mariana Gallo, and Alicia M. Seldes. "Cycloartane Derivatives fromTillandsia usneoides." Journal of Natural Products 59, no. 4 (1996): 343–47. http://dx.doi.org/10.1021/np960075+.

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2

Nyemba, Anne-Marie, Theophile Ngando Mpondo, Joseph D. Connolly, and David S. Rycroft. "Cycloartane derivatives from Garcinia lucida." Phytochemistry 29, no. 3 (1990): 994–97. http://dx.doi.org/10.1016/0031-9422(90)80067-q.

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3

Furlan, Maysa, Nídia Franca Roque, and Wilson Wolter Filho. "Cycloartane derivatives from Guarea trichilioides." Phytochemistry 32, no. 6 (1993): 1519–22. http://dx.doi.org/10.1016/0031-9422(93)85170-v.

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4

Kim, Nanyoung, SeonJu Park, Nguyen Xuan Nhiem, Jae-Hyoung Song, Hyun-Jeong Ko, and Seung Hyun Kim. "Cycloartane-type triterpenoid derivatives and a flavonoid glycoside from the burs of Castanea crenata." Phytochemistry 158 (February 28, 2019): 135–41. https://doi.org/10.1016/j.phytochem.2018.11.001.

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Kim, Nanyoung, Park, SeonJu, Nhiem, Nguyen Xuan, Song, Jae-Hyoung, Ko, Hyun-Jeong, Kim, Seung Hyun (2019): Cycloartane-type triterpenoid derivatives and a flavonoid glycoside from the burs of Castanea crenata. Phytochemistry 158: 135-141, DOI: 10.1016/j.phytochem.2018.11.001, URL: http://dx.doi.org/10.1016/j.phytochem.2018.11.001
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5

Nagashima, Fumihiro, Yuki Tabuchi, Takuya Ito, Liva Harinantenaina, and Yoshinori Asakawa. "Terpenoids, Flavonoids and Acetogenins from Some Malagasy Plants." Natural Product Communications 11, no. 2 (2016): 1934578X1601100. http://dx.doi.org/10.1177/1934578x1601100205.

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Humulanes, drimanes, ent-kaurane, lupane, cycloartane, flavanone, flavones and quinol derivatives were isolated from Malagasy Cussonia vantsilana, Helichrysum gymnocephalum, Phyllarthron madagascariense, Gomphocarpus fructicosus, Cinnamosma sp. and C. fragrans, and their structures elucidated by using extensive NMR analysis. A mixture of a few flavones and/or lupane triterpene showed antimicrobial activity against Mycobacterium smegmatis and Pseudomonas aeruginosa.
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6

Debelec-Butuner, Bilge, Mert Burak Ozturk, Ozgur Tag, Ismail Hakki Akgun, Erdal Bedir, and Kemal Sami Korkmaz. "Characterization of Cycloartane-Type Sapogenol Derivatives for Prostate Cancer Chemoprevention." Proceedings 1, no. 10 (2017): 985. http://dx.doi.org/10.3390/proceedings1100985.

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7

Watanabe, Kazuki, Yoshihiro Mimaki, Haruhiko Fukaya, and Yukiko Matsuo. "Cycloartane and Oleanane Glycosides from the Tubers of Eranthis cilicica." Molecules 24, no. 1 (2018): 69. http://dx.doi.org/10.3390/molecules24010069.

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Phytochemical analysis of the tubers of Eranthis cilicica was performed as part of our continuous study on the plants of the family Ranunculaceae, which resulted in the isolation of eleven new cycloartane glycosides (1–11) and one new oleanane glycoside (13), together with one known oleanane glycoside (12). The structures of the new compounds were determined by extensive spectroscopic analysis, including two-dimensional (2D) NMR, and enzymatic hydrolysis followed by either X-ray crystallographic or chromatographic analysis. The aglycone (1a) of 2 and its C-23 epimer (8a), and the oleanane glyc
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8

R., Banik, and Dinda B. "Chemical constituents of Artocarpus chaplasha." Journal of Indian Chemical Society 93, Mar 2016 (2016): 333–36. https://doi.org/10.5281/zenodo.5639088.

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Department of Chemistry, Tripura University, Suryamaninagar-799 022, Tripura, India <em>E-mail </em>: dindabtu@gmail.com <em>Manuscript received 05 September 2012, revised 29 May 2015, accepted 26 November 2015</em> Chemical investigation of the stem bark of Artocarpus chaplasha (Moraceae) afforded cycloartenyl acetate&nbsp;(1), 24-methylenecycloartanyl acetate (2), lupenyl acetate (3), (23E)-25-hydroxycycloart-23-en-3&beta;-ol (4), (23E)-25- methoxycycloart-23-en-3&beta;-ol (5), (23E)-25-hydroperoxycycloart-23-en-3&beta;-ol (6), &beta;-sitosterol (7) and stigmasterol (8). Compounds 2, 4-6 and
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9

Kim, Nanyoung, SeonJu Park, Nguyen Xuan Nhiem, Jae-Hyoung Song, Hyun-Jeong Ko, and Seung Hyun Kim. "Cycloartane-type triterpenoid derivatives and a flavonoid glycoside from the burs of Castanea crenata." Phytochemistry 158 (February 2019): 135–41. http://dx.doi.org/10.1016/j.phytochem.2018.11.001.

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10

Ning, Ruo-nan, Hong-min Wang, Yu Shen, et al. "Lithocarpic acids O–S, five homo-cycloartane derivatives from the cupules of Lithocarpus polystachyus." Bioorganic & Medicinal Chemistry Letters 24, no. 23 (2014): 5395–98. http://dx.doi.org/10.1016/j.bmcl.2014.10.036.

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