Antibacterial phloroglucinols derivatives from the leaves of Mallotus oppositifolius (Geisler) Müll. Arg. (Euphorbiaceae).

作者: Yvan Anderson Ngandjui Tchangoue , Joseph Tchamgoue , Paul Keilah Lunga , Janosch Knepper , Ramona Paltinean

DOI: 10.1016/J.FITOTE.2020.104527

关键词: Mallotus oppositifoliusMallotojaponinMinimum inhibitory concentrationEuphorbiaceaeStereochemistryChemistry

摘要: Abstract From the ethno-medicinally used leaves of Mallotus oppositifolius, four acylphloroglucinol derivatives, namely Acronyculatin S U (1–3) and Mallotojaponin D (4) were isolated along with seven known compounds (5–11). Structures elucidated by comprehensive spectroscopic analyses HRMS data. Absolute configurations assigned careful comparison their specific optical rotation those closely related compounds. Compounds 1, 2, 6 11 demonstrated inhibitory activity against bacterial strains E. coli, S. aureus, typhi, P. aeruginosa minimum concentration (MIC) values ranging from 3.125 to 50 μg/ml.

参考文章(38)
Faustin A. Kabran, Timothée A. Okpekon, François Roblot, Blandine Séon-Méniel, Karine Leblanc, Christian Bories, Pierre Champy, Séri F. Yolou, Philippe M. Loiseau, Léon A. Djakouré, Bruno Figadère, Alexandre Maciuk, Bioactive phloroglucinols from Mallotus oppositifolius Fitoterapia. ,vol. 107, pp. 100- 104 ,(2015) , 10.1016/J.FITOTE.2015.09.015
Eirini Kouloura, Maria Halabalaki, Marie-Christine Lallemand, Sangkil Nam, Richard Jove, Marc Litaudon, Khalijah Awang, Hamid A. Hadi, Alexios-Leandros Skaltsounis, Cytotoxic prenylated acetophenone dimers from Acronychia pedunculata. Journal of Natural Products. ,vol. 75, pp. 1270- 1276 ,(2012) , 10.1021/NP201007A
Tian-Ying An, Li-Hong Hu, Xiao-Fang Cheng, Zhong-Liang Chen, Two new benzopyran derivatives from Mallotus apelta. Natural Product Research. ,vol. 17, pp. 325- 328 ,(2003) , 10.1080/1057563031000072569
Jimmy Orjala, Anthony D. Wright, Henrik Behrends, Gerd Folkers, Otto Sticher, Heinz Rüegger, Topul Rali, Cytotoxic and antibacterial dihydrochalcones from Piper aduncum. Journal of Natural Products. ,vol. 57, pp. 18- 26 ,(1994) , 10.1021/NP50103A003
Zhong-yan Tang, Zheng-xiang Xia, Shi-ping Qiao, Chao Jiang, Guo-rong Shen, Mei-xiang Cai, Xiao-yan Tang, Four new cytotoxic xanthones from Garcinia nujiangensis. Fitoterapia. ,vol. 102, pp. 109- 114 ,(2015) , 10.1016/J.FITOTE.2015.02.011
Laurice Bracine Njanang Chenda, Simeon Fogue Kouam, Marc Lamshöft, Souvik Kusari, Ferdinand Mouafo Talontsi, Bonaventure Tchaleu Ngadjui, Michael Spiteller, Isolation and characterization of six labdane diterpenes and one pregnane steroid of Turraeanthus africanus. Phytochemistry. ,vol. 103, pp. 137- 144 ,(2014) , 10.1016/J.PHYTOCHEM.2014.03.022
Paul K Lunga, Xu-Jie Qin, Xing W Yang, Jules-Roger Kuiate, Zhi Z Du, Donatien Gatsing, Antimicrobial steroidal saponin and oleanane-type triterpenoid saponins from Paullinia pinnata. BMC Complementary and Alternative Medicine. ,vol. 14, pp. 369- 369 ,(2014) , 10.1186/1472-6882-14-369
Ya-Wen Sheu, Lien-Chai Chiang, Ih-Sheng Chen, Yu-Chang Chen, Ian-Lih Tsai, Cytotoxic flavonoids and new chromenes from Ficus formosana f. formosana. Planta Medica. ,vol. 71, pp. 1165- 1167 ,(2005) , 10.1055/S-2005-873163
K Kamanzi Atindehou, C Schmid, R Brun, M.W Koné, D Traore, Antitrypanosomal and antiplasmodial activity of medicinal plants from Côte d'Ivoire. Journal of Ethnopharmacology. ,vol. 90, pp. 221- 227 ,(2004) , 10.1016/J.JEP.2003.09.032