Phytochemical investigations of Campsis radicans L.
DOI:
https://doi.org/10.18231/j.joapr.2020.v.8.i.3.55.59Keywords:
Campsis radicans, Bignoniaceae, corosolic acid, arjunolic acid, maslinic acidAbstract
Petroleum ether, dichloromethane and ethyl acetate soluble fractions were obtained through partitioning the crude methanolic extract of the leaves of Campsis radicans L. (Family. Bignoniaceae) followed by the chromatographic separation of secondary metabolites from them. A total of five triterpene compounds i.e., corosolic acid methyl ester (1), β-amyrin (2), arjunolic acid (3), maslinic acid (4) and 28-O-[β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl]-2α,3α,19α-trihydroxy-12-en-28-ursolic acid (5) were isolated from the dichloromethane fractions and their structures were characterized by 1H NMR spectroscopy and compared the NMR data with published values.
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References
Wen J, Jansen RK. Morphological and molecular comparisons of Campsis grandiflora and C. radicans (Bignoniaceae), an Eastern Asian and Eastern North American vicariad species pair. Plant Systematics and Evolution 196, 173-83 (1995).
Uddin MZ, Hassan MA. Plant diversity of Dhaka University campus. Journal of Asiatic Society of Bangladesh Science, 42, 49-68 (2016).
Michael M. Medicinal Plants of the Desert and Canyon West, p. 124 (1989).
Islam M, Jannat T, Kuddus MR, Rashid MR, Haque MR. In vitro and in vivo evaluation of pharmacological potentials of Campsis radicans L. Clinical Phytoscience 5, 42 (2019).
Hashem FA. Investigation of free radical scavenging activity by ESR for coumarins isolated from Tecoma radicans. Journal of Medical Science, 7, 1027-32 (2007).
Hashem FA. Free radical scavenging activity of the flavonoids isolated from Tecoma radicans. Journal of Herbs, Spices & Medicinal Plants, 13,1-10 (2008).
Van-Wagenen BC, Larsen R, Cardellina JH, Randazzo D, Lidert ZC, Swithenbank C. Ulosantion, a potent insecticide from the sponge Ulosa ruetzleri. Journal of Organometallic Chemistry, 58, 335-7 (1993).
Kim DH, Han KM, Chung IS, Kim DK, Kim SH, Kwon BM, Jeong TS, Park MH, Ahn EM, Baek NI. Triterpenoids from the flower of Campsis grandiflora K. Schum. as human acyl-CoA: cholesterol acyltransferase inhibitors. Archives of Pharmacal Research, 28, 550-556 (2005).
Kuddus MR, Rumi F, Kaisar MA, Rahman MS, Hasan CM, Hassan MA, Rashid MA. Secondary metabolites from Melocanna baccifera (Roxb.). Asian Journal of Chemistry, 23, 85-88 (2011).
Ercil D, Sakar MK, Del Olmo E. and San Feliciano A. Chemical constituents of Linaria aucheri. Turkish Journal of Chemistry, 28, 133-140 (2004).
Woo KY, Han JY, Choi SU, Kim KH, Lee KR. Triterpenes from Perilla frutescens var. acuta and their cytotoxic activity. Natural Product Sciences, 20, 71-75 (2014).
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Copyright (c) 2020 Mirazul Islam, Md Ruhul Kuddus, Mohammad Abdur Rashid, Mohammad Rashedul Haque
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