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Pendulaosides A and B. Two acylated triterpenoid saponins from Harpullia pendula seed extract
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“Members of the genus Harpullia are known to be rich sources of saponins, triterpenes, tannins, flavonoids, and sterols [29,30,31,32,33,34].”
From Novel Green Biosynthesis of 5-Fluorouracil Chromium Nanoparticles Using Harpullia pendula Extract for Treatment of Colorectal Cancer (2021) · cites this paper as [32]
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Research works printed but not linked: 24
- Abdel-Gawad, 2004, Laboratory evaluation of the molluscicidal miracidicidal and cercaricidal properties of two Egyptian plants, Bull. Pharm. Sci., 27, 331
- Abdelkader, 2016, Harpulliasides A and B: Two new benzeneacetic acid derivatives from Harpullia pendula, Phytochem. Lett., 15, 131, 10.1016/j.phytol.2015.12.006 · DOI · Paper page
- Abri, 2016, Isolation and identification of gallic acid from the Elaeagnus angustifolia leaves and determination of total phenolics, flavonoid contents and investigation of antioxidant activity, Iran. Chem. Commun., 4, 146
- Agrawal, 1992, NMR spectroscopy in the structural elucidation of oligosaccharides and glycosides, Phytochemistry, 31, 3307, 10.1016/0031-9422(92)83678-R · DOI
- Bharathimatha, 2002, Inhibition of fungal plant pathogens by seed proteins of Harpullia cupanioides (Roxb), Acta Phytopathol. Entomol. Hung., 37, 75, 10.1556/APhyt.37.2002.1-3.8 · DOI
- Chakravarty, 2003, Bacopasides III-V: three new triterpenoid glycosides from Bacopa monniera, Chem. Phar. Bull., 51, 215, 10.1248/cpb.51.215 · DOI
- Cherry, 1977, Chemical constituents of Harpullia pendula: II Further constituents of the bark and leaves, Aust. J. Chem., 30, 1397, 10.1071/CH9771397 · DOI
- Devi, 2004, Antiviral action of harpullia cupanioides and Mirabilis jalapa against tomato spotted Wilt virus (TSWV) infecting tomato, Arch. Phytopathol. Plant Protect., 37, 245, 10.1080/03235400412331273313 · DOI
- dos Santos, 2012, Anti- trypanosomal activity of 1,2,3,4,6-penta-O-galloyl-β-D-glucose isolated from plectranthus barbatus Andrews (Lamiaceae), Quim. Nova, 35, 2229, 10.1590/S0100-40422012001100025 · DOI
- El Sayed, 1988, Phenolics and flavonoids of the pericarp of Harpullia pendula, Rev. Latinoamer. Quim., 19, 66
- El-Gohary, 2004, Phytochemical and biological study of seeds of Harpullia pendula planch. and Harpullia cupanioides Roxb. cultivated in Egypt, Bull. Fac. Pharm. Cairo Univ., 42, 95
- Gowri, 2009, Solvent based effectiveness of antibacterial and phytochemical derivatized from the seeds of Harpullia arborea (Blanco) Radlk. (Sapindaceae), J. Appl. Sci. Environ. Manage., 13, 99
- Hisham, 2011, Identification and isolation of methyl gallate as a polar chemical marker for labisia pumila Benth, J. Trop. Agric. Fd Sc., 39, 279
- Kandil, 2001, Polyphenols from Cornulaca monacantha, Phytochemistry, 58, 611, 10.1016/S0031-9422(01)00265-5 · DOI
- Khong, 1976, Chemical constituents of Harpullia pendula, Aust. J. Chem., 29, 1351, 10.1071/CH9761351 · DOI
- Melek, 2002, Triterpenoid saponins from Oreopanax guatemalensis, Phytochemistry, 60, 185, 10.1016/S0031-9422(02)00058-4 · DOI
- Mosmann, 1983, Colorimetric assay for cellular growth and survival application to proliferation and cytotoxicity assay, J. Immunol. Methods, 65, 55, 10.1016/0022-1759(83)90303-4 · DOI · Paper page
- Murakami, 1999, Bioactive saponins and glycosides XV1). Saponin constituents with gastroprotective effect from the seeds of tea plant, Camellia sinensis L. var. assamica Pierre, cultivated in Sri Lanka: structures of Assamsaponins A, B, C, D and E, Chem. Pharm. Bull., 47, 1759, 10.1248/cpb.47.1759 · DOI
- Ohtsuki, 2008, Acylated triterpenoid saponins from Schima noronhae and their growth inhibitory activity, J. Nat. Prod., 71, 918, 10.1021/np800036t · DOI
- Voutquenne, 1998, Saponins from Harpullia cupanioides, Phytochemistry, 49, 2081, 10.1016/S0031-9422(98)00406-3 · DOI
- Voutquenne, 2002, Triterpenoid saponins and acylated prosapogenins from Harpullia austro-caledonica, Phytochemistry, 59, 825, 10.1016/S0031-9422(01)00482-4 · DOI
- Voutquenne, 2005, Haemolytic acylated triterpenoid saponins from Harpullia austro-caledonica, Phytochemistry, 66, 825, 10.1016/j.phytochem.2005.02.009 · DOI
- Yoshikawa, 1994, Camelliasaponins B1, B2, C1 and C2, New type inhibitors of ethanol absorption in rats from the seeds of Camellia Japonica L, Chem. Pharm. Bull., 42, 742, 10.1248/cpb.42.742 · DOI
- Zhang, 2012, A new saponin from Tea seed Pomace (Camellia oleifera Abel) and its protective effect on PC12 cells, Molecules, 17, 11721, 10.3390/molecules171011721 · DOI
Cited by
Sorted by citations
Saddik, M. S., Elsayed, M. M. A., Abdelkader, M. S. A., El-Mokhtar, M. A., Abdel-Aleem, J. A., Abu-Dief, A. M., Al-Hakkani, M. F., Farghaly, H. S., & Abou-Taleb, H. A. (2021) · Pharmaceutics · doi:10.3390/pharmaceutics13020226 · Cited by 89
Metadata
- Authors
- Ghaly, N. S., Nabil, M., Grace, M. H., & Melek, F. R.
- Venue
- Phytochemistry Letters
- Publisher
- Elsevier BV
- Published
- 2017-09
- Volume
- 21
- Pages
- 278-282
- ISSN
- 1874-3900
- Cited by
- 4
- References
- 0
- Language
- en
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Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
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