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Harpulliasides A and B: Two new benzeneacetic acid derivatives from Harpullia pendula
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In the citing paper
“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 [31]
In the citing paper
“Different flavonoids and polyphenolic compounds have previously been isolated and characterized from the H. pendula plant, including rutin, vitexin, isovitexin, orientin, quercetin, and kaempferol quercetin-3-O-β-d-glucoside”
From Novel Green Biosynthesis of 5-Fluorouracil Chromium Nanoparticles Using Harpullia pendula Extract for Treatment of Colorectal Cancer (2021) · cites this paper as [31]
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Research works printed but not linked: 29
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- Cherry, 1977, Chemical constituents of Harpullia pendula. 11: further constituents of the Bark and Leaves, Aust. J. Chem., 30, 1397, 10.1071/CH9771397 · DOI
- Devi, 2004, Antiviral action of Harpulia cupanioides and Mirabilis jalapa against tomato spotted wilt virus (TSWV) infecting tomato viral action of Harpulia cupanioides and Mirabilis jalapa against tomato spotted wilt virus (TSWV) infecting tomato, Arch. Phytopathol. Plant Protect., 37, 245, 10.1080/03235400412331273313 · DOI
- Dimbi, 1983, Triterpenöides de Harpullia Cupaniöides, Bull. Soc. Chim. Belg., 92, 473, 10.1002/bscb.19830920509 · DOI
- Dizes, 1998, Harpuloside a triterpenoid saponin from Harpullia ramiflora, Phytochemistry, 48, 1229, 10.1016/S0031-9422(98)00166-6 · DOI · Paper page
- Hamburger, 1985, Flavonol glycosides from Securidaca diversifolia, Phytochemistry, 24, 2689, 10.1016/S0031-9422(00)80695-0 · DOI
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- Kazuma, 2003, Malonylated flavonol glycosides from the petals of Clitoria ternatea, Phytochemistry, 62, 229, 10.1016/S0031-9422(02)00486-7 · DOI
- Khong, 1976, Chemical constituents of Harpullia pendula, Aust. J. Chem., 29, 1351, 10.1071/CH9761351 · DOI
- Kim, 2008, Anti-oxidative and inhibitory activities on nitric oxide (NO) and prostaglandin E2 (COX-2) production of flavonoids from seeds of Prunus tomentosa Thunberg, Arch. Pharm. Res., 31, 424, 10.1007/s12272-001-1174-9 · DOI
- Kim, 2010, Fast identification of flavonoids in the roots of Sophora flavescens by on-flow LC-NMR, J. Med. Plant Res., 4, 2452, 10.5897/JMPR10.073 · DOI
- Kronvall, 1983, Single-strain regression analysis for determination of interpretive breakpoints for cefoperazone disk diffusion susceptibility testing, J. Clin. Microbiol., 17, 975, 10.1128/JCM.17.6.975-980.1983 · DOI
- Kuroyanagi, 1999, Antibacterial and antiandrogen flavonoids from Sophora flavescens, J. Nat. Prod., 62, 1595, 10.1021/np990051d · DOI
- Ma, 2009, Seven new benzeneacetic acid derivatives and their quinone reductase activity from Eurycorymbus cavaleriei, Phytochem. Lett., 2, 152, 10.1016/j.phytol.2009.05.003 · DOI
- Mohamed, 2014, New anti-inflammatory flavonoids from Cadaba glandulosa Forssk, Arch. Pharm. Res., 37, 459, 10.1007/s12272-013-0305-1 · DOI
- Mohamed, 2014, Mangostanaxanthones I and II, new xanthones from the pericarp of Garcinia mangostana, Fitoterapia, 98, 215, 10.1016/j.fitote.2014.08.014 · DOI
- Mohamed, 2015, Blepharisides A and B: new flavonol glycosides from Blepharis ciliaris growing in Saudi Arabia, Phytochem. Lett., 11, 177, 10.1016/j.phytol.2014.12.018 · DOI
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- Scodro, 2015, A new benzoic acid derivative from Piper diospyrifolium and its anti-mycobacterium tuberculosis activity, Phytochem. Lett., 11, 18, 10.1016/j.phytol.2014.10.015 · DOI
- Shyamala, 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
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- Voutquenne, 1998, Saponins from Harpullia cupanioides, Phytochemistry, 49, 2081, 10.1016/S0031-9422(98)00406-3 · DOI
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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
Self-citation
Metadata
- Authors
- Abdelkader, M. S. A., Rateb, M. E., Mohamed, G. A., & Jaspars, M.
- Venue
- Phytochemistry Letters
- Publisher
- Elsevier BV
- Published
- 2016-03
- Volume
- 15
- Pages
- 131-135
- ISSN
- 1874-3900
- Cited by
- 11
- 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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