2006
DOI: 10.1016/j.phytochem.2006.01.030
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Antiplatelet prenylflavonoids from Artocarpus communis

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Cited by 55 publications
(53 citation statements)
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“…A large number of phenolic compounds including flavonoids, stilbenoids, and 2-arylbenzofurons have been isolated from Artocarpus plants and possess a wide range of biological properties such as anti-inflammatory (Hsu et al, 2012;Lin et al, 2011), antiplatelet (Jagtap & Bapat, 2010;Weng et al, 2006), antimycobacterial (Loizzo et al, 2010;Siritapetawee et al, 2012), and antiprotozoal activities (Bourjot et al, 2010). Among these activities, the antioxidant actions of these polyphenols derived from Artocarpus species have been frequently reported in vivo and in vitro (Omar et al, 2011;Sidahmed et al, 2013).…”
Section: Discussionmentioning
confidence: 99%
“…A large number of phenolic compounds including flavonoids, stilbenoids, and 2-arylbenzofurons have been isolated from Artocarpus plants and possess a wide range of biological properties such as anti-inflammatory (Hsu et al, 2012;Lin et al, 2011), antiplatelet (Jagtap & Bapat, 2010;Weng et al, 2006), antimycobacterial (Loizzo et al, 2010;Siritapetawee et al, 2012), and antiprotozoal activities (Bourjot et al, 2010). Among these activities, the antioxidant actions of these polyphenols derived from Artocarpus species have been frequently reported in vivo and in vitro (Omar et al, 2011;Sidahmed et al, 2013).…”
Section: Discussionmentioning
confidence: 99%
“…In Cameroon, the fruits of A. communis are used as food; other parts of the plants are traditionally used to treat headache, infectious and associated diseases such as toothache, eye problems, ear infections, herpes, enlarged spleen, sprains, contusions, swelling [3-5]. Some scientific evidences of the bioactivity of A. communis were reported on the extract or isolated compounds [6-9]. However, few reports are related to the antimicrobial activity of this taxon.…”
Section: Introductionmentioning
confidence: 99%
“…The UV spectrum in MeOH displayed absorption bands at λ max 218, 261 and 363 nm, suggesting a flavonoid skeleton. 16,17 The IR spectrum showed absorption bands of hydroxy (3339 cm ). The molecular formula, C 17 H 12 O 8 , implying twelve double bond equivalents, was deduced from NMR data and by HR-ESIMS (see exp.…”
mentioning
confidence: 99%