2000
DOI: 10.1002/(sici)1099-1573(200005)14:3<203::aid-ptr565>3.0.co;2-r
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A study of the trypanocidal and analgesic properties from Lychnophora granmongolense (Duarte) Semir & Leit�o Filho

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Cited by 58 publications
(40 citation statements)
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“…This activity was initially proposed due to the presence of sesquiterpene lactones. 30 However, Grael and co-workers 31 reported that extracts of the aerial parts of Lychnophora granmongolense showed no analgesic activity in the writhing model of pain, even though the STLs goyazensolide (84) and centratherin (92) were isolated from those extracts. These results, in combination with those obtained for the L. salicifolia extracts, 32 suggested that not all the Lychnophora species could exhibit analgesic activity correlated to the accumulation of sesquiterpene lactones.…”
Section: Proteopsis Furnensismentioning
confidence: 99%
“…This activity was initially proposed due to the presence of sesquiterpene lactones. 30 However, Grael and co-workers 31 reported that extracts of the aerial parts of Lychnophora granmongolense showed no analgesic activity in the writhing model of pain, even though the STLs goyazensolide (84) and centratherin (92) were isolated from those extracts. These results, in combination with those obtained for the L. salicifolia extracts, 32 suggested that not all the Lychnophora species could exhibit analgesic activity correlated to the accumulation of sesquiterpene lactones.…”
Section: Proteopsis Furnensismentioning
confidence: 99%
“…The NOEDIFF experiments confirmed all relative stereochemistry for each structure and some previously ambiguous carbon assignments were also clarified. C NMR data for centratherin (2). 500MHz, CDCl 3 …”
Section: Resultsmentioning
confidence: 99%
“…[1][2][3][4][5] Their structures show significant variety and complexity, making structural elucidation a challenge. Since the first articles on isolation and identification of SL were published in the early 1960s, some published data has proven incomplete, inaccurate or even wrong, due to equipment limitations at the time.…”
Section: Introductionmentioning
confidence: 99%
“…It showed an IC50 of 3.57 and 8.06 µg/mL (Table 1) against U87-MG and U251 cell lines, respectively. Furanoheliangolides often exhibit antiinflammatory, trypanocidal, cytotoxic, and genotoxic activities (Grael et al, 2000;Sakamoto et al, 2003;Santos et al, 2004;Vasconcelos et al, 2007;). The furanoheliangolides possess two functionalities in the form of an α-methylene-γ-lactone and an α,β,γ,δ unsaturated carbonyl group (Rüngeler et al, 1999) that can react through a stereospecific Michael addition with biological nucleophiles (mainly with the thiol groups of cysteine residues present in proteins) forming stable adducts (Ghantous et al, 2010).…”
Section: Ms/ms Analysis (mentioning
confidence: 99%