2007
DOI: 10.1016/j.phytochem.2007.02.006
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Activity-guided isolation of antiplasmodial dihydrochalcones and flavanones from Piper hostmannianum var. berbicense

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Cited by 83 publications
(80 citation statements)
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“…C. DC. showed no cytotoxic activity against MCF-7 cell lines (Portet et al, 2007); ethanol extract of Piper sarmentosum Roxb. inhibited HepG2 cells and nonmalignant Chang's liver cell lines (Ariffin et al, 2009); dichloromethane and methanol extracts from fruits of Piper nigrum L. and Piper chaba Hunter were inactive against C32 and HeLa cell lines (Atjanasuppat et al, 2009); although, E-piplartine isolated from roots of P. chaba showed cytotoxicity against several cell lines (BC-8, PCC4, P388S1, IMR32), significantly increased by curcumin (Jyothi et al, 2009).…”
Section: Discussionmentioning
confidence: 94%
See 1 more Smart Citation
“…C. DC. showed no cytotoxic activity against MCF-7 cell lines (Portet et al, 2007); ethanol extract of Piper sarmentosum Roxb. inhibited HepG2 cells and nonmalignant Chang's liver cell lines (Ariffin et al, 2009); dichloromethane and methanol extracts from fruits of Piper nigrum L. and Piper chaba Hunter were inactive against C32 and HeLa cell lines (Atjanasuppat et al, 2009); although, E-piplartine isolated from roots of P. chaba showed cytotoxicity against several cell lines (BC-8, PCC4, P388S1, IMR32), significantly increased by curcumin (Jyothi et al, 2009).…”
Section: Discussionmentioning
confidence: 94%
“…By bioassay-guided purification from hexane extract of P. hostmannianum var. berbicense in vitro activity to P. falciparum (IC50 5.64 µM) and in vivo activity against Plasmodium vinckei petteri was demonstrated by (-)-methyllinderatin (Portet et al, 2007). From 94 species detected by ethnobotany in Peru, eight species of Piper were detected, P. aduncum showed activity against P. falciparum (9.6±1.7 µg/mL), and Piper dennisii Trel.…”
Section: Larvicidalmentioning
confidence: 99%
“…The infrared spectra were interpreted according to the literature data [37][38][39][40][41][42][43][44][45][46][47]. The FTIR spectra of our sample and the assignments of their infrared absorption bands are reported respectively in Fig.5 and Table 3.…”
Section: Fourier Transform Infrared Spectroscopy (Ftir)mentioning
confidence: 99%
“…The band at 1440 cm −1 due to in plane deformation of -CH 2 (CH 2 -C=C) (δ 1 H 2 ppm; δ 13 C 22-30 ppm), the peak at 1372 cm −1 corresponds to C-H bending of CH 3 groups or to COO − antisymmetric stretching [47,49]. The high band intensity at 1232 cm −1 corresponds to the stretching vibration of C ar -O aromatic and/or in plane deformation of CO 2 H in carboxylic acids or unsaturated ethers [37][38][39][40]. The absorption band at 1114 cm −1 corresponds to the vibrations in ether (C sp3 -O-C ar ), alcohols (C sp3 -OH), C sp3 -OH of the carboxylic acids and C sp3 -O of ester [50] as well the large peak around 1040 cm −1 due to carbohydrates of polysaccharides [43,[51][52].…”
Section: Fourier Transform Infrared Spectroscopy (Ftir)mentioning
confidence: 99%
“…Indeed, the vast majority of the existing anti-malaria chemotherapeutic agents are based on natural products and this fact anticipates that new anti-malaria may constantly emerge from our tropical plants sources if well harnessed, since biological chemo diversity continue to be an important source of molecular templates in the search for anti-malaria drugs (Portet et al, 2007). Further research to isolate, identify, elucidate and characterize the active ingredients, especially from the alkaloids, flavonoids, terpenoids and quinones from which most anti-malaria drugs have been isolated, are encouraged.…”
Section: Resultsmentioning
confidence: 99%