Abstract:Phytochemical investigation of the twigs of Garcinia nobilis led to the isolation of a new xanthone, named l-hydroxy-2,5-dimethoxyxanthone (1), together with 15 known compounds (2 -16). The structures of the new and known compounds were established by means of spectroscopic methods and by comparison with previously reported data. The structure of compound 1 was confirmed by X-ray diffraction data. Compounds 1 -16 were tested for their cytotoxic activity against human cervix carcinoma cell line KB-3-1. Compound… Show more
“…Based on an agar diffusion method, 15 the antibacterial activity of all compounds was tested against Escherichia coli DSMZ 1058, Bacillus subtilis DSMZ 704, Micrococcus luteus DSMZ 1605, Cell-based cytotoxicity assays of all isolated compounds against the human cervix carcinoma cell line KB-3-1 in a resazurin assay was undertaken according to our previous study. 16 However, all the tested compounds were found to be inactive against the KB-3-1 cell line.…”
Section: Resultsmentioning
confidence: 96%
“…Cell-based cytotoxicity assays of all isolated compounds against the human cervix carcinoma cell line KB-3-1 in a resazurin assay was undertaken according to our previous study. 16 However, all the tested compounds were found to be inactive against the KB-3-1 cell line.…”
Section: Resultsmentioning
confidence: 96%
“…The cytotoxicity of 1-3 against the human cervix carcinoma cell line KB-3-1 was evaluated as previously reported. 16 The KB-3-1 cells were cultivated in 1 layer in Dulbecco's Modified Eagle medium with glucose (4.5 g/L), l-glutamine, sodium pyruvate, and phenol red, supplemented with 10% fetal bovine serum (FBS). The cells were then maintained at 37 °C in 5.3% carbon dioxide (CO 2 ) humidified air.…”
One new polyketide derivative, heptacyclosordarianone (1), together with 2 known compounds, heptacyclosordariolone (2) and sordariol (3), were isolated from an extract of Sordaria sp. AM-71, an endophytic fungus inhabiting Garcinia polyantha. The structures of these compounds were elucidated based on intensive nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry and by comparison with literature data. All compounds were assayed for their antimicrobial and cytotoxic properties. Only compound 2 showed antimicrobial activities against Bacillus subtilis DSMZ 704 , Pseudomonas agarici DSMZ 11810, and Micrococcus luteus DSMZ 1605 with minimum inhibitory concentration values of 9.3, 15.5, and 16.9 µg/mL respectively. None of the isolated compounds showed a significant cytotoxic property.
“…Based on an agar diffusion method, 15 the antibacterial activity of all compounds was tested against Escherichia coli DSMZ 1058, Bacillus subtilis DSMZ 704, Micrococcus luteus DSMZ 1605, Cell-based cytotoxicity assays of all isolated compounds against the human cervix carcinoma cell line KB-3-1 in a resazurin assay was undertaken according to our previous study. 16 However, all the tested compounds were found to be inactive against the KB-3-1 cell line.…”
Section: Resultsmentioning
confidence: 96%
“…Cell-based cytotoxicity assays of all isolated compounds against the human cervix carcinoma cell line KB-3-1 in a resazurin assay was undertaken according to our previous study. 16 However, all the tested compounds were found to be inactive against the KB-3-1 cell line.…”
Section: Resultsmentioning
confidence: 96%
“…The cytotoxicity of 1-3 against the human cervix carcinoma cell line KB-3-1 was evaluated as previously reported. 16 The KB-3-1 cells were cultivated in 1 layer in Dulbecco's Modified Eagle medium with glucose (4.5 g/L), l-glutamine, sodium pyruvate, and phenol red, supplemented with 10% fetal bovine serum (FBS). The cells were then maintained at 37 °C in 5.3% carbon dioxide (CO 2 ) humidified air.…”
One new polyketide derivative, heptacyclosordarianone (1), together with 2 known compounds, heptacyclosordariolone (2) and sordariol (3), were isolated from an extract of Sordaria sp. AM-71, an endophytic fungus inhabiting Garcinia polyantha. The structures of these compounds were elucidated based on intensive nuclear magnetic resonance spectroscopy and high-resolution mass spectrometry and by comparison with literature data. All compounds were assayed for their antimicrobial and cytotoxic properties. Only compound 2 showed antimicrobial activities against Bacillus subtilis DSMZ 704 , Pseudomonas agarici DSMZ 11810, and Micrococcus luteus DSMZ 1605 with minimum inhibitory concentration values of 9.3, 15.5, and 16.9 µg/mL respectively. None of the isolated compounds showed a significant cytotoxic property.
“…nobilis is found in the Southwest Region of Cameroon and is known to be a rich source of bioactive xanthones [16,17]. Similar to the small peptides, polyketides constitute a large proportion of industrial antibiotics.…”
Isolated compounds from Penicillium sp. harbored in G. nobilis exhibited promising antimycobacterial activity against M. smegmatis thus supporting the immensity of the potential of antimycobacterial drug discovery from endophytes from medicinal plants. Penialidin C could further be investigated for antimycobacterial drug development.
“…Guttiferones have been reported as anti-HIV, trypanocidal and cytotoxic agents (Gustafson et al 1992;Komguem et al 2005;Merza et al 2006). Our previous studies of the chemistry of Garcinia nobilis led to the isolation of xanthones derivatives including the isolation from the leaves of d l-hydroxy-2,5-dimethoxyxanthone with cytotoxic activity against human cervix carcinoma cell line KB-3-1 (Fouotsa et al 2014). We also isolated caroxanthone from the stem bark of G. nobilis which exhibited a-glucosidase and antibacterial activities but did not showed any a-chymotrypsin inhibitory activity (Fouotsa et al 2012;.…”
A new xanthone, mboudiexanthone (1), together with five known compounds, euxanthone (2), isogarcinol (3), garcinol (4), betulinic acid (5) and zeorin (6) were isolated from the leaves of Garcinia nobilis Engl. The structures were determined by 1D and 2D NMR techniques and X-ray diffraction for 6. The in vitro antiproliferative properties of isolated compounds were evaluated against the human breast cancer cell line MCF-7. All compounds showed an antiproliferative activity with an IC 50 value down to $11 mM for isogarcinol.
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