2000
DOI: 10.1016/s0031-9422(00)00144-8
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Cytotoxic cardenolides and antibacterial terpenoids from Crossopetalum gaumeri

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Cited by 57 publications
(37 citation statements)
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“…Celastrol (65) was toxic to several human cancer cell lines (Kutney et al, 1981a;Figueiredo et al, 1998;González et al, 1998;Ankli et al, 2000;Zhou et al, 2002;Lee et al, 2004) and inhibited TPA-induced EBV-EA . Pristimerin (64) and tingenone (66) were also toxic to numerous cancer cell lines (Gonzalez et al, 1977;Kutney et al, 1981a,b;Itokawa et al, 1991;Ngassapa et al, 1994;Shirota et al, 1994;Figueiredo et al, 1998;González et al, 1998;Setzer et al, 1998Setzer et al, , 2001Lee et al, 2004).…”
Section: Cancermentioning
confidence: 99%
See 1 more Smart Citation
“…Celastrol (65) was toxic to several human cancer cell lines (Kutney et al, 1981a;Figueiredo et al, 1998;González et al, 1998;Ankli et al, 2000;Zhou et al, 2002;Lee et al, 2004) and inhibited TPA-induced EBV-EA . Pristimerin (64) and tingenone (66) were also toxic to numerous cancer cell lines (Gonzalez et al, 1977;Kutney et al, 1981a,b;Itokawa et al, 1991;Ngassapa et al, 1994;Shirota et al, 1994;Figueiredo et al, 1998;González et al, 1998;Setzer et al, 1998Setzer et al, , 2001Lee et al, 2004).…”
Section: Cancermentioning
confidence: 99%
“…Pristimerin (64) and tingenone (66) were also toxic to numerous cancer cell lines (Gonzalez et al, 1977;Kutney et al, 1981a,b;Itokawa et al, 1991;Ngassapa et al, 1994;Shirota et al, 1994;Figueiredo et al, 1998;González et al, 1998;Setzer et al, 1998Setzer et al, , 2001Lee et al, 2004). 22β-Hydroxy-tingenone (67) was about as cytotoxic as 64 and 66 (Kutney et al, 1981b;Bavovada et al, 1990;Itokawa et al, 1991;Shirota et al, 1994;Sattar et al, 1998;, which were generally more toxic than 65 (Ngassapa et al, 1994;Ankli et al, 2000;Chang et al, 2003).…”
Section: Cancermentioning
confidence: 99%
“…A further search for structurally interesting and bioactive compounds from this plant resulted in the isolation of the new phenolic triterpenes isoblepharodol (1), 7-oxo blepharodol (2), blepharotriol (3), and 6-deoxoblepharodol (4), together with the known phenolic triterpenes 6-oxopristimerol, 8 7-hydroxy-6-oxopristimerol, 9 demethyl zeylasteral and demethylzeylasterone. 10 Their structures were determined by spectroscopic methods, including 1 H-13 C heteronuclear correlation (HSQC), long-range correlation with inverse detection (HMBC), and ROESY NMR experiments.…”
Section: Introductionmentioning
confidence: 99%
“…Because tannins are polyphenolic compounds. This was confirmed by Harbourne, 18,19 classic way to detect simple phenol extract is added to a solution of FeCl3 1% in water, which cause the color green, red, purple, blue and black strong. Formation of green or blue-black ink on the extract after added with FeCl3 1% as tannins will form complexes with Fe 3+ ions.…”
Section: Results and Discussion Phytochemical Testsmentioning
confidence: 75%
“…This result indicates there are present of tannin. Tannins can be used as an antibacterial because it has a phenol group, so that the tannins have properties like alcohol is an antiseptic that can be used as an antimicrobial component 18 . These experiments show that the extract being extracted does contain antibacterial properties and can be used to formulate the antibacterial cream.…”
Section: Results and Discussion Phytochemical Testsmentioning
confidence: 99%