2011
DOI: 10.1016/j.bmc.2011.06.067
|View full text |Cite
|
Sign up to set email alerts
|

In vitro cytotoxic activity of abietane diterpenes from Peltodon longipes as well as Salvia miltiorrhiza and Salvia sahendica

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

2
55
0

Year Published

2012
2012
2019
2019

Publication Types

Select...
7
2

Relationship

0
9

Authors

Journals

citations
Cited by 84 publications
(57 citation statements)
references
References 28 publications
2
55
0
Order By: Relevance
“…The seven known compounds were identified as mandarone A (1) [11], taxusabietane A (2) [12], 12-O-demethylcrypto-japonol (3) [13], cryptojaponol (4) [14], 11,14-dihydroxy-8,11,13-abietatrien-7-one (5) [15], fortunin E (6) [16], fortunin F (7) [16], by comparison of their spectra with those reported in the literature. Phytochemical investigations on Clerodendrum species revealed various diterpenoids in the plants, which showed antibacterial and cytotoxic activities [8,9].…”
Section: Resultsmentioning
confidence: 99%
See 1 more Smart Citation
“…The seven known compounds were identified as mandarone A (1) [11], taxusabietane A (2) [12], 12-O-demethylcrypto-japonol (3) [13], cryptojaponol (4) [14], 11,14-dihydroxy-8,11,13-abietatrien-7-one (5) [15], fortunin E (6) [16], fortunin F (7) [16], by comparison of their spectra with those reported in the literature. Phytochemical investigations on Clerodendrum species revealed various diterpenoids in the plants, which showed antibacterial and cytotoxic activities [8,9].…”
Section: Resultsmentioning
confidence: 99%
“…The 1 H-and 13 C-NMR spectroscopic data ( The seven known compounds were identified as mandarone A (1) [11], taxusabietane A (2) [12], 12-O-demethylcrypto-japonol (3) [13], cryptojaponol (4) [14], 11,14-dihydroxy-8,11,13-abietatrien-7-one (5) [15], fortunin E (6) [16], fortunin F (7) [16], by comparison of their spectra with those reported in the literature. To investigate their cytotoxic activities, these compounds were evaluated using an MTT cytotoxicity assay against human myeloid leukemia (HL-60), hepatocellular carcinoma (SMMC-7721), lung cancer (A-549) and breast cancer (MCF-7) cell lines.…”
Section: Resultsmentioning
confidence: 99%
“…By means of this technique, it is possible to analyse and identify volatile compounds, such as terpenoids, which compose both EOs and volatile fractions of extracts obtained with apolar organic solvents, among them hexane (Fronza et al . ; Bandeira Junior et al . ).…”
Section: Methodsmentioning
confidence: 96%
“…Compounds 1 and 3 showed cytotoxic activity against human pancreatic cancer cell line; MIAPaCa-2 with IC 50 = 10.18 and 22.5 μg/mL, respectively (Fronza et al 2011), while compound 4 was the most active anticancer agent (IC 50 = 4.7 and 7.4 μg/mL) against both MIAPaCa-2 and melanoma (MV-3) cancer cell lines, respectively (Fronza et al 2011). Compound 3 showed cytotoxic activity against multidrug-resistant human CEM/ADR5000 leukaemia cells lines, comparable to those reported for established natural anticancer agents, paclitaxel and vincristine (Efferth et al 2008).…”
Section: Introductionmentioning
confidence: 98%