2016
DOI: 10.20307/nps.2016.22.2.122
|View full text |Cite
|
Sign up to set email alerts
|

Cytotoxic, Anti-Inflammatory and Adipogenic Effects of Inophyllum D, Calanone, Isocordato-oblongic acid, and Morelloflavone on Cell Lines

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1
1

Citation Types

1
16
0

Year Published

2017
2017
2022
2022

Publication Types

Select...
5
2

Relationship

0
7

Authors

Journals

citations
Cited by 30 publications
(17 citation statements)
references
References 12 publications
1
16
0
Order By: Relevance
“…Viability of cells for the extracts (1, 2.5, 5, 10, 25, 50, 100, and 200 μg/mL), compounds 1 – 8 (1, 2.5, 5, 10, 25, 50, 100, and 200 μ m ), and l ‐NMMA (50, 100, 200, 400, and 800 μ m ) as a positive control was determined by an Ez‐Cytox cell viability detection kit purchased from Dail Lab Service Co . (Seoul, Korea), as reported previously …”
Section: Methodssupporting
confidence: 66%
See 1 more Smart Citation
“…Viability of cells for the extracts (1, 2.5, 5, 10, 25, 50, 100, and 200 μg/mL), compounds 1 – 8 (1, 2.5, 5, 10, 25, 50, 100, and 200 μ m ), and l ‐NMMA (50, 100, 200, 400, and 800 μ m ) as a positive control was determined by an Ez‐Cytox cell viability detection kit purchased from Dail Lab Service Co . (Seoul, Korea), as reported previously …”
Section: Methodssupporting
confidence: 66%
“…Viability of cells for the extracts (1, 2.5, 5, 10, 25, 50, 100, and 200 lg/mL), compounds 1 -8 (1, 2.5, 5, 10, 25, 50, 100, and 200 lM), and L-NMMA (50, 100, 200, 400, and 800 lM) as a positive control was determined by an Ez-Cytox cell viability detection kit purchased from Dail Lab Service Co. (Seoul, Korea), as reported previously. [20] [21] Measurement of Nitric Oxide Production RAW264.7 cells were plated into a 96-well plate at a density of 3 9 10 4 cells/well and preincubated at 37°C for 24 h. After serum starvation for 12 h, cells were pretreated with the extracts (1, 2.5, 5, 10, 25, 50, 100, and 200 lg/mL), compounds 1 -8 (1, 2.5, 5, 10, 25, 50, 100, and 200 lM), and L-NMMA (50, 100, 200, 400, and 800 lM) as a positive control for 1 h, and then stimulated with 100 ng/mL of LPS for another 24 h. To evaluate NO levels in the culture media, nitrite, a soluble oxidation product of NO, was measured using the Griess reaction. [30] [31]…”
Section: Extraction and Isolationmentioning
confidence: 99%
“…The EtOH extract was then solvent-partitioned for bioassay-guided fractionation with hexane, dichloromethane (CH 2 Cl 2 ), ethyl acetate (EtOAc), and n -butanol, yielding soluble fractions of hexane (HX), CH 2 Cl 2 (DCM), EtOAc (EA), and n -butanol (BuOH), respectively. Prior to investigating the anti-inflammatory effects of the four solvent-partitioned fractions, we examined the cellular toxicity of these fractions in RAW264.7 cells with MTT assay [ 23 , 24 , 25 , 26 ]. No significant cell death was observed for the HX, DCM, and BuOH fractions up to concentrations of 50 μg/mL, while the EA fraction caused cell death at a concentration of 50 μg/mL (data not shown).…”
Section: Resultsmentioning
confidence: 99%
“…Compounds 1 , 2 , 3 and 7 at 100 μM had little or no toxicity, whereas compound 4 , 5 , and 6 inhibited the growth of cells at higher concentrations, the viability rate of all chemical constitutes did not exceed 65.0% at doses up to 100 μM, respectively ( Figure 8 ). Taher et al (2016) reported [ 27 ] that the biflavonoid, morelloflavone, isolated from Garcinia prainiana showed no obvious inhibition of RAW 264.7 macrophage cell viability [ 27 ]. Also, the cytotoxicity of the novel synthesized flavone derivatives was investigated in terms of the structure–anti-inflammatory activity relationship.…”
Section: Resultsmentioning
confidence: 99%