scholarly journals Cytotoxic Activity Screening of Fungal Extracts Derived from the West Sumatran Marine Sponge Haliclona fascigera to Several Human Cell Lines: Hela, WiDr, T47D and Vero

2018 ◽  
Keyword(s):  
Cytotoxic Activity ◽  
Cell Lines ◽  
Human Cell ◽  
Marine Sponge ◽  
Human Cell Lines ◽  
The West ◽  
Activity Screening ◽  
Fungal Extracts

Cytotoxic Activity of Pereskia bleo (Cactaceae) Against Selected Human Cell Lines

2007 ◽  
Vol 4 (1) ◽  
pp. 20-27 ◽  
Author(s):  
Sri Nurestri Abd Malek ◽  
Norhanom Abdul Wahab ◽  
Hashim Yaacob ◽  
Sim Kae Shin ◽  
Hong Sok Lai ◽  
...  
Keyword(s):  
Cytotoxic Activity ◽  
Cell Lines ◽  
Human Cell ◽  
Human Cell Lines

Cytotoxic activity of aquatic fungus Pseudohalonectria lignicola on two different human cell lines

Planta Medica ◽  
2014 ◽  
Vol 80 (16) ◽  
Author(s):  
S Schneider ◽  
N Srirangan ◽  
M Wurster ◽  
U Lindequist ◽  
M Lalk
Keyword(s):  
Cytotoxic Activity ◽  
Cell Lines ◽  
Human Cell ◽  
Human Cell Lines ◽  
Aquatic Fungus

scholarly journals Two New Alkylresorcinols from Homalomena wendlandii and Their Cytotoxic Activity

2012 ◽  
Vol 7 (8) ◽  
pp. 1934578X1200700 ◽  
Author(s):  
Luis A. Sánchez ◽  
Dionisio Olmedo ◽  
José Luis López-Pérez ◽  
Todd D. Williams ◽  
Mahabir P. Gupta
Keyword(s):  
Cytotoxic Activity ◽  
Cell Lines ◽  
Human Cell ◽  
2D Nmr ◽  
Human Cell Lines ◽  
Ir Spectroscopic ◽  
Mcf 7

In the course of our search for antineoplasic agents from Panamanian Flora, two new alkylresorcinols: 1-(2,6-dihydroxyphenyl)octan-1-one (1) and (+)-1-(3-(1-(2,6-dihydroxyphenyl)butyl)-2,6-dihydroxyphenyl)octan-1-one (2), together with three known compounds, (1 R, 2 R)-1-(benzo[ d][1,3]dioxol-5-yl)propane-1,2,3-triol (3), (+)-aptosimon (4) and (-)-sesamin (5), were identified from the leaves of Homalomena wendlandii Schott (Araceae). Their structures were established by 1D and 2D NMR and IR spectroscopic, and MS methods. Compound 2 exhibited IC50 values of 3.3, 5.8 and 4.0 μg/mL against MCF-7, SF-268 and H-460 cancer human cell lines, respectively.

scholarly journals Two New Kaempferol Glycosides from Matthiola Longipetala (subsp. livida) (Delile) Maire and Carcinogenic Evaluation of its Extract

2008 ◽  
Vol 3 (8) ◽  
pp. 1934578X0800300
Author(s):  
Mona M. Marzouk ◽  
Salwa A. Kawashty ◽  
Lamyaa F. Ibrahium ◽  
Nabiel A. M. Saleh ◽  
Abdel-Ssalam M. Al-Nowaihi
Keyword(s):  
Spectral Analysis ◽  
Cytotoxic Activity ◽  
Cell Lines ◽  
Human Cell ◽  
Carcinoma Cells ◽  
Alcoholic Extract ◽  
Human Cell Lines ◽  
Kaempferol Glycosides ◽  
Detailed Chemical

Two new kaempferol glycosides, kaempferol 3- O-(2″-α-L-rhamnopyranosyl)-β-L-arabinopyranoside-7- O-α-L-rhamnopyranoside and kaempferol 3- O-(2″-α-L-rhamnopyranosyl)-β-L-arabinopyranoside-7- O-α-L-rhamnopyranoside-4′- O-β-D-glucopyranoside were isolated along with four known flavonols from Matthiola longipetala (subsp. livida) (Delile) Maire growing in Egypt. Their structures were established on the basis of detailed chemical and spectral analysis. The cytotoxic activity of the alcoholic extract against Cervix (HELA) and Colon (HCT116) human cell lines showed IC50 values of 22.1 and 53.7 μg/mL, respectively. No activity was found against liver (HEPG2) carcinoma cells.

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