scholarly journals <i>In Vitro</i> Anti-Cancer Activity of Larval Hemolymph and Fat Body of Flesh Fly <i>Sarcophaga argyrostoma</i> (Diptera: Sarcophagidae)

2020 ◽  
Vol 08 (02) ◽  
pp. 93-105
Author(s):  
Shaymaa Mahmoud ◽  
Lina Abou El-Khashab ◽  
Walaa Moselhy ◽  
Abdelbaset Zayed ◽  
Mohamed Salama
Keyword(s):  
Fat Body ◽  
Flesh Fly ◽  
Anti Cancer ◽  
Larval Hemolymph ◽  
Sarcophaga Argyrostoma ◽  
Cancer Activity

Anti-cancer activity of quercetin, gallic acid, and ellagic acid against hepg2 and hct 116 cell lines: in vitro

2016 ◽  
Vol 7 (4) ◽  
Author(s):  
AHMED ABD-RABOU A ◽  
AZIZA SHALBY B ◽  
HANAA AHMED H
Keyword(s):  
Gallic Acid ◽  
Cell Lines ◽  
Ellagic Acid ◽  
Anti Cancer ◽  
Hct 116 ◽  
Cancer Activity

scholarly journals Evaluation of the anti-cancer activity of the triterpenoidal saponin fraction isolated from the traditional Chinese medicine Conyza blinii H. Lév.

RSC Advances ◽  
2017 ◽  
Vol 7 (6) ◽  
pp. 3408-3412 ◽  
Author(s):  
Long Ma ◽  
Haiyan Liu ◽  
Lingpei Meng ◽  
Ping Qin ◽  
Botao Zhang ◽  
...  
Keyword(s):  
Chinese Medicine ◽  
Traditional Chinese Medicine ◽  
Anti Cancer ◽  
Saponin Fraction ◽  
Cancer Activity

Triterpenoidal saponins fraction isolated from a traditional Chinese medicine Conyza blinii H. Lév. demonstrates anti-cancer activity both in vitro and in vivo.

Design and synthesis of novel benzimidazoles containing 1,2,3-triazolesas in vitro, anticancer and anti-oxidant agents

2021 ◽  
Vol 25 (11) ◽  
pp. 104-109
Author(s):  
Gullapelli Kumaraswamy ◽  
Ravichandar Maroju ◽  
Srinivas Bandari ◽  
Gouthami Dasari ◽  
Gullapelli Sadanandam
Keyword(s):  
Spectroscopic Methods ◽  
Moderate Activity ◽  
Design And Synthesis ◽  
Anti Cancer ◽  
Excellent Activity ◽  
Test Organisms ◽  
Anti Oxidant ◽  
High Yields ◽  
Cancer Activity

A novel series of 2-(1-((1-substitutedphenyl-1H-1,2,3- triazol-4-yl)methoxy)ethyl)-1-((1-substituted phenyl- 1H-1,2,3-triazol-4-yl)methyl)-1H-benzo[d]imidazole (3a-j)derivatives was synthesized in moderate to high yields. The structures of all the synthesized compounds were characterized by 1HNMR, 13CNMR and Mass spectroscopic methods. The title compounds were screened for their anti-oxidant activity and anti-cancer activity. The cancer activity results reveal that the compounds 3j, 3b and 3f are showing promising activity and remaining compounds exhibited moderate activity against all the tested cancer cell lines. The anti-oxidant activity also shows that the compounds 3c and 3d have shown excellent activity and remaining compounds were also found to exhibit moderate activity against the test organisms employed.

Synthesis, Electronic Structure and Anti-Cancer Activity of the Phenyl Substituted Pyrazolo[1,5-a][1,3,5]triazines

2021 ◽  
Vol 25 ◽  
Author(s):  
Evgenia S. Veligina ◽  
Nataliya V. Obernikhina ◽  
Stepan G. Pilyo ◽  
Oleksiy D. Kachkovsky ◽  
Volodymyr S. Brovarets
Keyword(s):  
Electronic Transition ◽  
Lone Electron Pair ◽  
Electron Pair ◽  
Anti Cancer ◽  
Protein Molecules ◽  
Biological Affinity ◽  
Cancer Types ◽  
Derivatives Of ◽  
Cancer Activity

: Background: Synthesis of a series of 2-(dichloromethyl)pyrazolo[1,5- a][1,3,5]triazines was carried out and evaluated in vitro for their anticancer activity against a panel of 60 cell lines derived from nine cancer types. The joint quantum-chemical and experimental study of the influence of the extended πconjugated phenyl substituents on the electron structure of the pyrazolo[1,5-a][1,3,5]triazines as Pharmacophores were performed. It is shown that the decrease in the barriers to the rotation of phenyl substituents in compounds 1-7 possibly leads to an increase in the anti-cancer activity, which is in agreement with the change in the parameter biological affinity ϕ0. Analysis of the S0 → S1 electronic transitions (π→π*) of the pyrazolo[1,5-a][1,3,5]triazines shows that an increase in their intensity correlates with anti-cancer activity. Thus, the introduction of phenyl substituents increases the likelihood of investigated pyrazolo[1,5-a][1,3,5]triazines interacting with protein molecules (Biomolecule) by the π stacking mechanism. In both methyl and phenyl derivatives of pyrazolo[1,5-a][1,3,5]triazines, the second electronic transition includes the n-MO (the level of the lone electron pair in two-coordinated nitrogen atoms). The highest intensity of the η→π* electronic transition is observed in pyrazolo[1,5-a][1,3,5]triazine with pyridine residue, which does not exhibit anti-cancer activity, but exhibits antiviral activity [13]. It can be assumed that the possibility of the formation of [Pharmacophore-Biomolecule] complex by hydrogen bonding ([H-B]) mechanism with protein molecules increases.

Isolation, Characterization, and In-vitro Anti-Cancer Activity of Bioactive Cassane Diterpenoids from the Roots of Mezoneuron benthamianum (Baill.)

2017 ◽  
Vol 7 (3) ◽  
pp. 157-165 ◽  
Author(s):  
Paul M. Osamudiamen ◽  
Olapeju O. Aiyelaagbe ◽  
Surrinder Koul ◽  
Payere L. Sangwan ◽  
Shagun Vaid ◽  
...  
Keyword(s):  
Anti Cancer ◽  
Cancer Activity

Poly(HPMA)–chlorambucil conjugate nanoparticles: facile fabrication and in vitro anti-cancer activity

2021 ◽  
Vol 45 (39) ◽  
pp. 18544-18551
Author(s):  
Guichen Li ◽  
Minzhi Zhao ◽  
Jia Zhang ◽  
Haining Li ◽  
Weibing Xu ◽  
...  
Keyword(s):  
Antitumor Effect ◽  
Anti Cancer ◽  
Facile Fabrication ◽  
Cancer Activity ◽  
Mcf 7

An acid-sensitive poly(HPMA)–Chl conjugate was developed and its antitumor effect towards HepG2 and MCF-7 cells was evaluated.

In vitro anti-cancer activity of ethanolic extract of Momordica charantia on cervical and breast cancer cell lines

2015 ◽  
Vol 4 (4) ◽  
pp. 210
Author(s):  
Prashant Vishwanath ◽  
CR Shobha ◽  
MN Suma ◽  
Akila Prashant ◽  
Chandini Rangaswamy ◽  
...  
Keyword(s):  
Breast Cancer ◽  
Cell Lines ◽  
Cancer Cell ◽  
Breast Cancer Cell ◽  
Ethanolic Extract ◽  
Cancer Cell Lines ◽  
Breast Cancer Cell Lines ◽  
Anti Cancer ◽  
Cancer Activity
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