In Vitro Cytotoxic Activity of Phenanthroindolizidine Alkaloids fromCynanchumvincetoxicumandTylophoratanakaeagainst Drug-Sensitive and Multidrug-Resistant Cancer Cells

2002 ◽  
Vol 65 (9) ◽  
pp. 1299-1302 ◽  
Author(s):  
Anne K. Lykkeberg ◽  
Jette Christensen ◽  
Bogdan A. Budnik ◽  
Fumiko Abe ◽  
Jerzy W. Jaroszewski
Author(s):  
Muhammad Jawad Nasim ◽  
Karolina Witek ◽  
Annamaria Kincses ◽  
Muhammad Sarfraz ◽  
Ewa Żesławska ◽  
...  

Selenocyanates form an interesting class of organic selenium compounds as they serve as multifunctional agents (being the precursors of seleninic acids and diselenides in synthetic chemistry and as antimicrobial and cytotoxic agent in biology) and, due to their similarity with better known thiocyanates promise high biological activity. Yet whilst selenocyanates are common in synthetic chemistry, they are rarely considered in pharmaceutical design. Arylmethyl selenocyanates (1-13) have been synthesized and an insight into their structural properties using X-ray crystallography has been obtained. The compounds subsequently have been evaluated for their potential antimicrobial, nematicidal and cytotoxic activity. ADMET properties in vitro, using mutagenicity (AMES) and permeability (PAMPA) tests, have been determined. The compounds exhibit pronounced activity against various strains of bacteria (both Gram-positive and Gram-negative) and yeasts. Among them, benzylselenocyanate (1) represents the most active anti-ESKAPE agent, with potent antibacterial activity, especially against multidrug resistant MRSA strains (HEMSA 5). Our results demonstrate that the arylmethyl selenocyantes are not only non-mutagenic but also possess moderate cytotoxic activity against cancer cells.


Molecules ◽  
2021 ◽  
Vol 26 (16) ◽  
pp. 4984
Author(s):  
Didi Nurhadi Illian ◽  
Ihsanul Hafiz ◽  
Okpri Meila ◽  
Ahmad Rusdan Handoyo Utomo ◽  
Arif Nuryawan ◽  
...  

In 2020, an estimated 19.3 million new cancer cases and nearly 10 million cancer deaths have occurred worldwide, with colorectal cancer ranking as the third most frequently diagnosed (10.0%). Several attempts have been conducted against cancer, including surgery, radiation, monoclonal antibodies, and chemotherapy. Many people choose natural products as alternatives against cancer. These products will not only help in human life preservation but also work as a source of up-to-date information, leading people away from incorrect information. We discuss the current status, distribution, and future implications of protecting populations with natural products as an alternative against colorectal cancer in Indonesia. Thirty-eight studies were included in this review for data extraction. The distribution of natural products in Indonesia that have potential activity against colorectal cancer cells was predominated by terpenoids, followed by phytosterols, phenolics, alkaloids, and polyisoprenoids. The type of cell line utilized in the cytotoxic activity analysis of natural products was the WiDr cell line, followed by HT-29 cells and HCT-116 cells. This review showed that MTT in vitro assay is a general method used to analyze the cytotoxic activity of a natural product against colorectal cancer cells, followed by other in vitro and in vivo methods. The systematic review provided predictions for several secondary metabolites to be utilized as an alternative treatment against colorectal cancer in Indonesia. It also might be a candidate for a future co-chemotherapy agent in safety, quality, and standardization. In addition, computational methods are being developed to predict the drug-likeness of compounds, thus, drug discovery is already on the road towards electronic research and development.


2013 ◽  
Vol 8 (1) ◽  
pp. 1934578X1300800
Author(s):  
Yu-Chang Su ◽  
Chen-Lung Ho

This study investigated the chemical composition and in-vitro cytotoxic activities of the essential oil isolated from the leaf of Beilschmiedia erythrophloia. The essential oil was isolated using hydrodistillation in a Clevenger-type apparatus, and characterized by GC-FID and GC-MS. Fifty-five compounds were identified, representing 100% of the oil. The main components identified were β-caryophyllene (22.6%), α-humulene (21.9%), terpinen-4-ol (5.3%), cis-β-ocimene (5.1%), sabinene (5.0%) and limonene (4.5%). The anticancer activities of oil were evaluated. The results showed that the oil exhibited cytotoxic activity against human oral, liver, lung, colon, melanoma, and leukemic cancer cells.


ChemMedChem ◽  
2018 ◽  
Vol 13 (17) ◽  
pp. 1744-1750 ◽  
Author(s):  
Giulio Bertuzzi ◽  
Simone Crotti ◽  
Pierpaolo Calandro ◽  
Bianca Flavia Bonini ◽  
Ilaria Monaco ◽  
...  

2018 ◽  
Vol 215 ◽  
pp. 233-240 ◽  
Author(s):  
Dominic O. Ochwang’i ◽  
Charles N. Kimwele ◽  
Jemimah A. Oduma ◽  
Peter K. Gathumbi ◽  
Stephen G. Kiama ◽  
...  

2020 ◽  
Vol 44 (47) ◽  
pp. 20574-20583
Author(s):  
Kandoth Kandy Jesna ◽  
Malaichamy Ilanchelian

In the present work, we have synthesized cetyltrimethyl ammonium bromide (CTAB) capped gold nanorods (Au NRs) to evaluate apparent binding affinities for the adsorption of trypsin (TRP).


MedChemComm ◽  
2014 ◽  
Vol 5 (1) ◽  
pp. 25-31 ◽  
Author(s):  
Peng Du ◽  
Uma M. Viswanathan ◽  
Khairan Khairan ◽  
Tomislav Buric ◽  
Nathaniel E. B. Saidu ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document