The selective cytotoxicity of new triazene compounds to human melanoma cells

A Sousa, F Santos, MM Gaspar, S Calado… - Bioorganic & Medicinal …, 2017 - Elsevier
Metastatic melanoma still remains one the most difficult cancers to overcome. The aim of our
research was the design of anti-tumour triazene compounds 3 for application to a melanoma …

N4‐aryl substituted thiosemicarbazones derived from 1‐indanones as potential anti‐tumor agents for breast cancer treatment

A Solimo, MC Soraires Santacruz… - Journal of Cellular …, 2018 - Wiley Online Library
Breast cancer is the first cause of cancer death in women. Many patients are resistant to
current therapies, and even those were sensitive at first may eventually become resistant …

Synthesis and anticancer activities of thiosemicarbazones derivatives of thiochromanones and related scaffolds

J Song, R Pan, G Li, W Su, X Song, J Li… - Medicinal Chemistry …, 2020 - Springer
A series of novel thiosemicarbazone analogs (4a–t, 6a–j) were synthesized and evaluated
for their cytotoxic activities. The obtained results showed that thiochromanone-based …

Effects of substituents on anticancer activity of thiosemicarbazone against MCF-7 human breast cancer cell line

BZ Sibuh, P Taneja, S Khanna - bioRxiv, 2020 - biorxiv.org
Abstract Background/Aim Breast cancer is one of the world's leading cause of deaths in
women. This study evaluated the in-vitro anticancer activity of different thiosemicarbazones …

Capsaicin-like analogue induced selective apoptosis in A2058 melanoma cells: Design, synthesis and molecular modeling

GJV Pereira, MT Tavares, RA Azevedo… - Bioorganic & medicinal …, 2019 - Elsevier
The use of molecules inspired by natural scaffolds has proven to be a very promising and
efficient method of drug discovery. In this work, capsaicin, a natural product from Capsicum …

[HTML][HTML] Redox effects and cytotoxic profiles of MJ25 and auranofin towards malignant melanoma cells

MCC Sachweh, WC Stafford, CJ Drummond… - Oncotarget, 2015 - ncbi.nlm.nih.gov
Malignant melanoma is the most dangerous type of skin cancer. Although recent progress in
treatment has been achieved, lack of response, drug resistance and relapse remain major …

Effective melanoma inhibition by synthetic pentacyclic triterpenoid 2-(3-phenylprop-2-en-1-ylidene)-22β-hydroxy-3-oxoolean-12-en-28-oic acid: An in vitro and in vivo …

NK Tailor, HB Lee, M Sharma - Journal of Environmental …, 2013 - dl.begellhouse.com
The C-2 arylidene analog (compound 3) of pentacyclic triterpenoid Lantadene A (compound
1) was synthesized and evaluated by the National Cancer Institute, USA, for in vitro …

Synthesis, spectroscopic characterization and biological properties of new natural aldehydes thiosemicarbazones

P Tarasconi, S Capacchi, G Pelosi, M Cornia… - Bioorganic & medicinal …, 2000 - Elsevier
As part of a research programme aimed at the synthesis of compounds with antiviral,
antibacterial and antitumor properties and their spectroscopic characterization, new …

Novel thiosemicarbazone derivatives as potential antitumor agents: Synthesis, physicochemical and structural properties, DNA interactions and antiproliferative …

I Đilović, M Rubčić, V Vrdoljak, SK Pavelić… - Bioorganic & medicinal …, 2008 - Elsevier
The paper describes synthesis of several novel thiosemicarbazone derivatives. Furthermore,
crystal and molecular structure of 4-diethylamino-salicylaldehyde 4 …

Anticancer potency of N (4)-ring incorporated-5-methoxyisatin thiosemicarbazones

U Chaudhary, D Dawa, I Banerjee, S Sharma… - Journal of Molecular …, 2023 - Elsevier
Abstract (Z)-N'-(5-methoxy-2-oxoindolin-3-ylidene) thiomorpholine-4-carbothiohydrazide
(MeOIstTmor),(Z)-N'-(5-methoxy-2-oxoindolin-3-ylidene)-2, 6-dimethylmorpholine-4 …