[HTML][HTML] Synthesis and cytotoxic activity of organotin (IV) diallyldithiocarbamate compounds as anticancer agent towards colon adenocarcinoma cells (HT-29)

FN Haezam, N Awang, NF Kamaludin… - Saudi Journal of …, 2021 - Elsevier
Context Diphenyltin (IV) diallyldithiocarbamate compound (Compound 1) and triphenyltin
(IV) diallyldithiocarbamate compound (Compound 2) are two newly synthesised compounds …

Biological activity, quantitative structure–activity relationship analysis, and molecular docking of xanthone derivatives as anticancer drugs

I Miladiyah, J Jumina, SM Haryana… - Drug design …, 2018 - Taylor & Francis
Background Xanthone derivatives have a wide range of pharmacological activities, such as
those involving antibacterial, antiviral, antimalarial, anthelmintic, anti-inflammatory …

[PDF][PDF] Pharmacological properties of Calophyllum inophyllum—Updated review

WM Oo - Int. J. Photochem. Photobiol, 2018 - researchgate.net
Natural products have been used as medicine since ancient times. With the advancement of
research methods nowadays, the pharmacological properties of herbal plants have become …

Triphenyltin (IV) dithiocarbamate compound induces genotoxicity and cytotoxicity in K562 human erythroleukemia cells primarily via mitochondria-mediated apoptosis

SNS Annuar, NF Kamaludin, N Awang… - Food and Chemical …, 2022 - Elsevier
The novel di-and triphenyltin (IV) dithiocarbamate compounds represented as R n SnL 2
(where R= C 4 H 9, C 6 H 5; n= 2, 3; L= N, N-dithiocarbamate), Ph 2 Sn (N, N …

Bioactive Coumarins and Xanthones from Calophyllum genus and analysis of their Druglikeness and toxicological properties

JC Gómez-Verjan, KD Rodríguez-Hernández… - Studies in Natural …, 2017 - Elsevier
Calophyllum spp.(Calophyllaceae) is a genus of tropical trees valued in the
chemopharmacological industry as an important source of biogenetically related coumarins …

Calophyllolide Content in Calophyllum inophyllum at Different Stages of Maturity and Its Osteogenic Activity

WH Liu, YW Liu, ZF Chen, WF Chiou, YC Tsai… - Molecules, 2015 - mdpi.com
Calophyllum inophyllum is a coastal plant rich in natural substances. Its ingredients have
been used for the development of an anti-human immunodeficiency virus (HIV) drug. In this …

[PDF][PDF] In silico molecular docking of xanthone derivatives as cyclooxygenase-2 inhibitor agents

I Miladiyah, J Jumina, SM Haryana… - Int J Pharm Pharm Sci, 2017 - academia.edu
Objective: To demonstrate the potential ofdifferent xanthone derivatives as cyclooxygenase-
2 (COX-2) inhibitor agents and their selectivity against cycloooxygenase-1 (COX-1) and …

Mangosenone F, A Furanoxanthone from Garciana mangostana, Induces Reactive Oxygen Species‐Mediated Apoptosis in Lung Cancer Cells and Decreases …

KH Seo, HW Ryu, MJ Park, KH Park… - Phytotherapy …, 2015 - Wiley Online Library
Mangosenone F (MSF), a natural xanthone, was isolated form Carcinia mangotana, and a
few studies have reported its glycosidase inhibitor effect. In this study we investigated the …

Herbal formulation C168 attenuates proliferation and induces apoptosis in HCT 116 human colorectal carcinoma cells: Role of oxidative stress and DNA damage

LM Leong, KM Chan, A Hamid, J Latip… - Evidence‐Based …, 2016 - Wiley Online Library
The use of herbal formulations has gained scientific interest, particularly in cancer treatment.
In this study, the herbal formulation of interest, denoted as C168, is a mixture of eight genera …

Cytoprotective effects of (E)-N-(2-(3, 5-dimethoxystyryl) phenyl) furan-2-carboxamide (BK3C231) against 4-nitroquinoline 1-oxide-induced damage in CCD-18Co …

HH Tan, NF Thomas, SH Inayat-Hussain, KM Chan - PLoS One, 2020 - journals.plos.org
Stilbenes are a group of chemicals characterized with the presence of 1, 2-
diphenylethylene. Previously, our group has demonstrated that synthesized (E)-N-(2-(3, 5 …