Lysine-specific demethylase 1 promises to be a novel target in cancer drug resistance: therapeutic implications

FF Yang, XL Xu, T Hu, JQ Liu, JZ Zhou… - Journal of Medicinal …, 2023 - ACS Publications
Chemotherapy, targeted therapy, and immunotherapy are effective against most tumors, but
drug resistance remains a barrier to successful treatment. Lysine-specific demethylase 1 …

Acridone alkaloids

JP Michael - The Alkaloids: Chemistry and Biology, 2017 - Elsevier
There have been substantial developments in the chemistry and biology of the acridone
alkaloids in the 16 years since the topic was last reviewed in this series of monographs …

Investigation of cytotoxic activity on human cancer cell lines of arborinine and furanoacridones isolated from Ruta graveolens

B Rethy, I Zupko, R Minorics, J Hohmann… - Planta …, 2007 - thieme-connect.com
The cytotoxic effects of a series of furanoacridones isolated from Ruta graveolens
L.(Rutaceae) and of two further acridone alkaloids (arborinine and evoxanthine) were …

Arborinine, a potential LSD1 inhibitor, inhibits epithelial-mesenchymal transition of SGC-7901 cells and adriamycin-resistant gastric cancer SGC-7901/ADR cells

Y Chu, Z Xiao, N Jing, W Yan, S Wang, B Ma… - Investigational New …, 2021 - Springer
Arborinine is a natural product isolated from G. parva leaf extracts, which displays potentially
antiproliferative activity against human cervical cancer cells. In contrast, its anticancer effects …

Survey of functional activities of alpha-fetoprotein derived growth inhibitory peptides: review and prospects

GJ Mizejewski, G Butterstein - Current Protein and Peptide …, 2006 - ingentaconnect.com
Alpha-fetoprotein (AFP), known largely as a growth-promoting agent, possesses a growth-
inhibitory motif recently identified as an occult epitopic segment in the third domain. The …

Crispenes F and G, cis-Clerodane Furanoditerpenoids from Tinospora crispa, Inhibit STAT3 Dimerization

MAA Noman, T Hossain, M Ahsan… - Journal of natural …, 2018 - ACS Publications
Two new cis-clerodane-type furanoditerpenes, crispenes F and G (1 and 2), together with
seven known compounds, were isolated from the stems of Tinospora crispa. Crispenes F …

Determination of antibacterial activity and metabolite profile of Ruta graveolens against Streptococcus mutans and Streptococcus sobrinus

HA Salman, S Venkatesh… - Journal of laboratory …, 2018 - thieme-connect.com
BACKGROUND: Ruta graveolens is one of the most used phytomedicines. To date, there is
no report of determining the bioactivity of R. graveolens against cariogenic causing bacteria …

Antitumour properties of acridone alkaloids on a murine lymphoma cell line

B Rethy, J Hohmann, R Minorics, A Varga… - Anticancer …, 2008 - ar.iiarjournals.org
The aim of the present study was to investigate the anticancer properties of a set of
furanoacridone alkaloids, arborinine and evoxanthine, including the inhibitory effect of P …

Indole alkaloids from the leaves of Ravenia spectabilis engl. with activity against pancreatic cancer cell line

F Tabassum, CM Hasan, MM Masud, S Jamshidi… - Phytochemistry, 2021 - Elsevier
Two previously undescribed indole alkaloids, 3-prenyl-5 (3-keto-but-1-enyl) indole and 3-
prenyl-indole-5-carbaldehyde, the structurally-related 3, 5-diprenyl indole and four known …

Plant natural products as a potential source for antibacterial agents: recent trends

M Shahid, A Shahzad, F Sobia, A Sahai… - Anti-Infective Agents …, 2009 - ingentaconnect.com
Pasteur and Joubert, in 1877, were among the first to recognize the potential of microbial
products as therapeutic agents and demonstrated that common microorganisms could …