Iridoid for drug discovery: Structural modifications and bioactivity studies
M Wang, X Zheng, M Yang, J Ni, Q **ao, H Han… - Medicinal Chemistry …, 2024 - Springer
Iridoid glycosides are a class of chemical structures with various pharmacological activities
and have excellent research potential. However, the poor stability, water solubility, and oral …
and have excellent research potential. However, the poor stability, water solubility, and oral …
Coumarins as potential inhibitors of DNA polymerases and reverse transcriptases. Searching new antiretroviral and antitumoral drugs
H A. Garro, C R. Pungitore - Current Drug Discovery …, 2015 - benthamdirect.com
Human Immunodeficiency Virus (HIV) is the viral agent of Acquired Immunodeficiency
Syndrome (AIDS), and at present, there is no effective vaccine against HIV. Reverse …
Syndrome (AIDS), and at present, there is no effective vaccine against HIV. Reverse …
Naphthoquinones inhibit formation and viability of Yersinia enterocolitica biofilm
NI Di Marco, PL Páez, CSM Lucero-Estrada… - World Journal of …, 2021 - Springer
The capacity of different naphthoquinones to inhibit and eradicate Yersinia enterocolitica
biofilm was investigated and possible mechanisms of action were evaluated. Inhibition of …
biofilm was investigated and possible mechanisms of action were evaluated. Inhibition of …
Catalpol suppresses proliferation and facilitates apoptosis of OVCAR-3 ovarian cancer cells through upregulating microRNA-200 and downregulating MMP-2 …
N Gao, JX Tian, YH Shang, DY Zhao, T Wu - International Journal of …, 2014 - mdpi.com
Catalpol is expected to possess diverse pharmacological actions including anti-cancer, anti-
inflammatory and hypoglycemic properties. Matrix metalloproteinase-2 (MMP-2) is closely …
inflammatory and hypoglycemic properties. Matrix metalloproteinase-2 (MMP-2) is closely …
Aporphinoid alkaloids inhibit biofilm formation of Yersinia enterocolitica isolated from sausages
NI Di Marco, CR Pungitore… - Journal of Applied …, 2020 - academic.oup.com
Aims of the study The ability of Yersinia enterocolitica strains to form biofilms and the
capacity of different alkaloids to inhibit biofilm formation were investigated. Methods and …
capacity of different alkaloids to inhibit biofilm formation were investigated. Methods and …
Study on the chemical reactivity difference of primary hydroxyl groups in iridoid glycosides
Y Kong, J Xu, P Zhu, S Wang, B Yang, J Zhang… - RSC …, 2023 - pubs.rsc.org
Iridoid glycoside, which belongs to the polyhydroxy compound, is a kind of active ingredient
of traditional Chinese medicine with a wide range of sources, and has many …
of traditional Chinese medicine with a wide range of sources, and has many …
A systematic review of a naturally occurring iridoid: catalpol
Z Liu, X Wen - Current Bioactive Compounds, 2013 - ingentaconnect.com
Catalpol is one of the most abundant naturally occurring iridoids. Catalpol appears to
possess many excellent biological and pharmacological activities as shown in recent …
possess many excellent biological and pharmacological activities as shown in recent …
DNA related enzymes as molecular targets for antiviral and antitumoral chemotherapy. A natural overview of the current perspectives
HA Garro, CR Pungitore - Current Drug Targets, 2019 - ingentaconnect.com
Background: The discovery of new chemotherapeutic agents still remains a continuous goal
to achieve. DNA polymerases and topoisomerases act in nucleic acids metabolism …
to achieve. DNA polymerases and topoisomerases act in nucleic acids metabolism …
Inhibition of Taq DNA polymerase by iridoid aglycone derivates
Faithful replication of DNA molecules by DNA polymerases is essential for genome integrity
and correct transmission of genetic information in all living organisms. DNA polymerases …
and correct transmission of genetic information in all living organisms. DNA polymerases …
Collection of alkenylcoumarin derivatives as Taq DNA polymerase inhibitors: SAR and in silico simulations
E Bruna-Haupt, HA Garro, L Gutiérrez… - Medicinal Chemistry …, 2018 - Springer
Using a feasible method, we generated a small focused library of structurally related
alkenylcoumarins. These compounds were evaluated as potential antitumoral agents …
alkenylcoumarins. These compounds were evaluated as potential antitumoral agents …