Peptide-drug conjugates: A new paradigm for targeted cancer therapy

M Wang, J Liu, M Xia, L Yin, L Zhang, X Liu… - European Journal of …, 2024 - Elsevier
Peptide-drug conjugates (PDCs) are the new hope for targeted therapy after antibody-drug
conjugates (ADCs). Compared with ADCs, the core advantages of PDCs are enhanced …

[HTML][HTML] Integrating artificial intelligence into the modernization of traditional Chinese medicine industry: a review

E Zhou, Q Shen, Y Hou - Frontiers in Pharmacology, 2024 - frontiersin.org
Traditional Chinese medicine (TCM) is the practical experience and summary of the
Chinese nation for thousands of years. It shows great potential in treating various chronic …

Vanadium (IV) complexes of salicylaldehyde-based furoic acid hydrazones: Synthesis, BSA binding and in vivo antidiabetic potential

A Zahirović, S Hadžalić, A Višnjevac, M Fočak… - Journal of inorganic …, 2023 - Elsevier
Solution synthesis afforded five novel neutral heteroleptic octahedral paramagnetic
mononuclear oxidovanadium (IV) complexes of general composition [VO (bpy) L], where L is …

Advanced network pharmacology study reveals multi-pathway and multi-gene regulatory molecular mechanism of Bacopa monnieri in liver cancer based on data …

M Sadaqat, M Qasim, MT ul Qamar, MS Masoud… - Computers in biology …, 2023 - Elsevier
Liver cancer is a malignant tumor that grows on the surface or inside the liver. The leading
cause is a viral infection with hepatitis B or C virus. Natural products and their structural …

[HTML][HTML] Mechanistic inhibition of gastric cancer-associated bacteria Helicobacter pylori by selected phytocompounds: A new cutting-edge computational approach

S Akash, I Bayıl, S Mahmood, N Mukerjee, TA Mili… - Heliyon, 2023 - cell.com
Background Helicobacter pylori (H. pylori) is a persistent bacterial inhabitant in the stomachs
of approximately half the global populace. This bacterium is directly linked to chronic …

Green and efficient one-pot three-component synthesis of novel drug-like furo [2, 3-d] pyrimidines as potential active site inhibitors and putative allosteric hotspots …

H Mousavi, B Zeynizadeh, M Rimaz - Bioorganic Chemistry, 2023 - Elsevier
In this paper, an environmentally benign, convenient, and efficient one-pot three-component
reaction has been developed for the regioselective synthesis of novel 5-aroyl (or …

[HTML][HTML] In vitro and in silico evaluation of the antimicrobial and antioxidant activities of spiropyrazoline oxindole congeners

M Chalkha, K Chebbac, H Nour, A Nakkabi… - Arabian Journal of …, 2024 - Elsevier
The search for novel powerful antimicrobial and antioxidant agents is considered a dynamic
field in medicinal chemistry. In this context, a series of spiropyrazoline indolin-3-one …

2-Amino Thiazole Derivatives as Prospective Aurora Kinase Inhibitors against Breast Cancer: QSAR, ADMET Prediction, Molecular Docking, and Molecular Dynamic …

S Bathula, M Sankaranarayanan, B Malgija… - ACS …, 2023 - ACS Publications
The aurora kinase is a key enzyme that is implicated in tumor growth. Research revealed
that small molecules that target aurora kinase have beneficial effects as anticancer agents …

[HTML][HTML] Synthesis and molecular docking simulations of novel azepines based on quinazolinone moiety as prospective antimicrobial and antitumor hedgehog …

AA Noser, AA El-Barbary, MM Salem, HAA El Salam… - Scientific Reports, 2024 - nature.com
A series of novel azepine derivatives based on quinazolinone moiety was synthesized
through the reaction of quinazolinone chalcones (2a–d) either with 2-amino aniline in acidic …

[HTML][HTML] Design, synthesis, and biological evaluation of indole-2-carboxamides as potential multi-target antiproliferative agents

LH Al-Wahaibi, AF Mohammed, MH Abdelrahman… - Pharmaceuticals, 2023 - mdpi.com
A small set of indole-based derivatives, IV and Va–I, was designed and synthesized.
Compounds Va–i demonstrated promising antiproliferative activity, with GI50 values ranging …