The purines: Potent and versatile small molecule inhibitors and modulators of key biological targets

M Legraverend, DS Grierson - Bioorganic & medicinal chemistry, 2006 - Elsevier
The goal of this review is to highlight the wide range of biological activities displayed by
purines, with particular emphasis on new purine-based agents which find potential …

[PDF][PDF] The interactome: predicting the protein-protein interactions in cells

D Plewczyński, K Ginalski - Cellular and Molecular Biology Letters, 2009 - degruyter.com
The term Interactome describes the set of all molecular interactions in cells, especially in the
context of protein-protein interactions. These interactions are crucial for most cellular …

Design, synthesis and biological evaluation of [1, 2, 3] triazolo [4, 5-d] pyrimidine derivatives possessing a hydrazone moiety as antiproliferative agents

ZH Li, DX Yang, PF Geng, J Zhang, HM Wei… - European journal of …, 2016 - Elsevier
Abstract A series of [1, 2, 3] triazolo [4, 5-d] pyrimidine derivatives bearing a hydrazone
moiety were designed, synthesized and evaluated for their antiproliferative activity against …

Synthesis and anti-tumor activities of novel [1, 2, 4] triazolo [1, 5-a] pyrimidines

XL Zhao, YF Zhao, SC Guo, HS Song, D Wang, P Gong - Molecules, 2007 - mdpi.com
In order to find novel anti-tumor compounds a series of novel [1, 2, 4] triazolo [1, 5-a]
pyrimidine derivatives has been designed and synthesized. The structures of all the …

Synthesis and biological evaluation of aminobenzamides containing purine moiety as class I histone deacetylases inhibitors

PT Mao, WB He, X Mai, LH Feng, N Li, YJ Liao… - Bioorganic & Medicinal …, 2022 - Elsevier
The aminobenzamide is selective to class I histone deacetylases (HDACs) and displays
unique tight-binding/slow-off HDAC-binding mechanism. Herein, we report a series of 9 …

Design, synthesis, and anticancer evaluation of N6‐hydrazone purine derivatives with potential antiplatelet aggregation activity

C Wei, L Zhou, Y Yang, L Niu… - Chemical Biology & Drug …, 2023 - Wiley Online Library
In our research on novel anticancer agents, a series of N 6‐hydrazone purine derivatives
were designed and synthesized by analysis of a pharmacophore model for ATP‐competitive …

[PDF][PDF] Local Anesthetics Transfer Across the Membrane: Reproducing Octanol-Water Partition Coefficients by Solvent Reaction Field Methods.

H Kavcic, N Umek, D Pregeljc, N Vintar… - Acta Chimica …, 2021 - researchgate.net
Local anesthetics are one of the most widely used drug classes in clinical practice. Like
many other biological molecules, their properties are altered depending on their protonation …

Scaffold-hopping and hybridization based design and building block strategic synthesis of pyridine-annulated purines: discovery of novel apoptotic anticancer agents

V Chaudhary, S Das, A Nayak, SK Guchhait… - RSC …, 2015 - pubs.rsc.org
A set of novel pyridine-annulated analogs of purinones, adenines and their oxo/thio
congeners, xanthines, guanines, and purine-2, 4-diamines as potential anticancer agents …

Synthesis and Biological Evaluation of New 4β-5-Fu-substituted 4'-Demethylepipodophyllotoxin Derivatives

FM Zhang, XJ Yao, X Tian, YQ Tu - Molecules, 2006 - mdpi.com
A series of new 4β-5-Fu-substituted 4'-demethylepipodophyllotoxin derivatives were
synthesized and evaluated, together with some previously prepared ones, for their cytotoxic …

The Determination of Partition Coefficient of 6‐Mercaptopurine Derivatives by Thin Layer Chromatography

A Czyrski, B Kupczyk - Journal of Chemistry, 2013 - Wiley Online Library
Mercaptopurine and its derivatives are used in the treatment of leukemia. To estimate their
lipophilicity, a simple and novel thin layer chromatography method was developed. The …