Queuosine modification of tRNA: its divergent role in cellular machinery

M Vinayak, C Pathak - Bioscience reports, 2010 - portlandpress.com
tRNAs possess a high content of modified nucleosides, which display an incredible
structural variety. These modified nucleosides are conserved in their sequence and have …

Therapeutic potential of pteridine derivatives: A comprehensive review

V Carmona‐Martínez, AJ Ruiz‐Alcaraz… - Medicinal Research …, 2019 - Wiley Online Library
Pteridines are aromatic compounds formed by fused pyrazine and pyrimidine rings. Many
living organisms synthesize pteridines, where they act as pigments, enzymatic cofactors, or …

[图书][B] Virtual screening in drug discovery

J Alvarez, B Shoichet - 2005 - taylorfrancis.com
Virtual screening can reduce costs and increase hit rates for lead discovery by eliminating
the need for robotics, reagent acquisition or production, and compound storage facilities …

Crystal structures of tRNA-guanine transglycosylase (TGT) in complex with novel and potent inhibitors unravel pronounced induced-fit adaptations and suggest dimer …

B Stengl, EA Meyer, A Heine, R Brenk… - Journal of molecular …, 2007 - Elsevier
The bacterial tRNA-guanine transglycosylase (TGT) is a tRNA modifying enzyme catalyzing
the exchange of guanine 34 by the modified base preQ1. The enzyme is involved in the …

Current status of virtual screening as analysed by target class

MJ Stoermer - Medicinal Chemistry, 2006 - ingentaconnect.com
In silico virtual screening for drug discovery has become a hot topic in medicinal chemistry
research during the last 5 years, growing from a largely academic pursuit concerned …

Crystallographic study of inhibitors of tRNA-guanine transglycosylase suggests a new structure-based pharmacophore for virtual screening

R Brenk, EA Meyer, K Reuter, MT Stubbs… - Journal of molecular …, 2004 - Elsevier
The enzyme tRNA-guanine transglycosylase (TGT) is involved in the pathogenicity of
Shigellae. As the crystal structure of this protein is known, it is a putative target for the …

Exploring the scope of DBU-promoted amidations of 7-methoxycarbonylpterin

AR Bockman, JM Pruet - Beilstein Journal of Organic …, 2020 - beilstein-journals.org
The synthetic utility of pterins is often hampered by the notorious insolubility of this
heterocycle, slowing the development of medicinally relevant pteridine derivatives …

A Case Study: Structure-Based Inhibitor Design for tRNA-Guanine Transglycosylase

G Klebe - Drug Design: From Structure and Mode-of-Action to …, 2025 - Springer
A case study should be considered before the numerous application examples are
presented in the last part of this book. Using the example of the tRNA-modifying enzyme …

Computational methods for the identification and optimisation of high quality leads

B Pirard - Combinatorial Chemistry & High Throughput …, 2004 - ingentaconnect.com
Lead identification and optimisation have evolved into multidimensional, multidisciplinary
and information-driven processes. Herein, we review the contribution of computational …

Synthesis of 4-hydroxyquinoline-2, 3-dicarboxylates using N-(2-aminobenzoyl) benzotriazoles

İ Çelik, F Yıldız - Tetrahedron, 2017 - Elsevier
A method for the preparation of 4-hydroxyquinoline-2, 3-dicarboxylates has been developed
by aza-Michael addition reaction of N-(2-aminobenzoyl) benzotriazoles with dimethyl …