Synthesis and bioevaluation of aryl hydroxamates distinguishing between NAD+ and ATP-dependent DNA ligases

Synthesis, in silico screening and bioevaluation of dispiro-cycloalkanones as antitubercular and mycobacterial NAD+-dependent DNA ligase inhibitors

(2011) Rama P. Tripathi et al.   MedChemComm

Dual inhibitors of inosine monophosphate dehydrogenase and histone deacetylase based on a cinnamic hydroxamic acid core structure

(2010) Liqiang Chen et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Modified Cap Group Suberoylanilide Hydroxamic Acid Histone Deacetylase Inhibitor Derivatives Reveal Improved Selective Antileukemic Activity

(2010) Chanaz Salmi-Smail et al.   JOURNAL OF MEDICINAL CHEMISTRY

Facile synthesis of salmochelin S1, S2, MGE, DGE, and TGE

(2010) Xiaolong Yu et al.   TETRAHEDRON

Azaindole Hydroxamic Acids are Potent HIV-1 Integrase Inhibitors

(2009) Michael B. Plewe et al.   JOURNAL OF MEDICINAL CHEMISTRY

N-O-Isopropyl Sulfonamido-Based Hydroxamates: Design, Synthesis and Biological Evaluation of Selective Matrix Metalloproteinase-13 Inhibitors as Potential Therapeutic Agents for Osteoarthritis

(2009) Elisa Nuti et al.   JOURNAL OF MEDICINAL CHEMISTRY

The pathways and outcomes of mycobacterial NHEJ depend on the structure of the broken DNA ends

(2008) J. Aniukwu et al.   GENES & DEVELOPMENT