Structural aspects of N-hydroxy-N′-aminoguanidine derivatives as inhibitors of L1210 cell growth and ribonucleotide reductase activity
Author:
Publisher
Elsevier BV
Subject
Cancer Research,Genetics,Molecular Biology,Molecular Medicine
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1. Synthesis of 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP);Tetrahedron;1998-06
2. Efficient synthesis of ribonucleotide reductase inhibitors 3-aminopyridine-2-carboxaldehyde thiosemicarbazone (3-AP) and 3-amino-4-methylpyridine-2-carboxaldehyde thiosemicarbazone (3-AMP) via palladium mediated cross-coupling reactions;Tetrahedron;1998-01
3. The Enzyme Ribonucleotide Reductase: Target for Antitumor and Anti-HIV Therapy;Critical Reviews in Clinical Laboratory Sciences;1997-01
4. 1 Chemical and Biological Properties of Cytotoxic α-(N)-Heterocyclic Carboxaldehyde Thiosemicarbazones;Progress in Medicinal Chemistry;1995
5. Inhibitors of ribonucleotide reductase;Biochemical Pharmacology;1994-07
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