| Literature DB >> 18475818 |
M C Miller1, A Sood, B F Spielvogel, I H Hall.
Abstract
Sodium N-[(trimethylamineboryl)-carbonyl]-L-phenylalanine 2 and {N-[(trimethylamineboryl)-carbonyl]-L-phenylalanyl- carbxylato}-bis-{N-[(trimethylaminebryl)-carbonyl]-L-phenylalanine} dicopper (II) 3 were successfully synthesized. The agents blocked L(1210) leukemic cell DNA and RNA syntheses by inhibiting multiple enzyme activities for nucleic acid synthesis, e.g. PRPP amido transferase, IMP dehydrogenase, DNA polymerase alpha, thymidine kinase, and TMP kinase. The copper (II) complex 3 demonstrated improved ability to inhibit L(1210) partially purified DNA topoisomerase II compared to the parent compound while the sodium salt was inactive at 100 muM.Entities:
Year: 1998 PMID: 18475818 PMCID: PMC2365097 DOI: 10.1155/MBD.1998.1
Source DB: PubMed Journal: Met Based Drugs ISSN: 0793-0291