SYNTHESIS AND BIOCHEMICAL-PROPERTIES OF P HOSPHONYL ACYCLIC ANALOGS OF 2'-DEOXYADENOSINE NUCLEOTIDES

Citation
Dv. Malakhov et al., SYNTHESIS AND BIOCHEMICAL-PROPERTIES OF P HOSPHONYL ACYCLIC ANALOGS OF 2'-DEOXYADENOSINE NUCLEOTIDES, Bioorganiceskaa himia, 21(7), 1995, pp. 539-544
Citations number
18
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
ISSN journal
01323423
Volume
21
Issue
7
Year of publication
1995
Pages
539 - 544
Database
ISI
SICI code
0132-3423(1995)21:7<539:SABOPH>2.0.ZU;2-L
Abstract
9-[2-(phosphonomethylcarbonylamino)ethyl]adenine, 9-[(2-phosphonoethyl )aminocarbonylmethyl]adenine, {2-[(2-phosphonoethyl)carbonylamino]ethy l}adenine, and their diphosphates were synthesized. All three diphosph ates were shown to incorporate into the 3'-terminus of the DNA chain d uring the synthesis of the avian myeloblastose virus catalyzed by reve rse transcriptase. However, they do not serve as substrates for DNA po lymerase beta from human placenta, polymerase beta from calf thymus, o r terminal deoxynucleotidyl transferase from calf thymus.