Nucleosides Nucleotides Nucleic Acids, 2007, 26(89):897-900

5′-carbamoylphosphonyl-[6-3H]-AZT as a tool for studying metabolic transformations of the nonradioactive counterpart, an inhibitor of HIV replication

An effective synthesis of 5′-carbamoylphosphonyl-[6-3H]-AZT was developed from [6-3H]-AZT.For the synthesized compound, chemical and enzymatic stability were determined and its penetrationa cross HL-60 cell membranes was studied. Copyright © Taylor & Francis Group, LLC.

Yanvarev DV, Shirokova EA, Astapova MV, Shram VI, Kukhanova MK, Skoblov YS

Изотопный блок

: 10.1080/15257770701505899
Scopus: 2-s2.0-36849045154
: 18058504
IBCH: 524
Ссылка на статью в журнале: https://www.tandfonline.com/doi/full/10.1080/15257770701505899
Кол-во цитирований на 01.2024: 1
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