FIELD: medicine; pharmacology.
SUBSTANCE: invention refers to new nucleoside analogues characterised as inhibitors of purinephosphoribosiletransferase, purinenucleosidephosphorylase, 5 '-methylthioadenosinephosphorylase, 5 '-methylthioadenosinenucleosidase and/or nucleosidehydrolase and can be applied for treatment of malignant neoplasm, bacterial infections, protozoal infections, T- cell mediated diseases. In formula V is selected of CH2 and NH, and W is selected of NR1 and NR2; X is selected of CH2 and CHOH in R or S - configurations; Y is selected of hydrogen and hydroxy; Z is selected of hydrogen, halogen and hydroxy, SQ and Q where Q is optionally substituted with halogen C1-C6alkyl or benzyl group; R1 is radical of formula ; R2 is radical of formula ; A is selected of N, CH; B is selected of OH, NH2 and halogen; D is selected of NH2 and hydrogen; E means N; G is selected of CH2 or G is absent. Invention also refers to based pharmaceutical composition, methods of disease or condition treatment requiring inhibition of purinephosphoribosiletransferase, purinenucleosidephosphorylase, 5 '-methylthioadenosinephosphorylase, 5 '-methylthioadenosinenucleosidase and/or nucleosidehydrolase, and to application of invention compounds for medical product preparation.
EFFECT: products are characterised with increased efficiency.
30 cl, 6 tbl, 19 dwg, 51 ex
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Authors
Dates
2008-07-27—Published
2003-08-21—Filed