Synthesis of nucleosides as potential inhibitors of purine biosynthesis.

Microwave-assisted synthesis of novel purine nucleosides as selective cholinesterase inhibitors.

Some pyrazoles as inhibitors of purine biosynthesis de novo.

Modular Synthesis of Constrained Ethyl (cEt) Purine and Pyrimidine Nucleosides.

Marine nucleosides: structure, bioactivity, synthesis and biosynthesis.

Synthesis of arabinose glycosyl sulfamides as potential inhibitors of mycobacterial cell wall biosynthesis.

A new synthesis of 5'-deoxy-8,5'-cyclo-adenosine and -inosine: conformationally-fixed purine nucleosides (nucleosides and nucleotides. XVI).

Acetylation and cleavage of purine nucleosides. Synthesis of 6-azauridine, 5-fluorouridine, and 5-methyluridine.

Synthesis of some purine and pyrimidine nucleosides of 3-amino-2,3,6-trideoxy-L-lyxo-hexopyranose (daunosamine).

Synthesis and Evaluation of 2,6-Modified Purine 2'-C-Methyl Ribonucleosides as Inhibitors of HCV Replication.

Synthesis of purine and pyrimidine bases and nucleosides under the cold plasma conditions (IX).

Discovery and Synthesis of C-Nucleosides as Potential New Anti-HCV Agents.

Versatile synthesis and biological evaluation of novel 3'-fluorinated purine nucleosides.

Synthesis and biological evaluation of novel C6-cyclo secondary amine substituted purine steroid-nucleosides analogues.

Synthesis and anticancer activity of novel C6-piperazine substituted purine steroid-nucleosides analogues.

Induction of HL-60 leukemia cell differentiation by tetrahydrofolate inhibitors of de novo purine nucleotide biosynthesis.

Synthesis and antitumor activity of a novel series of 6-substituted pyrrolo[2,3-d]pyrimidines as potential nonclassical antifolates targeting both thymidylate and purine nucleotide biosynthesis.

Synthesis and biochemical evaluation of inhibitors of estrogen biosynthesis.

Synthesis of N-acetyl Glucosamine Analogs as Inhibitors for Hyaluronan Biosynthesis.

Synthesis of 6,8,9 poly-substituted purine analogue libraries as pro-apoptotic inducers of human leukemic lymphocytes and DAPK-1 inhibitors.

Comparative study by circular dichroism of the conformation of deazapurine nucleosides and that of common purine nucleosides.

Pyrrolo[3,2-d]pyrimidines, a new class of purine nucleoside phosphorylase (PNP) inhibitors as potential T-cell selective immunosuppressive agents.

Cytotoxic Activities Toward Human and Rat Glioblastoma Cells.

Amino and carboxy functionalized modified nucleosides: a potential class of inhibitors for angiogenin.

Synthesis and anti-HIV activity of carbocyclic 2',3'-didehydro-2',3'-dideoxy 2,6-disubstituted purine nucleosides.

Suggest Documents

Microwave-assisted synthesis of novel purine nucleosides as selective cholinesterase inhibitors.

Some pyrazoles as inhibitors of purine biosynthesis de novo.

Modular Synthesis of Constrained Ethyl (cEt) Purine and Pyrimidine Nucleosides.

Marine nucleosides: structure, bioactivity, synthesis and biosynthesis.

Synthesis of arabinose glycosyl sulfamides as potential inhibitors of mycobacterial cell wall biosynthesis.

A new synthesis of 5'-deoxy-8,5'-cyclo-adenosine and -inosine: conformationally-fixed purine nucleosides (nucleosides and nucleotides. XVI).

Acetylation and cleavage of purine nucleosides. Synthesis of 6-azauridine, 5-fluorouridine, and 5-methyluridine.

Synthesis of some purine and pyrimidine nucleosides of 3-amino-2,3,6-trideoxy-L-lyxo-hexopyranose (daunosamine).

Synthesis and Evaluation of 2,6-Modified Purine 2'-C-Methyl Ribonucleosides as Inhibitors of HCV Replication.

Synthesis of purine and pyrimidine bases and nucleosides under the cold plasma conditions (IX).

Discovery and Synthesis of C-Nucleosides as Potential New Anti-HCV Agents.

Versatile synthesis and biological evaluation of novel 3'-fluorinated purine nucleosides.

Synthesis and biological evaluation of novel C6-cyclo secondary amine substituted purine steroid-nucleosides analogues.

Synthesis and anticancer activity of novel C6-piperazine substituted purine steroid-nucleosides analogues.

Induction of HL-60 leukemia cell differentiation by tetrahydrofolate inhibitors of de novo purine nucleotide biosynthesis.

Synthesis and antitumor activity of a novel series of 6-substituted pyrrolo[2,3-d]pyrimidines as potential nonclassical antifolates targeting both thymidylate and purine nucleotide biosynthesis.

Synthesis and biochemical evaluation of inhibitors of estrogen biosynthesis.

Synthesis of N-acetyl Glucosamine Analogs as Inhibitors for Hyaluronan Biosynthesis.

Synthesis of 6,8,9 poly-substituted purine analogue libraries as pro-apoptotic inducers of human leukemic lymphocytes and DAPK-1 inhibitors.

Comparative study by circular dichroism of the conformation of deazapurine nucleosides and that of common purine nucleosides.

Pyrrolo[3,2-d]pyrimidines, a new class of purine nucleoside phosphorylase (PNP) inhibitors as potential T-cell selective immunosuppressive agents.

Cytotoxic Activities Toward Human and Rat Glioblastoma Cells.

Amino and carboxy functionalized modified nucleosides: a potential class of inhibitors for angiogenin.

Synthesis and anti-HIV activity of carbocyclic 2',3'-didehydro-2',3'-dideoxy 2,6-disubstituted purine nucleosides.

Synthesis of nucleosides as potential inhibitors of purine biosynthesis.

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