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Cytostatic 6-Arylpurine Nucleosides. 6. † SAR in Anti-HCV and Cytostatic Activity of Extended Series of 6-Hetarylpurine Ribonucleosides

Journal of medicinal chemistry, 2005-09, Vol.48 (18), p.5869-5873

2005

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Lasioglossins: Three Novel Antimicrobial Peptides from the Venom of the Eusocial Bee Lasioglossum laticeps (Hymenoptera: Halictidae)

Chembiochem : a European journal of chemical biology, 2009-08, Vol.10 (12), p.2089-2099

2009

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Structural Basis for Inhibition of Mycobacterial and Human Adenosine Kinase by 7‑Substituted 7‑(Het)aryl-7-deazaadenine Ribonucleosides

Journal of medicinal chemistry, 2014-10, Vol.57 (20), p.8268-8279

2014

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2´-deoxy-5,6-dihydro-5-azacytidine - a less toxic alternative of 2´-deoxy-5-azacytidine: a comparative study of hypomethylating potential

Epigenetics, 2011-06, Vol.6 (6), p.769-776

2011

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Discovery of 5-Substituted-6-chlorouracils as Efficient Inhibitors of Human Thymidine Phosphorylase

Journal of medicinal chemistry, 2007-11, Vol.50 (24), p.6016-6023

2007

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In Vivo Modulation of Angiogenic Gene Expression by Acyclic Nucleoside Phosphonates PMEDAP and PMEG

Anticancer research, 2009-04, Vol.29 (4), p.1295-1302

2009

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Tenofovir Diphosphate Is a Poor Substrate and a Weak Inhibitor of Rat DNA Polymerases α, δ, and ε

Antimicrobial Agents and Chemotherapy, 2002-05, Vol.46 (5), p.1610-1613

2002

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In Vitro Activities of 3-(Halogenated Phenyl)-5-Acyloxymethyl- 2,5-Dihydrofuran-2-ones against Common and Emerging Yeasts and Molds

Antimicrobial Agents and Chemotherapy, 2004-03, Vol.48 (3), p.873-878

2004

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Synthesis and Significant Cytostatic Activity of 7-Hetaryl-7-deazaadenosines

Journal of medicinal chemistry, 2011-08, Vol.54 (15), p.5498-5507

2011

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Synthesis and Cytostatic Activity of Substituted 6-Phenylpurine Bases and Nucleosides: Application of the Suzuki−Miyaura Cross-Coupling Reactions of 6-Chloropurine Derivatives with Phenylboronic Acids

Journal of medicinal chemistry, 2000-05, Vol.43 (9), p.1817-1825

2000

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Sphingosine and clavaminol H derivatives bearing fluorinated chains and their cytotoxic activity

Journal of fluorine chemistry, 2012-09, Vol.141, p.49-57

2012

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6-(Het)aryl-7-Deazapurine Ribonucleosides as Novel Potent Cytostatic Agents

Journal of medicinal chemistry, 2010-01, Vol.53 (1), p.460-470

2010

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A novel and efficient one-pot synthesis of symmetrical diamide (bis-amidate) prodrugs of acyclic nucleoside phosphonates and evaluation of their biological activities

European journal of medicinal chemistry, 2011-09, Vol.46 (9), p.3748-3754

2011

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Sugar-modified derivatives of cytostatic 7-(het)aryl-7-deazaadenosines: 2′-C-methylribonucleosides, 2′-deoxy-2′-fluoroarabinonucleosides, arabinonucleosides and 2′-deoxyribonucleosides

Bioorganic & medicinal chemistry, 2012-09, Vol.20 (17), p.5202-5214

2012

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The Acyclic 2,4-Diaminopyrimidine Nucleoside Phosphonate Acts as a Purine Mimetic in HIV-1 Reverse Transcriptase DNA Polymerization

The Journal of biological chemistry, 2010-04, Vol.285 (16), p.12101-12108

2010

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Synthesis of 2'-deoxyadenosine nucleosides bearing bipyridine-type ligands and their Ru-complexes in position 8 through cross-coupling reactions

Organic & biomolecular chemistry, 2007-01, Vol.5 (17), p.2849

2007

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N 6-Methyl-AMP aminohydrolase activates N 6-substituted purine acyclic nucleoside phosphonates

Biochemical pharmacology, 2006-04, Vol.71 (9), p.1370-1376

2006

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Phosphoramidate pronucleotides of cytostatic 6-aryl-7-deazapurine ribonucleosides

Bioorganic & medicinal chemistry, 2011-01, Vol.19 (1), p.229-242

2011

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6-[2-(Phosphonomethoxy)alkoxy]pyrimidines with Antiviral Activity

Journal of medicinal chemistry, 2002-04, Vol.45 (9), p.1918-1929

2002

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Synthesis and antiviral activity of N⁹-[3-fluoro-2-(phosphonomethoxy)propyl] analogues derived from N⁶-substituted adenines and 2,6-diaminopurines

Bioorganic & medicinal chemistry, 2011-04, Vol.19 (7), p.2114-2124

2011

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8-Aza-7,9-dideazaxanthine acyclic nucleoside phosphonate inhibitors of thymidine phosphorylase

Bioorganic & medicinal chemistry letters, 2011-01, Vol.21 (2), p.652-654

2011

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Covalent analogues of DNA base-pairs and triplets. Part 2: Synthesis and cytostatic activity of bis(purin-6-yl)acetylenes, -diacetylenes and related compounds

Bioorganic & medicinal chemistry letters, 2002-04, Vol.12 (7), p.1055-1058

2002

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Inhibition of SAH-hydrolase activity during seed germination leads to deregulation of flowering genes and altered flower morphology in tobacco

Molecular genetics and genomics : MGG, 2011-03, Vol.285 (3), p.225-236

2011

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Facile and Efficient Synthesis of 6-(Hydroxymethyl)purines

Organic letters, 2004-09, Vol.6 (19), p.3225-3228

2004

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Synthesis and Cytostatic Activity of Novel 6-(Difluoromethyl)purine Bases and Nucleosides

Synthesis (Stuttgart), 2006-06, Vol.2006 (11), p.1848-1852

2006

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Cytostatic 6-Arylpurine Nucleosides. 6. † SAR in Anti-HCV and Cytostatic Activity of Extended Series of 6-Hetarylpurine Ribonucleosides

Lasioglossins: Three Novel Antimicrobial Peptides from the Venom of the Eusocial Bee Lasioglossum laticeps (Hymenoptera: Halictidae)

Structural Basis for Inhibition of Mycobacterial and Human Adenosine Kinase by 7‑Substituted 7‑(Het)aryl-7-deazaadenine Ribonucleosides

2´-deoxy-5,6-dihydro-5-azacytidine - a less toxic alternative of 2´-deoxy-5-azacytidine: a comparative study of hypomethylating potential

Discovery of 5-Substituted-6-chlorouracils as Efficient Inhibitors of Human Thymidine Phosphorylase

In Vivo Modulation of Angiogenic Gene Expression by Acyclic Nucleoside Phosphonates PMEDAP and PMEG

Tenofovir Diphosphate Is a Poor Substrate and a Weak Inhibitor of Rat DNA Polymerases α, δ, and ε

In Vitro Activities of 3-(Halogenated Phenyl)-5-Acyloxymethyl- 2,5-Dihydrofuran-2-ones against Common and Emerging Yeasts and Molds

Synthesis and Significant Cytostatic Activity of 7-Hetaryl-7-deazaadenosines

Synthesis and Cytostatic Activity of Substituted 6-Phenylpurine Bases and Nucleosides: Application of the Suzuki−Miyaura Cross-Coupling Reactions of 6-Chloropurine Derivatives with Phenylboronic Acids

Sphingosine and clavaminol H derivatives bearing fluorinated chains and their cytotoxic activity

6-(Het)aryl-7-Deazapurine Ribonucleosides as Novel Potent Cytostatic Agents

A novel and efficient one-pot synthesis of symmetrical diamide (bis-amidate) prodrugs of acyclic nucleoside phosphonates and evaluation of their biological activities

Sugar-modified derivatives of cytostatic 7-(het)aryl-7-deazaadenosines: 2′-C-methylribonucleosides, 2′-deoxy-2′-fluoroarabinonucleosides, arabinonucleosides and 2′-deoxyribonucleosides

The Acyclic 2,4-Diaminopyrimidine Nucleoside Phosphonate Acts as a Purine Mimetic in HIV-1 Reverse Transcriptase DNA Polymerization

Synthesis of 2'-deoxyadenosine nucleosides bearing bipyridine-type ligands and their Ru-complexes in position 8 through cross-coupling reactions

N 6-Methyl-AMP aminohydrolase activates N 6-substituted purine acyclic nucleoside phosphonates

Phosphoramidate pronucleotides of cytostatic 6-aryl-7-deazapurine ribonucleosides

6-[2-(Phosphonomethoxy)alkoxy]pyrimidines with Antiviral Activity

Synthesis and antiviral activity of N⁹-[3-fluoro-2-(phosphonomethoxy)propyl] analogues derived from N⁶-substituted adenines and 2,6-diaminopurines

8-Aza-7,9-dideazaxanthine acyclic nucleoside phosphonate inhibitors of thymidine phosphorylase

Covalent analogues of DNA base-pairs and triplets. Part 2: Synthesis and cytostatic activity of bis(purin-6-yl)acetylenes, -diacetylenes and related compounds

Inhibition of SAH-hydrolase activity during seed germination leads to deregulation of flowering genes and altered flower morphology in tobacco

Facile and Efficient Synthesis of 6-(Hydroxymethyl)purines

Synthesis and Cytostatic Activity of Novel 6-(Difluoromethyl)purine Bases and Nucleosides

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