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Analysis of electrodialysis water desalination costs by convective-diffusion model

Desalination, 1999-11, Vol.126 (1), p.207-211

1999

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Analysis of electrodialysis water desalination costs by convective-diffusion model

Desalination (Amsterdam), 1999, Vol.126 (1-3), p.207-211

1999

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Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the Potent Anti-HCV Agent 2‘-C-Methylcytidine

Journal of medicinal chemistry, 2006-11, Vol.49 (22), p.6614-6620

2006

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Conformationally Constrained Analogues of Diacylglycerol (DAG). 16. How Much Structural Complexity Is Necessary for Recognition and High Binding Affinity to Protein Kinase C?

Journal of medicinal chemistry, 2000-03, Vol.43 (5), p.921-944

2000

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Conformationally Constrained Analogues of Diacylglycerol. 18. The Incorporation of a Hydroxamate Moiety into Diacylglycerol-Lactones Reduces Lipophilicity and Helps Discriminate between sn-1 and sn-2 Binding Modes to Protein Kinase C (PK-C). Implications for Isozyme Specificity

Journal of medicinal chemistry, 2001-12, Vol.44 (25), p.4309-4312

2001

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Synthesis, in Vitro Antiviral Evaluation, and Stability Studies of Bis(S-acyl-2-thioethyl) Ester Derivatives of 9-[2-(Phosphonomethoxy)ethyl]adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability

Journal of medicinal chemistry, 1996-12, Vol.39 (25), p.4958-4965

1996

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The Transition from a Pharmacophore-Guided Approach to a Receptor-Guided Approach in the Design of Potent Protein Kinase C Ligands

Pharmacology & therapeutics (Oxford), 1999-05, Vol.82 (2), p.251-261

1999

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Conformationally Constrained Analogues of Diacylglycerol. 18. The Incorporation of a Hydroxamate Moiety into Diacylglycerol-Lactones Reduces Lipophilicity and Helps Discriminate between sn-1 and sn-2 Binding Modes to Protein Kinase C (PK-C). Implications for Isozyme Specificity

Journal of medicinal chemistry, 2003-06, Vol.46 (13), p.2794-2794

2003

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Equal inhibition of the replication of human immunodeficiency virus in human T-cell culture by ddA BIS(SATE)phosphotriester and 3′-azido-2′,3′-dideoxythymidine

Biochemical pharmacology, 1994-07, Vol.48 (1), p.11-14

1994

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Rational design for cytosolic delivery of nucleoside monophosphates : SATE and DTE as enzyme-labile transient phosphate protecting groups

Bioorganic & medicinal chemistry letters, 1993-12, Vol.3 (12), p.2521-2526

1993

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4′- C -Methyl-β-D-ribofuranosyl Purine and Pyrimidine Nucleosides Revisited

Nucleosides, nucleotides & nucleic acids, 2003-10, Vol.22 (5-8), p.707-709

2003

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Monoval-LdC: Efficient Prodrug of 2′-Deoxy-β-L-cytidine (L-dC), A Potent and Selective Anti-HBV Agent

Nucleosides, nucleotides & nucleic acids, 2003-10, Vol.22 (5-8), p.1003-1006

2003

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Comparison of the disposition of ester prodrugs of the antiviral agent 9-(2-phosphonylmethoxyethyl)adenine [PMEA] in Caco-2 monolayers

Pharmaceutical research, 1998-02, Vol.15 (2), p.239-245

1998

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Synthesis, physicochemical and pharmacokinetic studies of potential prodrugs of b-l-2'-deoxycytidine, a selective and specific anti-HBV agent

Antiviral chemistry & chemotherapy, 2004-09, Vol.15 (5), p.269-279

2004

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New insights regarding the potential of the pronucleotide approach in antiviral chemotherapy

Acta biochimica polonica, 1996-01, Vol.43 (1), p.196-208

1996

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bis(S-Acyl-2-thioethyl)esters of 2′,3′-Dideoxyadenosine 5′-Monophosphate Are Potent Anti-HIV Agents in Cell Culture

Nucleosides & nucleotides, 1995-05, Vol.14 (3-5), p.789-791

1995

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New Prodrugs of 9-(2-Phosphonomethoxyethyl)adenine [PMEA]: Synthesis and Stability Studies

Nucleosides & nucleotides, 1995-05, Vol.14 (3-5), p.563-565

1995

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Synthesis of 2′,3′,5′-trideoxyuridine-5′-methylphosphonic Acid and its Diphosphate Derivative. Study of the Interaction with HIV-1 reverse Transcriptase

Antiviral chemistry & chemotherapy, 1994-08, Vol.5 (4), p.221-228

1994

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New insights regarding the potential of the pronucleotide approach in antiviral chemotherapy

Acta biochimica polonica, 1996-01, Vol.43 (1), p.196-208

1996

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4′-C-Methyl-β-D-ribofuranosyl Purine and Pyrimidine Nucleosides Revisited

ChemInform, 2004-01, Vol.35 (3), p.no-no

2004

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Monoval-LdC: Efficient Prodrug of 2′-Deoxy-β-L-cytidine (L-dC), a Potent and Selective anti-HBV Agent

ChemInform, 2004-02, Vol.35 (5), p.no-no

2004

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Anti-human immunodeficiency virus type 1 activities of dideoxynucleoside phosphotriester derivatives in primary monocytes/macrophages

Research in virology (Paris), 1996-03, Vol.147 (2), p.155-163

1996

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ChemInform Abstract: Synthesis, in vitro Antiviral Evaluation, and Stability Studies of Bis( S-acyl-2-thioethyl) Ester Derivatives of 9-(2-(Phosphonomethoxy)ethyl) adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability

ChemInform, 1997-04, Vol.28 (14), p.no-no

1997

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ChemInform Abstract: New Prodrugs of 9-(2-Phosphonomethoxyethyl)adenine (PMEA): Synthesis and Stability Studies

ChemInform, 1995-10, Vol.26 (40), p.no-no

1995

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ChemInform Abstract: Bis(S-acyl-2-thioethyl)esters of 2′,3′-Dideoxyadenosine 5′- Monophosphate Are Potent Anti-HIV Agents in Cell Culture

ChemInform, 1995-09, Vol.26 (39), p.no-no

1995

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Analysis of electrodialysis water desalination costs by convective-diffusion model

Analysis of electrodialysis water desalination costs by convective-diffusion model

Synthesis and Pharmacokinetics of Valopicitabine (NM283), an Efficient Prodrug of the Potent Anti-HCV Agent 2‘-C-Methylcytidine

Conformationally Constrained Analogues of Diacylglycerol (DAG). 16. How Much Structural Complexity Is Necessary for Recognition and High Binding Affinity to Protein Kinase C?

Conformationally Constrained Analogues of Diacylglycerol. 18. The Incorporation of a Hydroxamate Moiety into Diacylglycerol-Lactones Reduces Lipophilicity and Helps Discriminate between sn-1 and sn-2 Binding Modes to Protein Kinase C (PK-C). Implications for Isozyme Specificity

Synthesis, in Vitro Antiviral Evaluation, and Stability Studies of Bis(S-acyl-2-thioethyl) Ester Derivatives of 9-[2-(Phosphonomethoxy)ethyl]adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability

The Transition from a Pharmacophore-Guided Approach to a Receptor-Guided Approach in the Design of Potent Protein Kinase C Ligands

Conformationally Constrained Analogues of Diacylglycerol. 18. The Incorporation of a Hydroxamate Moiety into Diacylglycerol-Lactones Reduces Lipophilicity and Helps Discriminate between sn-1 and sn-2 Binding Modes to Protein Kinase C (PK-C). Implications for Isozyme Specificity

Equal inhibition of the replication of human immunodeficiency virus in human T-cell culture by ddA BIS(SATE)phosphotriester and 3′-azido-2′,3′-dideoxythymidine

Rational design for cytosolic delivery of nucleoside monophosphates : SATE and DTE as enzyme-labile transient phosphate protecting groups

4′- C -Methyl-β-D-ribofuranosyl Purine and Pyrimidine Nucleosides Revisited

Monoval-LdC: Efficient Prodrug of 2′-Deoxy-β-L-cytidine (L-dC), A Potent and Selective Anti-HBV Agent

Comparison of the disposition of ester prodrugs of the antiviral agent 9-(2-phosphonylmethoxyethyl)adenine [PMEA] in Caco-2 monolayers

Synthesis, physicochemical and pharmacokinetic studies of potential prodrugs of b-l-2'-deoxycytidine, a selective and specific anti-HBV agent

New insights regarding the potential of the pronucleotide approach in antiviral chemotherapy

bis(S-Acyl-2-thioethyl)esters of 2′,3′-Dideoxyadenosine 5′-Monophosphate Are Potent Anti-HIV Agents in Cell Culture

New Prodrugs of 9-(2-Phosphonomethoxyethyl)adenine [PMEA]: Synthesis and Stability Studies

Synthesis of 2′,3′,5′-trideoxyuridine-5′-methylphosphonic Acid and its Diphosphate Derivative. Study of the Interaction with HIV-1 reverse Transcriptase

New insights regarding the potential of the pronucleotide approach in antiviral chemotherapy

4′-C-Methyl-β-D-ribofuranosyl Purine and Pyrimidine Nucleosides Revisited

Monoval-LdC: Efficient Prodrug of 2′-Deoxy-β-L-cytidine (L-dC), a Potent and Selective anti-HBV Agent

Anti-human immunodeficiency virus type 1 activities of dideoxynucleoside phosphotriester derivatives in primary monocytes/macrophages

ChemInform Abstract: Synthesis, in vitro Antiviral Evaluation, and Stability Studies of Bis( S-acyl-2-thioethyl) Ester Derivatives of 9-(2-(Phosphonomethoxy)ethyl) adenine (PMEA) as Potential PMEA Prodrugs with Improved Oral Bioavailability

ChemInform Abstract: New Prodrugs of 9-(2-Phosphonomethoxyethyl)adenine (PMEA): Synthesis and Stability Studies

ChemInform Abstract: Bis(S-acyl-2-thioethyl)esters of 2′,3′-Dideoxyadenosine 5′- Monophosphate Are Potent Anti-HIV Agents in Cell Culture

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