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A comprehensive review on pyrimidine analogs-versatile scaffold with medicinal and biological potential

Journal of molecular structure, 2021-12, Vol.1246, p.131168, Article 131168

2021

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Activity of acyclic 6-(phenylselenenyl)pyrimidine nucleosides against human immunodeficiency viruses in primary lymphocytes

Journal of medicinal chemistry, 1991-11, Vol.34 (11), p.3305-3309

1991

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Phenylselenenyl- and phenylthio-substituted pyrimidines as inhibitors of dihydrouracil dehydrogenase and uridine phosphorylase

Journal of medicinal chemistry, 1993-12, Vol.36 (26), p.4250-4254

1993

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Sodium perborate: a mild and convenient reagent for efficiently oxidizing organoboranes

Journal of organic chemistry, 1989-12, Vol.54 (25), p.5930-5933

1989

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5-phenylthioacyclouridine: a potent and specific inhibitor of uridine phosphorylase

Biochemical pharmacology, 2000-09, Vol.60 (6), p.851-856

2000

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Effect of administration of 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase, on the anti-tumor efficacy of 5-fluoro-2′-deoxyuridine against murine colon tumor C26–10

Biochemical pharmacology, 2000-09, Vol.60 (5), p.687-692

2000

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Unexpected formation of novel butenolides by thermolysis of o-carboranyl substituted cyclobutenones

Tetrahedron letters, 1998-04, Vol.39 (14), p.1869-1872

1998

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Sodium perborate: A mild and convenient reagent for efficiently oxidizing trialkylboranes

Tetrahedron letters, 1989, Vol.30 (12), p.1483-1486

1989

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Synthesis and anti-mirobial activity of thiazole substituted coumarins

Heterocyclic communications, 2009, Vol.15 (5), p.343-348

2009

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Synthesis and Biological Properties of5-o-Carboranyl-1-(2-deoxy-2-fluoro-.beta.-D-arabinofuranosyl)uracil

Journal of medicinal chemistry, 1994-08, Vol.37 (16), p.2583-2588

1994

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Reaction of organoboranes with olefinic .alpha.,.beta.-unsaturated nitro compounds

Organometallics, 1988-02, Vol.7 (2), p.493-495

1988

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Catabolism of 3'-azido-3'-deoxythymidine in hepatocytes and liver microsomes, with evidence of formation of 3'-amino-3'-deoxythymidine, a highly toxic catabolite for human bone marrow cells

Molecular pharmacology, 1991-02, Vol.39 (2), p.258-266

1991

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Cellular pharmacology and biological activity of 5-carboranyl-2′-deoxyuridine

International journal of radiation oncology, biology, physics, 1994-03, Vol.28 (5), p.1113-1120

1994

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Modulation of the pharmacokinetics of endogenous plasma uridine by 5-(phenylthio)acyclouridine, a uridine phosphorylase inhibitor: implications for chemotherapy

Cancer chemotherapy and pharmacology, 2001-08, Vol.48 (2), p.145-150

2001

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Modulation of plasma uridine concentration by 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase : relevance to chemotherapy

Cancer chemotherapy and pharmacology, 2000, Vol.45 (5), p.351-361

2000

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Effect of 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase, on plasma concentration of uridine released from 2', 3', 5'-tri-O-acetyluridine, a prodrug of uridine: relevance to uridine rescue in chemotherapy

Cancer chemotherapy and pharmacology, 2000, Vol.46 (3), p.235-240

2000

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Boron Containing Pyrimidines, Nucleosides, and Oligonucleotides for Neutron Capture Therapy

Nucleosides & nucleotides, 1994-03, Vol.13 (1-3), p.849-880

1994

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Synthesis and biological properties of 5-o-carboranyl-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)uracil

Journal of medicinal chemistry, 1994-08, Vol.37 (16), p.2583-2588

1994

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Catabolic disposition of 3'-azido-2',3'-dideoxyuridine in hepatocytes with evidence of azido reduction being a general catabolic pathway of 3'-azido-2',3'-dideoxynucleosides

Biochemical pharmacology, 1992-09, Vol.44 (5), p.973-980

1992

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The Reduction of α,β-Unsaturated Nitroalkenes to Nitroalkanes with Borohydride Supported on an Ion Exchange Resin

Synthetic communications, 1989-03, Vol.19 (5-6), p.805-811

1989

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A Facile Aldoxime Preparation Via the Reduction of α, β-Unsaturated Nitroalkenes Using Tin (II) Chloride

Synthetic communications, 1988-05, Vol.18 (7), p.693-697

1988

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The Reaction of Organoboranes with Trimethylsilyl Azide in a Neutral Medium: Synthesis of Primary Amines

Synthetic communications, 1988-08, Vol.18 (12), p.1363-1369

1988

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A General Synthetic Method of 5-Carboranyluracil Nucleosides with Potential Antiviral Activity and use in Neutron Capture Therapy

Nucleosides & nucleotides, 1997-12, Vol.16 (12), p.2133-2150

1997

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Effects of modifications in the pentose moiety and conformational changes on the binding of nucleoside ligands to uridine phosphorylase from Toxoplasma gondii

Biochemical pharmacology, 1996-06, Vol.51 (12), p.1687-1700

1996

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SYNTHESIS OF (2-BUTYL-3-BENZOFURANYL)[4-[2-(DIETHYLAMINO)ETHOXY]-3,5-DIIODOPHENYL)METHANE DERIVATIVES

Organic preparations and procedures international, 1989-06, Vol.21 (3), p.348-351

1989

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A comprehensive review on pyrimidine analogs-versatile scaffold with medicinal and biological potential

Activity of acyclic 6-(phenylselenenyl)pyrimidine nucleosides against human immunodeficiency viruses in primary lymphocytes

Phenylselenenyl- and phenylthio-substituted pyrimidines as inhibitors of dihydrouracil dehydrogenase and uridine phosphorylase

Sodium perborate: a mild and convenient reagent for efficiently oxidizing organoboranes

5-phenylthioacyclouridine: a potent and specific inhibitor of uridine phosphorylase

Effect of administration of 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase, on the anti-tumor efficacy of 5-fluoro-2′-deoxyuridine against murine colon tumor C26–10

Unexpected formation of novel butenolides by thermolysis of o-carboranyl substituted cyclobutenones

Sodium perborate: A mild and convenient reagent for efficiently oxidizing trialkylboranes

Synthesis and anti-mirobial activity of thiazole substituted coumarins

Synthesis and Biological Properties of5-o-Carboranyl-1-(2-deoxy-2-fluoro-.beta.-D-arabinofuranosyl)uracil

Reaction of organoboranes with olefinic .alpha.,.beta.-unsaturated nitro compounds

Catabolism of 3'-azido-3'-deoxythymidine in hepatocytes and liver microsomes, with evidence of formation of 3'-amino-3'-deoxythymidine, a highly toxic catabolite for human bone marrow cells

Cellular pharmacology and biological activity of 5-carboranyl-2′-deoxyuridine

Modulation of the pharmacokinetics of endogenous plasma uridine by 5-(phenylthio)acyclouridine, a uridine phosphorylase inhibitor: implications for chemotherapy

Modulation of plasma uridine concentration by 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase : relevance to chemotherapy

Effect of 5-(phenylselenenyl)acyclouridine, an inhibitor of uridine phosphorylase, on plasma concentration of uridine released from 2', 3', 5'-tri-O-acetyluridine, a prodrug of uridine: relevance to uridine rescue in chemotherapy

Boron Containing Pyrimidines, Nucleosides, and Oligonucleotides for Neutron Capture Therapy

Synthesis and biological properties of 5-o-carboranyl-1-(2-deoxy-2-fluoro-β-D-arabinofuranosyl)uracil

Catabolic disposition of 3'-azido-2',3'-dideoxyuridine in hepatocytes with evidence of azido reduction being a general catabolic pathway of 3'-azido-2',3'-dideoxynucleosides

The Reduction of α,β-Unsaturated Nitroalkenes to Nitroalkanes with Borohydride Supported on an Ion Exchange Resin

A Facile Aldoxime Preparation Via the Reduction of α, β-Unsaturated Nitroalkenes Using Tin (II) Chloride

The Reaction of Organoboranes with Trimethylsilyl Azide in a Neutral Medium: Synthesis of Primary Amines

A General Synthetic Method of 5-Carboranyluracil Nucleosides with Potential Antiviral Activity and use in Neutron Capture Therapy

Effects of modifications in the pentose moiety and conformational changes on the binding of nucleoside ligands to uridine phosphorylase from Toxoplasma gondii

SYNTHESIS OF (2-BUTYL-3-BENZOFURANYL)[4-[2-(DIETHYLAMINO)ETHOXY]-3,5-DIIODOPHENYL)METHANE DERIVATIVES

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