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Synthesis, in vitro and in vivo antifungal activity of 5-phenylthio-2,4-bisbenzyloxypyrimidine: a novel nucleobase

Indian journal of pharmaceutical sciences, 2010-11, Vol.72 (6), p.778-781

2010

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Synthesis and antimicrobial evaluation of 5-iodopyrimidine analogs

Indian journal of pharmaceutical sciences, 2009-11, Vol.71 (6), p.672-677

2009

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DESIGN, SYNTHESIS AND ANTIMICROBIAL EVALUATION OF NOVEL 1-(2-(4-FLUORO BENZYLTHIO)PYRIMIDIN-4-YL-AMINO)-4-(SUBSTITUTED PHENYL)AZETIDIN-2-ONES

International journal of pharmaceutical sciences and research, 2015-03, Vol.6 (3), p.1060-1060

2015

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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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SYNTHESIS AND ANTIMICROBIAL EVALUATION OF 2-(4-FLUORO BENZYLTHIO)-N-(SUBSTITUTED PHENYL)PYRIMIDINE-4-AMINES

International journal of pharmaceutical sciences and research, 2013-11, Vol.4 (11), p.4336-4336

2013

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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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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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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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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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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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Resistance of human immunodeficiency virus type 1 to acyclic 6-phenylselenenyl- and 6-phenylthiopyrimidines

Antimicrobial Agents and Chemotherapy, 1994-10, Vol.38 (10), p.2409-2414

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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1-(Ethoxymethyl)-6-(Phenylselenenyl)Pyrimidines with Activity against Human Immunodeficiency Virus Types 1 and 2

Antiviral chemistry & chemotherapy, 1992-10, Vol.3 (5), p.263-266

1992

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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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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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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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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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EFFICIENT SYNTHESIS OF NOVEL 6-PHENYLTHIO-2,4- DISUBSTITUTED PYRIMIDINES

Heterocyclic communications, 2008, Vol.14 (6), p.443-448

2008

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

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

1988

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ChemInform Abstract: Synthesis of 3-(Benzimidazol-2-yl-amino)-1- (4-bromophenyl)-2-thioxopyrimidin-4,6-dione Analogues and Their Antimicrobial Activity

ChemInform, 2011-03, Vol.42 (11), p.no-no

2011

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ChemInform Abstract: Synthesis and Antimicrobial Activities of Novel Formazans Incorporating Pyrimidine Ring

ChemInform, 2010-05, Vol.41 (19), p.no-no

2010

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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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Synthesis, in vitro and in vivo antifungal activity of 5-phenylthio-2,4-bisbenzyloxypyrimidine: a novel nucleobase

Synthesis and antimicrobial evaluation of 5-iodopyrimidine analogs

DESIGN, SYNTHESIS AND ANTIMICROBIAL EVALUATION OF NOVEL 1-(2-(4-FLUORO BENZYLTHIO)PYRIMIDIN-4-YL-AMINO)-4-(SUBSTITUTED PHENYL)AZETIDIN-2-ONES

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

SYNTHESIS AND ANTIMICROBIAL EVALUATION OF 2-(4-FLUORO BENZYLTHIO)-N-(SUBSTITUTED PHENYL)PYRIMIDINE-4-AMINES

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

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

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

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

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

Resistance of human immunodeficiency virus type 1 to acyclic 6-phenylselenenyl- and 6-phenylthiopyrimidines

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

1-(Ethoxymethyl)-6-(Phenylselenenyl)Pyrimidines with Activity against Human Immunodeficiency Virus Types 1 and 2

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

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

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

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

EFFICIENT SYNTHESIS OF NOVEL 6-PHENYLTHIO-2,4- DISUBSTITUTED PYRIMIDINES

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

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

ChemInform Abstract: Synthesis of 3-(Benzimidazol-2-yl-amino)-1- (4-bromophenyl)-2-thioxopyrimidin-4,6-dione Analogues and Their Antimicrobial Activity

ChemInform Abstract: Synthesis and Antimicrobial Activities of Novel Formazans Incorporating Pyrimidine Ring

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

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