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Novel Approaches to Cancer Chemotherapy

Sunkara, Prasad S

1, 1984

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Novel Approaches to Cancer Chemotherapy

Sunkara, Prasad S

2013

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Chalcones: a new class of antimitotic agents

Journal of medicinal chemistry, 1990-07, Vol.33 (7), p.1948-1954

1990

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Evaluation of (E)-2′-deoxy-2′-(fluoromethylene)cytidine on the 9L rat brain tumor model using MRI

NMR in biomedicine, 2003-04, Vol.16 (2), p.67-76

2003

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The synthesis of acyclonucleoside hydroxamic acids as inhibitors of ribonucleotide reductase

Journal of medicinal chemistry, 1989-08, Vol.32 (8), p.1879-1885

1989

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Antiretroviral activity of castanospermine and deoxynojirimycin, specific inhibitors of glycoprotein processing

Biochemical and biophysical research communications, 1987-10, Vol.148 (1), p.206-210

1987

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Stereospecific method to (E) and (Z) terminal fluoroolefins and its application to the synthesis of 2'-deoxy-2'-fluoromethylenenucleosides as potential inhibitors of ribonucleoside diphosphate reductase

Journal of the American Chemical Society, 1991-09, Vol.113 (19), p.7439-7440

1991

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4'-5'-Unsaturated 5'-halogenated nucleosides. Mechanism-based and competitive inhibitors of S-adenosyl-L-homocysteine hydrolase

Journal of medicinal chemistry, 1991-02, Vol.34 (2), p.647-656

1991

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EFFECT OF POLYAMINE DEPLETION ON DNA DAMAGE and REPAIR FOLLOWING UV IRRADIATION OF HeLa CELLS

Photochemistry and photobiology, 1990-09, Vol.52 (3), p.525-532

1990

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Potentiation of human lymphokine-activated killer cell activity by swainsonine, an inhibitor of glycoprotein processing

Cancer research (Chicago, Ill.), 1989-08, Vol.49 (15), p.4109-4113

1989

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Tumor Suppression with a Combination of $\alpha $-difluoromethyl Ornithine and Interferon

Science (American Association for the Advancement of Science), 1983-02, Vol.219 (4586), p.851-853

1983

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Effects of three irreversible inhibitors of ornithine decarboxylase on macrophage-mediated tumoricidal activity and antitumor activity in B16F1 tumor-bearing mice

Cancer research (Chicago, Ill.), 1990-08, Vol.50 (15), p.4510-4514

1990

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Intracellular polyamine biosynthesis is required for interleukin 2 responsiveness during lymphocyte mitogenesis

Cellular immunology, 1987-05, Vol.106 (2), p.420-427

1987

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4'-5'-Unsaturated 5'-halogenated nucleosides. Mechanism-based and competitive inhibitors of S-adenosyl-L-homocysteine hydrolase. [Erratum to document cited in CA114(21):207657n]

Journal of medicinal chemistry, 1993-02, Vol.36 (4), p.518-518

1993

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Stereospecific method to E and Z terminal fluoro olefins and its application to the synthesis of 2'-deoxy-2'-fluoromethylene nucleosides as potential inhibitors of ribonucleoside diphosphate reductase

Journal of the American Chemical Society, 1991-09, Vol.113 (19), p.7439-7440

1991

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4',5'-Unsaturated-5'-fluoro adenosine nucleosides: potent mechanism-based inhibitors of S-adenosyl-L-homocysteine hydrolase

Journal of the American Chemical Society, 1989-02, Vol.111 (3), p.1127-1128

1989

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6-0-Butanoylcastanospermine (MDL 28,574) inhibits glycoprotein processing and the growth of HIVs

AIDS (London), 1991-06, Vol.5 (6), p.693-698

1991

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Farnesyl-Derived Inhibitors of ras Farnesyl Transferase

Biochemical and biophysical research communications, 1995-12, Vol.217 (1), p.245-249

1995

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Synthesis of polyhydroxylated indolizidine and quinolizidine compounds--potent inhibitors of α-glucosidase I

Tetrahedron letters, 1991-10, Vol.32 (42), p.5853-5856

1991

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The ribonucleotide reductase inhibitor ( E)-2′-fluoromethylene-2′-deoxycytidine (MDL 101,731): a potential topical therapy for herpes simplex virus infection

Antiviral Research, 1995-08, Vol.27 (4), p.325-334

1995

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A potent inhibitor of β-N-acetylglucosaminidases : 6-acetamido-6-deoxycastanospermine

Tetrahedron letters, 1991-02, Vol.32 (6), p.719-720

1991

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Mitotic factors from mammalian cells: A preliminary characterization

Journal of supramolecular structure, 1979, Vol.11 (2), p.189-195

1979

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Castanospermine analogues: their inhibition of glycoprotein processing α-glucosidases from porcine kidney and B16F10 cells

Glycobiology (Oxford), 1995-02, Vol.5 (1), p.147-152

1995

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Swainsonine, an inhibitor of glycoprotein processing, enhances mitogen induced interleukin 2 production and receptor expression in human lymphocytes

Biochemical and biophysical research communications, 1988-03, Vol.151 (2), p.859-864

1988

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Mitotic Factors from Mammalian Cells Induce Germinal Vesicle Breakdown and Chromosome Condensation in Amphibian Oocytes

Proceedings of the National Academy of Sciences - PNAS, 1979-06, Vol.76 (6), p.2799-2802

1979

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Novel Approaches to Cancer Chemotherapy

Novel Approaches to Cancer Chemotherapy

Chalcones: a new class of antimitotic agents

Evaluation of (E)-2′-deoxy-2′-(fluoromethylene)cytidine on the 9L rat brain tumor model using MRI

The synthesis of acyclonucleoside hydroxamic acids as inhibitors of ribonucleotide reductase

Antiretroviral activity of castanospermine and deoxynojirimycin, specific inhibitors of glycoprotein processing

Stereospecific method to (E) and (Z) terminal fluoroolefins and its application to the synthesis of 2'-deoxy-2'-fluoromethylenenucleosides as potential inhibitors of ribonucleoside diphosphate reductase

4'-5'-Unsaturated 5'-halogenated nucleosides. Mechanism-based and competitive inhibitors of S-adenosyl-L-homocysteine hydrolase

EFFECT OF POLYAMINE DEPLETION ON DNA DAMAGE and REPAIR FOLLOWING UV IRRADIATION OF HeLa CELLS

Potentiation of human lymphokine-activated killer cell activity by swainsonine, an inhibitor of glycoprotein processing

Tumor Suppression with a Combination of $\alpha $-difluoromethyl Ornithine and Interferon

Effects of three irreversible inhibitors of ornithine decarboxylase on macrophage-mediated tumoricidal activity and antitumor activity in B16F1 tumor-bearing mice

Intracellular polyamine biosynthesis is required for interleukin 2 responsiveness during lymphocyte mitogenesis

4'-5'-Unsaturated 5'-halogenated nucleosides. Mechanism-based and competitive inhibitors of S-adenosyl-L-homocysteine hydrolase. [Erratum to document cited in CA114(21):207657n]

Stereospecific method to E and Z terminal fluoro olefins and its application to the synthesis of 2'-deoxy-2'-fluoromethylene nucleosides as potential inhibitors of ribonucleoside diphosphate reductase

4',5'-Unsaturated-5'-fluoro adenosine nucleosides: potent mechanism-based inhibitors of S-adenosyl-L-homocysteine hydrolase

6-0-Butanoylcastanospermine (MDL 28,574) inhibits glycoprotein processing and the growth of HIVs

Farnesyl-Derived Inhibitors of ras Farnesyl Transferase

Synthesis of polyhydroxylated indolizidine and quinolizidine compounds--potent inhibitors of α-glucosidase I

The ribonucleotide reductase inhibitor ( E)-2′-fluoromethylene-2′-deoxycytidine (MDL 101,731): a potential topical therapy for herpes simplex virus infection

A potent inhibitor of β-N-acetylglucosaminidases : 6-acetamido-6-deoxycastanospermine

Mitotic factors from mammalian cells: A preliminary characterization

Castanospermine analogues: their inhibition of glycoprotein processing α-glucosidases from porcine kidney and B16F10 cells

Swainsonine, an inhibitor of glycoprotein processing, enhances mitogen induced interleukin 2 production and receptor expression in human lymphocytes

Mitotic Factors from Mammalian Cells Induce Germinal Vesicle Breakdown and Chromosome Condensation in Amphibian Oocytes

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