Search Results - "Shaddix, Sue C"
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Structure-activity relationship for adenosine kinase from Mycobacterium tuberculosis II. Modifications to the ribofuranosyl moiety
Published in Biochemical pharmacology (15-04-2008)“…Adenosine kinase (Ado kinase) from Mycobacterium tuberculosis is structurally and biochemically unique from other known Ado kinases. This purine salvage enzyme…”
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Enhancement of the in vivo antitumor activity of clofarabine by 1-β-d-[4-thio-arabinofuranosyl]-cytosine
Published in Cancer chemotherapy and pharmacology (01-07-2009)“…Purpose Clofarabine increases the activation of 1-β-d-arabinofuranosyl cytosine (araC) in tumor cells, and combination of these two drugs has been shown to…”
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Structure–activity relationship for adenosine kinase from Mycobacterium tuberculosis
Published in Biochemical pharmacology (01-04-2008)“…Adenosine kinase (Ado kinase) from Mycobacterium tuberculosis is structurally and biochemically unique from other known Ado kinases. This purine salvage enzyme…”
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Metabolism and Metabolic Actions of 6-Methylpurine and 2-Fluoroadenine in Human Cells
Published in Biochemical pharmacology (15-05-1998)“…Activation of purine nucleoside analogs by Escherichia coli purine nucleoside phosphorylase (PNP) is being evaluated as a suicide gene therapy strategy for the…”
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Comparison of the mechanism of cytotoxicity of 2-chloro-9-(2-deoxy-2- fluoro-beta-D-arabinofuranosyl)adenine, 2-chloro-9-(2-deoxy-2-fluoro- beta-D-ribofuranosyl)adenine, and 2-chloro-9-(2-deoxy-2,2-difluoro- beta-D-ribofuranosyl)adenine in CEM cells
Published in Molecular pharmacology (01-03-1999)“…In an effort to understand biochemical features that are important to the selective antitumor activity of…”
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Phosphorylation of 4'-thio-beta-D-arabinofuranosylcytosine and its analogs by human deoxycytidine kinase
Published in The Journal of pharmacology and experimental therapeutics (01-03-2003)“…4'-thio-beta-D-arabinofuranosylcytosine (T-araC) exhibits excellent in vivo antitumor activity against a variety of solid tumors despite its structural…”
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Enhancement of Nucleoside Cytotoxicity through Nucleotide Prodrugs
Published in Journal of medicinal chemistry (26-09-2002)“…A common reason for the lack of cytotoxicity of certain nucleosides is thought to be their inability to be initially activated to the monophosphate level by a…”
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Metabolism of 4′-thio-β- d-arabinofuranosylcytosine in CEM cells
Published in Biochemical pharmacology (15-12-2000)“…Because of the excellent in vivo activity of 4′-thio-β- d-arabinofuranosylcytosine (T-araC) against a variety of human solid tumors, we have studied its…”
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Effects of 2-chloro-9-(3-deoxy-2-fluoro-β-D-arabinofuranosyl)adenine on K562 cellular metabolism and the inhibition of human ribonucleotide reductase and DNA polymerases by its 5'-triphosphate
Published in Cancer research (Chicago, Ill.) (01-05-1991)“…2-Chloro-9-(2-deoxy-2-fluoro-beta-D-arabinofuranosyl)-adenine (Cl-F-ara-A) has activity against the P388 tumor in mice on several different schedules…”
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Metabolism of 2-methyladenosine in Mycobacterium tuberculosis
Published in Tuberculosis (Edinburgh, Scotland) (2004)“…2-Methyladenosine (methyl-Ado) has selective activity against Mycobacterium tuberculosis ( M. tuberculosis). In an effort to better understand its mechanism of…”
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Metabolism and metabolic actions of 4′-thiothymidine in L1210 cells
Published in Biochemical pharmacology (25-08-1995)“…4′-Thiothymidine (S-dThd) is a potent inhibitor of L1210 cell growth and is active against P388 leukemia in mice. Because of these activities and its novel…”
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Enhancement of the in vivo antitumor activity of clofarabine by 1-[beta]-d-[4-thio-arabinofuranosyl]-cytosine
Published in Cancer chemotherapy and pharmacology (01-07-2009)“…Clofarabine increases the activation of 1-β-d-arabinofuranosyl cytosine (araC) in tumor cells, and combination of these two drugs has been shown to result in…”
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Nitrosoureido nucleosides as potential inhibitors of nucleotide biosynthesis
Published in Journal of medicinal chemistry (01-01-1988)“…Several nitrosoureido nucleosides (3a, 3b, 5a, 7a, 7c, and 10a) designed as inhibitors of enzymes that metabolize pyrimidine nucleotides have been prepared and…”
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Carbocyclic analogs of 5-fluorouracil nucleosides
Published in Journal of medicinal chemistry (01-09-1981)“…The carbocyclic analogues of 5-fluoro-2'-deoxyuridine (5-FdUrd, 1), 5-fluorouridine, and 5-fluoro-3 alpha-deoxyuridine were prepared by fluorination of the…”
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Metabolism and metabolic effects of 2-azahypoxanthine and 2-azaadenosine
Published in Biochemical pharmacology (15-04-1985)“…The metabolism and metabolic effects of 2-azahypoxanthine and 2-azaadenosine were studied to elucidate the biochemical basis for their known cytotoxicities…”
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Mechanism of inhibition of human immunodeficiency virus type 1 reverse transcriptase and human DNA polymerases alpha, beta, and gamma by the 5'-triphosphates of carbovir, 3'-azido-3'-deoxythymidine, 2',3'-dideoxyguanosine and 3'-deoxythymidine. A novel RNA template for the evaluation of antiretroviral drugs
Published in The Journal of biological chemistry (25-01-1991)“…Carbovir (the carbocyclic analog of 2'-3'-didehydro-2',3'-dideoxyguanosine) is a potent inhibitor of human immunodeficiency virus type 1 (HIV-1) replication…”
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Synthesis and Biological Evaluation of Some 4'-C-(Hydroxymethyl)-α- and -β-D-Arabinofuranosyl Pyrimidine and Adenine Nucleosides
Published in Collection of Czechoslovak chemical communications (01-01-2006)“…A series of 4'- C -(hydroxymethyl) analogs of pyrimidine and purine nucleosides have been prepared utilizing standard methodologies, and the α and β anomers…”
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Comparison of the effect of Carbovir, AZT, and dideoxynucleoside triphosphates on the activity of human immunodeficiency virus reverse transcriptase and selected human polymerases
Published in Biochemical and biophysical research communications (15-06-1989)“…Carbocylic 2',3'-didehydro-2',3'-dideoxyguanosine (Carbovir; NSC 614846) is an antiretroviral agent which may be useful in the treatment of AIDS. We have…”
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