Search Results - "Shaddix, Sue C"

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    Structure-activity relationship for adenosine kinase from Mycobacterium tuberculosis II. Modifications to the ribofuranosyl moiety by LONG, Mary C, SHADDIX, Sue C, MOUKHA-CHAFIQ, Omar, MADDRY, Joseph A, NAGY, Lisa, PARKER, William B

    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 by Parker, William B, Shaddix, Sue C, Gilbert, Karen S, Shepherd, Rodney V, Waud, William R

    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 by Long, Mary C., Shaddix, Sue C., Moukha-Chafiq, Omar, Maddry, Joseph A., Nagy, Lisa, Parker, William B.

    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 by Parker, William B, Allan, Paula W, Shaddix, Sue C, Rose, Lucy M, Speegle, Heath F, Gillespie, G.Yancey, Bennett, L.Lee

    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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    Phosphorylation of 4'-thio-beta-D-arabinofuranosylcytosine and its analogs by human deoxycytidine kinase by Someya, Hitoshi, Shaddix, Sue C, Tiwari, Kamal N, Secrist, 3rd, John A, Parker, William B

    “…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 by Rose, Jerry D, Parker, William B, Someya, Hitoshi, Shaddix, Sue C, Montgomery, John A, Secrist, John A

    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 by Parker, William B, Shaddix, Sue C, Rose, Lucy M, Waud, William R, Shewach, Donna S, Tiwari, Kamal N, Secrist, John A

    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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    Metabolism of 2-methyladenosine in Mycobacterium tuberculosis by Parker, William B, Barrow, Esther W, Allan, Paula W, Shaddix, Sue C, Long, Mary C, Barrow, William W, Bansal, Namita, Maddry, Joseph A

    “…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 by Parker, William B., Shaddix, Sue C., Rose, Lucy M., Tiwari, Kamal N., Montgomery, John A., Secrist, John A., Bennett, L.Lee

    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 by Parker, William B, Shaddix, Sue C, Gilbert, Karen S, Shepherd, Rodney V, Waud, William R

    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…”
    Get full text
    Journal Article
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    Nitrosoureido nucleosides as potential inhibitors of nucleotide biosynthesis by Elliott, Robert D, Thomas, H. Jeanette, Shaddix, Sue C, Adamson, Doris J, Brockman, R. Wallace, Riordan, James M, Montgomery, John A

    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 by Shealy, Y. Fulmer, Frye, Jerry L, DuBois, Nancy F, Shaddix, Sue C, Brockman, R. Wallace

    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 by Bennett, Jr, L L, Smithers, D, Rose, L M, Adamson, D J, Shaddix, S C, Thomas, H J

    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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    Synthesis and Biological Evaluation of Some 4'-C-(Hydroxymethyl)-α- and -β-D-Arabinofuranosyl Pyrimidine and Adenine Nucleosides by Griffon, Jean-François, Shaddix, Sue C., Parker, William B., Al-Madhoun, Ashraf S., Eriksson, Staffan, Montgomery, John A., Secrist III, John A.

    “…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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