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Radiolabeled Cyclosaligenyl Monophosphates of 5-Iodo-2′-deoxyuridine, 5-Iodo-3′-fluoro-2′,3′-dideoxyuridine, and 3′-Fluorothymidine for Molecular Radiotherapy of Cancer: Synthesis and Biological Evaluation

机译：5-Iodo-2'-脱氧尿苷，5-Iodo-3'-Fluoro-2'，3'-二氧化脲和3'-含有癌症的3'-氟脲酰基的甲基水环氧酯：合成和生物学评估

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Zbigniew P. Kortylewicz; Yu Kimura; Kotaro Inoue; Elizabeth Mack; Janina Baranowska-Kortylewicz;
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1. Radiolabeled cyclosaligenyl monophosphates of 5-iodo-2′-deoxyuridine, 5-iodo-3′-fluoro-2′,3′-dideoxyuridine, and 3′-fluorothymidine for molecular radiotherapy of cancer: Synthesis and biological evaluation [J] . Kortylewicz Z.P., Kimura Y., Inoue K., Journal of Medicinal Chemistry . 2012,第6期

机译：放射性标记的5-碘-2'-脱氧尿苷，5-碘-3'-氟-2'，3'-二脱氧尿苷和3'-氟胸苷的环saligenyl单磷酸酯的合成及生物学评价
2. Radiolabeled 5-Iodo-3 '-O-(17 beta-succinyl-5 alpha-androstan-3-one)-2 '-deoxyuridine and Its 5 '-Monophosphate for Imaging and Therapy of Androgen Receptor-Positive Cancers: Synthesis and Biological Evaluation [J] . Kortylewicz ZP, Nearman J, Baranowska-Kortylewicz J Journal of Medicinal Chemistry . 2009,第16期

机译：放射性标记的5-碘-3'-O-（17β-琥珀酰基-5α-雄烷-3-酮）-2'-脱氧尿苷及其5'-单磷酸盐用于雄激素受体阳性癌症的成像和治疗：合成与生物学评价
3. A new tiazofurin pronucleotide: synthesis and biological evaluation of cyclosaligenyl-tiazofurin monophosphate. [J] . Cappellacci L, Barboni G, Franchetti P, Nucleosides, nucleotides and nucleic acids . 2003,第5a8期

机译：一种新的噻唑呋林原核苷酸：环saligenyl-tiazofurin一磷酸的合成和生物学评估。
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5. Design, synthesis and biological evaluation of human inosine 5'-monophosphate dehydrogenase inhibitors: 1,5-diazabicyclo(3.1.0)hexane-2,4-diones, as novel isozyme-selective cancer chemotherapeutic agents. [D] . Barnes, Betsy Jo. 1999

机译：人肌苷5'-单磷酸脱氢酶抑制剂的设计，合成和生物学评估：1,5-二氮杂双环（3.1.0）己烷-2,4-二酮，作为新型的同工酶选择性癌症化学治疗剂。
6. Radiolabeled cycloSaligenyl Monophosphates of 5-Iodo-2′-deoxyuridine 5-Iodo-3′-fluoro-2′ 3′-dideoxyuridine and 3′-Fluorothymidine for Molecular Radiotherapy of Cancer: Synthesis and Biological Evaluation [O] . Zbigniew P. Kortylewicz, Yu Kimura, Kotaro Inoue, -1

机译：5-碘-2-脱氧尿苷的放射性标记的环saligenyl单磷酸盐5-碘3-氟-23-二脱氧尿苷和-3-氟癌症的分子放射治疗：合成和生物学评价
7. Synthesis and Evaluation of 6-Aza-2′-deoxyuridine Monophosphate Analogs as Inhibitors of Thymidylate Synthases, and as Substrates or Inhibitors of Thymidine Monophosphate Kinase in Mycobacterium tuberculosis [O] . Martin Kögler, Roger Busson, Steven De Jonghe, 2012

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Radiolabeled Cyclosaligenyl Monophosphates of 5-Iodo-2′-deoxyuridine, 5-Iodo-3′-fluoro-2′,3′-dideoxyuridine, and 3′-Fluorothymidine for Molecular Radiotherapy of Cancer: Synthesis and Biological Evaluation

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