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Synthesis and evaluation of radiolabeled AGI-5198 analogues as candidate radiotracers for imaging mutant IDH1 expression in tumors

机译：放射性标记的AGI-5198类似物作为候选反氨酸酸盐的合成与评价，用于肿瘤成像突变体IDH1表达的

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Satish K. Chitneni; Zachary J. Reitman; Rebecca Spicehandler; David M. Gooden; Hai Yan; Michael R. Zalutsky;
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1. Synthesis and evaluation of radiolabeled AGI-5198 analogues as candidate radiotracers for imaging mutant IDH1 expression in tumors [J] . Chitneni Satish K., Reitman Zachary J., Spicehandler Rebecca, Bioorganic and Medicinal Chemistry Letters . 2018,第4期

机译：放射性标记的AGI-5198类似物作为候选突变体IDH1表达的候选反氨酸酯的合成与评价
2. Synthesis, Radiolabeling, and Biological Evaluation of 5-Hydroxy-2-[F-18]fluoroalkyl-tryptophan Analogues as Potential PET Radiotracers for Tumor Imaging [J] . Chiotellis Aristeidis, Herde Adrienne Muller, Rossler Simon L., Journal of Medicinal Chemistry . 2016,第11期

机译：5-羟基-2- [F-18]氟烷基色氨酸类似物作为肿瘤成像的潜在PET示踪剂的合成，放射性标记和生物学评估。
3. Radiolabeled inhibitors as probes for imaging mutant IDH1 expression in gliomas: Synthesis and preliminary evaluation of labeled butyl-phenyl sulfonamide analogs [J] . Chitneni Satish K., Reitman Zachary J., Gooden David M., European Journal of Medicinal Chemistry: Chimie Therapeutique . 2016,第Null期

机译：放射性标记的抑制剂作为胶质瘤中突变IDH1表达成像的探针：标记的丁基苯基磺酰胺类似物的合成和初步评估
4. Solid-phase synthesis and radiolabeling of a bombesin peptide analog for diagnostic imaging of tumors:a preliminary report [C] . Subhani M.Okarvi the International Peptide Symposium . 2001

机译：庞贝蛋白肽类似物肿瘤诊断成像的固相合成和放射性标记：初步报告
5. Design and synthesis of molecular probes to modulate cell membrane permeation: I. Design, synthesis, and biological evaluation of novel chicoric acid analogues as inhibitors of HIV-1 integrase. II. Design, synthesis, and biological evaluation of novel estradiol analogues targeting the membrane estrogen receptor. [D] . Charvat, Trevor Thomas. 2004

机译：设计和合成的分子探针，可调节细胞膜的渗透性：I.设计，合成和生物评价作为抗HIV-1整合酶抑制剂的新型菊苣酸类似物。二。针对膜雌激素受体的新型雌二醇类似物的设计，合成和生物学评估。
6. Synthesis and evaluation of radiolabeled AGI-5198 analogues as candidate radiotracers for imaging mutant IDH1 expression in tumors [O] . Satish K. Chitneni, Zachary J. Reitman, Rebecca Spicehandler, -1

机译：放射标记的AGI-5198类似物的合成和评估作为在肿瘤中突变IDH1表达成像的候选放射性示踪剂
7. Radiolabeled inhibitors as probes for imaging mutant IDH1 expression in gliomas: Synthesis and preliminary evaluation of labeled butyl-phenyl sulfonamide analogs. [O] . Chitneni, SK, Reitman, ZJ, Gooden, DM, 2016

机译：放射性标记的抑制剂作为用于在神经胶质瘤中成像突变体IDH1表达的探针：标记的丁基 - 苯基磺酰胺类似物的合成和初步评估。

Synthesis and evaluation of radiolabeled AGI-5198 analogues as candidate radiotracers for imaging mutant IDH1 expression in tumors

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