俞鐘山 教授 (詳閱請點標題進入)
| 期刊論文 |
| 1. Chun-Ping Chang, Ho-Lien Huang, Jing-Kai Huang, Ming-Shiu Hung, Chien-Huang Wu,Jen-Shin Song, Chia-Jui Lee, Chung-Shan Yu* and Kak-Shan Shia,* “Fluorine-18 isotope labeling for positron emission tomography imaging. Direct evidence for DBPR211 as a peripherally restricted CBI inverse agonist”Bioorg. Med. Chem. 2019, 27(1), 216-223 |
| 2. Chi-Wei Chang, Chun-Nan Yeh, I-Shio Chung, Yong-Ren Chen, Shi-Wei Tien, You-Cheng Chou, Tsung-Wen Chen, Ming-Huang Chen, Kun-Chun Chiang, Ying-Cheng Huang, Hsin-Er Wang, Shi-Jen Wang, Wen-Sheng Huang and Chung-Shan Yu* “Synthesis and Evaluation of ortho-[18F]Fluorocelecoxib for COX-2 Cholangiocarcinoma Imaging” Drug Des. Dev. Ther. 2018, 12,1467-1478 |
| 3. Ying-Cheng Huang, Chiou-Shiow Farn, Yo-Cheng Chou, Chun-Nan Yeh, Chi-Wei Chang, Yi-Hsiu Chung, Tsong-Wen Chen, Wen-Sheng Huang and Chung-Shan Yu* “Synthesis of para-[18F]Fluorofenbufen Octylamide fot PET Imaging of Brain Tumors” J. Chin. Chem. Soc. 2018, 65, 780-792 |
| 4. Chun-Nan Yeh, Chi-Wei Chang, I-Shio Chung, Yong-Ren Chen, Shi-Wei Tien, You-Cheng Chou, Tsung-Wen Chen, Ming-Huang Chen, Kun-Chun Chiang, Ying-Cheng Huang, Hsin-Er Wang, Shi-Jen Wang, Wen-Sheng Huang and Chung-Shan Yu* “Toward a Probe for Assessing COX-2 Expression: Synthesis and Evaluation of [18F]Fluorocelecoxib for Imaging Cholangio Carcinoma” Eur. J. Pharm. Sci. 2017, 107, 217-229 |
| 5. Ying-Cheng Huang, In-Min Liu, Yo-Cheng Chou, Chun-Nan Yeh, Chi-Wei Chang, Yi-Hsiu Chung, Tsong-Wen Chen, Shi-Wei Tien, Wen-Sheng Huang and Chung-Shan Yu* “Octyl-para-[18F]Fluorofenbufen Amide as a Surrogate of NSAIDs for PET Imaging of Brain Tumors” |
| 6. Chun-Nan Yeh, Chi-Wei Chang, I-Shio Chung, Yong-Ren Chen, Shi-Wei Tien, You-Cheng Chou, Tsung-Wen Chen, Ming-Huang Chen, Kun-Chun Chiang, Ying-Cheng Huang, Hsin-Er Wang, Shi-Jen Wang, Wen-Sheng Huang and Chung-Shan Yu* “Synthesis and characterization of boron fenbufen and its F-18 labeled homolog for boron neutron capture therapy of COX-2 overexpressed cholangiocarcinoma” Eur. J. Pharm. Sci. 2017, 107, 217-229. |
| 7. Shiou-Shiow Farn, Yuen-Han Yeh, Chang-Chin Li, Ching-Shiuann Yang, Jenn-Tzong Chen, Chung- Shan Yu,* Wuu-Jyh Lin* “Development and validation of a reversed-phase HPLC method for analysis of radiochemical purity in [123I]IBZM” Appl. Radiat. Isot. 2017, 127, 61-67 (SCI). |
| 8. Huang, H.-L.; Chiang, L.-W.; Chen, J.-R.; Huang, C.-W.; Yang, W.-K.; Chiang, C.-S.; Jeng, K.-C.; Lin, W.-Z.; Fan, S.-S.; Chen, J.-Z.; Yu, C.-S.* "Study of [18F]FLT and [123I]IaraU for cellular imaging in HSV1 tk-transfected murine fibrosarcoma cells: Evaluation of the tracer uptake using 5-fluoro, 5-iodo and 5-iodovinyl arabinosyl uridines as competitive probes", Nucl. Med. Biol. In press, 2011, xx-xx. |
| 9. Su, Y.-H.; Chiang, L.-W.; Jeng, K.-C.; Huang, H.-L.; Chen, J.-Z.; Lin, W.-Z.; Huang, C.-W.; Yu, C.-S.*, "Solution-phase parallel synthesis and screening of anti-tumor activities from fenbufen and ethacrynic acid libraries", Bioorg. Med. Chem. Lett. 2011, 21, 1320-1324. |
| 10. Lin, K.-I.; Yang, C.-H.; Huang, C.-W.; Jian, J.-Y.; Huang, Y.-C.*; Yu, C.-S.*, "Synthesis and structure-activity relationships of fenbufen amide analogs", Molecules 2010, 15, 8796-8803. |
| 11. Chiang, L.-W.; Pei, K.; Chen, S.-W.; Huang, H.-L.; Lin, K.-J.; Yen, T.-C.; Yu, C.-S.*, "Combining a solution-phase derived library with in-situ cellular bioassay: Prompt screening of amide-forming minilibraries using MTT assay", Chem. Pharm. Bull. 2009, 57, 714-718. |
| 12. Yu, C.-S.*; Wang, R.-T.; Chiang, L.-W.; Lee, M.-S. “Synthesis of 4',4'-C-diaminomethyl nucleoside derivative as a building block for constructing libraries via amide bond formation.” Tetrahedron Lett. 2007, 48, 2979-2982. (SCI) (Granted by NSC 94-2113-M-007-005) |
| 13. Yu, C.-S.*; Wang, H.-Y.; Chiang L.-W.; Pei, K. “Synthesis of rhamnosyl trisaccharide repeating unit to mimic the antigen determinant of Pseudomonas syringae lipopolysaccharide.” Synthesis, 2007, 1412-1419. (SCI) (Granted by NSC 94-2113-M-007-005) |
| 14. Lin, K.-I.; Chiang, L.-W.; Wu, C.-H.; Chen, S.-W.; Yu, C.-S.*. “Synthesis of 5-radioiodoarabinosyl uridine analog for probing HSV-1 thymidine kinase gene.” J. Chin. Chem. Soc. Taipei. 2007, 54, 563-568. (SCI) (Granted by NSC 94-2113-M-007-005). |
| 15. Yu C.-S.*; Wu, C.-H.; Chiang, L.-W.; Pei, K.; Hsu, Z.-K. “Synthesis of (E)-5-(2-fluorovinyl)arabinosyl uridine analog as a potential probe for HSV-1 thymidine kinase gene” Synthesis, 2006, 3835-3840 (SCI). (Granted by NSC 94-2113-M-007-005) |
| 16. Yu, C.-S.*; Chiang, L.-W.; Wu, C.-H.; Wang, R.-T.; Chen, S.-W.; Wang, H.-Y.; Yeh, C.-H. “Synthesis of 5-radioiodoarbinosyl uridine analogs for Probing HSV TK gene: An unexpected chelating effect” Nucl. Med. Biol. 2006, 33, 367-370 (SCI). (Granted by 93-2113-M-007-038) |
| 17. Yu, C.-S.*, Wu, C.-H.; Chiang, L.-W.; Wang, R.-T.; Wang, H.-Y.; Yeh, C.-H., Lin, K.-I. “Synthesis of (E)-5-(2-radioiodovinyl)arabinosyl Uridine Analog for Probing HSV-1 Thymidine Kinase Gene” Chemistry Letters 2005, 34 (10), 1390-1391 (SCI). (Granted by NSC 93-2113-M-007-038) |
| 18. Yu, C.-S.*; Oberdorfer, F. “Synthesis of a Novel Aldehyde: 4-O-methyl-5-formylmethyl-2’-deoxyuridine Derivatives” Nucleosides, Nucleotides Nucleic Acids 2003, 22 (1), 71-84. (SCI) |
| 19. Yu, C.-S.*; Zeisler, S.; Eisenbarth, J.; Weber, K.; Runz, A.; Oberdorfer, F. “Synthesis of 5-(2-radiohaloethyl)- and 5-(2-radiohalovinyl)-2’-deoxyuridines. Novel Types of Radiotracer for Monitoring Cancer Gene Therapy with PET” J. Labelled Compd. Radiopharm. 2003, 46, 1-19 (SCI) |
| 20. Yu, C.-S.; Niikura, K.; Lin, C.-C.*; Wong, C.-H*. “The Thioglycoside and Glycosyl Phosphite of 5-Azido Sialic Acid: Excellent Donors for the a-Glycosylation of Primary Hydroxy Groups” Angewandte Chemie 2001, 40, 86-88. |
| 21. Yu, C.-S.; Oberdorfer, F.* “Synthesis of €-5-[2-(tri-n-butylstannyl)vinyl] substituted 2’-deoxyuridine derivatives for use in halogenation and radiohalogenation reactions” Synlett 2000, 86-88. Yu, C.-S.; Oberdorfer, F.* “Synthesis of 4-O-methyl-protected 5-(2-hydroxyethy)-2’-deoxyuridine derivatives and their nucleophilic fluorination to 5-(2-fluoroethyl)-2’-deoxyuridine” Synthesis 1999, 2057-2064. |
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