메뉴 건너뛰기




Volumn 69, Issue 2, 2011, Pages 410-414

Automated radiochemical synthesis of [18F]FBEM: A thiol reactive synthon for radiofluorination of peptides and proteins

Author keywords

18F FBEM; Fluorine 18; PET; Thiol reactive synthon

Indexed keywords

[18F]FBEM; ACIDIC CONDITIONS; FLUORINE-18; FLUOROBENZOIC ACIDS; MALEIMIDES; NUCLEOPHILIC DISPLACEMENT; PET; PROSTHETIC GROUPS; RADIOCHEMICAL SYNTHESIS; RADIOFLUORINATION; RADIOLABELING; SPECIFIC ACTIVITY; SULFHYDRYL GROUPS; SYNTHONS;

EID: 78650304774     PISSN: 09698043     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.apradiso.2010.09.023     Document Type: Article
Times cited : (46)

References (14)
  • 1
    • 72449192291 scopus 로고    scopus 로고
    • Direct one-step[18]F-labeling of peptides via nucleophilic aromatic substitution
    • Becaud J., et al. Direct one-step[18]F-labeling of peptides via nucleophilic aromatic substitution. Bioconjug. Chem. 2009, 20:2254-2261.
    • (2009) Bioconjug. Chem. , vol.20 , pp. 2254-2261
    • Becaud, J.1
  • 2
    • 33845933484 scopus 로고    scopus 로고
    • Labeling of low-density lipoproteins using the F-18-labeled thiol-reactive N-[6-(4-[F-18]fluorobenzylidene)aminooxyhexyl]maleimide
    • Berndt M., Pietzsch J., Wuest F. Labeling of low-density lipoproteins using the F-18-labeled thiol-reactive N-[6-(4-[F-18]fluorobenzylidene)aminooxyhexyl]maleimide. Nucl. Med. Biol. 2007, 34:5-15.
    • (2007) Nucl. Med. Biol. , vol.34 , pp. 5-15
    • Berndt, M.1    Pietzsch, J.2    Wuest, F.3
  • 3
    • 33747150885 scopus 로고    scopus 로고
    • A thiol-reactive F-18-labeling agent, N-[2-(4-F-18-fluorobenzamido)ethyl]maleimide, and synthesis of RGD peptide-based tracer for PET imaging of alpha(v)beta(3) integrin expression
    • Cai W.B., Zhang X.Z., Wu Y., Chen X. A thiol-reactive F-18-labeling agent, N-[2-(4-F-18-fluorobenzamido)ethyl]maleimide, and synthesis of RGD peptide-based tracer for PET imaging of alpha(v)beta(3) integrin expression. J. Nucl. Med. 2006, 47:1172-1180.
    • (2006) J. Nucl. Med. , vol.47 , pp. 1172-1180
    • Cai, W.B.1    Zhang, X.Z.2    Wu, Y.3    Chen, X.4
  • 4
    • 20144364601 scopus 로고    scopus 로고
    • 1-[3-(2-[F-18]fluoropyridin-3-yloxy)propyl]pyrrole-2,5-dione: design, synthesis, and radiosynthesis of a new[F-18]fluoropyridine-based maleimide reagent for the labeling of peptides and proteins
    • de Bruin B., et al. 1-[3-(2-[F-18]fluoropyridin-3-yloxy)propyl]pyrrole-2,5-dione: design, synthesis, and radiosynthesis of a new[F-18]fluoropyridine-based maleimide reagent for the labeling of peptides and proteins. Bioconjug. Chem. 2005, 16:406-420.
    • (2005) Bioconjug. Chem. , vol.16 , pp. 406-420
    • de Bruin, B.1
  • 6
    • 0037213044 scopus 로고    scopus 로고
    • Fluoro-, bromo-, and iodopaclitaxel derivatives: synthesis and biological evaluation
    • Kiesewetter D.O., et al. Fluoro-, bromo-, and iodopaclitaxel derivatives: synthesis and biological evaluation. Nucl. Med. Biol. 2003, 30:11-24.
    • (2003) Nucl. Med. Biol. , vol.30 , pp. 11-24
    • Kiesewetter, D.O.1
  • 8
    • 0033529043 scopus 로고    scopus 로고
    • Development of fluorine-18-labeled 5-HT1A antagonists
    • Lang L.X., et al. Development of fluorine-18-labeled 5-HT1A antagonists. J. Med. Chem. 1999, 42:1576-1586.
    • (1999) J. Med. Chem. , vol.42 , pp. 1576-1586
    • Lang, L.X.1
  • 9
    • 0037213374 scopus 로고    scopus 로고
    • Direct electrophilic radiofluorination of a cyclic RGD peptide for in vivo alpha(v)beta(3) integrin related tumor imaging
    • Ogawa M., et al. Direct electrophilic radiofluorination of a cyclic RGD peptide for in vivo alpha(v)beta(3) integrin related tumor imaging. Nucl. Med. Biol. 2003, 30:1-9.
    • (2003) Nucl. Med. Biol. , vol.30 , pp. 1-9
    • Ogawa, M.1
  • 11
    • 0344013630 scopus 로고    scopus 로고
    • Synthesis of a new heterobifunctional linker, N-[4-(aminooxy)butyl]maleimide, for facile access to a thiol-reactive F-18-labeling agent
    • Toyokuni T., et al. Synthesis of a new heterobifunctional linker, N-[4-(aminooxy)butyl]maleimide, for facile access to a thiol-reactive F-18-labeling agent. Bioconjug. Chem. 2003, 14:1253-1259.
    • (2003) Bioconjug. Chem. , vol.14 , pp. 1253-1259
    • Toyokuni, T.1
  • 12
    • 34248632788 scopus 로고    scopus 로고
    • Synthesis of N-succinimidyl 4-[F-18] fluorobenzoate, an agent for labeling proteins and peptides with F-18
    • Vaidyanathan G., Zalutsky M.R. Synthesis of N-succinimidyl 4-[F-18] fluorobenzoate, an agent for labeling proteins and peptides with F-18. Nat. Protocols 2006, 1:1655-1661.
    • (2006) Nat. Protocols , vol.1 , pp. 1655-1661
    • Vaidyanathan, G.1    Zalutsky, M.R.2
  • 13
    • 39049192745 scopus 로고    scopus 로고
    • Fluorine-18 labeling of peptides and proteins
    • Springer-Verlag, Berlin-Heidelberg, P.A. Schubiger, L. Lehmann, M. Friebe (Eds.)
    • Wester K., Schottelius M. Fluorine-18 labeling of peptides and proteins. PET Chemistry: The Driving Force in Molecular Imaging 2007, 79-111. Springer-Verlag, Berlin-Heidelberg. P.A. Schubiger, L. Lehmann, M. Friebe (Eds.).
    • (2007) PET Chemistry: The Driving Force in Molecular Imaging , pp. 79-111
    • Wester, K.1    Schottelius, M.2
  • 14
    • 45749108297 scopus 로고    scopus 로고
    • Synthesis and application of [F-18]FDG-maleimidehexyloxime ([F-18]FDG-MHO): a [F-18]FDG-based prosthetic group for the chemoselective F-18-labelling of peptides and proteins
    • Wuest F., Berndt M., Bergmann R., van den Hoff J., Pietzsch J. Synthesis and application of [F-18]FDG-maleimidehexyloxime ([F-18]FDG-MHO): a [F-18]FDG-based prosthetic group for the chemoselective F-18-labelling of peptides and proteins. Bioconjug. Chem. 2008, 19:1202-1210.
    • (2008) Bioconjug. Chem. , vol.19 , pp. 1202-1210
    • Wuest, F.1    Berndt, M.2    Bergmann, R.3    van den Hoff, J.4    Pietzsch, J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.