메뉴 건너뛰기




Volumn 20, Issue 6, 2009, Pages 1139-1145

17-[4-(2-[18F]fluoroethyl)-1H-1,2,3-triazol-1-yl]-6-thia- heptadecanoic acid: A potential radiotracer for the evaluation of myocardial fatty acid metabolism

Author keywords

[No Author keywords available]

Indexed keywords

CHLORINE COMPOUNDS; RADIATION; RADIOACTIVE TRACERS; RADIOACTIVITY; TISSUE; UREA;

EID: 67649203351     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc800472a     Document Type: Article
Times cited : (15)

References (27)
  • 1
    • 0032812589 scopus 로고    scopus 로고
    • Fatty acids for myocardial imaging
    • DOI 10.1016/S0001-2998(99)80013-0
    • Corbett, J. R. (1999) Fatty acids for myocardial imaging. Sem. Nucl. Med. 29, 237-258. (Pubitemid 29337182)
    • (1999) Seminars in Nuclear Medicine , vol.29 , Issue.3 , pp. 237-258
    • Corbett, J.R.1
  • 4
    • 0026665432 scopus 로고
    • Fatty acid kinetics in aerobic myocardium: Characteristics of tracer carbon entry and washout and influence of metabolic demand
    • Nellis, S. H., Liedtke, A. J., and Renstrom, B. (1992) Fatty acid kinetics in aerobic myocardium: characteristics of tracer carbon entry and washout and influence of metabolic demand. J. Nucl. Med. 33, 1864-1874.
    • (1992) J. Nucl. Med. , vol.33 , pp. 1864-1874
    • Nellis, S.H.1    Liedtke, A.J.2    Renstrom, B.3
  • 6
    • 0022999856 scopus 로고
    • Radioiodinated free fatty acids; can we measure myocardial metabolism?
    • Visser, F. C., van Eenige, M. J., Duwel, C. M., and Roos, J. P. (1986) Radioiodinated free fatty acids; can we measure myocardial metabolism? Eur. J. Nucl. Med. 12, S20-23.
    • (1986) Eur. J. Nucl. Med. , vol.12
    • Visser, F.C.1    Van Eenige, M.J.2    Duwel, C.M.3    Roos, J.P.4
  • 11
    • 0021319962 scopus 로고    scopus 로고
    • Synthesis of radioiodinated ω-(p-iodophenyl)-substituted methyl-branched long-chain fatty acids
    • Goodman, M. M., Kirsch, G., and Knapp, F. F., Jr. (2003) Synthesis of radioiodinated ω-(p-iodophenyl)-substituted methyl-branched long-chain fatty acids. J. Med. Chem. 27, 390-397.
    • (2003) J. Med. Chem. , vol.27 , pp. 390-397
    • Goodman, M.M.1    Kirsch, G.2    Knapp Jr., F.F.3
  • 14
    • 0025745452 scopus 로고
    • 18F]fluoro-6-thia-heptadecanoic acid (FTHA)
    • 18F]fluoro-6-thia- heptadecanoic acid (FTHA). J. Labelled Comp. Radiopharm. 29, 989-995.
    • (1991) J. Labelled Comp. Radiopharm. , vol.29 , pp. 989-995
    • DeGrado, T.R.1
  • 15
    • 0025944969 scopus 로고
    • 18F]Fluoro-6-thia-heptadecanoic acid (FTHA): Evaluation in mouse of a new probe of myocardial utilization of long chain fatty acids
    • 18F]Fluoro-6-thia-heptadecanoic acid (FTHA): evaluation in mouse of a new probe of myocardial utilization of long chain fatty acids. J. Nucl. Med. 32, 1888-1896.
    • (1991) J. Nucl. Med. , vol.32 , pp. 1888-1896
    • DeGrado, T.R.1    Coenen, H.H.2    Stöcklin, G.3
  • 17
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • Rostovtsev, V. V., Green, L. G., Foskin, V. V., and Sharpless, K. B. (2002) A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew. Chem., Int. Ed. 41, 2596-2599.
    • (2002) Angew. Chem., Int. Ed. , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Foskin, V.V.3    Sharpless, K.B.4
  • 20
    • 34447502169 scopus 로고    scopus 로고
    • Quick assembly of 1,4-diphenyltriazoles as probes targeting β-amyloid aggregates in Alzheimer's disease
    • DOI 10.1021/jm070467l
    • Qu, W., Kung, M. P., Hou, C., Oya, S., and Kung, H. F. (2007) Quick assembly of 1,4-diphenyltriazoles as probes targeting β-amyloid aggregates in Alzheimer's disease. J. Med. Chem. 50, 3380-3387. (Pubitemid 47065987)
    • (2007) Journal of Medicinal Chemistry , vol.50 , Issue.14 , pp. 3380-3387
    • Qu, W.1    Kung, M.-P.2    Hou, C.3    Oya, S.4    Kung, H.F.5
  • 22
    • 38749121328 scopus 로고    scopus 로고
    • Discovery of a dopamine D4 selective PET ligand candidate taking advantage of a click chemistry based REM linker
    • DOI 10.1016/j.bmcl.2007.12.026, PII S0960894X07014680
    • Tietze, R., Lober, S., Hubner, H., Gmeiner, P., Kuwert, T., and Prante, O. (2008) Discovery of a dopamine D4 selective PET ligand candidate taking advantage of a click chemistry based REM linker. Bioorg. Med. Chem. Lett. 18, 983-988. (Pubitemid 351179345)
    • (2008) Bioorganic and Medicinal Chemistry Letters , vol.18 , Issue.3 , pp. 983-988
    • Tietze, R.1    Lober, S.2    Hubner, H.3    Gmeiner, P.4    Kuwert, T.5    Prante, O.6
  • 24
    • 0036235635 scopus 로고    scopus 로고
    • Syntheses and first crystal structures of rhenium complexes derived from ω-functionalized fatty acids as model compounds of technetium tracers for myocardial metabolism imaging
    • Jung, C. M., Kraus, W., Leibnitz, P., Pietzsch, H. J., Kropp, J., and Spies, H. (2002) Syntheses and first crystal structures of rhenium complexes derived from ω-functionalized fatty acids as model compounds of technetium tracers for myocardial metabolism imaging. Eur. J. Inorg. Chem. 2002, 1219-1225.
    • (2002) Eur. J. Inorg. Chem. , vol.2002 , pp. 1219-1225
    • Jung, C.M.1    Kraus, W.2    Leibnitz, P.3    Pietzsch, H.J.4    Kropp, J.5    Spies, H.6
  • 25
    • 36949069995 scopus 로고
    • Propargyl fluoride and its microwave spectrum
    • Job, B. E., and Sheridan, J. (1962) Propargyl fluoride and its microwave spectrum. Nature 193, 677.
    • (1962) Nature , vol.193 , pp. 677
    • Job, B.E.1    Sheridan, J.2
  • 26
    • 0018703105 scopus 로고
    • Long-chain F-18 fatty acids for the study of regional metabolism in heart and liver; odd-even effects of metabolism in mice
    • Knust, E. J., Kupfernagel, Ch., and Stöcklin, G. (1979) Longchain F-18 fatty acids for the study of regional metabolism in heart and liver; odd-even effects of metabolism in mice. J. Nucl. Med. 20, 1170-1175. (Pubitemid 10209201)
    • (1979) Journal of Nuclear Medicine , vol.20 , Issue.11 , pp. 1170-1175
    • Knust, E.J.1    Kupfernagel, Ch.2    Stoecklin, G.3
  • 27
    • 0024462021 scopus 로고
    • 4-Thia-trans-2-alkenoyl-CoA derivatives: Properties and enzymatic reactions
    • Lau, S.-M., Brantley, R. K., and Thorpe, C. (1989) 4-Thia-trans-2- alkenoyl-CoA derivatives: Properties and enzymatic reactions. Biochemistry 28, 8255-8262. (Pubitemid 19252910)
    • (1989) Biochemistry , vol.28 , Issue.20 , pp. 8255-8262
    • Lau, S.-M.1    Brantley, R.K.2    Thorpe, C.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.