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Volumn 54, Issue 3, 2013, Pages 859-868

Cobalt carbonyl complexes as probes for alkyne-tagged lipids

Author keywords

Alkyne cobalt carbonyl complexes; Alkynylated fatty acids; Lipid electrophiles; Proteinlipid adducts

Indexed keywords

ALKYNE; AMINO ACID DERIVATIVE; COBALT CARBONYL COMPLEX; COBALT COMPLEX; ESTER DERIVATIVE; FUNCTIONAL GROUP; HEXADEC 15 YNOIC ACID; HEXADEC 7 YNOIC ACID; LIPID; PHOSPHINE; PHOSPHOCHOLINE ESTER; SILICON DIOXIDE; UNCLASSIFIED DRUG;

EID: 84874034344     PISSN: 00222275     EISSN: 15397262     Source Type: Journal    
DOI: 10.1194/jlr.D033332     Document Type: Article
Times cited : (12)

References (23)
  • 1
    • 0034677879 scopus 로고    scopus 로고
    • Cell surface engineering by a modifi ed Staudinger reaction
    • Saxon, E., and C. R. Bertozzi. 2000. Cell surface engineering by a modifi ed Staudinger reaction. Science. 287 : 2007-2010.
    • (2000) Science. , vol.287 , pp. 2007-2010
    • Saxon, E.1    Bertozzi, C.R.2
  • 3
    • 50249085119 scopus 로고    scopus 로고
    • Second-generation difl uorinated cyclooctynes for copper-free click chemistry
    • Codelli, J. A., J. M. Baskin, N. J. Agard, and C. R. Bertozzi. 2008. Second-generation difl uorinated cyclooctynes for copper-free click chemistry. J. Am. Chem. Soc. 130 : 11486-11493.
    • (2008) J. Am. Chem. Soc. , vol.130 , pp. 11486-11493
    • Codelli, J.A.1    Baskin, J.M.2    Agard, N.J.3    Bertozzi, C.R.4
  • 4
    • 0000096835 scopus 로고    scopus 로고
    • Click chemistry: Diverse chemical function from a few good reactions
    • Kolb, H. C., M. G. Finn, and K. B. Sharpless. 2001. Click chemistry: diverse chemical function from a few good reactions. Angew. Chem. Int. Ed. Engl. 40 : 2004-2021.
    • (2001) Angew. Chem. Int. Ed. Engl. , vol.40 , pp. 2004-2021
    • Kolb, H.C.1    Finn, M.G.2    Sharpless, K.B.3
  • 5
    • 0037099395 scopus 로고    scopus 로고
    • A stepwise Huisgen cycloaddition process: Copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes
    • Rostovtsev, V. V., L. G. Green, V. V. Fokin, and K. B. Sharpless. 2002. A stepwise Huisgen cycloaddition process: copper(I)-catalyzed regioselective "ligation" of azides and terminal alkynes. Angew. Chem. Int. Ed. Engl. 41 : 2596-2599.
    • (2002) Angew. Chem. Int. Ed. Engl. , vol.41 , pp. 2596-2599
    • Rostovtsev, V.V.1    Green, L.G.2    Fokin, V.V.3    Sharpless, K.B.4
  • 6
    • 0002490493 scopus 로고
    • 1,3-Dipolar cycloadditions-introduction, survey, mechanism
    • A. Padwa, editor. Wiley, NY
    • Husigen, R. 1984. 1,3-Dipolar Cycloadditions-Introduction, Survey, Mechanism. In 1,3-Dipolar Cycloaddition Chemistry. Vol. 1. A. Padwa, editor. Wiley, NY. 1-176.
    • (1984) 1,3-Dipolar Cycloaddition Chemistry , vol.1 , pp. 1-176
    • Husigen, R.1
  • 7
    • 67650474557 scopus 로고    scopus 로고
    • Click chemistry and bioorthogonal reactions: Unprecedented selectivity in the labeling of biological molecules
    • Best, M. D. 2009. Click chemistry and bioorthogonal reactions: unprecedented selectivity in the labeling of biological molecules. Biochemistry. 48 : 6571-6584.
    • (2009) Biochemistry. , vol.48 , pp. 6571-6584
    • Best, M.D.1
  • 8
    • 0037462106 scopus 로고    scopus 로고
    • Activity-based protein profi ling in vivo using a copper(I)-catalyzed azide-alkyne [3+2] cycloaddition
    • Speers, A. E., G. C. Adam, and B. F. Cravatt. 2003. Activity-based protein profi ling in vivo using a copper(I)-catalyzed azide-alkyne [3+2] cycloaddition. J. Am. Chem. Soc. 125 : 4686-4687.
    • (2003) J. Am. Chem. Soc. , vol.125 , pp. 4686-4687
    • Speers, A.E.1    Adam, G.C.2    Cravatt, B.F.3
  • 9
    • 22244445882 scopus 로고    scopus 로고
    • A tandem orthogonal proteolysis strategy for high-content chemical proteomics
    • Speers, A. E., and B. F. Cravatt. 2005. A tandem orthogonal proteolysis strategy for high-content chemical proteomics. J. Am. Chem. Soc. 127 : 10018-10019.
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 10018-10019
    • Speers, A.E.1    Cravatt, B.F.2
  • 10
    • 47049095632 scopus 로고    scopus 로고
    • Routes to 4-hydroxynonenal: Fundamental issues in the mechanisms of lipid peroxidation
    • Schneider, C., N. Porter, and A. Brash. 2008. Routes to 4-hydroxynonenal: fundamental issues in the mechanisms of lipid peroxidation. J. Biol. Chem. 283 : 15539-15543.
    • (2008) J. Biol. Chem. , vol.283 , pp. 15539-15543
    • Schneider, C.1    Porter, N.2    Brash, A.3
  • 11
    • 41649118986 scopus 로고    scopus 로고
    • Identifi cation of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives
    • Vila, A., K. Tallman, A. Jacobs, D. Liebler, N. Porter, and L. Marnett. 2008. Identifi cation of protein targets of 4-hydroxynonenal using click chemistry for ex vivo biotinylation of azido and alkynyl derivatives. Chem. Res. Toxicol. 21 : 432-444.
    • (2008) Chem. Res. Toxicol. , vol.21 , pp. 432-444
    • Vila, A.1    Tallman, K.2    Jacobs, A.3    Liebler, D.4    Porter, N.5    Marnett, L.6
  • 12
    • 71049139267 scopus 로고    scopus 로고
    • An azidobiotin reagent for use in the isolation of protein adducts of lipidderived electrophiles by streptavidin catch and photorelease
    • Kim, H-Y., K. Tallman, D. Liebler, and N. Porter. 2009. An azidobiotin reagent for use in the isolation of protein adducts of lipidderived electrophiles by streptavidin catch and photorelease. Mol. Cell. Proteomics. 8 : 2080-2089.
    • (2009) Mol. Cell. Proteomics. , vol.8 , pp. 2080-2089
    • Kim, H.-Y.1    Tallman, K.2    Liebler, D.3    Porter, N.4
  • 14
    • 0001267873 scopus 로고
    • An alkyne protecting group
    • Nicholas, K. M., and R. Pettit. 1971. An alkyne protecting group. Tetrahedron Lett. 37 : 3475-3478.
    • (1971) Tetrahedron Lett. , vol.37 , pp. 3475-3478
    • Nicholas, K.M.1    Pettit, R.2
  • 15
    • 37049121676 scopus 로고
    • Organocobalt complexes. Part 1. Arene complexes derived from dodecacarbonyltetracobalt
    • Khand, I. U., G. R. Knox, P. L. Pauson, and W. E. Watts. 1973. Organocobalt complexes. Part 1. Arene complexes derived from dodecacarbonyltetracobalt. J. Chem. Soc. Perkin Trans. 1 : 975-977.
    • (1973) J. Chem. Soc. Perkin Trans. , vol.1 , pp. 975-977
    • Khand, I.U.1    Knox, G.R.2    Pauson, P.L.3    Watts, W.E.4
  • 16
    • 0000312277 scopus 로고
    • Organocobalt cluster complexes. 18. Freidel-Crafts acylation of diarlyacetlenedicobalt hexacarbonyl complexes. Dicobalt hexacarbonyl unit as a protecting group for acetylene function
    • Seyferth, D., M. O. Nestle, and A. T. Wehman. 1975. Organocobalt cluster complexes. 18. Freidel-Crafts acylation of diarlyacetlenedicobalt hexacarbonyl complexes. Dicobalt hexacarbonyl unit as a protecting group for acetylene function. J. Am. Chem. Soc. 97 : 7417-7426.
    • (1975) J. Am. Chem. Soc. , vol.97 , pp. 7417-7426
    • Seyferth, D.1    Nestle, M.O.2    Wehman, A.T.3
  • 17
    • 0031008503 scopus 로고    scopus 로고
    • Improved synthesis of 10,20-bis-and 5,10,15,20-tetraethynylporphyrins via ethynyl protection with dicobalt octacarbonyl
    • Milgrom, L., R. Rees, and G. Yahioglu. 1997. Improved synthesis of 10,20-bis-and 5,10,15,20-tetraethynylporphyrins via ethynyl protection with dicobalt octacarbonyl. Tetrahedron Lett. 38 : 4905-4908.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 4905-4908
    • Milgrom, L.1    Rees, R.2    Yahioglu, G.3
  • 18
    • 0033592567 scopus 로고    scopus 로고
    • Polymer supported cobalt carbonyl complexes as novel traceless alkyne linkers for solidphase synthesis
    • Comely, A., S. Gibson, and N. Hales. 1999. Polymer supported cobalt carbonyl complexes as novel traceless alkyne linkers for solidphase synthesis. Chem. Commun. 1999: 2075-2076.
    • (1999) Chem. Commun. , vol.1999 , pp. 2075-2076
    • Comely, A.1    Gibson, S.2    Hales, N.3
  • 19
    • 0034696214 scopus 로고    scopus 로고
    • Polymer-supported cobalt carbonyl complexes as novel solid-phase catalysts of the Pauson-Khand reaction
    • Comely, A., S. Gibson, and N. Hales. 2000. Polymer-supported cobalt carbonyl complexes as novel solid-phase catalysts of the Pauson-Khand reaction. Chem. Commun. 2000: 305-306.
    • (2000) Chem. Commun. , vol.2000 , pp. 305-306
    • Comely, A.1    Gibson, S.2    Hales, N.3
  • 20
    • 0038264253 scopus 로고    scopus 로고
    • The application of polymer-bound carbonylcobalt(0) species in linker chemistry and catalysis
    • Comely, A., S. Gibson, N. Hales, C. Johnstone, and A. Stevenazzi. 2003. The application of polymer-bound carbonylcobalt(0) species in linker chemistry and catalysis. Org. Biomol. Chem. 1 : 1959-1968.
    • (2003) Org. Biomol. Chem. , vol.1 , pp. 1959-1968
    • Comely, A.1    Gibson, S.2    Hales, N.3    Johnstone, C.4    Stevenazzi, A.5
  • 21
    • 33845261493 scopus 로고
    • A rapid method of total lipid extraction and purifi cation
    • Bligh, E. G., and W. J. Dyer. 1959. A rapid method of total lipid extraction and purifi cation. Can. J. Biochem. Physiol. 37 : 911-917.
    • (1959) Can. J. Biochem. Physiol. , vol.37 , pp. 911-917
    • Bligh, E.G.1    Dyer, W.J.2
  • 22
    • 41249101849 scopus 로고    scopus 로고
    • Glycerophospholipid identifi cation and quantitation by electrospray ionization mass spectrometry
    • H. A. Brown, editor. Academic Press, San Diego, CA
    • Ivanova, P. T., S. B. Milne, M. O. Byrne, Y. Xiang, and H. A. Brown. 2007. Glycerophospholipid identifi cation and quantitation by electrospray ionization mass spectrometry. In Lipidomics and Bioactive Lipids: Mass-Spectrometry-Based Lipid Analysis. Vol. 432. H. A. Brown, editor. Academic Press, San Diego, CA. 21-57.
    • (2007) Lipidomics and Bioactive Lipids: Mass-Spectrometry-Based Lipid Analysis , vol.432 , pp. 21-57
    • Ivanova, P.T.1    Milne, S.B.2    Byrne, M.O.3    Xiang, Y.4    Brown, H.A.5
  • 23
    • 69249136669 scopus 로고    scopus 로고
    • Working towards an exegesis for lipids in biology
    • Brown, H. A., and R. C. Murphy. 2009. Working towards an exegesis for lipids in biology. Nat. Chem. Biol. 5 : 602-606.
    • (2009) Nat. Chem. Biol. , vol.5 , pp. 602-606
    • Brown, H.A.1    Murphy, R.C.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.