Nomenclature systems for the neuroprostanes and for the neurofurans

Prostaglandins and Other Lipid Mediators

Volumn 78, Issue 1-4, 2005, Pages 14-18

  Taber, Douglass F ^a   Jackson Roberts II, L ^b  

^a UNIVERSITY OF DELAWARE   (United States)

^b VANDERBILT UNIVERSITY   (United States)

Author keywords

Neurofurans; Neuroprostanes; Nomenclature

Indexed keywords

ALKYL GROUP; DOCOSAHEXAENOIC ACID; ISOPROSTANE; LONG CHAIN FATTY ACID; NEUROFURAN; NEUROPROSTANE; PROSTAGLANDIN; UNCLASSIFIED DRUG;

ARTICLE; CHEMICAL ANALYSIS; CHEMICAL STRUCTURE; CIS ISOMER; COMPARATIVE STUDY; DIASTEREOISOMER; ENANTIOMER; FATTY ACID OXIDATION; ISOMER; LIPID PEROXIDATION; NOMENCLATURE; STRUCTURE ANALYSIS; TRANS ISOMER;

DOCOSAHEXAENOIC ACIDS; FURANS; HUMANS; MOLECULAR STRUCTURE; TERMINOLOGY;

EID: 27744562522     PISSN: 10988823     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.prostaglandins.2005.07.002     Document Type: Article

References (13)

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3. S.E. Browne, L.J. Roberts II, and P.A. Dennery Free Rad Biol Med 36 2004 938
4. For synthetic efforts reported to date toward NeuroP type structures, see
5. T. Durand, A. Guy, J.-P. Vidal, J. Viala, and J.-C. Rossi Tetrahedron Lett 41 2000 3859
6. L.G. Quan, and J.K. Cha J Am Chem Soc 124 2002 12424
7. L.G. Quan, and J.K. Cha Chem Phys Lip 128 2004 3
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9. T. Durand, A. Guy, and O. Henry Chem Phys Lip 128 2004 14
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11. D.F. Taber, J.D. Morrow, and L.J. Roberts II Prostaglandins 53 1997 63
12. D.F. Taber, J.P. Fessel, and L.J. Roberts II Prostaglandins Other Lipid Mediators 73 2004 47
13. No synthesis of a neurofuran has yet been reported.