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Volumn 10, Issue 29, 2012, Pages 5514-5517

Attack of radicals and protons on ladderane lipids: Quantum chemical calculations and biological implications

Author keywords

[No Author keywords available]

Indexed keywords

BIOLOGICAL IMPLICATIONS; CYCLOBUTANE RING; DECOMPOSITION PROCESS; HYDROGEN ATOM ABSTRACTION; QUANTUM CHEMICAL CALCULATIONS;

EID: 84863611744     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c2ob25717c     Document Type: Article
Times cited : (14)

References (29)
  • 20
    • 84863625353 scopus 로고    scopus 로고
    • Ph.D. dissertation, University of California-Davis
    • D. H. Nouri, Ph.D. dissertation, University of California-Davis, 2007
    • (2007)
    • Nouri, D.H.1
  • 25
    • 84859857546 scopus 로고    scopus 로고
    • 2NOH Volumes were calculated at the B3LYP/6-31G(d) level using the "volume = tight" command in GAUSSIAN09 The heteroatom-containing products of hydrogen atom abstraction may themselves be toxic, but given their increased polarity, they are probably less likely to pass through the membrane. In addition, they may react with the resulting polyenes
    • J. M. Fukuto S. J. Carrington D. J. Tantillo J. G. Harrison L. J. Ignarro B. A. Freeman A. Chen D. A. Wink Chem. Res. Toxicol. 2012 25 769 793
    • (2012) Chem. Res. Toxicol. , vol.25 , pp. 769-793
    • Fukuto, J.M.1    Carrington, S.J.2    Tantillo, D.J.3    Harrison, J.G.4    Ignarro, L.J.5    Freeman, B.A.6    Chen, A.7    Wink, D.A.8
  • 27
    • 84863621674 scopus 로고
    • 12 of
    • Issue 12 of Acc. Chem. Res. 1983, 16
    • (1983) Acc. Chem. Res. , vol.16
  • 28
    • 0004135609 scopus 로고
    • Plenum, New York, (with comments by v. R. Schleyer)
    • H. C. Brown, The Nonclassical Ion Problem, Plenum, New York, 1977 (with comments by P. v. R. Schleyer)
    • (1977) The Nonclassical Ion Problem
    • Brown, H.C.1
  • 29
    • 30744479220 scopus 로고    scopus 로고
    • -1 of experimentally determined values; see, for example M. R. Siebert, D. J. Tantillo, J. Org. Chem., 2006, 71, 645-654, which discusses the proton affinities of other strained hydrocarbons Protonation at other positions also leads to nonclassical carbocations similar in energy (see ESI for details), but it is likely that the bond that is protonated in Fig. 3 is the internal ladderane bond that will be closest to the outer surface of the anammoxosome membrane (i.e., it is closest to the lipid head group)
    • -1 of experimentally determined values; see, for example M. R. Siebert, D. J. Tantillo, J. Org. Chem., 2006, 71, 645-654, which discusses the proton affinities of other strained hydrocarbons
    • , vol.27 , pp. 413


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.