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Volumn 127, Issue 4, 2005, Pages 1114-1115

Anionic fullerenes, calixarenes, coronenes, and pyrenes as activators of oligo/polyarginines in model membranes and live cells

Author keywords

[No Author keywords available]

Indexed keywords

AMPHOPHILE; ANION; ARGININE DERIVATIVE; BUTYRIC ACID DERIVATIVE; CALIXARENE; CELL PROTEIN; CORONENEBUTYRATE; FULLERENE DERIVATIVE; PHOSPHATIDYLGLYCEROL; POLYARGININE; PYRENE DERIVATIVE; PYRENEBUTYRATE; UNCLASSIFIED DRUG;

EID: 13644271605     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja043633c     Document Type: Article
Times cited : (130)

References (21)
  • 3
    • 3543051871 scopus 로고    scopus 로고
    • 8) into octanol using laurate as a counter-anion has recently been reported: (a) Rothbard, J. B.; Jessop, T. C.; Lewis, R. S.; Murray, B. A.; Wender, P. A. J. Am. Chem. Soc. 2004, 126, 9506-9507. Compare also: (b) Dom, G.; Shaw-Jackson, C.; Matis, C.; Bouffioux, O.; Picard, J. J.; Prochiantz, A.; Mingeot-Leclercq, M. P.; Brasseur, R.; Rezsohazy, R. Nucleic Acids Res. 2003, 31, 556-561.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 9506-9507
    • Rothbard, J.B.1    Jessop, T.C.2    Lewis, R.S.3    Murray, B.A.4    Wender, P.A.5
  • 5
    • 13644259585 scopus 로고    scopus 로고
    • note
    • 1,2 cannot be excluded in vesicles either, although activity in DPPC vesicles below phase transition was poor and neither ion-channel formation nor membrane disruption could be observed in planar EYPC/EYPG-bilayer experiments.
  • 8
    • 13644258154 scopus 로고    scopus 로고
    • note
    • Please see the Supporting Information.
  • 9
    • 13644268250 scopus 로고    scopus 로고
    • note
    • max depended on nature as well as concentration of oligo/polyarginine (not shown); the possibility of systematic batch-to-batch errors required attention to eventually necessary calibration.
  • 10
    • 13644264457 scopus 로고    scopus 로고
    • note
    • 1
  • 11
    • 13644258155 scopus 로고    scopus 로고
    • note
    • Inactivity of alcohols corresponding to all sulfates and some carboxylates listed in Figure 1 confirmed, however, that low-affinity ion pairing is essential.
  • 18
    • 13644259584 scopus 로고    scopus 로고
    • note
    • Whereas ring expansion to calix[6]arenes reduced activator efficiency, additional carboxylates on one face and alkyls on the other face of calix-[4]arenes were tolerated. Several calix[4]arene carboxylates with sulfates at the upper rim were inactive, presumably because the resulting complexes were too hydrophilic.
  • 19
    • 0001396269 scopus 로고
    • (a) Bingel, C. Chem. Ber. 1993, 126, 1957-1959.
    • (1993) Chem. Ber. , vol.126 , pp. 1957-1959
    • Bingel, C.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.