-
2
-
-
13644249563
-
-
in press, and references therein
-
Sakai, N.; Takeuchi, T.; Futaki, S.; Matile, S. ChemBioChem, in press, and references therein.
-
ChemBioChem
-
-
Sakai, N.1
Takeuchi, T.2
Futaki, S.3
Matile, S.4
-
3
-
-
3543051871
-
-
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
-
4
-
-
0037440187
-
-
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.
-
(2003)
Nucleic Acids Res.
, vol.31
, pp. 556-561
-
-
Dom, G.1
Shaw-Jackson, C.2
Matis, C.3
Bouffioux, O.4
Picard, J.J.5
Prochiantz, A.6
Mingeot-Leclercq, M.P.7
Brasseur, R.8
Rezsohazy, R.9
-
5
-
-
13644259585
-
-
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
-
-
note
-
Please see the Supporting Information.
-
-
-
-
9
-
-
13644268250
-
-
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
-
-
note
-
1
-
-
-
-
11
-
-
13644258155
-
-
note
-
Inactivity of alcohols corresponding to all sulfates and some carboxylates listed in Figure 1 confirmed, however, that low-affinity ion pairing is essential.
-
-
-
-
12
-
-
0026557830
-
-
(a) Schiffer, M.; Chang, C. H.; Stevens, F. J. Protein Eng. 1992, 5, 213-214.
-
(1992)
Protein Eng.
, vol.5
, pp. 213-214
-
-
Schiffer, M.1
Chang, C.H.2
Stevens, F.J.3
-
13
-
-
0032552880
-
-
(b) Yau, W. M.; Wimley, W. C.; Gawrisch, K.; White, S. H. Biochemistry 1998, 37, 14713-14718.
-
(1998)
Biochemistry
, vol.37
, pp. 14713-14718
-
-
Yau, W.M.1
Wimley, W.C.2
Gawrisch, K.3
White, S.H.4
-
15
-
-
0037016255
-
-
(b) Orner, B. P.; Salvatella. X.; Sánchez-Quesada, J.; de Mendoza, J.; Giralt, E.; Hamilton, A. D. Angew. Chem., Int. Ed. 2002, 41, 117-119.
-
(2002)
Angew. Chem., Int. Ed.
, vol.41
, pp. 117-119
-
-
Orner, B.P.1
Salvatella, X.2
Sánchez-Quesada, J.3
De Mendoza, J.4
Giralt, E.5
Hamilton, A.D.6
-
16
-
-
0035084196
-
-
Davenport, L.; Shen, B.; Joseph, T. W.; Straher, M. P. Chem. Phys. Lipids 2001, 109, 145-156.
-
(2001)
Chem. Phys. Lipids
, vol.109
, pp. 145-156
-
-
Davenport, L.1
Shen, B.2
Joseph, T.W.3
Straher, M.P.4
-
17
-
-
1842479070
-
-
Da Silva, E.; Lazar, A. N.; Coleman, A. W. J. Drug Del. Sci. Technol. 2004, 14, 3-20.
-
(2004)
J. Drug Del. Sci. Technol.
, vol.14
, pp. 3-20
-
-
Da Silva, E.1
Lazar, A.N.2
Coleman, A.W.3
-
18
-
-
13644259584
-
-
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
-
-
(a) Bingel, C. Chem. Ber. 1993, 126, 1957-1959.
-
(1993)
Chem. Ber.
, vol.126
, pp. 1957-1959
-
-
Bingel, C.1
-
21
-
-
0036293102
-
-
(c) Foley, S.; Crowley, C.; Smaihi, M.; Bonfils, C.; Erlanger, B. F.; Seta, P.; Larroque, C. Biochem. Biophys. Res. Commun. 2002, 294, 116-119.
-
(2002)
Biochem. Biophys. Res. Commun.
, vol.294
, pp. 116-119
-
-
Foley, S.1
Crowley, C.2
Smaihi, M.3
Bonfils, C.4
Erlanger, B.F.5
Seta, P.6
Larroque, C.7
|