-
6
-
-
0024593497
-
-
Winquist R.J., Heaney L.A., Wallace A.A., Baskin E.P., Stein R.B., Garcia M.L., and Kaczorowsk G.J. J. Pharmacol. Exp. Ther. 248 (1989) 149
-
(1989)
J. Pharmacol. Exp. Ther.
, vol.248
, pp. 149
-
-
Winquist, R.J.1
Heaney, L.A.2
Wallace, A.A.3
Baskin, E.P.4
Stein, R.B.5
Garcia, M.L.6
Kaczorowsk, G.J.7
-
7
-
-
1242337465
-
-
and references cited therein
-
Mannhold R. Med. Res. Rev. 24 (2004) 213 and references cited therein
-
(2004)
Med. Res. Rev.
, vol.24
, pp. 213
-
-
Mannhold, R.1
-
15
-
-
15444378025
-
-
For some recent examples of medicinally interesting polyamine-conjugates see:
-
For some recent examples of medicinally interesting polyamine-conjugates see:. Camps P., Formosa X., Muñoz-Torrero D., Petrignet J., Badia A., and Clos M.V. J. Med. Chem. 48 (2005) 1701
-
(2005)
J. Med. Chem.
, vol.48
, pp. 1701
-
-
Camps, P.1
Formosa, X.2
Muñoz-Torrero, D.3
Petrignet, J.4
Badia, A.5
Clos, M.V.6
-
16
-
-
21244436057
-
-
Cholody W.M., Kosakowska-Cholody T., Hollingshead M.G., Hariprakasha H.K., and Michejda C.J. J. Med. Chem. 48 (2005) 4474
-
(2005)
J. Med. Chem.
, vol.48
, pp. 4474
-
-
Cholody, W.M.1
Kosakowska-Cholody, T.2
Hollingshead, M.G.3
Hariprakasha, H.K.4
Michejda, C.J.5
-
17
-
-
33747470312
-
-
Nagarajan M., Morrell A., Antony S., Kohlhagen G., Agama K., Pommier Y., Ragazzon P.A., Garbett N.C., Chaires J.B., Hollingshead M., and Cushman M. J. Med. Chem. 49 (2006) 5129
-
(2006)
J. Med. Chem.
, vol.49
, pp. 5129
-
-
Nagarajan, M.1
Morrell, A.2
Antony, S.3
Kohlhagen, G.4
Agama, K.5
Pommier, Y.6
Ragazzon, P.A.7
Garbett, N.C.8
Chaires, J.B.9
Hollingshead, M.10
Cushman, M.11
-
18
-
-
33749253527
-
-
Oves D., Fernández S., Verlinden L., Bouillon R., Verstuyf A., Ferrero M., and Gotor V. Bioorg. Med. Chem. 14 (2006) 7512
-
(2006)
Bioorg. Med. Chem.
, vol.14
, pp. 7512
-
-
Oves, D.1
Fernández, S.2
Verlinden, L.3
Bouillon, R.4
Verstuyf, A.5
Ferrero, M.6
Gotor, V.7
-
19
-
-
33644981818
-
-
Battaglia A., Guerrini A., Baldelli E., Fontana G., Varchi G., Samori C., and Bombardelli E. Tetrahedron Lett. 47 (2006) 2667
-
(2006)
Tetrahedron Lett.
, vol.47
, pp. 2667
-
-
Battaglia, A.1
Guerrini, A.2
Baldelli, E.3
Fontana, G.4
Varchi, G.5
Samori, C.6
Bombardelli, E.7
-
20
-
-
34247895612
-
-
Wu D., Ji S., Wu Y., Ju Y., and Zhao Y. Bioorg. Med. Chem. Lett. 17 (2007) 2983
-
(2007)
Bioorg. Med. Chem. Lett.
, vol.17
, pp. 2983
-
-
Wu, D.1
Ji, S.2
Wu, Y.3
Ju, Y.4
Zhao, Y.5
-
22
-
-
41549083307
-
-
Recently, solubility studies of minoxidil in water in the form of inclusion complexes with β-CD have been described in:
-
Recently, solubility studies of minoxidil in water in the form of inclusion complexes with β-CD have been described in:. Calderini A., and Pessine F.B.T. J. Incl. Phemon. Macrocycl. Chem. 60 (2008) 369
-
(2008)
J. Incl. Phemon. Macrocycl. Chem.
, vol.60
, pp. 369
-
-
Calderini, A.1
Pessine, F.B.T.2
-
23
-
-
35148886772
-
-
Olsen E.A., Whiting D., Bergfeld W., Miller J., Hordinsky M., Wanser R., Zhang P., and Kohut B. J. Am. Acad. Dermatol. 57 (2007) 767
-
(2007)
J. Am. Acad. Dermatol.
, vol.57
, pp. 767
-
-
Olsen, E.A.1
Whiting, D.2
Bergfeld, W.3
Miller, J.4
Hordinsky, M.5
Wanser, R.6
Zhang, P.7
Kohut, B.8
-
24
-
-
0021040644
-
-
For selected examples of other minoxidil derivatives, their synthesis and mode of action, see:
-
For selected examples of other minoxidil derivatives, their synthesis and mode of action, see:. McCall J.M., Aiken J.W., Chidester C.G., DuCharme D.W., and Wendling M.G. J. Med. Chem. 26 (1983) 1791
-
(1983)
J. Med. Chem.
, vol.26
, pp. 1791
-
-
McCall, J.M.1
Aiken, J.W.2
Chidester, C.G.3
DuCharme, D.W.4
Wendling, M.G.5
-
29
-
-
77649270435
-
-
note
-
Part of this work was presented in the form of a poster at the 10th Tetrahedron Symposium, Paris, 2009, Abstract Book (P C132).
-
-
-
-
31
-
-
0036532331
-
-
The preparation, in only 31% yield (see however Supplementary data), and the characterization of 2 was subsequently described in:
-
The preparation, in only 31% yield (see however Supplementary data), and the characterization of 2 was subsequently described in:. Vassis S., Govaris I., Voyatzi K., Mamos P., and Papaioannou D. Tetrahedron Lett. 43 (2002) 2597
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 2597
-
-
Vassis, S.1
Govaris, I.2
Voyatzi, K.3
Mamos, P.4
Papaioannou, D.5
-
32
-
-
60149107206
-
-
McCarthy O., Musso-Buendia A., Kaiser M., Brun R., Ruiz-Perez L.M., Gunnar Johansson N., Gonzalez Pacanowska D., and Gilbert I.H. Eur. J. Med. Chem. 44 (2009) 678
-
(2009)
Eur. J. Med. Chem.
, vol.44
, pp. 678
-
-
McCarthy, O.1
Musso-Buendia, A.2
Kaiser, M.3
Brun, R.4
Ruiz-Perez, L.M.5
Gunnar Johansson, N.6
Gonzalez Pacanowska, D.7
Gilbert, I.H.8
-
34
-
-
0029044308
-
-
The preparation of this compound (see Supplementary data) initially required selective protection of the primary amino functions using the trifluoroacetyl group as described in:
-
The preparation of this compound (see Supplementary data) initially required selective protection of the primary amino functions using the trifluoroacetyl group as described in:. O'Sullivan M.C., and Dalrymple D.M. Tetrahedron Lett. 36 (1995) 3451
-
(1995)
Tetrahedron Lett.
, vol.36
, pp. 3451
-
-
O'Sullivan, M.C.1
Dalrymple, D.M.2
-
39
-
-
77649275778
-
-
Allaigre, J. P.; Desbois, J. FR. Patent 2,632,954, 1989; Chem. Abstr. 1989, 113, 212009.
-
Allaigre, J. P.; Desbois, J. FR. Patent 2,632,954, 1989; Chem. Abstr. 1989, 113, 212009.
-
-
-
-
43
-
-
29744450738
-
-
Buscemi S., Pace A., Piccionello A.P., Vivona N., and Pani M. Tetrahedron 62 (2006) 1158
-
(2006)
Tetrahedron
, vol.62
, pp. 1158
-
-
Buscemi, S.1
Pace, A.2
Piccionello, A.P.3
Vivona, N.4
Pani, M.5
|