-
4
-
-
33845961059
-
-
Musiol R., Jampilek J., Kralova K., Richardson D.R., Kalinowski D., Podeszwa B., Finster J., Niedabala H., Palka A., and Polanski J. Bioorg. Med. Chem. 15 (2007) 1280
-
(2007)
Bioorg. Med. Chem.
, vol.15
, pp. 1280
-
-
Musiol, R.1
Jampilek, J.2
Kralova, K.3
Richardson, D.R.4
Kalinowski, D.5
Podeszwa, B.6
Finster, J.7
Niedabala, H.8
Palka, A.9
Polanski, J.10
-
5
-
-
0037193150
-
-
Simons S.R., Gerrison J.C., Kofron W.G., Tessier C.A., and Youngs W.J. Tetrahedron Lett. 43 (2002) 3423
-
(2002)
Tetrahedron Lett.
, vol.43
, pp. 3423
-
-
Simons, S.R.1
Gerrison, J.C.2
Kofron, W.G.3
Tessier, C.A.4
Youngs, W.J.5
-
6
-
-
0035929299
-
-
Garrison J.C., Simons R.S., Kofron W.G., Tessier C.A., and Youngs W. J. Chem. Commun. (2001) 1780
-
(2001)
J. Chem. Commun.
, pp. 1780
-
-
Garrison, J.C.1
Simons, R.S.2
Kofron, W.G.3
Tessier, C.A.4
Youngs, W.5
-
7
-
-
0033531369
-
-
Alcalde E., Alvarez-Rua C., Garcia-Rodriguez S., Mesquida N., and Perez-Garcia L. J. Chem. Soc., Chem. Commun. (1999) 295
-
(1999)
J. Chem. Soc., Chem. Commun.
, pp. 295
-
-
Alcalde, E.1
Alvarez-Rua, C.2
Garcia-Rodriguez, S.3
Mesquida, N.4
Perez-Garcia, L.5
-
8
-
-
33846100324
-
-
Dallas A., Kuhtz H., Farrell A., Quilty B., and Nolan K. Tetrahedron Lett. 48 (2007) 1017
-
(2007)
Tetrahedron Lett.
, vol.48
, pp. 1017
-
-
Dallas, A.1
Kuhtz, H.2
Farrell, A.3
Quilty, B.4
Nolan, K.5
-
9
-
-
0033582512
-
-
Cabildo P., Sanz D., Claramunt R.M., Bourne S.A., Alkorta I., and Elguero J. Tetrahedron 55 (1999) 2327
-
(1999)
Tetrahedron
, vol.55
, pp. 2327
-
-
Cabildo, P.1
Sanz, D.2
Claramunt, R.M.3
Bourne, S.A.4
Alkorta, I.5
Elguero, J.6
-
12
-
-
66349102258
-
-
U.S. Patent, 3,853,907
-
Edwards, P. N. U.S. Patent 1974, 3,853,907.
-
(1974)
-
-
Edwards, P.N.1
-
13
-
-
1342279565
-
-
Demberelnyamba D., Kim K., Choi S., Park S., Lee H., Kim C., and Yoo I. Bioorg. Med. Chem. 12 (2004) 853
-
(2004)
Bioorg. Med. Chem.
, vol.12
, pp. 853
-
-
Demberelnyamba, D.1
Kim, K.2
Choi, S.3
Park, S.4
Lee, H.5
Kim, C.6
Yoo, I.7
-
16
-
-
13944252829
-
-
Melaiye A., Sun Z., Hindi K., Milsted A., Ely D., Rencker D.H., Tessier C.A., and Younges W.J. J. Am. Chem. Soc. 127 (2005) 2285
-
(2005)
J. Am. Chem. Soc.
, vol.127
, pp. 2285
-
-
Melaiye, A.1
Sun, Z.2
Hindi, K.3
Milsted, A.4
Ely, D.5
Rencker, D.H.6
Tessier, C.A.7
Younges, W.J.8
-
25
-
-
0031603012
-
-
Rosa J.C., Galanakis D., Ganellin C.R., Dunn P.M., and Jenkinson D.H. J. Med. Chem. 41 (1998) 2
-
(1998)
J. Med. Chem.
, vol.41
, pp. 2
-
-
Rosa, J.C.1
Galanakis, D.2
Ganellin, C.R.3
Dunn, P.M.4
Jenkinson, D.H.5
-
26
-
-
3142664644
-
-
Galanakis D., Ganellin C.R., Chen J.Q., Gunasekera D., and Dunn P.M. Bioorg. Med. Chem. Lett. 14 (2004) 4231
-
(2004)
Bioorg. Med. Chem. Lett.
, vol.14
, pp. 4231
-
-
Galanakis, D.1
Ganellin, C.R.2
Chen, J.Q.3
Gunasekera, D.4
Dunn, P.M.5
-
27
-
-
22144470168
-
-
Conejo-Garcia A., Campos J., Elder C., Entrena A., Gallo M.A., and Espinosa A.J. Org. Chem. 70 (2005) 5748
-
(2005)
Org. Chem.
, vol.70
, pp. 5748
-
-
Conejo-Garcia, A.1
Campos, J.2
Elder, C.3
Entrena, A.4
Gallo, M.A.5
Espinosa, A.J.6
-
28
-
-
41849092643
-
-
Liverton N.J., Holloway M.K., McCauley J.A., Rudd M.T., Butcher J.W., Carroll S.S., DiMuzio J., Fandozzi C., Golbert K.F., Mao S., Mclntyre C.J., Nguyen K.T., Romano J.J., Stahlhut M., Wan B., Olsen D.B., and Vacca J.P. J. Am. Chem. Soc. 130 (2008) 4607
-
(2008)
J. Am. Chem. Soc.
, vol.130
, pp. 4607
-
-
Liverton, N.J.1
Holloway, M.K.2
McCauley, J.A.3
Rudd, M.T.4
Butcher, J.W.5
Carroll, S.S.6
DiMuzio, J.7
Fandozzi, C.8
Golbert, K.F.9
Mao, S.10
Mclntyre, C.J.11
Nguyen, K.T.12
Romano, J.J.13
Stahlhut, M.14
Wan, B.15
Olsen, D.B.16
Vacca, J.P.17
-
30
-
-
66349115075
-
-
note
-
2: C, 80.98; H, 4.53; N, 10.49. Found: C, 80.85; H, 4.59; N, 10.63.
-
-
-
-
31
-
-
66349115633
-
-
note
-
2: C, 76.91; H, 4.52; N, 13.45. Found: C, 76.74; H, 4.65; N, 13.54.
-
-
-
-
32
-
-
66349097216
-
-
note
-
2: C, 78.84; H, 4.60; N, 11.99. Found: C, 78.93; H, 4.48; N, 12.07.
-
-
-
-
33
-
-
66349132820
-
-
note
-
2: C, 73.27; H, 4.61; N, 16.02. Found: C, 73.40; H, 4.69; N, 15.87.
-
-
-
-
34
-
-
66349087977
-
-
note
-
2: C, 68.74; H, 4.07; N, 9.20. Found: C, 68.65; H, 4.16; N, 9.09.
-
-
-
-
35
-
-
66349111176
-
-
note
-
2: C, 69.93; H, 4.16; N, 7.89. Found: C, 69.79; H, 4.29; N, 7.81.
-
-
-
-
36
-
-
66349130179
-
-
note
-
2: C, 63.45; H, 3.97; N, 11.02. Found: C, 63.66; H, 3.76; N, 11.15.
-
-
-
-
37
-
-
66349128885
-
-
note
-
2: C, 64.88; H, 4.08; N, 9.46. Found: C, 64.75; H, 4.02; N, 9.54.
-
-
-
-
38
-
-
66349131919
-
-
note
-
2: C, 65.92; H, 4.07; N, 10.15. Found: C, 65.78; H, 4.19; N, 10.01.
-
-
-
-
39
-
-
66349087369
-
-
note
-
2: C, 67.23; H, 4.18; N, 8.71. Found: C, 67.34; H, 4.37; N, 8.63.
-
-
-
-
40
-
-
66349096629
-
-
note
-
2: C, 59.33; H, 3.96; N, 12.42. Found: C, 59.41; H, 3.83; N, 12.51.
-
-
-
-
41
-
-
66349109986
-
-
note
-
2: C, 60.93; H, 4.09; N, 10.66. Found: C, 61.09; H, 4.17; N, 10.52.
-
-
-
-
43
-
-
66349137064
-
-
note
-
Antibacterial activity: Antibacterial activity of the cyclophanes against the selected human pathogens was evaluated by the agar well diffusion method. About 1 ml of inoculums of each test pathogen was added to the molten NA medium and poured into sterile Petri plates under aseptic conditions. After solidification, a 5 mm well was made in four wells of each plate using a sterile cork borer. Each compound was dissolved in 10% DMSO to get different concentrations and filtered using 0.25 μm sterilized filter paper. Each well received 50 μl solutions of each compound and the plates incubated at room temperature. Sterile DMSO (10%) was used as control. After 48 h, the appearance of inhibition zone around the well was observed. The plates were incubated overnight at 37 °C. Microbial growth was determined by measuring the minimum inhibitory concentration in μl/ml. For each bacterial strain, controls and commercial antibiotics were maintained.
-
-
-
|