-
2
-
-
0025799785
-
-
(b) Woodcock J., Moazed D., Cannon M., Davies J., Noller H.F. EMBO J. 10:1991;3099
-
(1991)
EMBO J.
, vol.10
, pp. 3099
-
-
Woodcock, J.1
Moazed, D.2
Cannon, M.3
Davies, J.4
Noller, H.F.5
-
4
-
-
0034699519
-
-
(a) Carter A.P., Clemons W.M., Brodersen D.E., Morgan-Warren R.J., Wimberly B.T., Ramakrishnan V. Nature. 407:2000;340
-
(2000)
Nature
, vol.407
, pp. 340
-
-
Carter, A.P.1
Clemons, W.M.2
Brodersen, D.E.3
Morgan-Warren, R.J.4
Wimberly, B.T.5
Ramakrishnan, V.6
-
5
-
-
0034704217
-
-
(b) Brodersen D.E., Clemons W.M., Carter A.P., Morgan-Warren R.J., Wimberly B.T., Ramakrishnan V. Cell. 103:2000;1143
-
(2000)
Cell
, vol.103
, pp. 1143
-
-
Brodersen, D.E.1
Clemons, W.M.2
Carter, A.P.3
Morgan-Warren, R.J.4
Wimberly, B.T.5
Ramakrishnan, V.6
-
6
-
-
0035805229
-
-
(c) Ogle J.M., Bordersen D.E., Clemons W.M., Tarry M.J., Carter A.P., Ramakrishnan V. Science. 292:2001;897.
-
(2001)
Science
, vol.292
, pp. 897
-
-
Ogle, J.M.1
Bordersen, D.E.2
Clemons, W.M.3
Tarry, M.J.4
Carter, A.P.5
Ramakrishnan, V.6
-
7
-
-
0002346798
-
-
Rosen, B. P., Mobashery, S., Eds; Plenum: New York, and references cited therein.
-
Wright, G. D.; Berghuis, A. M.; Mobashery, S. In Resolving the Antibiotic Paradox: Progress in Understanding Drug Resistance and Development of New Antibiotics; Rosen, B. P., Mobashery, S., Eds; Plenum: New York, 1998; p 27, and references cited therein.
-
(1998)
Resolving the Antibiotic Paradox: Progress in Understanding Drug Resistance and Development of New Antibiotics
, pp. 27
-
-
Wright, G.D.1
Berghuis, A.M.2
Mobashery, S.3
-
11
-
-
1842388479
-
-
(a) Recht M.I., Fourmy D., Blanchard S.C., Dahlquist K.D., Puglisi J.D. J. Mol. Biol. 262:1996;421
-
(1996)
J. Mol. Biol.
, vol.262
, pp. 421
-
-
Recht, M.I.1
Fourmy, D.2
Blanchard, S.C.3
Dahlquist, K.D.4
Puglisi, J.D.5
-
18
-
-
0033591922
-
-
Greenberg W.A., Priestley E.S., Sears P.S., Alper P.B., Rosenbohm C., Hendrix M., Hung S.-C., Wong C.-H. J. Am. Chem. Soc. 121:1999;6527.
-
(1999)
J. Am. Chem. Soc.
, vol.121
, pp. 6527
-
-
Greenberg, W.A.1
Priestley, E.S.2
Sears, P.S.3
Alper, P.B.4
Rosenbohm, C.5
Hendrix, M.6
Hung, S.-C.7
Wong, C.-H.8
-
20
-
-
0037012422
-
-
Haddad J., Kotra L.P., Llano-Sotelo B., Kim C., Azucena E.F., Liu M., Vakulenko S.B., Chow C.S., Mobashery S. J. Am. Chem. Soc. 124:2002;3229.
-
(2002)
J. Am. Chem. Soc.
, vol.124
, pp. 3229
-
-
Haddad, J.1
Kotra, L.P.2
Llano-Sotelo, B.3
Kim, C.4
Azucena, E.F.5
Liu, M.6
Vakulenko, S.B.7
Chow, C.S.8
Mobashery, S.9
-
31
-
-
33846403202
-
-
In press
-
Simonsen, K. B. Ayida, B.; Vourloumis, D.; Takahashi, M.; Winters, G. C.; Barluenga, S.; Qamar, S.; Shandrick, S.; Zhao, Q.; Hermann, T. ChemBioChem. In press.
-
ChemBioChem
-
-
Simonsen, K.B.1
Ayida, B.2
Vourloumis, D.3
Takahashi, M.4
Winters, G.C.5
Barluenga, S.6
Qamar, S.7
Shandrick, S.8
Zhao, Q.9
Hermann, T.10
-
32
-
-
0003026045
-
-
Chaiken, I. M., Janda K. D., Eds.; American Chemical Society: Washington, DC
-
Wuonola, M. A.; Powers D. G. In Use of Combinatorial Libraries in the Discovery of Novel Antiinfectives; Chaiken, I. M., Janda K. D., Eds.; American Chemical Society: Washington, DC, 1996; p 284.
-
(1996)
Use of Combinatorial Libraries in the Discovery of Novel Antiinfectives
, pp. 284
-
-
Wuonola, M.A.1
Powers, D.G.2
-
34
-
-
0011248318
-
-
Kurisu T., Yamashita M., Nishimura Y., Miyake T., Tsuchiya T., Umezawa S. Bull. Chem. Soc. Jpn. 49:1976;285.
-
(1976)
Bull. Chem. Soc. Jpn.
, vol.49
, pp. 285
-
-
Kurisu, T.1
Yamashita, M.2
Nishimura, Y.3
Miyake, T.4
Tsuchiya, T.5
Umezawa, S.6
-
36
-
-
0033535566
-
-
2 and high-resolution crystal structures of a synthetic 35 nt RNA construct containing the bacterial decoding site internal loop (Q. Zhao, Q. Han, T. Hermann, unpublished). The conformational space available to the 6′-hydroxyl group of paromamine docked to the decoding site RNA was explored using Insight/Discover (Accelrys) and the AMBER force field following established protocols: Hermann T., Westhof E. J. Med. Chem. 42:1999;1250.
-
(1999)
J. Med. Chem.
, vol.42
, pp. 1250
-
-
Hermann, T.1
Westhof, E.2
-
43
-
-
0011248942
-
-
note
-
3) δ 191.7, 155.6, 155.6, 148.0, 140.0, 137.2, 136.2, 136.1, 128.4 (3C), 128.0 (6C), 75.1, 71.8, 66.9, 55.5, 50.3, 44.8, 32.6.
-
-
-
-
45
-
-
0011206023
-
-
note
-
6 sulfoxide) δ 167.7, 156.6, 156.3, 139.3, 139.0, 138.2, 138.1, 134.7, 129.3, 129.2, 129.1, 128.7, 128.6, 128.6, 128.5, 128.4, 128.4, 77.2, 71.6, 66.2, 66.0, 51.5, 47.3, 31.3.
-
-
-
-
46
-
-
0011249097
-
-
note
-
For amines 16c and 16i the final hydrogenation step resulted in cleavage of the furane or partial reduction of the pyrazine ring, respectively, leading to the formation of products 17c and 17i.
-
-
-
-
48
-
-
0011211209
-
-
note
-
3, (M+H): 243.2, found 243.2.
-
-
-
|