-
2
-
-
23444440823
-
Inactivation of antibiotics and the dissemination of resistance genes
-
(b) Davies, J. Inactivation of Antibiotics and the Dissemination of Resistance Genes. Science 1994, 264, 375-382.
-
(1994)
Science
, vol.264
, pp. 375-382
-
-
Davies, J.1
-
3
-
-
0028420272
-
Resistance to antibiotics mediated by target alterations
-
(c) Spratt, B. G. Resistance to Antibiotics Mediated by Target Alterations. Science 1994, 264, 388-393.
-
(1994)
Science
, vol.264
, pp. 388-393
-
-
Spratt, B.G.1
-
4
-
-
0037678042
-
-
Oxford University Press: New York, Chapter 7
-
(d) Pratt, W. B.; Fekety, R. The Antimicrobial Drugs; Oxford University Press: New York, 1986; Chapter 7, pp 153-183.
-
(1986)
The Antimicrobial Drugs
, pp. 153-183
-
-
Pratt, W.B.1
Fekety, R.2
-
5
-
-
2342463112
-
Streptomycin causes misreading of natural messenger by interacting with ribosomes after initiation
-
Tai, P.-C.; Wallace, B. J.; Davis, B. D. Streptomycin Causes Misreading of Natural Messenger by Interacting with Ribosomes after Initiation. Proc. Natl. Acad. Sci. U.S.A. 1978, 75, 275-279.
-
(1978)
Proc. Natl. Acad. Sci. U.S.A.
, vol.75
, pp. 275-279
-
-
Tai, P.-C.1
Wallace, B.J.2
Davis, B.D.3
-
6
-
-
0344627267
-
-
Unpublished results
-
Blyn, L.; Risen, L.; et al. Unpublished results.
-
-
-
Blyn, L.1
Risen, L.2
-
7
-
-
0345057729
-
New pyrazine derivatives. Their preparation and their use as ingredients in drugs
-
WO 9304048
-
(a) Koeppe, H.; Speck, G.; Stockhaus, K. New Pyrazine Derivatives. Their Preparation and their Use as Ingredients in Drugs. PCT Int. Appl., WO 9304048.
-
PCT Int. Appl.
-
-
Koeppe, H.1
Speck, G.2
Stockhaus, K.3
-
8
-
-
0023214496
-
Pyridonecarboxylic acids as antibacterial agents. VIII. An alternative synthesis of enoxacin via fluoronicotinic acid derivatives
-
(b) Miyamoto, T.; Egawa, H.; Matsumoto, J.-I. Pyridonecarboxylic Acids as Antibacterial Agents. VIII. An Alternative Synthesis of Enoxacin via Fluoronicotinic Acid Derivatives. Chem. Pharm. Bull. 1987, 35, 2280-2285.
-
(1987)
Chem. Pharm. Bull.
, vol.35
, pp. 2280-2285
-
-
Miyamoto, T.1
Egawa, H.2
Matsumoto, J.-I.3
-
9
-
-
0025973691
-
Synthesis and anti-HIV-1 activity of 4,5,6,7-tetrahydro-5-methylimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one (TIBO) derivatives
-
(c) Kukla, M. J.; Breslin, H. J.; Pauwels, R.; Fedde, C. L.; Miranda, M.; Scott, M. K.; Sherrill, R. G.; Raeymaekers, A.; Van Gelder, J.; Andries, K.; Janssen, M. A. C.; De Clerq, E.; Janssen, P. A. J. Synthesis and Anti-HIV-1 Activity of 4,5,6,7-Tetrahydro-5-methylimidazo[4,5,1-jk][1,4]benzodiazepin-2(1H)-one (TIBO) Derivatives. J. Med. Chem. 1991, 34, 746-751.
-
(1991)
J. Med. Chem.
, vol.34
, pp. 746-751
-
-
Kukla, M.J.1
Breslin, H.J.2
Pauwels, R.3
Fedde, C.L.4
Miranda, M.5
Scott, M.K.6
Sherrill, R.G.7
Raeymaekers, A.8
Van Gelder, J.9
Andries, K.10
Janssen, M.A.C.11
De Clerq, E.12
Janssen, P.A.J.13
-
10
-
-
0029905037
-
The synthesis of aminopyridines: A method employing palladium-catalyzed carbon-nitrogen bond formation
-
(a) Wagaw, S.; Buchwald, S. L. The Synthesis of Aminopyridines: A Method Employing Palladium-Catalyzed Carbon-Nitrogen Bond Formation. J. Org. Chem. 1996, 61, 7240-7241.
-
(1996)
J. Org. Chem.
, vol.61
, pp. 7240-7241
-
-
Wagaw, S.1
Buchwald, S.L.2
-
11
-
-
0029743317
-
An improved catalyst system for aromatic carbon-nitrogen bond formation: The possible involvement of bis(phosphine) palladium complexes as key intermediates
-
(b) Wolfe, J. P.; Wagaw, S.; Buchwald, S. L. An Improved Catalyst System for Aromatic Carbon-Nitrogen Bond Formation: The Possible Involvement of Bis(Phosphine) Palladium Complexes as Key Intermediates. J. Am. Chem. Soc. 1996, 118, 7215-7216.
-
(1996)
J. Am. Chem. Soc.
, vol.118
, pp. 7215-7216
-
-
Wolfe, J.P.1
Wagaw, S.2
Buchwald, S.L.3
-
12
-
-
0027915421
-
2 receptor with positron emission tomography
-
2 Receptor with Positron Emission Tomography. J. Med. Chem. 1993, 36, 3707-3720.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 3707-3720
-
-
Mach, R.H.1
Luedtke, R.R.2
Unsworth, C.D.3
Boundy, V.A.4
Nowak, P.A.5
Scripko, J.G.6
Elder, S.D.7
Jackson, J.R.8
Hoffman, P.L.9
Evora, P.H.10
Rao, A.V.11
Molinoff, P.B.12
Childers, S.R.13
Ehrenkaufer, R.L.14
-
13
-
-
0027405060
-
Structure-activity relationships in prazosin-related compounds. 2. Role of the piperazine ring on α-blocking activity
-
(a) Giardina, D.; Gulini, U.; Massi, M.; Piloni, M. G.; Pompei, P.; Rafaiani, G.; Melchiorre, C. Structure-Activity Relationships in Prazosin-Related Compounds. 2. Role of the Piperazine Ring on α-Blocking Activity. J. Med. Chem. 1993, 36, 690-698.
-
(1993)
J. Med. Chem.
, vol.36
, pp. 690-698
-
-
Giardina, D.1
Gulini, U.2
Massi, M.3
Piloni, M.G.4
Pompei, P.5
Rafaiani, G.6
Melchiorre, C.7
-
14
-
-
0017349724
-
Synthesis and identification of the major metabolites if prazosin formed in dog and rat. Synthesis and identification of the major metabolites if prazosin formed in dog and rat
-
(b) Althuis, T. H.; Hess, H.-J. Synthesis and Identification of the Major Metabolites if Prazosin Formed in Dog and Rat. Synthesis and Identification of the Major Metabolites if Prazosin Formed in Dog and Rat. J. Med. Chem. 1977, 20, 146-149.
-
(1977)
J. Med. Chem.
, vol.20
, pp. 146-149
-
-
Althuis, T.H.1
Hess, H.-J.2
-
15
-
-
0001347492
-
Selective removal of an N-BOC protecting group in the presence of a tert-butyl ester and other acid-sensitive groups
-
Gibson, F. S.; Bergmeier, S. C.; Rapoport, H. Selective Removal of an N-BOC Protecting Group in the Presence of a tert-Butyl Ester and Other Acid-Sensitive Groups. J. Org. Chem. 1994, 59, 3216-3218.
-
(1994)
J. Org. Chem.
, vol.59
, pp. 3216-3218
-
-
Gibson, F.S.1
Bergmeier, S.C.2
Rapoport, H.3
-
16
-
-
0024358248
-
Convergent and efficient palladium-effected synthesis of 5,10-dideaza-5,6,7,8-tetrahydrofolic acid (DDATHF)
-
Taylor, E. C.; Wong, G. S. K. Convergent and Efficient Palladium-Effected Synthesis of 5,10-Dideaza-5,6,7,8-tetrahydrofolic Acid (DDATHF). J. Org. Chem. 1989, 54, 3618-3624.
-
(1989)
J. Org. Chem.
, vol.54
, pp. 3618-3624
-
-
Taylor, E.C.1
Wong, G.S.K.2
-
17
-
-
0030845978
-
Improved functional group compatibility in the palladium-catalyzed amination of aryl bromides
-
Wolfe, J. P.; Buchwald, S. L. Improved Functional Group Compatibility in the Palladium-Catalyzed Amination of Aryl Bromides. Tetrahedron Lett. 1997, 38, 6359-6362.
-
(1997)
Tetrahedron Lett.
, vol.38
, pp. 6359-6362
-
-
Wolfe, J.P.1
Buchwald, S.L.2
-
18
-
-
0345489441
-
Preparation of 2-(1-piperazinyl)pyrimidines as agents for treating neuropathy
-
WO 8704928
-
(a) Awaya, A.; Nakano, T.; Kobayashi, H.; Tan, K.; Horikomi, K.; Sasaki, T.; Yokoyama, K.; Ohno, H.; Kato, K. Preparation of 2-(1-piperazinyl)pyrimidines as Agents for Treating Neuropathy. PCT Int. Appl., WO 8704928.
-
PCT Int. Appl.
-
-
Awaya, A.1
Nakano, T.2
Kobayashi, H.3
Tan, K.4
Horikomi, K.5
Sasaki, T.6
Yokoyama, K.7
Ohno, H.8
Kato, K.9
-
19
-
-
0345489440
-
Quinazoline derivatives and antihypertensive preparations containing
-
EP 188094
-
(b) Yokoyama, K.; Kato, K.; Kitahara, T.; Ohno, H.; Nishina, T.; Awaya, A.; Nakano, T.; Watanabe, K.; Saruta, S.; Kumakura, M. Quinazoline Derivatives and Antihypertensive Preparations Containing Them. Eur. Pat. Appl., EP 188094.
-
Them. Eur. Pat. Appl.
-
-
Yokoyama, K.1
Kato, K.2
Kitahara, T.3
Ohno, H.4
Nishina, T.5
Awaya, A.6
Nakano, T.7
Watanabe, K.8
Saruta, S.9
Kumakura, M.10
-
20
-
-
0014233521
-
Antihypertensive 2-amino-4(3H)-quinazolines
-
Hess, H. J.; Cronin, T. H.; Scriabine, A. Antihypertensive 2-amino-4(3H)-quinazolines. J. Med. Chem. 1968, 11, 130-136.
-
(1968)
J. Med. Chem.
, vol.11
, pp. 130-136
-
-
Hess, H.J.1
Cronin, T.H.2
Scriabine, A.3
-
21
-
-
0030220783
-
Tyrphostins IV-highly potent inhibitors of EGF receptor kinase. Structure-activity relationship study of 4-anilidoquinazolines
-
Gazit, A.; Chen, J.; App, H.; McMahon, G.; Hirth, P.; Chen, I.; Levitzki, A. Tyrphostins IV-Highly Potent Inhibitors of EGF Receptor Kinase. Structure-Activity Relationship Study of 4-Anilidoquinazolines. Bioorg. Med. Chem. 1996, 4, 1203-1207.
-
(1996)
Bioorg. Med. Chem.
, vol.4
, pp. 1203-1207
-
-
Gazit, A.1
Chen, J.2
App, H.3
McMahon, G.4
Hirth, P.5
Chen, I.6
Levitzki, A.7
-
24
-
-
0002714675
-
Rapid chromatographic technique for preparative separations with moderate resolution
-
Still, W. C.; Kahn, M.; Mitra, A. Rapid Chromatographic Technique for Preparative Separations with Moderate Resolution. J. Org. Chem. 1978, 43, 2923-2925.
-
(1978)
J. Org. Chem.
, vol.43
, pp. 2923-2925
-
-
Still, W.C.1
Kahn, M.2
Mitra, A.3
-
25
-
-
0024690869
-
Identification and characterization of a new gene of Escherichia coli K-12 involved in outer membrane permeability
-
Sampson, B. A.; Misra, R.; Benson, S. A. Identification and Characterization of a New Gene of Escherichia coli K-12 Involved in Outer Membrane Permeability. Genetics 1989, 122, 491-501.
-
(1989)
Genetics
, vol.122
, pp. 491-501
-
-
Sampson, B.A.1
Misra, R.2
Benson, S.A.3
-
26
-
-
0025737880
-
Use of invitro protein synthesis from polymerase chain reaction-generated templates to study interaction of Escherichia coli transcription factors with core RNA polymerase and for epitope mapping of monoclonal antibodies
-
Lesley, S. A.; Brow, M. A. D.; Burgess, R. R. Use of inVitro Protein Synthesis from Polymerase Chain Reaction-generated Templates to Study Interaction of Escherichia coli Transcription Factors with Core RNA Polymerase and for Epitope Mapping of Monoclonal Antibodies. J. Biol. Chem. 1991, 266, 2632-2638.
-
(1991)
J. Biol. Chem.
, vol.266
, pp. 2632-2638
-
-
Lesley, S.A.1
Brow, M.A.D.2
Burgess, R.R.3
-
27
-
-
0019852290
-
Comparison of the misreading induced by streptomycin and neomycin
-
(a) Grise-Miron, L.; Noreau, J.; Melancon, P.; Brakier-Gingras, L. Comparison of the Misreading Induced by Streptomycin and Neomycin. Biochim. Biophys. Acta 1981, 656, 103-110.
-
(1981)
Biochim. Biophys. Acta
, vol.656
, pp. 103-110
-
-
Grise-Miron, L.1
Noreau, J.2
Melancon, P.3
Brakier-Gingras, L.4
-
28
-
-
0014429801
-
Misreading of ribonucleic acid code words induced by aminoglycoside antibiotics (the effect of drug concentration)
-
(b) Davies, J.; Davis, B. D. Misreading of Ribonucleic Acid Code Words Induced by Aminoglycoside Antibiotics (The Effect of Drug Concentration). J. Biol. Chem. 1968, 243, 3312-3316.
-
(1968)
J. Biol. Chem.
, vol.243
, pp. 3312-3316
-
-
Davies, J.1
Davis, B.D.2
-
29
-
-
0023656339
-
Gene synthesis, expression, structures, and functional activities of site-specific mutants of ubiquitin
-
Ecker, D. J.; Butt, T. R.; Marsh, J.; Sternberg, E. J.; Margolis, N.; Monia, B. P.; Jonnalagadda, S.; Khan, M. I.; Weber, P. L.; Mueller, L.; Crooke, S. T. Gene Synthesis, Expression, Structures, and Functional Activities of Site-specific Mutants of Ubiquitin. J. Biol. Chem. 1987, 262, 14213-14221.
-
(1987)
J. Biol. Chem.
, vol.262
, pp. 14213-14221
-
-
Ecker, D.J.1
Butt, T.R.2
Marsh, J.3
Sternberg, E.J.4
Margolis, N.5
Monia, B.P.6
Jonnalagadda, S.7
Khan, M.I.8
Weber, P.L.9
Mueller, L.10
Crooke, S.T.11
|