-
1
-
-
0019252702
-
Structure-Activity Relationships of Antibacterial 6,7- and 7,8-Disubstituted 1-Alkyl-1,4-dihydro-4-oxoquinolone-3-carboxylic Acids
-
Koga, H.; Itoh, A.; Murayama, S.; Suzue, S.; Irikura, T. Structure-Activity Relationships of Antibacterial 6,7- and 7,8-Disubstituted 1-Alkyl-1,4-dihydro-4-oxoquinolone-3-carboxylic Acids. J. Med. Chem. 1980, 23, 1358-1363.
-
(1980)
J. Med. Chem
, vol.23
, pp. 1358-1363
-
-
Koga, H.1
Itoh, A.2
Murayama, S.3
Suzue, S.4
Irikura, T.5
-
2
-
-
44949232927
-
Antibacterial Activity of AM-1155
-
Atlanta, GA, Abstract 385
-
(a) Hirai, K.; Hosaka, M.; Niwata, Y.; Yasue, T.; Fukuda, H.; Ishizaki, T.; Suzue, S.; Nishino, K. Antibacterial Activity of AM-1155, a New Quinolone. Presented at the30th Meeting of the ICAAC, Atlanta, GA, 1990; Abstract 385.
-
(1990)
a New Quinolone. Presented at the30th Meeting of the ICAAC
-
-
Hirai, K.1
Hosaka, M.2
Niwata, Y.3
Yasue, T.4
Fukuda, H.5
Ishizaki, T.6
Suzue, S.7
Nishino, K.8
-
3
-
-
0026658475
-
In Vitro and in Vivo Antibacterial Activities of AM-1155, a New 6-Fluoro-8-Methoxy quinolone
-
(b) Hosaka, M.; Yasue, T.; Fukuda, H.; Tomizawa, H.; Aoyama, H.; Hirai, K. In Vitro and in Vivo Antibacterial Activities of AM-1155, a New 6-Fluoro-8-Methoxy quinolone. Antimicrob. Agents Chemother. 1992, 36, 2108-2117.
-
(1992)
Antimicrob. Agents Chemother
, vol.36
, pp. 2108-2117
-
-
Hosaka, M.1
Yasue, T.2
Fukuda, H.3
Tomizawa, H.4
Aoyama, H.5
Hirai, K.6
-
4
-
-
0010423242
-
Synthesis and in Vitro Activity of BAY 12-8039, a New 8-Methoxy-Quinlone
-
Presented at the, New Orleans, LA, Abstract F1
-
Peterson, U.; Bremm, K. D.; Dalhoff, A.; Endermann, R.; Heilmann, W.; Krebs, A.; Schenke, T. Synthesis and in Vitro Activity of BAY 12-8039, a New 8-Methoxy-Quinlone. Presented at the 36th Meeting of the ICAAC, New Orleans, LA, 1996; Abstract F1.
-
(1996)
36th Meeting of the ICAAC
-
-
Peterson, U.1
Bremm, K.D.2
Dalhoff, A.3
Endermann, R.4
Heilmann, W.5
Krebs, A.6
Schenke, T.7
-
5
-
-
0343529226
-
Vitro Activity and Synthesis of CP-99219, a Novel 7-(3-Azabicyclo[3.1.0]hexyl)naphthyridine
-
Presented at the, Anaheim, CA, Abstract 751
-
Gootz, T. D.; Brighty, K. E.; Anderson, M. R.; Haskell, S. L.; Sutcliffe, J. A.; Castaldi, M. J.; Miller, S. A. In Vitro Activity and Synthesis of CP-99219, a Novel 7-(3-Azabicyclo[3.1.0]hexyl)naphthyridine. Presented at the 32th Meeting of the ICAAC, Anaheim, CA, 1992; Abstract 751.
-
(1992)
32th Meeting of the ICAAC
-
-
Gootz, T.D.1
Brighty, K.E.2
Anderson, M.R.3
Haskell, S.L.4
Sutcliffe, J.A.5
Castaldi, M.J.6
Miller, S.A.7
-
6
-
-
0001765560
-
Novel Fluoroquinolone Antibacterial Agents Containing Oxime-Substituted (Aminomethyl)pyrrolidines: Synthesis and Antibacterial Activity of 7-(4-(Aminomethyl)-3-(methoxyimino)pyrrolidin-1-yl)-1-cyclopropyl-6- fluoro-4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxylic Acid (LB20304)
-
Hong, C. Y.; Kim, Y. K.; Chang, J. H.; Kim, S. H.; Choi, H.; Nam, D. H.; Kim, Y. Z.; Kwak, J. H. Novel Fluoroquinolone Antibacterial Agents Containing Oxime-Substituted (Aminomethyl)pyrrolidines: Synthesis and Antibacterial Activity of 7-(4-(Aminomethyl)-3-(methoxyimino)pyrrolidin-1-yl)-1-cyclopropyl-6- fluoro-4-oxo-1,4-dihydro[1,8]naphthyridine-3-carboxylic Acid (LB20304). J. Med. Chem. 1997, 40, 3584-3593.
-
(1997)
J. Med. Chem
, vol.40
, pp. 3584-3593
-
-
Hong, C.Y.1
Kim, Y.K.2
Chang, J.H.3
Kim, S.H.4
Choi, H.5
Nam, D.H.6
Kim, Y.Z.7
Kwak, J.H.8
-
7
-
-
0025740347
-
Emergence of quinolone resistance among clinical isolates of methicillin-resistant Staphylococcus aureus in Ontario, Canada
-
(a) Harnett, N.; Brown, S.; Krishnan, C. Emergence of quinolone resistance among clinical isolates of methicillin-resistant Staphylococcus aureus in Ontario, Canada. Antimicrob. Agents Chemother. 1991, 35, 1911-1913.
-
(1991)
Antimicrob. Agents Chemother
, vol.35
, pp. 1911-1913
-
-
Harnett, N.1
Brown, S.2
Krishnan, C.3
-
8
-
-
0032758083
-
-
Piddock, L. J. Mechanism of fluoroquinolone resistance: an update 1994-1998. Drags 1999, 58, 11-18. (c) Appelbaum, P. C.; Hunter, P. A. The fluoroquinolone antibacterials: past, present and future perspectives. Int. J. Antimicrob. Agents 2000, 16, 5-15.
-
(b) Piddock, L. J. Mechanism of fluoroquinolone resistance: an update 1994-1998. Drags 1999, 58, 11-18. (c) Appelbaum, P. C.; Hunter, P. A. The fluoroquinolone antibacterials: past, present and future perspectives. Int. J. Antimicrob. Agents 2000, 16, 5-15.
-
-
-
-
9
-
-
0026590968
-
Recent advance in structure activity relationships in new quinolones
-
Mitsuhashi, S, Junker, E, Eds, Birkhauser Verlag: Basel, Switzerland
-
(a) Asahina, Y.; Ishizaki, T.; Suzue, S.; Recent advance in structure activity relationships in new quinolones. In Fluorinated Quinolones-New Quinolones Antimicrobials; Progress in Drug Research, Vol. 38; Mitsuhashi, S., Junker, E., Eds.; Birkhauser Verlag: Basel, Switzerland, 1992; pp 57-106.
-
(1992)
Fluorinated Quinolones-New Quinolones Antimicrobials; Progress in Drug Research
, vol.38
, pp. 57-106
-
-
Asahina, Y.1
Ishizaki, T.2
Suzue, S.3
-
10
-
-
0028316927
-
Structure-activity and structure-side-effect relationships for the quinolone antibacterials
-
(b) Domagara, J. M. Structure-activity and structure-side-effect relationships for the quinolone antibacterials. J. Antimicrob. Chemother. 1994, 33, 685-706.
-
(1994)
J. Antimicrob. Chemother
, vol.33
, pp. 685-706
-
-
Domagara, J.M.1
-
11
-
-
14844347928
-
Bacterial Topoisomerase Inhibitors: Quinolone and Pyridone Antibacterial Agents
-
(c) Mitscher, L. A. Bacterial Topoisomerase Inhibitors: Quinolone and Pyridone Antibacterial Agents. Chem. Rev. 2005, 105, 559-592.
-
(2005)
Chem. Rev
, vol.105
, pp. 559-592
-
-
Mitscher, L.A.1
-
12
-
-
0022449871
-
1-Ethyl-7-[3-[(ethylamino)methyl]-1-pyrrolidinyl]-6,8-difluoro-1, 4-dihydro-3-quinolinecarboxylic Acid. New Quinolone Antibacterial with Potent Gram-Positive Activity
-
Domagala, J. M.; Heifetz, C. L.; Mich, T. F.; Nichols, J. B. 1-Ethyl-7-[3-[(ethylamino)methyl]-1-pyrrolidinyl]-6,8-difluoro-1, 4-dihydro-3-quinolinecarboxylic Acid. New Quinolone Antibacterial with Potent Gram-Positive Activity. J. Med. Chem. 1986, 29, 445-448.
-
(1986)
J. Med. Chem
, vol.29
, pp. 445-448
-
-
Domagala, J.M.1
Heifetz, C.L.2
Mich, T.F.3
Nichols, J.B.4
-
13
-
-
0023939458
-
Quinolone Antibacterial Agents. Synthesis and Structure-Activity Relationships of 8-Substituted Quinolone-3-carboxylic Acids and 1,8-Naphthyridine-3-carboxylic Acids
-
(a) Sanchez, J. P.; Domagala, J. M.; Hagen, S. E.; Heifetz, C. L.; Hutt, M. P.; Nichols, J. B.; Trehan, A. K. Quinolone Antibacterial Agents. Synthesis and Structure-Activity Relationships of 8-Substituted Quinolone-3-carboxylic Acids and 1,8-Naphthyridine-3-carboxylic Acids. J. Med. Chem. 1988, 31, 983-991.
-
(1988)
J. Med. Chem
, vol.31
, pp. 983-991
-
-
Sanchez, J.P.1
Domagala, J.M.2
Hagen, S.E.3
Heifetz, C.L.4
Hutt, M.P.5
Nichols, J.B.6
Trehan, A.K.7
-
14
-
-
0023885198
-
1-Substituted 7-[3-[(Ethylamino)methyl]-1- pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acids. New Quantitative Structure-Activity Relationships at Ni for the Quinolone Antibacterials
-
(b) Domagala, J. M.; Heifetz, C. L.; Hutt, M. P.; Mich, T. F.; Nichols, J. B.; Solomon, M.; Worth, D. F. 1-Substituted 7-[3-[(Ethylamino)methyl]-1- pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acids. New Quantitative Structure-Activity Relationships at Ni for the Quinolone Antibacterials. J. Med. Chem. 1988, 31, 991-1001.
-
(1988)
J. Med. Chem
, vol.31
, pp. 991-1001
-
-
Domagala, J.M.1
Heifetz, C.L.2
Hutt, M.P.3
Mich, T.F.4
Nichols, J.B.5
Solomon, M.6
Worth, D.F.7
-
15
-
-
0027070672
-
Fluoroquinolones: Relationships between Structural Variations, Mammalian Cell Cytotoxicity, and Antimicrobial Activity
-
Suto, M. J.; Domagala, J. M.; Roland, G. E.; Mailloux, G. B.; Cohen, M. A. Fluoroquinolones: Relationships between Structural Variations, Mammalian Cell Cytotoxicity, and Antimicrobial Activity. J. Med. Chem. 1992, 35, 4745-4750.
-
(1992)
J. Med. Chem
, vol.35
, pp. 4745-4750
-
-
Suto, M.J.1
Domagala, J.M.2
Roland, G.E.3
Mailloux, G.B.4
Cohen, M.A.5
-
16
-
-
0033915250
-
Antimycobacterial Activities of Novel Levofloxacin Analogues
-
Kawakami, K.; Namba, K.; Tanaka, M.; Matsuhashi, N.; Sato, K.; Takemura, M. Antimycobacterial Activities of Novel Levofloxacin Analogues. Antimicrob. Agents Chemother. 2000, 44, 2126-2129.
-
(2000)
Antimicrob. Agents Chemother
, vol.44
, pp. 2126-2129
-
-
Kawakami, K.1
Namba, K.2
Tanaka, M.3
Matsuhashi, N.4
Sato, K.5
Takemura, M.6
-
17
-
-
0031970342
-
Comparative Activities of Clinafloxacin against Gram-Positive and Gram-Negative Bacteria
-
(a) Edine, L. M.; Jacobs, M. R.; Appelbaum, P. C. Comparative Activities of Clinafloxacin against Gram-Positive and Gram-Negative Bacteria. Antimicrob. Agents Chemother. 1998, 42, 1269-1273.
-
(1998)
Antimicrob. Agents Chemother
, vol.42
, pp. 1269-1273
-
-
Edine, L.M.1
Jacobs, M.R.2
Appelbaum, P.C.3
-
18
-
-
0030951636
-
Comparative in-vitro activities of PR59500 (quinupristin/dalfopristin), CL329998, CL331002, trovafloxacin, clinafloxacin, teicoplanin and vancomycin against Gram-positive bacteria
-
(b) Shonekan, D.; Handwerger, S.; Mildvan, D. Comparative in-vitro activities of PR59500 (quinupristin/dalfopristin), CL329998, CL331002, trovafloxacin, clinafloxacin, teicoplanin and vancomycin against Gram-positive bacteria. J. Antimicrob. Chemother. 1997, 39, 405-409.
-
(1997)
J. Antimicrob. Chemother
, vol.39
, pp. 405-409
-
-
Shonekan, D.1
Handwerger, S.2
Mildvan, D.3
-
19
-
-
0025343827
-
Fluoronaphthyridines and Quinolones as Antibacterial Agents. 2. Synthesis and Structure-Activity Relationships of New 1-tert-Bulyl 7-Substituted Derivatives
-
(a) Bouzard, M.; Cesare, P. D.; Essiz, M.; Jacquet, J. P.; Kiechel, J. R.; Remuzon, P.; Weber, A.; Oki, T.; Masuyoshi, M.; Kessler, R. E.; Fung-Tomc, J.; Desiderio, J. Fluoronaphthyridines and Quinolones as Antibacterial Agents. 2. Synthesis and Structure-Activity Relationships of New 1-tert-Bulyl 7-Substituted Derivatives. J. Med. Chem. 1990, 33, 1344-1352.
-
(1990)
J. Med. Chem
, vol.33
, pp. 1344-1352
-
-
Bouzard, M.1
Cesare, P.D.2
Essiz, M.3
Jacquet, J.P.4
Kiechel, J.R.5
Remuzon, P.6
Weber, A.7
Oki, T.8
Masuyoshi, M.9
Kessler, R.E.10
Fung-Tomc, J.11
Desiderio, J.12
-
20
-
-
0026499635
-
Fluoronaphthyridines and -quinolones as Antibacterial Agents. 5. Synthesis and Antibacterial Activity of Chiral 1-tert-Butyl-6-fluoro-7-substituted- naphthyridones
-
(b) Cesare, P. D.; Bouzard, M.; Essiz, M.; Jacquet, J. P.; Ledoussal, B.; Kiechel, J. R.; Remuzon, P.; Kessler, R. E.; Fung-Tomc, J.; Desiderio, J. Fluoronaphthyridines and -quinolones as Antibacterial Agents. 5. Synthesis and Antibacterial Activity of Chiral 1-tert-Butyl-6-fluoro-7-substituted- naphthyridones. J. Med. Chem. 1992, 35, 4205-4213.
-
(1992)
J. Med. Chem
, vol.35
, pp. 4205-4213
-
-
Cesare, P.D.1
Bouzard, M.2
Essiz, M.3
Jacquet, J.P.4
Ledoussal, B.5
Kiechel, J.R.6
Remuzon, P.7
Kessler, R.E.8
Fung-Tomc, J.9
Desiderio, J.10
-
21
-
-
0008821147
-
Studies on Quinolone Antibacterials. V. Synthesis and Antibacterial Activity of Chiral 5-Amino-7-(4-substituted-3-amino-1-pyrrolidinyl)-6-fluoro-1,4-dihydro-8-methyl- 4-oxoquinoline-3-carboxylic Acids and Derivatives
-
(c) Yoshida, T.; Yamamoto, Y.; Orita, H.; Kakiuchi, M.; Takahashi, Y.; Itakura, M.; Kado, N.; Yasuda, S.; Kato, H.; Itoh, Y. Studies on Quinolone Antibacterials. V. Synthesis and Antibacterial Activity of Chiral 5-Amino-7-(4-substituted-3-amino-1-pyrrolidinyl)-6-fluoro-1,4-dihydro-8-methyl- 4-oxoquinoline-3-carboxylic Acids and Derivatives. Chem. Pharm. Bull. 1996, 44, 1376-1386.
-
(1996)
Chem. Pharm. Bull
, vol.44
, pp. 1376-1386
-
-
Yoshida, T.1
Yamamoto, Y.2
Orita, H.3
Kakiuchi, M.4
Takahashi, Y.5
Itakura, M.6
Kado, N.7
Yasuda, S.8
Kato, H.9
Itoh, Y.10
-
22
-
-
0037435067
-
-
Inagaki, H.; Miyauchi, S.; Miyauchi, R. N.; Kawato, H. C.; Ohki, H.; Matsuhashi, N.; Kawakami, K.; Takahashi, H.; Takemura, M. Synthesis and Structure-Activity Relationships of 5-Amino-6-fluoro-1-[(1R,2S)-2- fluorocyclopropan-1-yl]-8-methylquinolonecarboxylic Acid Antibacterials Having Fluorinated 7-[(3R)-3-(Aminocyclopropan-1-yl)pyrrolidin-1-yl] Substituents. J. Med. Chem. 2003, 46, 1005-1015.
-
Inagaki, H.; Miyauchi, S.; Miyauchi, R. N.; Kawato, H. C.; Ohki, H.; Matsuhashi, N.; Kawakami, K.; Takahashi, H.; Takemura, M. Synthesis and Structure-Activity Relationships of 5-Amino-6-fluoro-1-[(1R,2S)-2- fluorocyclopropan-1-yl]-8-methylquinolonecarboxylic Acid Antibacterials Having Fluorinated 7-[(3R)-3-(Aminocyclopropan-1-yl)pyrrolidin-1-yl] Substituents. J. Med. Chem. 2003, 46, 1005-1015.
-
-
-
-
23
-
-
0025118545
-
Synthesis and Antibacterial Activity of the Metabolites of 9-Fluoro-6,7-dihydro-8-(4-hydroxy-1-piperidyl)-5-methoxy-1-oxo-1H, 5H-benzo[i,j]quinolidine-2-carboxylic Acid (OPC-7251)
-
Morita, S.; Otsubo, K.; Uchida, M.; Kawabata, S.; Tamaoka, H.; Shimizu, T. Synthesis and Antibacterial Activity of the Metabolites of 9-Fluoro-6,7-dihydro-8-(4-hydroxy-1-piperidyl)-5-methoxy-1-oxo-1H, 5H-benzo[i,j]quinolidine-2-carboxylic Acid (OPC-7251). Chem. Pharm. Bull. 1990, 38, 2027-2099.
-
(1990)
Chem. Pharm. Bull
, vol.38
, pp. 2027-2099
-
-
Morita, S.1
Otsubo, K.2
Uchida, M.3
Kawabata, S.4
Tamaoka, H.5
Shimizu, T.6
-
24
-
-
44949265051
-
-
European Patent 172651, 97485
-
Mich, T. F.; Sanchez, J. P.; Domagala, J. M. European Patent 172651, 1986; Chem. Abstr. 1986, 105, 97485.
-
(1986)
Chem. Abstr
, vol.105
-
-
Mich, T.F.1
Sanchez, J.P.2
Domagala, J.M.3
-
25
-
-
44949259749
-
-
European Patent 443498, 256018j
-
Asahina, Y.; Fukuda, Y.; Fukuda, H. European Patent 443498, 1992; Chem. Abstr., 1992, 115, 256018j.
-
(1992)
Chem. Abstr
, vol.115
-
-
Asahina, Y.1
Fukuda, Y.2
Fukuda, H.3
-
26
-
-
0344699370
-
Enantio- and Diastereocontrolled Dopamine D1, D2, D3, and D4 Receptor Binding of N-(3-Pyrrolidinylmethyl) benzamides Synthesized from Aspartic Acid
-
Thomas, C.; Hubner, H.; Gmeiner, P. Enantio- and Diastereocontrolled Dopamine D1, D2, D3, and D4 Receptor Binding of N-(3-Pyrrolidinylmethyl) benzamides Synthesized from Aspartic Acid. Bioorg. Med. Chem. Lett. 1999, 9, 841-846.
-
(1999)
Bioorg. Med. Chem. Lett
, vol.9
, pp. 841-846
-
-
Thomas, C.1
Hubner, H.2
Gmeiner, P.3
-
27
-
-
0029132257
-
A Simple Method for the Formation of Cyclopropylamines: The First Synthesis of Tricyclopropylamine
-
Gillaspy, M. L.; Lefker, B. L.; Hada, W. A.; Hoover, D. J. A Simple Method for the Formation of Cyclopropylamines: The First Synthesis of Tricyclopropylamine. Tetrahedron Lett. 1995, 36, 7399-7402.
-
(1995)
Tetrahedron Lett
, vol.36
, pp. 7399-7402
-
-
Gillaspy, M.L.1
Lefker, B.L.2
Hada, W.A.3
Hoover, D.J.4
-
28
-
-
0030909024
-
Asymmetric dipolar cycloaddition reactions: A practical, convergent synthesis of chiral pyrrolidines
-
Ma, Z.; Wang, S.; Cooper, C. S.; Fung, A.; Lynch, J. K.; Plagge, F.; Chu, D. T. W. Asymmetric dipolar cycloaddition reactions: a practical, convergent synthesis of chiral pyrrolidines. Tetrahedron Asymm. 1997, 8, 883-887.
-
(1997)
Tetrahedron Asymm
, vol.8
, pp. 883-887
-
-
Ma, Z.1
Wang, S.2
Cooper, C.S.3
Fung, A.4
Lynch, J.K.5
Plagge, F.6
Chu, D.T.W.7
-
29
-
-
0035859709
-
Synthesis of enantiomerically pure 4-substituted pyrrolidin-3-ols via asymmetric 1,3-dipolar cycloadition
-
(a) Karsson, S.; Hoggerg, H.-E. Synthesis of enantiomerically pure 4-substituted pyrrolidin-3-ols via asymmetric 1,3-dipolar cycloadition. Tetrahedron Asymm. 2001, 12, 1977-1982.
-
(2001)
Tetrahedron Asymm
, vol.12
, pp. 1977-1982
-
-
Karsson, S.1
Hoggerg, H.-E.2
-
30
-
-
17144418234
-
-
Kotian, P. L.; Lin, T.-H.; El-Kattan, Y.; Chand, P. A Practical Large-Scale Synthesis of (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol via Asymmetric 1,3-Dipolar Cycloaddition. Org. Process Res. Dev. 2005, 9, 193-197.
-
(b) Kotian, P. L.; Lin, T.-H.; El-Kattan, Y.; Chand, P. A Practical Large-Scale Synthesis of (3R,4R)-4-(Hydroxymethyl)pyrrolidin-3-ol via Asymmetric 1,3-Dipolar Cycloaddition. Org. Process Res. Dev. 2005, 9, 193-197.
-
-
-
-
31
-
-
0002667764
-
The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products
-
Mitsunobu, O. The Use of Diethyl Azodicarboxylate and Triphenylphosphine in Synthesis and Transformation of Natural Products. Synthesis 1980, 1, 28.
-
(1980)
Synthesis
, vol.1
, pp. 28
-
-
Mitsunobu, O.1
-
32
-
-
0023340780
-
Synthesis and Antibacterial Activity of Optically Active Ofloxacin and Its Fluoromethyl Derivative
-
(a) Atarashi, S.; Yokohama, S.; Yamazaki, K.; Sakano, K.; Imamura, M.; Hayakawa, I. Synthesis and Antibacterial Activity of Optically Active Ofloxacin and Its Fluoromethyl Derivative. Chem. Pharm. Bull. 1987, 35, 1896-1902.
-
(1987)
Chem. Pharm. Bull
, vol.35
, pp. 1896-1902
-
-
Atarashi, S.1
Yokohama, S.2
Yamazaki, K.3
Sakano, K.4
Imamura, M.5
Hayakawa, I.6
-
33
-
-
18244403477
-
Synthesis and Antibacterial Activity of Optically Active Ofloxacin
-
(b) Une, T.; Fujimoto, T.; Sato, K.; Osada, Y. Synthesis and Antibacterial Activity of Optically Active Ofloxacin. Antimicrob. Agents Chemother. 1988, 32, 559-564.
-
(1988)
Antimicrob. Agents Chemother
, vol.32
, pp. 559-564
-
-
Une, T.1
Fujimoto, T.2
Sato, K.3
Osada, Y.4
-
34
-
-
0023028275
-
-
Egawa, H.; Miyamoto, T.; Matsumoto, J. A New Synthesis of 7H-Pyrido[1,2,3-de][1,4]benzoxazine derivatives including an antibacterial agent, ofloxacin. Chem. Pharm. Bull. 1986, 34, 4098-4102.
-
(a) Egawa, H.; Miyamoto, T.; Matsumoto, J. A New Synthesis of 7H-Pyrido[1,2,3-de][1,4]benzoxazine derivatives including an antibacterial agent, ofloxacin. Chem. Pharm. Bull. 1986, 34, 4098-4102.
-
-
-
-
35
-
-
0023628552
-
-
Mitscher, L. A.; Sharma, P. N.; Chu, D. T. W.; Shen, L. L.; Pernet, A. G. Chiral DNA Gyrase Inhibitors. 2. Asymmetric Synthesis and Biological Activity of the Enantiomers of 9-Fluoro-3-methyl-10-(4-methyl-1-piperazinyl)-7- oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic Acid (Ofloxacin). J. Med. Chem. 1987, 30, 2283-2286.
-
(b) Mitscher, L. A.; Sharma, P. N.; Chu, D. T. W.; Shen, L. L.; Pernet, A. G. Chiral DNA Gyrase Inhibitors. 2. Asymmetric Synthesis and Biological Activity of the Enantiomers of 9-Fluoro-3-methyl-10-(4-methyl-1-piperazinyl)-7- oxo-2,3-dihydro-7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic Acid (Ofloxacin). J. Med. Chem. 1987, 30, 2283-2286.
-
-
-
-
36
-
-
0035180501
-
Target Preference of 15 Quinolones against Staphylococcus aureus Based on Antibacterial Activity and Target Inhibition
-
Takei, M.; Fukuda, H.; Kishii, R.; Hosaka, M. Target Preference of 15 Quinolones against Staphylococcus aureus Based on Antibacterial Activity and Target Inhibition. Antimicrob. Agents Chemother. 2001, 45, 3544-3547.
-
(2001)
Antimicrob. Agents Chemother
, vol.45
, pp. 3544-3547
-
-
Takei, M.1
Fukuda, H.2
Kishii, R.3
Hosaka, M.4
-
37
-
-
0031879199
-
Antibacterial Activity of Gatifloxacin (AM-1155, CG5501, BMS-206584), a Newly Developed Fluoroquinolone, against Sequentially Acquired Quionolone-Resistant Mutants and the norA Transformant of Staphylococcus aureus
-
Fukuda, H.; Hori, S.; Hiramatsu, K. Antibacterial Activity of Gatifloxacin (AM-1155, CG5501, BMS-206584), a Newly Developed Fluoroquinolone, against Sequentially Acquired Quionolone-Resistant Mutants and the norA Transformant of Staphylococcus aureus. Antimicrob. Agents Chemother. 1998, 42, 1917-1922.
-
(1998)
Antimicrob. Agents Chemother
, vol.42
, pp. 1917-1922
-
-
Fukuda, H.1
Hori, S.2
Hiramatsu, K.3
-
38
-
-
44949241216
-
-
Method for dilution antibacterial susceptibility test for bacteria that grow aerobically, 4th ed.; approved standard M7-A4; NCCLS: Wayne, PA, 1997; 17, no. 2.
-
Method for dilution antibacterial susceptibility test for bacteria that grow aerobically, 4th ed.; approved standard M7-A4; NCCLS: Wayne, PA, 1997; Vol. 17, no. 2.
-
-
-
|