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Volumn 57, Issue 8, 2004, Pages 518-527

In vitro and in vivo antibacterial activities of the tricyclic ketolide TE-802 and its analogs

Author keywords

[No Author keywords available]

Indexed keywords

AZITHROMYCIN; CLARITHROMYCIN; KETOLIDE; MACROLIDE; ROKITAMYCIN; TE 802; TE 806; TE 935; TE 943; UNCLASSIFIED DRUG;

EID: 4544293607     PISSN: 00218820     EISSN: None     Source Type: Journal    
DOI: 10.7164/antibiotics.57.518     Document Type: Article
Times cited : (21)

References (15)
  • 1
    • 0021329213 scopus 로고
    • Chemical modification of erythromycins I. Synthesis and antibacterial activity of 6-O-methylerythromycin A
    • Morimoto, S.; Y. Takahashi, Y. Watanabe & S. Omura: Chemical modification of erythromycins I. Synthesis and antibacterial activity of 6-O-methylerythromycin A. J. Antibiotics 37: 187-189, 1984
    • (1984) J. Antibiotics , vol.37 , pp. 187-189
    • Morimoto, S.1    Takahashi, Y.2    Watanabe, Y.3    Omura, S.4
  • 4
    • 1642572519 scopus 로고
    • Preparation of 5-O-deososaminyl erythronolide A derivatives as antibacterial agents
    • WO 9321200
    • Asaka, T.; M. Kashimura, Y. Misawa, S. Morimoto & K. Hatayama: Preparation of 5-O-deososaminyl erythronolide A derivatives as antibacterial agents. WO 9321200, 1993
    • (1993)
    • Asaka, T.1    Kashimura, M.2    Misawa, Y.3    Morimoto, S.4    Hatayama, K.5
  • 5
    • 0034824275 scopus 로고    scopus 로고
    • Synthesis and antibacterial activity of the tricyclic ketolides TE-802 and its analogs
    • Kashimura, M.; T. Asaka, Y. Misawa, K. Matsumoto & S. Morimoto: Synthesis and antibacterial activity of the tricyclic ketolides TE-802 and its analogs. J. Antibiotics 54: 664-678, 2001
    • (2001) J. Antibiotics , vol.54 , pp. 664-678
    • Kashimura, M.1    Asaka, T.2    Misawa, Y.3    Matsumoto, K.4    Morimoto, S.5
  • 6
    • 1642462119 scopus 로고    scopus 로고
    • The synthesis and antibacterial activity of tetracyclic macrolides
    • Kashimura, M.; T. Asaka, K. Suzuki & S. Morimoto: The synthesis and antibacterial activity of tetracyclic macrolides. J. Antibiotics 56: 1062-1066, 2003
    • (2003) J. Antibiotics , vol.56 , pp. 1062-1066
    • Kashimura, M.1    Asaka, T.2    Suzuki, K.3    Morimoto, S.4
  • 7
    • 26744476630 scopus 로고    scopus 로고
    • Preparation of multicyclic erythromycins as bactericides
    • WO 98541979
    • Or, Y. S.; G. W. Griesgraber & D. T. Chu: Preparation of multicyclic erythromycins as bactericides. WO 98541979, 1998
    • (1998)
    • Or, Y.S.1    Griesgraber, G.W.2    Chu, D.T.3
  • 8
    • 1642572517 scopus 로고    scopus 로고
    • Preparation of 9a,11b-dehydro derivatives of 9-oxime-3-keto-6-O-methylerythromycin as bactericides
    • EP 952157
    • Wu, Y. J.: Preparation of 9a,11b-dehydro derivatives of 9-oxime-3-keto-6-O-methylerythromycin as bactericides. EP 952157, 1999
    • (1999)
    • Wu, Y.J.1
  • 9
    • 1642531757 scopus 로고    scopus 로고
    • Preparation of erythromycins as antibacterial agents
    • WO 9851696
    • Wu, Y. J.: Preparation of erythromycins as antibacterial agents. WO 9851696, 1998
    • (1998)
    • Wu, Y.J.1
  • 11
    • 0010670648 scopus 로고    scopus 로고
    • 2-Substituted tricyclic ketolides: New antibacterial macrolides-synthesis and biological activity
    • 38th Intersci. Conf. Antimicrob. Agents Chemother. San Diego, CA Abstr. F-127
    • Phan, L. T.; Y. S. Or, Y. Chen, D. T. W. Chu, P. Ewing, A. M. Nilius, M. H. Bui, P. M. Raney, D. Hensey-Rudloff, M. Mitten & J. J. Plattner: 2-Substituted tricyclic ketolides: New antibacterial macrolides-synthesis and biological activity. 38th Intersci. Conf. Antimicrob. Agents Chemother. San Diego, CA, 1998; Abstr. F-127
    • (1998)
    • Phan, L.T.1    Or, Y.S.2    Chen, Y.3    Chu, D.T.W.4    Ewing, P.5    Nilius, A.M.6    Bui, M.H.7    Raney, P.M.8    Hensey-Rudloff, D.9    Mitten, M.10    Plattner, J.J.11
  • 12
    • 0019858719 scopus 로고
    • Acyl derivatives of 16-membered macrolides. I. Synthesis and biological properties of 3″-O-propionylleucomycin A5 (TMS-19-Q)
    • Sakakibara, H.; O. Okekawa, T. Fujiwara, M. Otani & S. Omura: Acyl derivatives of 16-membered macrolides. I. Synthesis and biological properties of 3″-O-propionylleucomycin A5 (TMS-19-Q). J. Antibiotics 34: 1001-1010, 1981
    • (1981) J. Antibiotics , vol.34 , pp. 1001-1010
    • Sakakibara, H.1    Okekawa, O.2    Fujiwara, T.3    Otani, M.4    Omura, S.5
  • 13
    • 0002292977 scopus 로고
    • Japan Society of Chemotherapy: Revised method for determining the minimun inhibitory concentration (MIC)
    • Japan Society of Chemotherapy: Revised method for determining the minimun inhibitory concentration (MIC). Chemotherapy (Tokyo) 29: 76-79, 1981
    • (1981) Chemotherapy (Tokyo) , vol.29 , pp. 76-79
  • 14
    • 4544310473 scopus 로고
    • The maximum likehood solution
    • 2nd. Ed. Ed., D. J. Finney, Cambridge University Press
    • Finney, D. J.: The maximum likehood solution. In Probit Analysis. 2nd. Ed. Ed., D. J. Finney, pp. 48-64, Cambridge University Press, 1952
    • (1952) Probit Analysis , pp. 48-64
    • Finney, D.J.1
  • 15
    • 0003262335 scopus 로고    scopus 로고
    • Molecular basis of ABT-773 activity against ermcontaining macrolide resistant S. pneumoniae
    • 5th ICMAS-KO. Seville, Spain, Poster No. 02.16
    • Zhong, P.; R. Hammond, Z. Cao, Y. Chen, D. Shortridge, A. Nilius, R. K. Flamm & Y. S. Or: Molecular basis of ABT-773 activity against ermcontaining macrolide resistant S. pneumoniae. 5th ICMAS-KO. Seville, Spain, 2000; Poster No. 02.16
    • (2000)
    • Zhong, P.1    Hammond, R.2    Cao, Z.3    Chen, Y.4    Shortridge, D.5    Nilius, A.6    Flamm, K.7    Or, Y.S.8


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.