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Volumn 94, Issue , 2014, Pages 48-54

Potential targets by pentacyclic triterpenoids from Callicarpa farinosa against methicillin-resistant and sensitive Staphylococcus aureus

Author keywords

Antimicrobial activity; Callicarpa farinosa; Mechanisms of action; Pentacyclic triterpenoids; Staphylococcus aureus

Indexed keywords

ABC TRANSPORTER; ALPHA AMYRIN [3BETA HYDROXY URS 12 EN 3 OL]; AMINO ACID TRANSFER RNA LIGASE; ANTIINFECTIVE AGENT; BETULINALDEHYDE [3BETA HYDROXY 20(29) LUPEN 28 AL]; BETULINIC ACID [3BETA HYDROXY 20(29) LUPAENE 28 OIC ACID]; CHLOROFORM; METHANOL; METICILLIN; PEPTIDOGLYCAN; TRITERPENOID; UNCLASSIFIED DRUG; VANCOMYCIN; AMYRIN; BETULIC ACID; OLEANOLIC ACID; PENTACYCLIC TRITERPENE; PLANT EXTRACT; TRANSCRIPTOME; TRITERPENE;

EID: 84894231634     PISSN: 0367326X     EISSN: 18736971     Source Type: Journal    
DOI: 10.1016/j.fitote.2014.01.026     Document Type: Article
Times cited : (43)

References (58)
  • 1
    • 33845711756 scopus 로고    scopus 로고
    • Prospects for plant-derived antibacterials
    • DOI 10.1038/nbt1206-1504, PII NBT12061504
    • K. Lewis, and F.M. Ausubel Prospects for plant-derived antibacterials Nat Biotechnol 24 2006 1504 1507 (Pubitemid 44967470)
    • (2006) Nature Biotechnology , vol.24 , Issue.12 , pp. 1504-1507
    • Lewis, K.1    Ausubel, F.M.2
  • 2
    • 33644636159 scopus 로고    scopus 로고
    • Genome of an epidemic community-acquired MRSA
    • DOI 10.1016/S0140-6736(06)68233-0, PII S0140673606682330
    • M.C. Enright Genome of an epidemic community-acquired MRSA Lancet 367 2006 705 706 (Pubitemid 43326270)
    • (2006) Lancet , vol.367 , Issue.9512 , pp. 705-706
    • Enright, M.C.1
  • 3
    • 1942502195 scopus 로고    scopus 로고
    • Anti-staphylococcal plant natural products
    • DOI 10.1039/b212695h
    • S. Gibbons Anti-staphylococcal plant natural products Nat Prod Rep 21 2004 263 277 (Pubitemid 38527319)
    • (2004) Natural Product Reports , vol.21 , Issue.2 , pp. 263-277
    • Gibbons, S.1
  • 4
    • 0033737532 scopus 로고    scopus 로고
    • Activity of tea component epicatechin gallate and analogues against methicillin-resistant Staphylococcus aureus
    • J.M. Hamilton-Miller, and S. Shah Activity of tea component epicatechin gallate and analogues against methicillin-resistant Staphylococcus aureus J Antimicrob Chemother 46 2000 852 853
    • (2000) J Antimicrob Chemother , vol.46 , pp. 852-853
    • Hamilton-Miller, J.M.1    Shah, S.2
  • 5
    • 0032820601 scopus 로고    scopus 로고
    • Potentiation of methicillin activity against methicillin-resistant Staphylococcus aureus by diterpenes
    • DOI 10.1016/S0378-1097(99)00417-6, PII S0378109799004176
    • K. Nicholson, G. Evans, and P.W. O'Toole Potentiation of methicillin activity against methicillin-resistant Staphylococcus aureus by diterpene FEMS Microbiol Lett 179 1999 233 239 (Pubitemid 29460683)
    • (1999) FEMS Microbiology Letters , vol.179 , Issue.2 , pp. 233-239
    • Nicolson, K.1    Evans, G.2    O'Toole, P.W.3
  • 6
    • 0034780297 scopus 로고    scopus 로고
    • Marked potentiation of activity of β-lactams against methicillin-resistant Staphylococcus aureus by corilagin
    • M. Shimizu, S. Shiota, and T. Mizushima et al. Marked potentiation of activity of β-lactams against methicillin-resistant Staphylococcus aureus by corilagin Antimicrob Agents Chemother 45 2001 3198 3210
    • (2001) Antimicrob Agents Chemother , vol.45 , pp. 3198-3210
    • Shimizu, M.1    Shiota, S.2    Mizushima, T.3
  • 7
    • 0034656247 scopus 로고    scopus 로고
    • Mechanism of action of corilagin and tellimagrandin i that remarkably potentiate the activity of β-lactams against methicillin-resistant Staphylococcus aureus
    • S. Shiota, M. Shimizu, and T. Mizusima et al. Mechanism of action of corilagin and tellimagrandin I that remarkably potentiate the activity of β-lactams against methicillin-resistant Staphylococcus aureus FEMS Microbiol Lett 185 2000 135 138
    • (2000) FEMS Microbiol Lett , vol.185 , pp. 135-138
    • Shiota, S.1    Shimizu, M.2    Mizusima, T.3
  • 9
    • 21644464831 scopus 로고    scopus 로고
    • Antimicrobial activity of some pentacyclic triterpenes and their synthesized 3-O-lipophilic chains
    • DOI 10.1248/bpb.27.1576
    • U.V. Mallavadhani, A. Mahapatra, K. Jamil, and P.S. Reddy Antimicrobial activity of some pentacyclic triterpenes and their synthesized 3-O-lipophilic chain Biol Pharm Bull 27 2004 1576 1579 (Pubitemid 41701642)
    • (2004) Biological and Pharmaceutical Bulletin , vol.27 , Issue.10 , pp. 1576-1579
    • Mallavadhani, U.V.1    Mahapatra, A.2    Jamil, K.3    Reddy, P.S.4
  • 10
    • 0037328647 scopus 로고    scopus 로고
    • Isolation, characterization and biological activity of betulinic acid and ursolic acid from Vitex negundo L.
    • DOI 10.1002/ptr.1088
    • C. Chandramu, R.D. Manohar, D.G. Krupadanam, and R.V. Dashavantha Isolation, characterization and biological activity of betulinic acid and ursolic acid from Vitex negundo L Phytother Res 17 2003 129 134 (Pubitemid 36262260)
    • (2003) Phytotherapy Research , vol.17 , Issue.2 , pp. 129-134
    • Chandramu, C.1    Manohar, R.D.2    Krupadanam, D.G.L.3    Dashavantha, R.V.4
  • 11
    • 0041474914 scopus 로고    scopus 로고
    • Antimicrobial activity of terpenoids from Trichodesma amplexicaule Roth.
    • DOI 10.1002/ptr.1202
    • B. Singh, and S. Singh Antimicrobial activity of terpenoids from Trichodesma amplexicaule Roth Phytother Res 17 2003 814 816 (Pubitemid 37020938)
    • (2003) Phytotherapy Research , vol.17 , Issue.7 , pp. 814-816
    • Singh, B.1    Singh, S.2
  • 12
    • 18744405406 scopus 로고    scopus 로고
    • Antimicrobial activity of 6-oxophenolic triterpenoids. Mode of action against Bacillus subtilis
    • DOI 10.1055/s-2005-864096
    • L. de Leon, B. Beltran, and L. Moujir Antimicrobial activity of 6-oxophenolic triterpenoids: mode of action against Bacillus subtilis Planta Med 71 2005 313 319 (Pubitemid 40676454)
    • (2005) Planta Medica , vol.71 , Issue.4 , pp. 313-319
    • De Leon, L.1    Beltran, B.2    Moujir, L.3
  • 13
    • 0037403328 scopus 로고    scopus 로고
    • Antimicrobial activity of pentacyclic triterpenes isolated from African Combretaceae
    • DOI 10.1016/S0031-9422(02)00726-4, PII S0031942202007264
    • D.R. Katerere, A.I. Gray, R.J. Nash, and R.D. Waigh Antimicrobial activity of pentacyclic triterpenes isolated from African Combretaceae Phytochemistry 63 2003 81 88 (Pubitemid 36427443)
    • (2003) Phytochemistry , vol.63 , Issue.1 , pp. 81-88
    • Katerere, D.R.1    Gray, A.I.2    Nash, R.J.3    Waigh, R.D.4
  • 14
    • 0033060031 scopus 로고    scopus 로고
    • Antimicrobial triterpenes from Ilex integra and the mechanism of antifungal action
    • DOI 10.1002/(SICI)1099-1573(199903)13:2<151::AID-PTR391>3.0.CO;2-C
    • H. Haraguchi, S. Kataoka, S. Okamoto, M. Hanafi, and K. Shibata Antimicrobial triterpenes from Ilex integra and the mechanism of antifungal action Phytother Res 13 1999 151 156 (Pubitemid 29129451)
    • (1999) Phytotherapy Research , vol.13 , Issue.2 , pp. 151-156
    • Haraguchi, H.1    Kataoka, S.2    Okamoto, S.3    Hanafi, M.4    Shibata, K.5
  • 15
    • 0029567968 scopus 로고
    • Pharmacology of oleanolic acid and ursolic acid
    • DOI 10.1016/0378-8741(95)01310-5
    • J. Liu Pharmacology of oleanolic acid and ursolic acid J Ethnopharmacol 49 1995 57 68 (Pubitemid 26010740)
    • (1995) Journal of Ethnopharmacology , vol.49 , Issue.2 , pp. 57-68
    • Liu, J.1
  • 16
    • 58649094196 scopus 로고    scopus 로고
    • Antimicrobial activity of pentacyclic triterpenes isolated from Acacia mellifera
    • C. Mutai, C. Bii, and G. Rukunga et al. Antimicrobial activity of pentacyclic triterpenes isolated from Acacia mellifera Afr J Tradit Complement Alternat Med 6 2009 42 48
    • (2009) Afr J Tradit Complement Alternat Med , vol.6 , pp. 42-48
    • Mutai, C.1    Bii, C.2    Rukunga, G.3
  • 17
    • 0033884057 scopus 로고    scopus 로고
    • Inhibitors of aminoacyl-tRNA synthetases as novel anti-infectives
    • J. Tao, and P. Schimmel Inhibitors of amino-acyl tRNA synthetase as novel anti-infectives Expert Opin Invest Drugs 9 2000 1767 1775 (Pubitemid 30639327)
    • (2000) Expert Opinion on Investigational Drugs , vol.9 , Issue.8 , pp. 1767-1775
    • Tao, J.1    Schimmel, P.2
  • 21
    • 18744405406 scopus 로고    scopus 로고
    • Antimicrobial activity of 6-oxophenolic triterpenoids. Mode of action against Bacillus subtilis
    • DOI 10.1055/s-2005-864096
    • L. de Leon, B. Beltran, and L. Moujir Antimicrobial activity of 6-oxophenolic triterpenoids. Mode of action against Bacillus subtilis Planta Med 71 2005 313 319 (Pubitemid 40676454)
    • (2005) Planta Medica , vol.71 , Issue.4 , pp. 313-319
    • De Leon, L.1    Beltran, B.2    Moujir, L.3
  • 23
    • 84874282682 scopus 로고    scopus 로고
    • Transcriptional profiles of the response of methicillin-resistant Staphylococcus aureus to pentacyclic triterpenoids
    • P.Y. Chung, L.Y. Chung, and P. Navaratnam Transcriptional profiles of the response of methicillin-resistant Staphylococcus aureus to pentacyclic triterpenoids PLoS One 8 2013 e56687
    • (2013) PLoS One , vol.8 , pp. 56687
    • Chung, P.Y.1    Chung, L.Y.2    Navaratnam, P.3
  • 24
    • 84876964599 scopus 로고    scopus 로고
    • Identification of novel gene targets in Staphylococcus aureus treated with betulinaldehyde by gene expression profiling analysis
    • P.Y. Chung, L.Y. Chung, and P. Navaratnam Identification of novel gene targets in Staphylococcus aureus treated with betulinaldehyde by gene expression profiling analysis Res Microbiol 164 2013 319 326
    • (2013) Res Microbiol , vol.164 , pp. 319-326
    • Chung, P.Y.1    Chung, L.Y.2    Navaratnam, P.3
  • 25
    • 3042636640 scopus 로고    scopus 로고
    • Constituents from the non-polar fraction of Artemisia apiacea
    • S. Lee, K.S. Kim, S.H. Shim, Y.M. Park, and B.K. Kim Constituents from the non-polar fraction of Artemisia apiacea Arch Pharm Res 26 2003 902 905
    • (2003) Arch Pharm Res , vol.26 , pp. 902-905
    • Lee, S.1    Kim, K.S.2    Shim, S.H.3    Park, Y.M.4    Kim, B.K.5
  • 26
    • 0035068929 scopus 로고    scopus 로고
    • Diospyros melanoxylon leaves: A rich source of pentacyclic triterpenes
    • DOI 10.1076/phbi.39.1.20.5941
    • U.V. Mallavadhni, A.K. Panda, and Y.R. Rao Diospyros melanoxylon leaves: a rich source of pentacyclic triterpenes Pharm Biol 39 2001 20 24 (Pubitemid 32234171)
    • (2001) Pharmaceutical Biology , vol.39 , Issue.1 , pp. 20-24
    • Mallavadhani, U.V.1    Panda, A.K.2    Rao, Y.R.3
  • 27
    • 33646479939 scopus 로고    scopus 로고
    • Cytotoxic terpenes and lignans from the roots of Ainsliaea acerifolia
    • S.Z. Choi, M.C. Yang, S.U. Choi, and K.R. Lee Cytotoxic terpenes and lignans from the roots of Ainsliaea acerifolia Arch Pharm Res 29 2006 203 208
    • (2006) Arch Pharm Res , vol.29 , pp. 203-208
    • Choi, S.Z.1    Yang, M.C.2    Choi, S.U.3    Lee, K.R.4
  • 28
    • 0642312371 scopus 로고    scopus 로고
    • A new acylglycosyl sterol from Quisqualis fructus
    • H.C. Kwon, Y.D. Min, and K.R. Kim et al. A new acylglycosyl sterol from Quisqualis fructus Arch Pharm Res 26 2003 275 278
    • (2003) Arch Pharm Res , vol.26 , pp. 275-278
    • Kwon, H.C.1    Min, Y.D.2    Kim, K.R.3
  • 29
    • 0033831223 scopus 로고    scopus 로고
    • Biotransformation of the antimelanoma agent betulinic acid by Bacillus megaterium ATCC 13368
    • P. Chatterjee, S.A. Kouzi, J.M. Pezzuto, and M.T. Hamann Biotransformation of the antimelanoma agent betulinic acid by Bacillus megaterium ATCC 13368 Appl Environ Microbiol 66 2000 3850 3855
    • (2000) Appl Environ Microbiol , vol.66 , pp. 3850-3855
    • Chatterjee, P.1    Kouzi, S.A.2    Pezzuto, J.M.3    Hamann, M.T.4
  • 30
    • 0028248808 scopus 로고
    • 13C NMR spectra of pentacyclic triterpenoids - A compilation and some salient features
    • 13C NMR spectra of pentacyclic triterpenoids - a compilation and some salient features Phytochemistry 37 1994 1517 1575
    • (1994) Phytochemistry , vol.37 , pp. 1517-1575
    • Mahato, S.B.1    Kundu, A.P.2
  • 31
    • 0019166638 scopus 로고
    • 13C nuclear magnetic resonance of lupane-type triterpenes, lupeol, betulin and betulinic acid
    • 13C nuclear magnetic resonance of lupane-type triterpenes, lupeol, betulin and betulinic acid Chem Pharm Bull (Tokyo) 28 1980 1006 1008 (Pubitemid 11248173)
    • (1980) Chemical and Pharmaceutical Bulletin , vol.28 , Issue.3 , pp. 1006-1008
    • Sholichin, M.1    Yamasaki, K.2    Kasai, R.3
  • 32
    • 0001573973 scopus 로고
    • Betulinic acid from Arbutus menziesii
    • F.P. Robinson, and H. Martel Betulinic acid from Arbutus menziesii Phytochemistry 9 1970 907 909
    • (1970) Phytochemistry , vol.9 , pp. 907-909
    • Robinson, F.P.1    Martel, H.2
  • 33
    • 0034946241 scopus 로고    scopus 로고
    • Cytotoxic activity of moronic acid and identification of the new triterpene 3,4-seco-olean-18-ene-3,28-dioic acid from Phoradendron reichenbachianum
    • DOI 10.1055/s-2001-15823
    • M.Y. Rios, D. Salina, and M.L. Villarreal Cytotoxic activity of moronic acid and identification of the new triterpene 3,4-seco-olean-18-ene-3,28-dioic acid from Phoradendron reichenbachianum Planta Med 67 2001 443 446 (Pubitemid 32652581)
    • (2001) Planta Medica , vol.67 , Issue.5 , pp. 443-446
    • Rios, M.Y.1    Salinas, D.2    Villarreal, M.L.3
  • 34
    • 0028131980 scopus 로고
    • Antibacterial triterpenoid acids from Dillenia papuana
    • DOI 10.1021/np50111a009
    • A. Nick, A.D. Wright, O. Sticher, and T. Rali Antibacterial triterpenoid acids from Dillenia papuana J Nat Prod 57 1994 1245 1250 (Pubitemid 24333035)
    • (1994) Journal of Natural Products , vol.57 , Issue.9 , pp. 1245-1250
    • Nick, A.1    Wright, A.D.2    Sticher, O.3
  • 35
    • 0018120172 scopus 로고
    • The constituents of Scirpus fluviatilis (Torr.) A. Gray. I. The structures of two new hydroxystilbene dimers, scirpusin A and B
    • K. Nakajima, K.H. Taguchi, T. Endo, and I. Yosioka The constituents of Scirpus fluviatilis (Torr.) A. Gray. I. The structures of two new hydroxystibene dimers, Scirpusin A and B Chem Pharm Bull (Tokyo) 26 1978 3050 3057 (Pubitemid 9050293)
    • (1978) Chemical and Pharmaceutical Bulletin , vol.26 , Issue.10 , pp. 3050-3057
    • Nakajima, K.1    Taguchi, H.2    Endo, T.3    Yosioka, I.4
  • 36
    • 49549136090 scopus 로고
    • The isolation from Sarracenia flava and partial synthesis of betulinaldehyde
    • J. Bhattacharyya, U. Kokpol, and D.H. Miles The isolation from Sarracenia flava and partial synthesis of betulinaldehyde Phytochemistry 15 1976 432 433
    • (1976) Phytochemistry , vol.15 , pp. 432-433
    • Bhattacharyya, J.1    Kokpol, U.2    Miles, D.H.3
  • 39
    • 54749137299 scopus 로고    scopus 로고
    • Biologically active natural products of the genus Callicarpa
    • W.P. Jones, and A.D. Kinghorn Biologically active natural products of the genus Callicarpa Curr Bioactive Comp 4 2008 5 32
    • (2008) Curr Bioactive Comp , vol.4 , pp. 5-32
    • Jones, W.P.1    Kinghorn, A.D.2
  • 40
    • 84875226527 scopus 로고    scopus 로고
    • The medicinal uses of Callicarpa L. in traditional Chinese medicine: An ethnopharmacological, phytochemical and pharmacological review
    • Y. Tu, L. Sun, M. Guo, and W. Chen The medicinal uses of Callicarpa L. in traditional Chinese medicine: an ethnopharmacological, phytochemical and pharmacological review J Ethnopharmacol 146 2013 465 481
    • (2013) J Ethnopharmacol , vol.146 , pp. 465-481
    • Tu, Y.1    Sun, L.2    Guo, M.3    Chen, W.4
  • 41
    • 9144249001 scopus 로고    scopus 로고
    • Allochemical potential of Callicarpa acuminata
    • A.L. Anaya, R. Mata, and J.J. Sims et al. Allochemical potential of Callicarpa acuminata J Chem Ecol 29 2003 2761 2776
    • (2003) J Chem Ecol , vol.29 , pp. 2761-2776
    • Anaya, A.L.1    Mata, R.2    Sims, J.J.3
  • 42
    • 54749129112 scopus 로고    scopus 로고
    • Chemical constituents of Callicarpa pedunculata
    • X. Gao, Z. Li, and R. Zhang Chemical constituents of Callicarpa pedunculata Huaxi Yaoxue Zashi 15 2000 358 359
    • (2000) Huaxi Yaoxue Zashi , vol.15 , pp. 358-359
    • Gao, X.1    Li, Z.2    Zhang, R.3
  • 43
    • 23444460416 scopus 로고    scopus 로고
    • Studies on flavonoids from leaves of Callicarpa bodinieri
    • F. Ren, X. Luan, Y. Zhao, and H. Qu Studies on flavonoids from leaves of Callicarpa bodinieri Zhongguo Zhong Yao Za Zhi 26 2001 841 844
    • (2001) Zhongguo Zhong Yao Za Zhi , vol.26 , pp. 841-844
    • Ren, F.1    Luan, X.2    Zhao, Y.3    Qu, H.4
  • 44
    • 0001277056 scopus 로고
    • Terpenoids and related compounds. Part 32. Calliphyllin, a new diterpene from the leaves of Callicarpa macrophylla
    • S.K. Talapatra, M. Polley, and B. Talapatra Terpenoids and related compounds. Part 32. Calliphyllin, a new diterpene from the leaves of Callicarpa macrophylla J Ind Chem Soc 71 1994 527 532
    • (1994) J Ind Chem Soc , vol.71 , pp. 527-532
    • Talapatra, S.K.1    Polley, M.2    Talapatra, B.3
  • 45
    • 0040138101 scopus 로고
    • Chemical examination of Callicarpa macrophylla, Lagerstromea lanceolata, Ficus palmata, and Taxodium mucronatum
    • S.A. Ahmad, S.A. Siddiqui, and A. Zaman Chemical examination of Callicarpa macrophylla, Lagerstromea lanceolata, Ficus palmata, and Taxodium mucronatum J Ind Chem Soc 53 1976 1165 1166
    • (1976) J Ind Chem Soc , vol.53 , pp. 1165-1166
    • Ahmad, S.A.1    Siddiqui, S.A.2    Zaman, A.3
  • 46
    • 0033850007 scopus 로고    scopus 로고
    • Four new clerodane diterpenoids from Callicarpa pentandra
    • J. Xu, L.J. Harrison, J.J. Vittal, Y. Xu, and S. Goh Four new clerodane diterpenoids from Callicarpa pentandra J Nat Prod 63 2000 1062 1065
    • (2000) J Nat Prod , vol.63 , pp. 1062-1065
    • Xu, J.1    Harrison, L.J.2    Vittal, J.J.3    Xu, Y.4    Goh, S.5
  • 47
    • 28044446224 scopus 로고
    • Vedantham TNC terpenoids and flavones of Callicarpa macrophylla and C. Longifolia
    • S.S. Subramaniam, and A.G.R. Nair Vedantham TNC terpenoids and flavones of Callicarpa macrophylla and C. longifolia Phytochemistry 13 1974 306 307
    • (1974) Phytochemistry , vol.13 , pp. 306-307
    • Subramaniam, S.S.1    Nair, A.G.R.2
  • 48
    • 79958067241 scopus 로고    scopus 로고
    • Synergistic antimicrobial activity between pentacyclic triterpenoids and antibiotics against Staphylococcus aureus strains
    • P.Y. Chung, P. Navaratnam, and L.Y. Chung Synergistic antimicrobial activity between pentacyclic triterpenoids and antibiotics against Staphylococcus aureus strains Ann Clin Microbiol Antimicrob 10 2011 25
    • (2011) Ann Clin Microbiol Antimicrob , vol.10 , pp. 25
    • Chung, P.Y.1    Navaratnam, P.2    Chung, L.Y.3
  • 49
    • 9144263033 scopus 로고    scopus 로고
    • New aminoacyl-tRNA synthetase inhibitors as antibacterial agents
    • DOI 10.2174/1568005043340515
    • J. Pohlmann, and H. Brotz-Oesterhelt New aminoacyl-tRNA synthetase inhibitors as antibacterial agents Curr Drug Targets Infect Disord 4 2004 261 272 (Pubitemid 39539181)
    • (2004) Current Drug Targets - Infectious Disorders , vol.4 , Issue.4 , pp. 261-272
    • Pohlmann, J.1    Brotz-Oesterhelt, H.2
  • 50
    • 0029126262 scopus 로고
    • Occurrence of the regulatory nucleotides ppGpp and pppGpp following induction of the stringent response in staphylococci
    • R. Cassels, B. Olivia, and D. Knowles Occurrence of the regulatory nucleotides ppGpp and pppGpp following induction of the stringent response in staphylococci J Bacteriol 177 1995 5161 5165
    • (1995) J Bacteriol , vol.177 , pp. 5161-5165
    • Cassels, R.1    Olivia, B.2    Knowles, D.3
  • 51
    • 39149115737 scopus 로고    scopus 로고
    • Membrane lipid homeostasis in bacteria
    • DOI 10.1038/nrmicro1839, PII NRMICRO1839
    • Y. Zhang, and C.O. Rock Membrane lipid homeostasis in bacteria Nat Rev Microbiol 6 2008 222 233 (Pubitemid 351256317)
    • (2008) Nature Reviews Microbiology , vol.6 , Issue.3 , pp. 222-233
    • Zhang, Y.-M.1    Rock, C.O.2
  • 52
    • 68549092791 scopus 로고    scopus 로고
    • Targeting FtsZ for antibacterial therapy: A promising avenue
    • S. Kapoor, and D. Panda Targeting FtsZ for antibacterial therapy: a promising avenue Expert Opin Ther Targets 13 2009 1037 1051
    • (2009) Expert Opin Ther Targets , vol.13 , pp. 1037-1051
    • Kapoor, S.1    Panda, D.2
  • 53
    • 73649122749 scopus 로고    scopus 로고
    • An oldie but goodie - Cell wall biosynthesis as antibiotic target pathway
    • T. Schneider, and H. Sahl An oldie but goodie - cell wall biosynthesis as antibiotic target pathway Int J Med Microbiol 300 2010 161 169
    • (2010) Int J Med Microbiol , vol.300 , pp. 161-169
    • Schneider, T.1    Sahl, H.2
  • 54
    • 0043166886 scopus 로고    scopus 로고
    • Two-component system VraSR positively modulates the regulation of cell-wall biosynthesis pathway in Staphylococcus aureus
    • DOI 10.1046/j.1365-2958.2003.03599.x
    • M. Kuroda, H. Kuroda, and T. Oshima et al. Two-component system VraSR positively modulates the regulation of cell-wall biosynthesis pathway in Staphylococcus aureus Mol Microbiol 49 2003 807 821 (Pubitemid 36918698)
    • (2003) Molecular Microbiology , vol.49 , Issue.3 , pp. 807-821
    • Kuroda, M.1    Kuroda, H.2    Oshima, T.3    Takeuchi, F.4    Mori, H.5    Hiramatsu, K.6
  • 55
    • 77950685616 scopus 로고    scopus 로고
    • In the Staphylococcus aureus two-component system sae, the response regulator SaeR binds to a direct repeat sequence and DNA binding requires phosphorylation by the sensor kinase SaeS
    • F. Sun, C. Li, and D. Jeong et al. In the Staphylococcus aureus two-component system sae, the response regulator SaeR binds to a direct repeat sequence and DNA binding requires phosphorylation by the sensor kinase SaeS J Bacteriol 192 2010 2111 2127
    • (2010) J Bacteriol , vol.192 , pp. 2111-2127
    • Sun, F.1    Li, C.2    Jeong, D.3
  • 57
    • 36248994803 scopus 로고    scopus 로고
    • The targets of currently used antibacterial agents: Lessons for drug discovery
    • DOI 10.2174/138161207782110408
    • R.P. Lange, H.H. Locher, P.C. Wyss, and R.L. Then The targets of currently used antibacterial agents: lessons for drug discovery Curr Pharm Des 13 2007 3140 3154 (Pubitemid 350130963)
    • (2007) Current Pharmaceutical Design , vol.13 , Issue.30 , pp. 3140-3154
    • Lange, R.P.1    Locher, H.H.2    Wyss, P.C.3    Then, R.L.4
  • 58
    • 33845894155 scopus 로고    scopus 로고
    • Multi-targeting by monotherapeutic antibacterials
    • DOI 10.1038/nrd2202, PII NRD2202
    • L.L. Silver Multi-targeting by monotherapeutic antibacterials Nat Rev Drug Disc 6 2007 41 55 (Pubitemid 46020285)
    • (2007) Nature Reviews Drug Discovery , vol.6 , Issue.1 , pp. 41-55
    • Silver, L.L.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.