메뉴 건너뛰기




Volumn 35, Issue 5, 2012, Pages 791-795

Chalcomoracin and moracin C, new inhibitors of Staphylococcus aureus enoyl-acyl carrier protein reductase from Morus alba

Author keywords

Chalcomoracin; Enoyl acyl carrier protein reductase; FabI; Fatty acid synthesis; Moracin C; Staphylococcus aureus

Indexed keywords

ANTIINFECTIVE AGENT; CHALCOMORACIN; ENOYL ACYL CARRIER PROTEIN REDUCTASE (NADH); MORACIN C; MULBERRY EXTRACT; UNCLASSIFIED DRUG;

EID: 84861206271     PISSN: 09186158     EISSN: 13475215     Source Type: Journal    
DOI: 10.1248/bpb.35.791     Document Type: Article
Times cited : (42)

References (25)
  • 3
    • 28044455908 scopus 로고    scopus 로고
    • Antimicrobial activity of 2-aryl-benzofurans from Morus species against methicillin-resistant Staphylococcus aureus
    • Fukai T, Kaitou K, Terada S. Antimicrobial activity of 2-aryl-benzofurans from Morus species against methicillin-resistant Staphylococcus aureus. Fitoterapia, 76, 708-711 (2005).
    • (2005) Fitoterapia , vol.76 , pp. 708-711
    • Fukai, T.1    Kaitou, K.2    Terada, S.3
  • 4
    • 0034780806 scopus 로고    scopus 로고
    • Bacterial fatty acid biosynthesis: Targets for antibacterial drug discovery
    • Campbell JW, Cronan JE Jr. Bacterial fatty acid biosynthesis: targets for antibacterial drug discovery. Annu. Rev. Microbiol., 55, 305-332 (2001).
    • (2001) Annu. Rev. Microbiol. , vol.55 , pp. 305-332
    • Campbell, J.W.1    Cronan Jr., J.E.2
  • 5
    • 3042764816 scopus 로고    scopus 로고
    • Fatty acid biosynthesis as a target for novel antibacterials
    • Heath RJ, Rock CO. Fatty acid biosynthesis as a target for novel antibacterials. Curr. Opin. Investig. Drugs, 5, 146-153 (2004).
    • (2004) Curr. Opin. Investig. Drugs , vol.5 , pp. 146-153
    • Heath, R.J.1    Rock, C.O.2
  • 6
    • 26844550453 scopus 로고    scopus 로고
    • Identification of inhibitors of bacterial enoyl-acyl carrier protein reductase
    • Moir DT. Identification of inhibitors of bacterial enoyl-acyl carrier protein reductase. Curr. Drug Targets Infect. Disord., 5, 297-305 (2005).
    • (2005) Curr. Drug Targets Infect. Disord. , vol.5 , pp. 297-305
    • Moir, D.T.1
  • 7
    • 33745817391 scopus 로고    scopus 로고
    • Inhibiting bacterial fatty acid synthesis
    • Zhang YM, White SW, Rock CO. Inhibiting bacterial fatty acid synthesis. J. Biol. Chem., 281, 17541-17544 (2006).
    • (2006) J. Biol. Chem. , vol.281 , pp. 17541-17544
    • Zhang, Y.M.1    White, S.W.2    Rock, C.O.3
  • 8
    • 0032490937 scopus 로고    scopus 로고
    • Triclosan targets lipid synthesis
    • McMurry LM, Oethinger M, Levy SB. Triclosan targets lipid synthesis. Nature, 394, 531-532 (1998).
    • (1998) Nature , vol.394 , pp. 531-532
    • McMurry, L.M.1    Oethinger, M.2    Levy, S.B.3
  • 16
    • 64649097918 scopus 로고    scopus 로고
    • Vinaxanthone, a new FabI inhibitor from Penicillium sp
    • Zheng CJ, Sohn M-J, Kim W-G. Vinaxanthone, a new FabI inhibitor from Penicillium sp. J. Antimicrob. Chemother., 63, 949-953 (2009).
    • (2009) J. Antimicrob. Chemother. , vol.63 , pp. 949-953
    • Zheng, C.J.1    Sohn, M.-J.2    Kim, W.-G.3
  • 17
    • 33744819176 scopus 로고    scopus 로고
    • Inhibition of Plasmodium falciparum fatty acid biosynthesis: Evaluation of FabG, FabZ, and FabI as drug targets for flavonoids
    • Tasdemir D, Lack G, Brun R, Rüedi P, Scapozza L, Perozzo R. Inhibition of Plasmodium falciparum fatty acid biosynthesis: evaluation of FabG, FabZ, and FabI as drug targets for flavonoids. J. Med. Chem., 49, 3345-3353 (2006).
    • (2006) J. Med. Chem. , vol.49 , pp. 3345-3353
    • Tasdemir, D.1    Lack, G.2    Brun, R.3    Rüedi, P.4    Scapozza, L.5    Perozzo, R.6
  • 18
    • 3843101649 scopus 로고    scopus 로고
    • Evaluation of epigallocatechin gallate and related plant polyphenols as inhibitors of the FabG and FabI reductases of bacterial type II fatty-acid synthase
    • Zhang YM, Rock CO. Evaluation of epigallocatechin gallate and related plant polyphenols as inhibitors of the FabG and FabI reductases of bacterial type II fatty-acid synthase. J. Biol. Chem., 279, 30994-31001 (2004).
    • (2004) J. Biol. Chem. , vol.279 , pp. 30994-31001
    • Zhang, Y.M.1    Rock, C.O.2
  • 19
    • 0038779197 scopus 로고    scopus 로고
    • Genetic strategies for antibacterial drug discovery
    • Miesel L, Greene J, Black TA. Genetic strategies for antibacterial drug discovery. Nat. Rev. Genet., 4, 442-456 (2003).
    • (2003) Nat. Rev. Genet. , vol.4 , pp. 442-456
    • Miesel, L.1    Greene, J.2    Black, T.A.3
  • 20
  • 23
    • 24944448678 scopus 로고    scopus 로고
    • Fatty acid synthesis is a target for antibacterial activity of unsaturated fatty acids
    • Zheng CJ, Yoo J-S, Lee T-G, Cho H-Y, Kim Y-H, Kim W-G. Fatty acid synthesis is a target for antibacterial activity of unsaturated fatty acids. FEBS Lett., 579, 5157-5162 (2005).
    • (2005) FEBS Lett. , vol.579 , pp. 5157-5162
    • Zheng, C.J.1    Yoo, J.-S.2    Lee, T.-G.3    Cho, H.-Y.4    Kim, Y.-H.5    Kim, W.-G.6
  • 24
    • 79955540636 scopus 로고    scopus 로고
    • Whole-genome sequencing of Staphylococcus aureus strain RN4220, a key laboratory strain used in virulence research, identifies mutations that affect not only virulence factors but also the fitness of the strain
    • Nair D, Memmi G, Hernandez D, Bard J, Beaume M, Gill S, Francois P, Cheung AL. Whole-genome sequencing of Staphylococcus aureus strain RN4220, a key laboratory strain used in virulence research, identifies mutations that affect not only virulence factors but also the fitness of the strain. J. Bacteriol., 193, 2332-2335 (2011).
    • (2011) J. Bacteriol. , vol.193 , pp. 2332-2335
    • Nair, D.1    Memmi, G.2    Hernandez, D.3    Bard, J.4    Beaume, M.5    Gill, S.6    Francois, P.7    Cheung, A.L.8
  • 25
    • 0037461276 scopus 로고    scopus 로고
    • Structureactivity studies of the inhibition of FabI, the enoyl reductase from Escherichia coli, by triclosan: Kinetic analysis of mutant FabIs
    • Sivaraman S, Zwahlen J, Bell AF, Hedstrom L, Tonge PJ. Structureactivity studies of the inhibition of FabI, the enoyl reductase from Escherichia coli, by triclosan: kinetic analysis of mutant FabIs. Biochemistry, 42, 4406-4413 (2003).
    • (2003) Biochemistry , vol.42 , pp. 4406-4413
    • Sivaraman, S.1    Zwahlen, J.2    Bell, A.F.3    Hedstrom, L.4    Tonge, P.J.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.