메뉴 건너뛰기




Volumn 13, Issue 24, 2013, Pages 3118-3130

Exploration of structure-based on Imidazole core as antibacterial agents

Author keywords

Antibacterial activity; Antibacterial agents; Docking; Imidazole; Kinase inhibitor; QSAR; Resistance to antibiotics; Structure activity relationship

Indexed keywords

ANTIINFECTIVE AGENT; BENZIMIDAZOLE DERIVATIVE; BETA LACTAMASE INHIBITOR; DNA TOPOISOMERASE (ATP HYDROLYSING); DNA TOPOISOMERASE INHIBITOR; FATTY ACID SYNTHASE INHIBITOR; GLUTAMATE RACEMASE INHIBITOR; GYRASE INHIBITOR; IMIDAZOLE DERIVATIVE; ISOMERASE INHIBITOR; UNCLASSIFIED DRUG; UREASE INHIBITOR;

EID: 84890907215     PISSN: 15680266     EISSN: 18734294     Source Type: Journal    
DOI: 10.2174/15680266113136660222     Document Type: Review
Times cited : (24)

References (117)
  • 1
    • 73549121712 scopus 로고    scopus 로고
    • Synthesis of nitroimidazole derived oxazolidinones as antibacterial agents
    • Varshney, V.; Mishra, N.N.; Shukla, P.K.; Sahu, D.P. Synthesis of nitroimidazole derived oxazolidinones as antibacterial agents. Eur. J. Med. Chem., 2010, 45(2), 661-666.
    • (2010) Eur. J. Med. Chem , vol.45 , Issue.2 , pp. 661-666
    • Varshney, V.1    Mishra, N.N.2    Shukla, P.K.3    Sahu, D.P.4
  • 2
    • 33644504461 scopus 로고    scopus 로고
    • Antibacterial drug discovery-then, now and the genomics future
    • Monaghan, R.L.; Barrett, J.F. Antibacterial drug discovery-then, now and the genomics future. Biochem. Pharmacol., 2006, 71(7), 901-909.
    • (2006) Biochem. Pharmacol , vol.71 , Issue.7 , pp. 901-909
    • Monaghan, R.L.1    Barrett, J.F.2
  • 3
    • 17844368362 scopus 로고    scopus 로고
    • Mortality risk factors with nosocomial Staphylococcus aureus infections in intensive care units: Results from the German Nosocomial Infection Surveillance System (KISS)
    • Gastmeier, P.; Sohr, D.; Geffers, C.; Behnke, M.; Daschner, F.; Ruden, H. Mortality risk factors with nosocomial Staphylococcus aureus infections in intensive care units: results from the German Nosocomial Infection Surveillance System (KISS). Infection, 2005, 33(2), 50-55.
    • (2005) Infection , vol.33 , Issue.2 , pp. 50-55
    • Gastmeier, P.1    Sohr, D.2    Geffers, C.3    Behnke, M.4    Daschner, F.5    Ruden, H.6
  • 4
    • 79957482244 scopus 로고    scopus 로고
    • 3-(1,3,4-Thiadiazole-2-yl)quinoline derivatives: Synthesis, characterization and anti-microbial activity
    • Bhat, A.R.; Tazeem; Azam, A.; Choi, I.; Athar, F. 3-(1,3,4-Thiadiazole-2-yl)quinoline derivatives: synthesis, characterization and anti-microbial activity. Eur. J. Med. Chem., 2011, 46(7), 3158-3166.
    • (2011) Eur. J. Med. Chem , vol.46 , Issue.7 , pp. 3158-3166
    • Bhat, A.R.1    Tazeem2    Azam, A.3    Choi, I.4    Athar, F.5
  • 5
    • 53349162138 scopus 로고    scopus 로고
    • 1,2,3-Thiadiazole thioacetanilides as a novel class of potent HIV-1 non-nucleoside reverse transcriptase inhibitors
    • Zhan, P.; Liu, X.; Cao, Y.; Wang, Y.; Pannecouque, C.; De Clercq, E. 1,2,3-Thiadiazole thioacetanilides as a novel class of potent HIV-1 non-nucleoside reverse transcriptase inhibitors. Bioorg. Med. Chem. Lett., 2008, 18 (20), 5368-5371.
    • (2008) Bioorg. Med. Chem. Lett , vol.18 , Issue.20 , pp. 5368-5371
    • Zhan, P.1    Liu, X.2    Cao, Y.3    Wang, Y.4    Pannecouque, C.5    de Clercq, E.6
  • 6
    • 23644459481 scopus 로고    scopus 로고
    • Designer antibacterial peptides kill fluoroquinolone-resistant clinical isolates
    • Otvos, L.; Wade, J.D.; Lin, F.; Condie, B.A.; Hanrieder, J.; Hoffmann, R. Designer antibacterial peptides kill fluoroquinolone-resistant clinical isolates. J. Med. Chem., 2005, 48(16), 5349-5359.
    • (2005) J. Med. Chem , vol.48 , Issue.16 , pp. 5349-5359
    • Otvos, L.1    Wade, J.D.2    Lin, F.3    Condie, B.A.4    Hanrieder, J.5    Hoffmann, R.6
  • 7
    • 0036732849 scopus 로고    scopus 로고
    • Increasing prevalence of antimicrobial resistance among isolates of Streptococcus pneumoniae from the PROTEKT surveillance study, and compatative in vitro activity of the ketolide, telithromycin
    • Felmingham, D.; Reinert, R.R.; Hirakata, Y.; Rodloff, A. Increasing prevalence of antimicrobial resistance among isolates of Streptococcus pneumoniae from the PROTEKT surveillance study, and compatative in vitro activity of the ketolide, telithromycin. J. Antimicrob. Chemother., 2002, 50(suppl 2), 25-37.
    • (2002) J. Antimicrob. Chemother , vol.50 , Issue.SUPPL. 1 , pp. 25-37
    • Felmingham, D.1    Reinert, R.R.2    Hirakata, Y.3    Rodloff, A.4
  • 8
    • 0034999522 scopus 로고    scopus 로고
    • Antimicrobial resistance among clinical isolates of Streptococcus pneumoniae in the United States during 1999-2000, including a comparison of resistance rates since 1994-1995
    • Doern, G.V.; Heilmann, K.P.; Huynh, H.K.; Rhomberg, P.R.; Coffman, S.L.; Brueggemann, A.B. Antimicrobial resistance among clinical isolates of Streptococcus pneumoniae in the United States during 1999-2000, including a comparison of resistance rates since 1994-1995. Antimicrob. Agents Chemother., 2001, 45(6), 1721-1729.
    • (2001) Antimicrob. Agents Chemother , vol.45 , Issue.6 , pp. 1721-1729
    • Doern, G.V.1    Heilmann, K.P.2    Huynh, H.K.3    Rhomberg, P.R.4    Coffman, S.L.5    Brueggemann, A.B.6
  • 9
    • 79960561354 scopus 로고    scopus 로고
    • Design, synthesis and biological evaluation of urea derivatives from o-hydroxybenzylamines and phenylisocyanate as potential FabH inhibitors
    • Li, Z.-L.; Li, Q.-S.; Zhang, H.-J.; Hu, Y.; Zhu, D.-D.; Zhu, H.-L. Design, synthesis and biological evaluation of urea derivatives from o-hydroxybenzylamines and phenylisocyanate as potential FabH inhibitors. Bioorg. Med. Chem., 2011, 19(15), 4413-4420.
    • (2011) Bioorg. Med. Chem , vol.19 , Issue.15 , pp. 4413-4420
    • Li, Z.-L.1    Li, Q.-S.2    Zhang, H.-J.3    Hu, Y.4    Zhu, D.-D.5    Zhu, H.-L.6
  • 10
    • 41649098151 scopus 로고    scopus 로고
    • N-substituted 3-acetyltetramic acid derivatives as antibacterial agents
    • Yendapally, R.; Hurdle, J.G.; Carson, E.I.; Lee, R.B.; Lee, R.E. N-substituted 3-acetyltetramic acid derivatives as antibacterial agents. J. Med. Chem., 2008, 5 (5), 1487-1491.
    • (2008) J. Med. Chem , vol.5 , Issue.5 , pp. 1487-1491
    • Yendapally, R.1    Hurdle, J.G.2    Carson, E.I.3    Lee, R.B.4    Lee, R.E.5
  • 12
    • 84871855345 scopus 로고    scopus 로고
    • Various approaches for synthesis of imidazole derivatives
    • Ashish, B.; Pandeya, S. Various approaches for synthesis of imidazole derivatives. IJRAP, 2011, 2(4), 1124-1129.
    • (2011) IJRAP , vol.2 , Issue.4 , pp. 1124-1129
    • Ashish, B.1    Pandeya, S.2
  • 13
    • 84874631208 scopus 로고    scopus 로고
    • Review of imidazole heterocyclic ring containing compounds with their biological activity
    • Kumar, J.R. Review of imidazole heterocyclic ring containing compounds with their biological activity. Hypertension, 2010, 1(3), 167-177.
    • (2010) Hypertension , vol.1 , Issue.3 , pp. 167-177
    • Kumar, J.R.1
  • 15
    • 68649112417 scopus 로고    scopus 로고
    • Synthesis and antibacterial activities of new metronidazole and imidazole derivatives
    • Atia, A.J.K. Synthesis and antibacterial activities of new metronidazole and imidazole derivatives. Molecules, 2009, 14(7), 2431-2446.
    • (2009) Molecules , vol.14 , Issue.7 , pp. 2431-2446
    • Atia, A.J.K.1
  • 16
    • 84876488006 scopus 로고    scopus 로고
    • Syntheses and biological activity of chalcones-imidazole derivatives
    • Liu, Y.-T.; Sun, X.-M.; Yin, D.-W.; Yuan, F. Syntheses and biological activity of chalcones-imidazole derivatives. Res. on Chem. Intermed., 2013,3(39), 1-12.
    • (2013) Res. On Chem. Intermed , vol.3 , Issue.39 , pp. 1-12
    • Liu, Y.-T.1    Sun, X.-M.2    Yin, D.-W.3    Yuan, F.4
  • 17
    • 26844492143 scopus 로고    scopus 로고
    • Self-assembly of hydrogen-bonded molecules: Discotic and elliptical mesogens
    • Foster, E.J.; Lavigueur, C.; Ke, Y. C.; Williams, V.E. Self-assembly of hydrogen-bonded molecules: discotic and elliptical mesogens. J. Mater. Chem., 2005, 15(37), 4062-4068.
    • (2005) J. Mater. Chem , vol.15 , Issue.37 , pp. 4062-4068
    • Foster, E.J.1    Lavigueur, C.2    Ke, Y.C.3    Williams, V.E.4
  • 19
    • 33644853786 scopus 로고    scopus 로고
    • Naturally occurring and synthetic imidazoles: Their chemistry and their biological activities
    • Luca, L.D. Naturally occurring and synthetic imidazoles: Their chemistry and their biological activities. Curr. Med. Chem., 2006, 13(1), 1-23.
    • (2006) Curr. Med. Chem , vol.13 , Issue.1 , pp. 1-23
    • Luca, L.D.1
  • 20
    • 0026635203 scopus 로고
    • New antiinflammatory agents. 2. 5-Phenyl-3H-imidazo [4, 5- c][1, 8] naphthyridin-4 (5H)-ones: A new class of nonsteroidal antiinflammatory agents with potent activity like glucocorticoids
    • Suzuki, F.; Kuroda, T.; Tamura, T.; Sato, S.; Ohmori, K.; Ichikawa, S. New antiinflammatory agents. 2. 5-Phenyl-3H-imidazo [4, 5- c][1, 8] naphthyridin-4 (5H)-ones: a new class of nonsteroidal antiinflammatory agents with potent activity like glucocorticoids. J. Med. Chem., 1992, 35(15), 2863-2870.
    • (1992) J. Med. Chem , vol.35 , Issue.15 , pp. 2863-2870
    • Suzuki, F.1    Kuroda, T.2    Tamura, T.3    Sato, S.4    Ohmori, K.5    Ichikawa, S.6
  • 21
    • 0027771510 scopus 로고
    • Synthesis and pharmacological activity of a series of dihydro-1H-pyrrolo [1, 2-a] imidazole-2, 5 (3H, 6H)-diones, a novel class of potent cognition enhancers
    • Pinza, M.; Farina, C.; Cerri, A.; Pfeiffer, U.; Riccaboni, M.T.; Banfi, S.; Biagetti, R.; Pozzi, O.; Magnani, M.; Dorigotti, L. Synthesis and pharmacological activity of a series of dihydro-1H-pyrrolo [1, 2-a] imidazole-2, 5 (3H, 6H)-diones, a novel class of potent cognition enhancers. J. Med. Chem., 1993, 36(26), 4214-4220.
    • (1993) J. Med. Chem , vol.36 , Issue.26 , pp. 4214-4220
    • Pinza, M.1    Farina, C.2    Cerri, A.3    Pfeiffer, U.4    Riccaboni, M.T.5    Banfi, S.6    Biagetti, R.7    Pozzi, O.8    Magnani, M.9    Dorigotti, L.10
  • 24
    • 0032544143 scopus 로고    scopus 로고
    • Novel imidazole derivatives with subtype-selective antimuscarinic activity
    • Miyachi, H.; Kiyota, H.; Segawa, M. Novel imidazole derivatives with subtype-selective antimuscarinic activity. Bioorg. Med. Chem. Lett., 1998, 8(16), 2163-2168.
    • (1998) Bioorg. Med. Chem. Lett , vol.8 , Issue.16 , pp. 2163-2168
    • Miyachi, H.1    Kiyota, H.2    Segawa, M.3
  • 26
    • 19944432264 scopus 로고    scopus 로고
    • Aminoimidazolylmethyluracil Analogues As Potent Inhibitors of Thymidine Phosphorylase and Their Bioreductive Nitroimidazolyl Prodrugs
    • Reigan, P.; Edwards, P.N.; Gbaj, A.; Cole, C.; Barry, S.T.; Page, K.M.; Ashton, S.E.; Luke, R.W.; Douglas, K.T.; Stratford, I.J. Aminoimidazolylmethyluracil analogues as potent inhibitors of thymidine phosphorylase and their bioreductive nitroimidazolyl prodrugs. J. Med. Chem., 2005, 48(2), 392-402.
    • (2005) J. Med. Chem , vol.48 , Issue.2 , pp. 392-402
    • Reigan, P.1    Edwards, P.N.2    Gbaj, A.3    Cole, C.4    Barry, S.T.5    Page, K.M.6    Ashton, S.E.7    Luke, R.W.8    Douglas, K.T.9    Stratford, I.J.10
  • 27
    • 14744271290 scopus 로고    scopus 로고
    • Inducible metronidazole resistance and nim genes in clinical Bacteroides fragilis group isolates
    • Löfmark, S.; Fang, H.; Hedberg, M.; Edlund, C. Inducible metronidazole resistance and nim genes in clinical Bacteroides fragilis group isolates. Antimicrob. Agents Chemother., 2005, 49(3), 1253-1256.
    • (2005) Antimicrob. Agents Chemother , vol.49 , Issue.3 , pp. 1253-1256
    • Löfmark, S.1    Fang, H.2    Hedberg, M.3    Edlund, C.4
  • 28
  • 29
    • 0029796373 scopus 로고    scopus 로고
    • New directions in antibacterial research
    • Chu, D.T.; Plattner, J.J.; Katz, L. New directions in antibacterial research. J. Med. Chem., 1996, 39(20), 3853-3874.
    • (1996) J. Med. Chem , vol.39 , Issue.20 , pp. 3853-3874
    • Chu, D.T.1    Plattner, J.J.2    Katz, L.3
  • 30
    • 12844274375 scopus 로고    scopus 로고
    • Antibiotics: Where Did We Go Wrong
    • Overbye, K.M.; Barrett, J.F. Antibiotics: where did we go wrong. Drug Discov. Today, 2005, 10(1), 45-52.
    • (2005) Drug Discov. Today , vol.10 , Issue.1 , pp. 45-52
    • Overbye, K.M.1    Barrett, J.F.2
  • 32
    • 78650831436 scopus 로고    scopus 로고
    • Genetic methods for detection of antibiotic resistance: Focus on extended-spectrum P-lactamases
    • Chroma, M.; Kolar, M. Genetic methods for detection of antibiotic resistance: focus on extended-spectrum P-lactamases. Biomed. Pap. Med. Fac. Univ. Palacky Olomouc Czech. Repub., 2010, 154(4), 289-296.
    • (2010) Biomed. Pap. Med. Fac. Univ. Palacky Olomouc Czech. Repub , vol.154 , Issue.4 , pp. 289-296
    • Chroma, M.1    Kolar, M.2
  • 33
    • 67349120688 scopus 로고    scopus 로고
    • Current applications and future trends of molecular diagnostics in clinical bacteriology
    • Weile, J.; Knabbe, C. Current applications and future trends of molecular diagnostics in clinical bacteriology. Analy. Bioanaly. Chem., 2009, 394(3), 731-742.
    • (2009) Analy. Bioanaly. Chem , vol.394 , Issue.3 , pp. 731-742
    • Weile, J.1    Knabbe, C.2
  • 34
    • 25844529374 scopus 로고    scopus 로고
    • Prevalence of antimicrobial resistance genes in Listeria monocytogenes isolated from dairy farms
    • Srinivasan, V.; Nam, H.; Nguyen, L.; Tamilselvam, B.; Murinda, S.; Oliver, S. Prevalence of antimicrobial resistance genes in Listeria monocytogenes isolated from dairy farms. Foodbourne Path. & Dis., 2005, 2(3), 201-211.
    • (2005) Foodbourne Path. & Dis , vol.2 , Issue.3 , pp. 201-211
    • Srinivasan, V.1    Nam, H.2    Nguyen, L.3    Tamilselvam, B.4    Murinda, S.5    Oliver, S.6
  • 35
    • 22144476125 scopus 로고    scopus 로고
    • Bacterial resistance to antibiotics: Enzymatic degradation and modification
    • Wright, G.D. Bacterial resistance to antibiotics: enzymatic degradation and modification. Adv. Drug Deliv. Rev., 2005, 57(10), 1451-1470.
    • (2005) Adv. Drug Deliv. Rev , vol.57 , Issue.10 , pp. 1451-1470
    • Wright, G.D.1
  • 36
    • 22144437663 scopus 로고    scopus 로고
    • Bacterial resistance to antibiotics: Modified target sites
    • Lambert, P.A. Bacterial resistance to antibiotics: modified target sites. Advanced drug delivery reviews, 2005, 57(10), 1471-1485.
    • (2005) Advanced Drug Delivery Reviews , vol.57 , Issue.10 , pp. 1471-1485
    • Lambert, P.A.1
  • 37
    • 22144471145 scopus 로고    scopus 로고
    • Bacterial resistance to antibiotics: Active efflux and reduced uptake
    • Kumar, A.; Schweizer, H.P. Bacterial resistance to antibiotics: active efflux and reduced uptake. Adv. Drug Deliv. Rev., 2005, 57(10), 1486-1513.
    • (2005) Adv. Drug Deliv. Rev , vol.57 , Issue.10 , pp. 1486-1513
    • Kumar, A.1    Schweizer, H.P.2
  • 38
    • 0032870940 scopus 로고    scopus 로고
    • The biological cost of antibiotic resistance
    • Andersson, D.I.; Levin, B.R. The biological cost of antibiotic resistance. Curr. Opin. Microbiol, 1999, 2(5), 489-493.
    • (1999) Curr. Opin. Microbiol , vol.2 , Issue.5 , pp. 489-493
    • Andersson, D.I.1    Levin, B.R.2
  • 39
    • 79959888707 scopus 로고    scopus 로고
    • Synthesis and activities of naphthalimide azoles as a new type of antibacterial and antifungal agents
    • Zhang, Y.Y.; Zhou, C.H. Synthesis and activities of naphthalimide azoles as a new type of antibacterial and antifungal agents. Bioorg. Med. Chem. Lett, 2011, 21(14), 4349-4352.
    • (2011) Bioorg. Med. Chem. Lett , vol.21 , Issue.14 , pp. 4349-4352
    • Zhang, Y.Y.1    Zhou, C.H.2
  • 40
    • 79953187564 scopus 로고    scopus 로고
    • Synthesis, spectral, crystal structure and in vitro antimicrobial evaluation of imidazole/benzotriazole substituted piperidin-4-one derivatives
    • Ramachandran, R.; Rani, M.; Senthan, S.; Jeong, Y.T.; Kabilan, S. Synthesis, spectral, crystal structure and in vitro antimicrobial evaluation of imidazole/benzotriazole substituted piperidin-4-one derivatives. Eur. J. Med. Chem., 2011, 46(5), 1926-1934.
    • (2011) Eur. J. Med. Chem , vol.46 , Issue.5 , pp. 1926-1934
    • Ramachandran, R.1    Rani, M.2    Senthan, S.3    Jeong, Y.T.4    Kabilan, S.5
  • 41
    • 77649233952 scopus 로고    scopus 로고
    • Synthesis, antibacterial and antifungal activities of some carbazole derivatives
    • Zhang, F.-F.; Gan, L.L.; Zhou, C.H. Synthesis, antibacterial and antifungal activities of some carbazole derivatives. Bioorg. Med. Chem. Lett., 2010, 20(6), 1881-1884.
    • (2010) Bioorg. Med. Chem. Lett , vol.20 , Issue.6 , pp. 1881-1884
    • Zhang, F.-F.1    Gan, L.L.2    Zhou, C.H.3
  • 43
    • 0015412753 scopus 로고
    • Antiparasitic nitroimidazoles. 1. 2-Styryl-5-nitroimidazoles
    • Ross, W.J.; Jamieson, W.B.; McCowen, M.C. Antiparasitic nitroimidazoles. 1. 2-Styryl-5-nitroimidazoles. J. Med. Chem., 1972, 15(10), 1035-1040.
    • (1972) J. Med. Chem , vol.15 , Issue.10 , pp. 1035-1040
    • Ross, W.J.1    Jamieson, W.B.2    McCowen, M.C.3
  • 44
    • 84865112654 scopus 로고    scopus 로고
    • Design of inhibitors of Helicobacter pylori glutamate racemase as selective antibacterial agents: Incorporation of imidazoles onto a core pyrazolopyrimidinedione scaffold to improve bioavailabilty
    • Basarab, G.S.; Hill, P.; Eyermann, C.J.; Gowravaram, M.; Käck, H.; Osimoni, E. Design of inhibitors of Helicobacter pylori glutamate racemase as selective antibacterial agents: Incorporation of imidazoles onto a core pyrazolopyrimidinedione scaffold to improve bioavailabilty. Bioorg. Med. Chem. Lett, 2012, 22(17), 5600-5607.
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , Issue.17 , pp. 5600-5607
    • Basarab, G.S.1    Hill, P.2    Eyermann, C.J.3    Gowravaram, M.4    Käck, H.5    Osimoni, E.6
  • 45
    • 3142698398 scopus 로고    scopus 로고
    • Synthesis and QSAR studies of pyrimido [4, 5- d] pyrimidine-2, 5-dione derivatives as potential antimicrobial agents
    • Sharma, P.; Rane, N.; Gurram, V. Synthesis and QSAR studies of pyrimido [4, 5- d] pyrimidine-2, 5-dione derivatives as potential antimicrobial agents. Bioorg. Med. Chem. Lett, 2004, 14(16), 4185-4190.
    • (2004) Bioorg. Med. Chem. Lett , vol.14 , Issue.16 , pp. 4185-4190
    • Sharma, P.1    Rane, N.2    Gurram, V.3
  • 46
    • 84884247676 scopus 로고    scopus 로고
    • Potentiating 1-(2-hydroxypropyl)-2-styryl-5-nitroimidazole derivatives against antibacterial agents: Design, synthesis and biology analysis
    • Wang, Z.C.; Duan, Y.T.; Qin, Y.J.; Wang, P.F.; Luo, Y.; Wen, Q.; Yang, Y.A.; Sun, J.; Hu, Y.; Sang, Y.L.; Zhu, H.L. Potentiating 1-(2-hydroxypropyl)-2-styryl-5-nitroimidazole derivatives against antibacterial agents: Design, synthesis and biology analysis. Eur. J. Med. Chem., 2013, 65(2013), 456-463.
    • (2013) Eur. J. Med. Chem , vol.2013 , Issue.65 , pp. 456-463
    • Wang, Z.C.1    Duan, Y.T.2    Qin, Y.J.3    Wang, P.F.4    Luo, Y.5    Wen, Q.6    Yang, Y.A.7    Sun, J.8    Hu, Y.9    Sang, Y.L.10    Zhu, H.L.11
  • 47
    • 84872769325 scopus 로고    scopus 로고
    • Synthesis and characterization of new imidazole and fluorene-bisphenol based polyamides: Thermal, photophysical and antibacterial properties
    • Ghaemy, M.; Aghakhani, B.; Taghavi, M.; Nasab, S.M.A.; Mohseni, M. Synthesis and characterization of new imidazole and fluorene-bisphenol based polyamides: Thermal, photophysical and antibacterial properties. Reactive Funct. Polym., 2013, 73(3), 555-563.
    • (2013) Reactive Funct. Polym , vol.73 , Issue.3 , pp. 555-563
    • Ghaemy, M.1    Aghakhani, B.2    Taghavi, M.3    Nasab, S.M.A.4    Mohseni, M.5
  • 48
    • 84863217489 scopus 로고    scopus 로고
    • Design, synthesis and antimicrobial activities of nitroimidazole derivatives containing 1,3,4-oxadiazole scaffold as FabH inhibitors
    • Li, Y.; Luo, Y.; Hu, Y.; Zhu, D.D.; Zhang, S.; Liu, Z.J.; Gong, H.B.; Zhu, H.L. Design, synthesis and antimicrobial activities of nitroimidazole derivatives containing 1,3,4-oxadiazole scaffold as FabH inhibitors. Bioorg. Med. Chem., 2012, 20(14), 4316-4322.
    • (2012) Bioorg. Med. Chem , vol.20 , Issue.14 , pp. 4316-4322
    • Li, Y.1    Luo, Y.2    Hu, Y.3    Zhu, D.D.4    Zhang, S.5    Liu, Z.J.6    Gong, H.B.7    Zhu, H.L.8
  • 49
    • 84870399271 scopus 로고    scopus 로고
    • A new synthetic approach and in vitro antimicrobial evaluation of novel imidazole incorporated 4-thiazolidinone motifs
    • Desai, N.C.; Joshi, V.V.; Rajpara, K.M.; Makwana, A.H. A new synthetic approach and in vitro antimicrobial evaluation of novel imidazole incorporated 4-thiazolidinone motifs. Arabian Journal of Chemistry, 2012, http://dx.doi.org/10.1016/j.arabjc.2012.10.020.
    • (2012) Arabian Journal of Chemistry
    • Desai, N.C.1    Joshi, V.V.2    Rajpara, K.M.3    Makwana, A.H.4
  • 50
    • 79958258686 scopus 로고    scopus 로고
    • Synthesis, characterization and antimicrobial studies of some new pyrazole incorporated imidazole derivatives
    • Vijesh, A.M.; Isloor, A.M.; Telkar, S.; Peethambar, S.K.; Rai, S.; Isloor, N. Synthesis, characterization and antimicrobial studies of some new pyrazole incorporated imidazole derivatives. Eur. J. Med. Chem., 2011, 46(8), 3531-3536.
    • (2011) Eur. J. Med. Chem , vol.46 , Issue.8 , pp. 3531-3536
    • Vijesh, A.M.1    Isloor, A.M.2    Telkar, S.3    Peethambar, S.K.4    Rai, S.5    Isloor, N.6
  • 51
    • 79953184219 scopus 로고    scopus 로고
    • Synthesis, antimicrobial, antioxidant, anti-hemolytic and cytotoxic evaluation of new imidazole-based heterocycles
    • Abdel-Wahab, B.F.; Awad, G.E.; Badria, F.A. Synthesis, antimicrobial, antioxidant, anti-hemolytic and cytotoxic evaluation of new imidazole-based heterocycles. Eur. J. Med. Chem., 2011, 46(5), 1505-1511.
    • (2011) Eur. J. Med. Chem , vol.46 , Issue.5 , pp. 1505-1511
    • Abdel-Wahab, B.F.1    Awad, G.E.2    Badria, F.A.3
  • 52
    • 73949119252 scopus 로고    scopus 로고
    • Synthesis, molecular docking and biological evaluation of metronidazole derivatives as potent Helicobacter pylori urease inhibitors
    • Mao, W.J.; Lv, P.C; Shi, L.; Li, H.Q.; Zhu, H.L. Synthesis, molecular docking and biological evaluation of metronidazole derivatives as potent Helicobacter pylori urease inhibitors. Bioorg. Med. Chem., 2009, 17(21), 7531-7536.
    • (2009) Bioorg. Med. Chem , vol.17 , Issue.21 , pp. 7531-7536
    • Mao, W.J.1    Lv, P.C.2    Shi, L.3    Li, H.Q.4    Zhu, H.L.5
  • 54
    • 13844307282 scopus 로고    scopus 로고
    • Design, synthesis, antibacterial and QSAR studies of benzimidazole and imidazole chloroaryloxyalkyl derivatives
    • Khalafi-Nezhad, A.; Soltani Rad, M.N.; Mohabatkar, H.; Asrari, Z.; Hemmateenejad, B. Design, synthesis, antibacterial and QSAR studies of benzimidazole and imidazole chloroaryloxyalkyl derivatives. Bioorg. Med. Chem., 2005,13(6), 1931-1938.
    • (2005) Bioorg. Med. Chem , vol.13 , Issue.6 , pp. 1931-1938
    • Khalafi-Nezhad, A.1    Soltani Rad, M.N.2    Mohabatkar, H.3    Asrari, Z.4    Hemmateenejad, B.5
  • 56
    • 84879684285 scopus 로고    scopus 로고
    • Microwave-assisted synthesis and antimicrobial screening of new imidazole derivatives bearing 4-thiazolidinone nucleus
    • Desai, N.C.; Joshi, V.V.; Rajpara, K.M.; Vaghani, H.V.; Satodiya, H.M. Microwave-assisted synthesis and antimicrobial screening of new imidazole derivatives bearing 4-thiazolidinone nucleus. Med. Chem. Res., 2012, 22(4), 1893-1908.
    • (2012) Med. Chem. Res , vol.22 , Issue.4 , pp. 1893-1908
    • Desai, N.C.1    Joshi, V.V.2    Rajpara, K.M.3    Vaghani, H.V.4    Satodiya, H.M.5
  • 57
    • 84922592981 scopus 로고    scopus 로고
    • Green synthesis of novel quinoline based imidazole derivatives and evaluation of their antimicrobial activity
    • Desai, N.C.; Maheta, A.S.; Rajpara, K.M.; Joshi, V.V.; Vaghani, H.V.; Satodiya, H.M. Green synthesis of novel quinoline based imidazole derivatives and evaluation of their antimicrobial activity. J. Saudi Chem. Soci., 2011, http://dx.doi.org/10.1016/jjscs. 2011.11.021.
    • (2011) J. Saudi Chem. Soci
    • Desai, N.C.1    Maheta, A.S.2    Rajpara, K.M.3    Joshi, V.V.4    Vaghani, H.V.5    Satodiya, H.M.6
  • 58
    • 77953984445 scopus 로고    scopus 로고
    • Synthesis and antibacterial evaluation of 2-substituted-4, 5-diphenyl-N-alkyl imidazole derivatives
    • Jain, A.K.; Ravichandran, V.; Sisodiya, M.; Agrawal, R. Synthesis and antibacterial evaluation of 2-substituted-4, 5-diphenyl-N-alkyl imidazole derivatives. Asian Pac. J. Trop. Med., 2010, 3(6), 471-474.
    • (2010) Asian Pac. J. Trop. Med , vol.3 , Issue.6 , pp. 471-474
    • Jain, A.K.1    Ravichandran, V.2    Sisodiya, M.3    Agrawal, R.4
  • 59
    • 68649112417 scopus 로고    scopus 로고
    • Synthesis and antibacterial activities of new metronidazole and imidazole derivatives
    • Atia, A.J. Synthesis and antibacterial activities of new metronidazole and imidazole derivatives. Molecules, 2009, 14(7), 2431-2446.
    • (2009) Molecules , vol.14 , Issue.7 , pp. 2431-2446
    • Atia, A.J.1
  • 61
    • 0028896551 scopus 로고
    • Total syntheses of de-branched nagstatin and its analogs having glycosidase inhibiting activities
    • Tatsuta, K.; Miura, S.; Ohta, S.; Gunji, H. Total syntheses of de-branched nagstatin and its analogs having glycosidase inhibiting activities. Tetrahedron Lett., 1995,36(7), 1085-1088.
    • (1995) Tetrahedron Lett , vol.36 , Issue.7 , pp. 1085-1088
    • Tatsuta, K.1    Miura, S.2    Ohta, S.3    Gunji, H.4
  • 62
    • 0026778637 scopus 로고
    • Benastatins A and B, new inhibitors of glutathione S-transferase, produced by Streptomyces sp. MI384-DF12. II: Structure determination of benastatins A and B
    • Aoyama, T.; Naganawa, H.; Muroka, Y.; Nakamura, H.; Aoyagi, T.; Takeuchi, T.; Iitaka, Y. Benastatins A and B, new inhibitors of glutathione S-transferase, produced by Streptomyces sp. MI384-DF12. II: Structure determination of benastatins A and B. J. Antibiot. (Tokyo), 1992,45(9), 1391-1396.
    • (1992) J. Antibiot. (Tokyo) , vol.45 , Issue.9 , pp. 1391-1396
    • Aoyama, T.1    Naganawa, H.2    Muroka, Y.3    Nakamura, H.4    Aoyagi, T.5    Takeuchi, T.6    Iitaka, Y.7
  • 63
    • 0026778638 scopus 로고
    • Nagstatin, a new inhibitor of N-acetyl-beta-D-glucosaminidase, produced by Streptomyces amakusaensis MG846-fF3. Taxonomy, production, isolation, physico-chemical properties and biological activities
    • Aoyagi, T.; Suda, H.; Uotani, K.; Kojima, F.; Aoyama, T.; Horiguchi, K.; Hamada, M.; Takeuchi, T. Nagstatin, a new inhibitor of N-acetyl-beta-D-glucosaminidase, produced by Streptomyces amakusaensis MG846-fF3. Taxonomy, production, isolation, physico-chemical properties and biological activities. J. Antibiot., 1992,45(9), 1404-1408.
    • (1992) J. Antibiot , vol.45 , Issue.9 , pp. 1404-1408
    • Aoyagi, T.1    Suda, H.2    Uotani, K.3    Kojima, F.4    Aoyama, T.5    Horiguchi, K.6    Hamada, M.7    Takeuchi, T.8
  • 64
    • 0029835371 scopus 로고    scopus 로고
    • Synthesis and Antiviral Evaluation of Certain Disubstituted Benzimidazole Ribonucleosides 1
    • Zou, R.; Ayres, K.R.; Drach, J.C.; Townsend, L.B. Synthesis and Antiviral Evaluation of Certain Disubstituted Benzimidazole Ribonucleosides 1. J. Med. Chem., 1996, 39(18), 3477-3482.
    • (1996) J. Med. Chem , vol.39 , Issue.18 , pp. 3477-3482
    • Zou, R.1    Ayres, K.R.2    Drach, J.C.3    Townsend, L.B.4
  • 65
    • 0025355351 scopus 로고
    • The synthesis and chemistry of certain anthelmintic benzimidazoles
    • Townsend, L.B.; Wise, D.S. The synthesis and chemistry of certain anthelmintic benzimidazoles. Parasitol. Today, 1990, 6(4), 107-112.
    • (1990) Parasitol. Today , vol.6 , Issue.4 , pp. 107-112
    • Townsend, L.B.1    Wise, D.S.2
  • 67
    • 0018188546 scopus 로고
    • 1-[4-(4-Chlorophenyl)-2-(2, 6-dichlorophenylthio)-n-butyl]-1H-imidazole nitrate, a new potent antifungal agent
    • Walker, K.A.; Braemer, A.C.; Hitt, S.; Jones, R.E.; Matthews, T.R. 1-[4-(4-Chlorophenyl)-2-(2, 6-dichlorophenylthio)-n-butyl]-1H-imidazole nitrate, a new potent antifungal agent. J. Med. Chem., 1978, 21(8), 840-843.
    • (1978) J. Med. Chem , vol.21 , Issue.8 , pp. 840-843
    • Walker, K.A.1    Braemer, A.C.2    Hitt, S.3    Jones, R.E.4    Matthews, T.R.5
  • 68
    • 84872555882 scopus 로고    scopus 로고
    • Synthesis and evaluation of antibacterial activity of 7-alkyloxy-4,5-dihydro-imidazo[1,2-a]quinoline derivatives
    • Sun, X.Y.; Wu, R.; Wen, X.; Guo, L.; Zhou, C.P.; Li, J.; Quan, Z.S.; Bao, J. Synthesis and evaluation of antibacterial activity of 7-alkyloxy-4,5-dihydro-imidazo[1,2-a]quinoline derivatives. Eur. J. Med. Chem., 2013, 60(2013), 451-455.
    • (2013) Eur. J. Med. Chem , vol.2013 , Issue.60 , pp. 451-455
    • Sun, X.Y.1    Wu, R.2    Wen, X.3    Guo, L.4    Zhou, C.P.5    Li, J.6    Quan, Z.S.7    Bao, J.8
  • 70
    • 84859540299 scopus 로고    scopus 로고
    • Design, Synthesis, Antibacterial and Antifungal Activity of Novel 2-[(E)-2-aryl-1-ethenyl]-3-(2- sulfanyl-1H-benzo [d] imidazole-5-yl)-3, 4-dihydro-4-quinolinones
    • Nath, A.R.; Reddy, M.S. Design, Synthesis, Antibacterial and Antifungal Activity of Novel 2-[(E)-2-aryl-1-ethenyl]-3-(2- sulfanyl-1H-benzo [d] imidazole-5-yl)-3, 4-dihydro-4-quinolinones. J. Chem., 2012,9(3), 1481-1489.
    • (2012) J. Chem , vol.9 , Issue.3 , pp. 1481-1489
    • Nath, A.R.1    Reddy, M.S.2
  • 71
    • 0036263032 scopus 로고    scopus 로고
    • Resistance to beta-lactam antibiotics: Structure and mechanism based design of beta-lactamase inhibitors
    • Sandanayaka, V.P.; Prashad, A.S. Resistance to beta-lactam antibiotics: structure and mechanism based design of beta-lactamase inhibitors. Curr. Med. Chem., 2002, 9(12), 1145-1165.
    • (2002) Curr. Med. Chem , vol.9 , Issue.12 , pp. 1145-1165
    • Sandanayaka, V.P.1    Prashad, A.S.2
  • 74
    • 0029071785 scopus 로고
    • A functional classification scheme for beta-lactamases and its correlation with molecular structure
    • Bush, K.; Jacoby, G.A.; Medeiros, A.A. A functional classification scheme for beta-lactamases and its correlation with molecular structure. Antimicrob. Agents Chemother., 1995,39(6), 1211.
    • (1995) Antimicrob. Agents Chemother , vol.39 , Issue.6 , pp. 1211
    • Bush, K.1    Jacoby, G.A.2    Medeiros, A.A.3
  • 77
    • 0035980230 scopus 로고    scopus 로고
    • Structure of β- ketoacyl-[acyl carrier protein] reductase from Escherichia coli: Negative cooperativity and its structural basis
    • Price, A.C.; Zhang, Y.M.; Rock, CO.; White, S.W. Structure of β- ketoacyl-[acyl carrier protein] reductase from Escherichia coli: negative cooperativity and its structural basis. Biochemistry, 2001,40(43), 12772-12781.
    • (2001) Biochemistry , vol.40 , Issue.43 , pp. 12772-12781
    • Price, A.C.1    Zhang, Y.M.2    Rock, C.O.3    White, S.W.4
  • 78
    • 0034780806 scopus 로고    scopus 로고
    • Bacterial fatty acid biosynthesis: Targets for antibacterial drug discovery
    • Campbell, J.W.; Cronan Jr, J.E. Bacterial fatty acid biosynthesis: targets for antibacterial drug discovery. Annual Reviews in Microbiology, 2001, 55(1), 305-332.
    • (2001) Annual Reviews In Microbiology , vol.55 , Issue.1 , pp. 305-332
    • Campbell, J.W.1    Cronan, J.E.2
  • 79
    • 0033986294 scopus 로고    scopus 로고
    • P-Ketoacyl-acyl carrier protein synthase III (FabH) is a determining factor in branched-chain fatty acid biosynthesis
    • Choi, K.-H.; Heath, R.J.; Rock, CO. P-Ketoacyl-acyl carrier protein synthase III (FabH) is a determining factor in branched-chain fatty acid biosynthesis. J. Bacteriol, 2000,182(2), 365-370.
    • (2000) J. Bacteriol , vol.182 , Issue.2 , pp. 365-370
    • Choi, K.-H.1    Heath, R.J.2    Rock, C.O.3
  • 80
    • 0037304783 scopus 로고    scopus 로고
    • Bacterial beta-ketoacyl-acyl carrier protein synthases as targets for antibacterial agents
    • Khandekar, S.S.; Daines, R.A.; Lonsdale, J.T. Bacterial beta-ketoacyl-acyl carrier protein synthases as targets for antibacterial agents. Current Protein and Peptide Science, 2003, 4(1), 21-29.
    • (2003) Current Protein and Peptide Science , vol.4 , Issue.1 , pp. 21-29
    • Khandekar, S.S.1    Daines, R.A.2    Lonsdale, J.T.3
  • 81
    • 0036775842 scopus 로고    scopus 로고
    • The Claisen condensation in biology
    • Heath, R.J.; Rock, CO. The Claisen condensation in biology. Nat. Prod. Rep., 2002, 19(5), 581-596.
    • (2002) Nat. Prod. Rep , vol.19 , Issue.5 , pp. 581-596
    • Heath, R.J.1    Rock, C.O.2
  • 82
    • 0026669362 scopus 로고
    • Purification and characterization of 3-ketoacyl-acyl carrier protein synthase III from spinach. A condensing enzyme utilizing acetyl-coenzyme A to initiate fatty acid synthesis
    • Clough, R.; Matthis, A.; Barnum, S.; Jaworski, J. Purification and characterization of 3-ketoacyl-acyl carrier protein synthase III from spinach. A condensing enzyme utilizing acetyl-coenzyme A to initiate fatty acid synthesis. J. Biol. Chem., 1992, 267(29), 20992-20998.
    • (1992) J. Biol. Chem , vol.267 , Issue.29 , pp. 20992-20998
    • Clough, R.1    Matthis, A.2    Barnum, S.3    Jaworski, J.4
  • 83
    • 0030033704 scopus 로고    scopus 로고
    • Regulation of fatty acid elongation and initiation by acyl-acyl carrier protein in Escherichia coli
    • Heath, R.J.; Rock, CO. Regulation of fatty acid elongation and initiation by acyl-acyl carrier protein in Escherichia coli. J. Biol. Chem., 1996, 271(4), 1833-1836.
    • (1996) J. Biol. Chem , vol.271 , Issue.4 , pp. 1833-1836
    • Heath, R.J.1    Rock, C.O.2
  • 84
    • 84867795001 scopus 로고    scopus 로고
    • Novel FabH inhibitors: A patent and article literature review (2000-2012)
    • Luo, Y.; Yang, Y.S.; Fu, J.; Zhu, H.L. Novel FabH inhibitors: a patent and article literature review (2000-2012). Expert Opin. Ther. Pat., 2012,22(11), 1325-1336.
    • (2012) Expert Opin. Ther. Pat , vol.22 , Issue.11 , pp. 1325-1336
    • Luo, Y.1    Yang, Y.S.2    Fu, J.3    Zhu, H.L.4
  • 86
    • 0031880789 scopus 로고    scopus 로고
    • Patents on DNA gyrase inhibitors: January 1995 to March 1998
    • Kim, O.K.; Ohemeng, K.A. Patents on DNA gyrase inhibitors: January 1995 to March 1998. Expert Opin. Ther. Pat., 1998, 8(8), 959-969.
    • (1998) Expert Opin. Ther. Pat , vol.8 , Issue.8 , pp. 959-969
    • Kim, O.K.1    Ohemeng, K.A.2
  • 87
    • 0027956736 scopus 로고
    • Cloning and primary structure of Staphylococcus aureus DNA topoisomerase IV: A primary target of fluoroquinolones
    • Ferrero, L.; Cameron, B.; Manse, B.; Lagneaux, D.; Crouzet, J.; Famechon, A.; Blanche, F. Cloning and primary structure of Staphylococcus aureus DNA topoisomerase IV: a primary target of fluoroquinolones. Mol. Microbiol, 1994, 13(4), 641-653.
    • (1994) Mol. Microbiol , vol.13 , Issue.4 , pp. 641-653
    • Ferrero, L.1    Cameron, B.2    Manse, B.3    Lagneaux, D.4    Crouzet, J.5    Famechon, A.6    Blanche, F.7
  • 89
    • 0024603181 scopus 로고
    • Chromosome partitioning in Escherichia coli: Novel mutants producing anucleate cells
    • Hiraga, S.; Niki, H.; Ogura, T.; Ichinose, C; Mori, H.; Ezaki, B.; Jaffe, A. Chromosome partitioning in Escherichia coli: novel mutants producing anucleate cells. J. Bacteriol, 1989, 171(3), 1496-1505.
    • (1989) J. Bacteriol , vol.171 , Issue.3 , pp. 1496-1505
    • Hiraga, S.1    Niki, H.2    Ogura, T.3    Ichinose, C.4    Mori, H.5    Ezaki, B.6    Jaffe, A.7
  • 91
    • 54849407182 scopus 로고    scopus 로고
    • Who's winning the war Molecular mechanisms of antibiotic resistance in Helicobacter pylori
    • Jones, K.R.; Cha, J.-H.; Merrell, D.S. Who's winning the war Molecular mechanisms of antibiotic resistance in Helicobacter pylori. Curr. Drug Ther., 2008, 3(3), 190.
    • (2008) Curr. Drug Ther , vol.3 , Issue.3 , pp. 190
    • Jones, K.R.1    Cha, J.-H.2    Merrell, D.S.3
  • 92
    • 79955478213 scopus 로고    scopus 로고
    • Helicobacter pylori in the pathogenesis of gastric cancer and gastric lymphoma
    • Kim, S.S.; Ruiz, V.E.; Carroll, J.D.; Moss, S.F. Helicobacter pylori in the pathogenesis of gastric cancer and gastric lymphoma. Cancer Lett., 2011, 305(2), 228-238.
    • (2011) Cancer Lett , vol.305 , Issue.2 , pp. 228-238
    • Kim, S.S.1    Ruiz, V.E.2    Carroll, J.D.3    Moss, S.F.4
  • 93
    • 76349118567 scopus 로고    scopus 로고
    • Role of Helicobacter pylori infection in gastric cancer pathogenesis: A chance for prevention
    • Malfertheiner, P.; Bornschein, J.; Selgrad, M. Role of Helicobacter pylori infection in gastric cancer pathogenesis: a chance for prevention. J. Dig. Dis., 2010, 11(1), 2-11.
    • (2010) J. Dig. Dis , vol.11 , Issue.1 , pp. 2-11
    • Malfertheiner, P.1    Bornschein, J.2    Selgrad, M.3
  • 94
    • 52449114589 scopus 로고    scopus 로고
    • Design, synthesis, and evaluation of novel organophosphorus inhibitors of bacterial ureases
    • Vassiliou, S.; Grabowiecka, A.; Kosikowska, P.; Yiotakis, A.; Kafarski, P.; Berlicki, L. Design, synthesis, and evaluation of novel organophosphorus inhibitors of bacterial ureases. J. Med. Chem., 2008, 51(18), 5736-5744.
    • (2008) J. Med. Chem , vol.51 , Issue.18 , pp. 5736-5744
    • Vassiliou, S.1    Grabowiecka, A.2    Kosikowska, P.3    Yiotakis, A.4    Kafarski, P.5    Berlicki, L.6
  • 97
    • 2942530702 scopus 로고    scopus 로고
    • Kinetics of novel competitive inhibitors of urease enzymes by a focused library of oxadiazoles/thiadiazoles and triazoles
    • Amtul, Z.; Rasheed, M.; Choudhary, M.I.; Rosanna, S.; Khan, K.M. Kinetics of novel competitive inhibitors of urease enzymes by a focused library of oxadiazoles/thiadiazoles and triazoles. Biochem. Biophys. Res. Commun., 2004, 319(3), 1053-1063.
    • (2004) Biochem. Biophys. Res. Commun , vol.319 , Issue.3 , pp. 1053-1063
    • Amtul, Z.1    Rasheed, M.2    Choudhary, M.I.3    Rosanna, S.4    Khan, K.M.5
  • 99
    • 0036635133 scopus 로고    scopus 로고
    • Chemistry and mechanism of urease inhibition
    • Amtul, Z.; Siddiqui, R.; Choudhary, M. Chemistry and mechanism of urease inhibition. Curr. Med. Chem., 2002, 9(14), 1323-1348.
    • (2002) Curr. Med. Chem , vol.9 , Issue.14 , pp. 1323-1348
    • Amtul, Z.1    Siddiqui, R.2    Choudhary, M.3
  • 100
    • 0034762821 scopus 로고    scopus 로고
    • Recent advances in the formation of the bacterial peptidoglycan monomer unit
    • Van Heijenoort, J. Recent advances in the formation of the bacterial peptidoglycan monomer unit. Nat. Prod. Rep., 2001, 18(5), 503-519.
    • (2001) Nat. Prod. Rep , vol.18 , Issue.5 , pp. 503-519
    • van Heijenoort, J.1
  • 101
    • 0035967535 scopus 로고    scopus 로고
    • Active site residues of glutamate racemase
    • Glavas, S.; Tanner, M.E. Active site residues of glutamate racemase. Biochemistry, 2001, 40(21), 6199-6204.
    • (2001) Biochemistry , vol.40 , Issue.21 , pp. 6199-6204
    • Glavas, S.1    Tanner, M.E.2
  • 102
    • 0028198913 scopus 로고
    • The glutamate racemase activity from Escherichia coli is regulated by peptidoglycan precursor UDP-N-acetylmuramoyl-L-alanine
    • Doublet, P.; van Heijenoort, J.; Mengin-Lecreulx, D. The glutamate racemase activity from Escherichia coli is regulated by peptidoglycan precursor UDP-N-acetylmuramoyl-L-alanine. Biochemistry, 1994, 33(17), 5285-5290.
    • (1994) Biochemistry , vol.33 , Issue.17 , pp. 5285-5290
    • Doublet, P.1    van Heijenoort, J.2    Mengin-Lecreulx, D.3
  • 103
    • 0026669824 scopus 로고
    • Identification of the Escherichia coli murI gene, which is required for the biosynthesis of D-glutamic acid, a specific component of bacterial peptidoglycan
    • Doublet, P.; van Heijenoort, J.; Mengin-Lecreulx, D. Identification of the Escherichia coli murI gene, which is required for the biosynthesis of D-glutamic acid, a specific component of bacterial peptidoglycan. J. Bacteriol, 1992, 174(18), 5772-5779.
    • (1992) J. Bacteriol , vol.174 , Issue.18 , pp. 5772-5779
    • Doublet, P.1    van Heijenoort, J.2    Mengin-Lecreulx, D.3
  • 104
    • 58949092833 scopus 로고    scopus 로고
    • Glutamate racemase as a target for drug discovery
    • Fisher, S.L. Glutamate racemase as a target for drug discovery. Microb. Biotechnol, 2008, 1(5), 345-360.
    • (2008) Microb. Biotechnol , vol.1 , Issue.5 , pp. 345-360
    • Fisher, S.L.1
  • 105
    • 34248671094 scopus 로고    scopus 로고
    • Novel targets against Helicobacter pylori: A bioinformatic approach
    • Supuran, C.T. Novel targets against Helicobacter pylori: a bioinformatic approach. Future Microbiol, 2007, 2(2), 111-114.
    • (2007) Future Microbiol , vol.2 , Issue.2 , pp. 111-114
    • Supuran, C.T.1
  • 108
    • 84865112654 scopus 로고    scopus 로고
    • Design of inhibitors of Helicobacter pylori glutamate racemase as selective antibacterial agents: Incorporation of imidazoles onto a core pyrazolopyrimidinedione scaffold to improve bioavailabilty
    • Basarab, G.S.; Hill, P.; Eyermann, C.J.; Gowravaram, M.; Kack, H.; Osimoni, E. Design of inhibitors of Helicobacter pylori glutamate racemase as selective antibacterial agents: incorporation of imidazoles onto a core pyrazolopyrimidinedione scaffold to improve bioavailabilty. Bioorg. Med. Chem. Lett., 2012, 22(17), 5600-5607.
    • (2012) Bioorg. Med. Chem. Lett , vol.22 , Issue.17 , pp. 5600-5607
    • Basarab, G.S.1    Hill, P.2    Eyermann, C.J.3    Gowravaram, M.4    Kack, H.5    Osimoni, E.6
  • 109
    • 70349766733 scopus 로고    scopus 로고
    • Multi-target spectral moments for QSAR and Complex Networks study of antibacterial drugs
    • Prado-Prado, F.J.; Uriarte, E.; Borges, F.; González-Díaz, H. Multi-target spectral moments for QSAR and Complex Networks study of antibacterial drugs. Eur. J. Med. Chem., 2009, 44(11), 4516-4521.
    • (2009) Eur. J. Med. Chem , vol.44 , Issue.11 , pp. 4516-4521
    • Prado-Prado, F.J.1    Uriarte, E.2    Borges, F.3    González-Díaz, H.4
  • 110
    • 56449126519 scopus 로고    scopus 로고
    • Development of linear and nonlinear predictive QSAR models and their external validation using molecular similarity principle for anti-HIV indolyl aryl sulfones
    • Roy, K.; Mandal, A.S. Development of linear and nonlinear predictive QSAR models and their external validation using molecular similarity principle for anti-HIV indolyl aryl sulfones. J. Enzy. Inhib. Med. Chem., 2008, 23(6), 980-995.
    • (2008) J. Enzy. Inhib. Med. Chem , vol.23 , Issue.6 , pp. 980-995
    • Roy, K.1    Mandal, A.S.2
  • 111
    • 15244343496 scopus 로고    scopus 로고
    • Atom, atom-type, and total nonstochastic and stochastic quadratic fingerprints: A promising approach for modeling of antibacterial activity
    • Marrero-Ponce, Y.; Medina-Marrero, R.; Torrens, F.; Martinez, Y.; Romero-Zaldivar, V.; Castro, E.A. Atom, atom-type, and total nonstochastic and stochastic quadratic fingerprints: a promising approach for modeling of antibacterial activity. Bioorg. Med. Chem., 2005, 13(8), 2881-2899.
    • (2005) Bioorg. Med. Chem , vol.13 , Issue.8 , pp. 2881-2899
    • Marrero-Ponce, Y.1    Medina-Marrero, R.2    Torrens, F.3    Martinez, Y.4    Romero-Zaldivar, V.5    Castro, E.A.6
  • 113
    • 0031197192 scopus 로고    scopus 로고
    • Antimicrobial agents
    • Bush, K. Antimicrobial agents. Curr. Opin. Chem. Biol, 1997, 1(2), 169-175.
    • (1997) Curr. Opin. Chem. Biol , vol.1 , Issue.2 , pp. 169-175
    • Bush, K.1
  • 114
    • 33846455846 scopus 로고    scopus 로고
    • Assigning wave functions to graphs: A way to introduce novel topological indices
    • Galvez, J.; Garcia-Domenech, R.; de Julian-Ortiz, J. Assigning wave functions to graphs: A way to introduce novel topological indices. Commun. Mathem. Comp. Chem./MATCH, 2006, 56(3), 509-518.
    • (2006) Commun. Mathem. Comp. Chem./MATCH , vol.56 , Issue.3 , pp. 509-518
    • Galvez, J.1    Garcia-Domenech, R.2    de Julian-Ortiz, J.3
  • 115
    • 34547347534 scopus 로고    scopus 로고
    • Computational Chemistry Comparison of Stable/nonstable Protein Mutants Classification Models Based On 3D and Topological Indices
    • González - Díaz, H.; Pérez - castillo, Y.; Podda, G.; Uriarte, E. Computational chemistry comparison of stable/nonstable protein mutants classification models based on 3D and topological indices. J. Comput. Chem., 2007, 28(12), 1990-1995.
    • (2007) J. Comput. Chem , vol.28 , Issue.12 , pp. 1990-1995
    • González-Díaz, H.1    Pérez-castillo, Y.2    Podda, G.3    Uriarte, E.4
  • 116
    • 25844496945 scopus 로고    scopus 로고
    • Markovian chemicals "in silico" design (MARCH-INSIDE), a promising approach for computer-aided molecular design III: 2.5 D indices for the discovery of antibacterials
    • González-Díaz, H.; Torres-Gómez, L.A.; Guevara, Y.; Almeida, M.S.; Molina, R.; Castañedo, N.; Santana, L.; Uriarte, E. Markovian chemicals "in silico" design (MARCH-INSIDE), a promising approach for computer-aided molecular design III: 2.5 D indices for the discovery of antibacterials. J. Mol. Model, 2005, 11(2), 116-123.
    • (2005) J. Mol. Model , vol.11 , Issue.2 , pp. 116-123
    • González-Díaz, H.1    Torres-Gómez, L.A.2    Guevara, Y.3    Almeida, M.S.4    Molina, R.5    Castañedo, N.6    Santana, L.7    Uriarte, E.8
  • 117
    • 84875734003 scopus 로고    scopus 로고
    • Novel 1,3,4-oxadiazole thioether derivatives targeting thymidylate synthase as dual anticancer/antimicrobial agents
    • Du, Q.R.; Li, D.D.; Pi, Y.Z.; Li, J.R.; Sun, J.; Fang, F.; Zhong, W.Q.; Gong, H.B.; Zhu, H.L. Novel 1,3,4-oxadiazole thioether derivatives targeting thymidylate synthase as dual anticancer/antimicrobial agents. Bioorg. Med. Chem., 2013, 21(8), 2286-2297.
    • (2013) Bioorg. Med. Chem , vol.21 , Issue.8 , pp. 2286-2297
    • Du, Q.R.1    Li, D.D.2    Pi, Y.Z.3    Li, J.R.4    Sun, J.5    Fang, F.6    Zhong, W.Q.7    Gong, H.B.8    Zhu, H.L.9


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.