-
1
-
-
7244245763
-
Antibiotics at the crossroads
-
Nathan, C. Antibiotics at the crossroads. Nature, 2004, 431, 899-902.
-
(2004)
Nature
, vol.431
, Issue.899
, pp. 902
-
-
Nathan, C.1
-
2
-
-
62249124522
-
-
Frechette, R. In Ann. Rep. Med. Chem., Elsevier, 2007, pp. 349-64.
-
Frechette, R. In Ann. Rep. Med. Chem., Elsevier, 2007, pp. 349-64.
-
-
-
-
3
-
-
33746001269
-
Antibacterial natural products in medicinal chemistry-exodus or revival?
-
Von Nussbaum, F.; Brands, M.; Hinzen, B.; Weigand, S.; Häbich, D. Antibacterial natural products in medicinal chemistry-exodus or revival? Angew. Chem. Int. Ed. Engl., 2006, 45, 5072-129.
-
(2006)
Angew. Chem. Int. Ed. Engl
, vol.45
, pp. 5072-5129
-
-
Von Nussbaum, F.1
Brands, M.2
Hinzen, B.3
Weigand, S.4
Häbich, D.5
-
4
-
-
15444377930
-
What can a chemist learn from nature's macrocycles? A brief, conceptual view
-
Wessjohann, L.A.; Ruijter, E.; Garcia-Rivera, D.; Brandt, W. What can a chemist learn from nature's macrocycles? A brief, conceptual view. Mol. Divers., 2005, 9, 171-86.
-
(2005)
Mol. Divers
, vol.9
, pp. 171-186
-
-
Wessjohann, L.A.1
Ruijter, E.2
Garcia-Rivera, D.3
Brandt, W.4
-
5
-
-
0042844744
-
Natural products as sources of new drugs over the period 1981-2002
-
Newman, D.J.; Cragg, G.M.; Snader, K.M. Natural products as sources of new drugs over the period 1981-2002. J. Nat. Prod., 2003, 66, 1022-37.
-
(2003)
J. Nat. Prod
, vol.66
, pp. 1022-1037
-
-
Newman, D.J.1
Cragg, G.M.2
Snader, K.M.3
-
6
-
-
37549071045
-
Drug discovery beyond the 'rule-of-five'
-
Zhang, M.Q.; Wilkinson, B. Drug discovery beyond the 'rule-of-five'. Curr. Opin. Biotechnol., 2007, 18, 478-88.
-
(2007)
Curr. Opin. Biotechnol
, vol.18
, pp. 478-488
-
-
Zhang, M.Q.1
Wilkinson, B.2
-
8
-
-
0034470558
-
Combinatorial biomimetic chemistry: Parallel synthesis of a small library of ß-hairpin mimetics based on loop III from human platelet-derived growth factor B
-
Jiang, L.; Moehle, K.; Dhanapal, B.; Obrecht, D.; Robinson, J.A. Combinatorial biomimetic chemistry: Parallel synthesis of a small library of ß-hairpin mimetics based on loop III from human platelet-derived growth factor B. Helv. Chem. Acta, 2000, 83, 3097-112.
-
(2000)
Helv. Chem. Acta
, vol.83
, pp. 3097-3112
-
-
Jiang, L.1
Moehle, K.2
Dhanapal, B.3
Obrecht, D.4
Robinson, J.A.5
-
9
-
-
54049134708
-
The design, structures and therapeutic potential of protein epitope mimetics
-
Robinson, J.A.; DeMarco, S.J.; Gombert, F.O.; Moehle, K.; Obrecht, D. The design, structures and therapeutic potential of protein epitope mimetics. Drug Disc. Today, 2008, 13, 944-951.
-
(2008)
Drug Disc. Today
, vol.13
, pp. 944-951
-
-
Robinson, J.A.1
DeMarco, S.J.2
Gombert, F.O.3
Moehle, K.4
Obrecht, D.5
-
10
-
-
33750527761
-
Discovery of novel, highly potent and selective beta-hairpin mimetic CXCR4 inhibitors with excellent anti-HIV activity and pharmacokinetic profiles
-
DeMarco, S.J.; Henze, H.; Lederer, A.; Moehle, K.; Mukherjee, R.; Romagnoli, B.; Robinson, J.A.; Brianza, F.; Gombert, F.O.; Lociuro, S.; Ludin, C.; Vrijbloed, J.W.; Zumbrunn, J.; Obrecht, J.P.; Obrecht, D.; Brondani, V.; Hamy, F.; Klimkait, T. Discovery of novel, highly potent and selective beta-hairpin mimetic CXCR4 inhibitors with excellent anti-HIV activity and pharmacokinetic profiles. Bioorg. Med. Chem., 2006, 14, 8396-404.
-
(2006)
Bioorg. Med. Chem
, vol.14
, pp. 8396-8404
-
-
DeMarco, S.J.1
Henze, H.2
Lederer, A.3
Moehle, K.4
Mukherjee, R.5
Romagnoli, B.6
Robinson, J.A.7
Brianza, F.8
Gombert, F.O.9
Lociuro, S.10
Ludin, C.11
Vrijbloed, J.W.12
Zumbrunn, J.13
Obrecht, J.P.14
Obrecht, D.15
Brondani, V.16
Hamy, F.17
Klimkait, T.18
-
11
-
-
0037021328
-
Macrocyclic hairpin mimetics of the cationic antimicrobial peptide protegrin I: A new family of broad-spectrum antibiotics
-
Shankaramma, S.C.; Athanassiou, Z.; Zerbe, O.; Moehle, K.; Mouton, C.; Bernardini, F.; Vrijbloed, J.W.; Obrecht, D.; Robinson, J.A. Macrocyclic hairpin mimetics of the cationic antimicrobial peptide protegrin I: A new family of broad-spectrum antibiotics. Chembiochem., 2002, 3, 1126-33.
-
(2002)
Chembiochem
, vol.3
, pp. 1126-1133
-
-
Shankaramma, S.C.1
Athanassiou, Z.2
Zerbe, O.3
Moehle, K.4
Mouton, C.5
Bernardini, F.6
Vrijbloed, J.W.7
Obrecht, D.8
Robinson, J.A.9
-
12
-
-
34548810386
-
A call to arms
-
Hopwood, D.; Levy, S.; Wenzel, R.P.; Georgopapadakou, N.; Baltz, R.H.; Bhavnani, S.; Cox, E. A call to arms. Nat. Rev. Drug Discov., 2007, 6, 8-12.
-
(2007)
Nat. Rev. Drug Discov
, vol.6
, pp. 8-12
-
-
Hopwood, D.1
Levy, S.2
Wenzel, R.P.3
Georgopapadakou, N.4
Baltz, R.H.5
Bhavnani, S.6
Cox, E.7
-
13
-
-
35748958975
-
Late stage antibacterial drugs in the clinical pipeline
-
Projan, S.J.; Bradford, P.A. Late stage antibacterial drugs in the clinical pipeline. Curr. Opin. Microbiol., 2007, 10, 441-46.
-
(2007)
Curr. Opin. Microbiol
, vol.10
, pp. 441-446
-
-
Projan, S.J.1
Bradford, P.A.2
-
14
-
-
33144473431
-
Bad bugs need drugs: An update on the development pipeline from the antimicrobial availability task force of the infectious diseases Society of America
-
Talbot, G.H.; Bradley, J.; Edwards, J.E., Jr.; Gilbert, D.; Scheld, M.; Bartlett, J.G. Bad bugs need drugs: An update on the development pipeline from the antimicrobial availability task force of the infectious diseases Society of America. Clin. Infect. Dis., 2006, 42, 657-68.
-
(2006)
Clin. Infect. Dis
, vol.42
, pp. 657-668
-
-
Talbot, G.H.1
Bradley, J.2
Edwards Jr., J.E.3
Gilbert, D.4
Scheld, M.5
Bartlett, J.G.6
-
15
-
-
34447560960
-
Toxicity of polymyxins: A systematic review of the evidence from old and recent studies
-
Falagas, M.E.; Kasiakou, S.K. Toxicity of polymyxins: A systematic review of the evidence from old and recent studies. Crit. Care, 2006, 10, R27.
-
(2006)
Crit. Care
, vol.10
-
-
Falagas, M.E.1
Kasiakou, S.K.2
-
16
-
-
13844306055
-
Thiopeptide antibiotics
-
Bagley, M.C.; Dale, J.W.; Merritt, E.A.; Xiong, X. Thiopeptide antibiotics. Chem. Rev., 2005, 105, 685-714.
-
(2005)
Chem. Rev
, vol.105
, pp. 685-714
-
-
Bagley, M.C.1
Dale, J.W.2
Merritt, E.A.3
Xiong, X.4
-
17
-
-
35648951171
-
From amino acids to heteroaromatics - thiopeptide antibiotics, nature's heterocyclic peptides
-
Hughes, R.A.; Moody, C.J. From amino acids to heteroaromatics - thiopeptide antibiotics, nature's heterocyclic peptides. Angew. Chem. Int. Ed. Engl., 2007, 46, 7930-54.
-
(2007)
Angew. Chem. Int. Ed. Engl
, vol.46
, pp. 7930-7954
-
-
Hughes, R.A.1
Moody, C.J.2
-
18
-
-
27544455748
-
Discovery of a biologically active thiostrepton fragment
-
Nicolaou, K.C.; Zak, M.; Rahimipour, S.; Estrada, A.A.; Lee, S.H.; O'Brate, A.; Giannakakou, P.; Ghadiri, M.R. Discovery of a biologically active thiostrepton fragment. J. Am. Chem. Soc., 2005, 127, 15042-44.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 15042-15044
-
-
Nicolaou, K.C.1
Zak, M.2
Rahimipour, S.3
Estrada, A.A.4
Lee, S.H.5
O'Brate, A.6
Giannakakou, P.7
Ghadiri, M.R.8
-
19
-
-
41549163979
-
Translational regulation via L11: Molecular switches on the ribosome turned on and off by thiostrepton and micrococcin
-
Harms, J.M.; Wilson, D.N.; Schluenzen, F.; Connell, S.R.; Stachelhaus, T.; Zaborowska, Z.; Spahn, C.M.; Fucini, P. Translational regulation via L11: Molecular switches on the ribosome turned on and off by thiostrepton and micrococcin. Mol. Cell, 2008, 30, 26-38.
-
(2008)
Mol. Cell
, vol.30
, pp. 26-38
-
-
Harms, J.M.1
Wilson, D.N.2
Schluenzen, F.3
Connell, S.R.4
Stachelhaus, T.5
Zaborowska, Z.6
Spahn, C.M.7
Fucini, P.8
-
20
-
-
0032548821
-
The antibiotic thiostrepton inhibits a functional transition within protein L11 at the ribosomal GTPase centre
-
Porse, B.T.; Leviev, I.; Mankin, A.S.; Garrett, R.A. The antibiotic thiostrepton inhibits a functional transition within protein L11 at the ribosomal GTPase centre. J. Mol. Biol., 1998, 276, 391-404.
-
(1998)
J. Mol. Biol
, vol.276
, pp. 391-404
-
-
Porse, B.T.1
Leviev, I.2
Mankin, A.S.3
Garrett, R.A.4
-
21
-
-
33744951325
-
Structural basis of the action of pulvomycin and GE2270 A on elongation factor Tu
-
Parmeggiani, A.; Krab, I.M.; Okamura, S.; Nielsen, R.C.; Nyborg, J.; Nissen, P. Structural basis of the action of pulvomycin and GE2270 A on elongation factor Tu. Biochemistry, 2006, 45, 6846-57.
-
(2006)
Biochemistry
, vol.45
, pp. 6846-6857
-
-
Parmeggiani, A.1
Krab, I.M.2
Okamura, S.3
Nielsen, R.C.4
Nyborg, J.5
Nissen, P.6
-
22
-
-
10744233763
-
Combinatorial modification of natural products: Synthesis and in vitro analysis of derivatives of thiazole peptide antibiotic GE2270 A: A-ring modifications
-
Clough, J.; Chen, S.; Gordon, E.M.; Hackbarth, C.; Lam, S.; Trias, J.; White, R.J.; Candiani, G.; Donadio, S.; Romano, G.; Ciabatti, R.; Jacobs, J.W. Combinatorial modification of natural products: Synthesis and in vitro analysis of derivatives of thiazole peptide antibiotic GE2270 A: A-ring modifications. Bioorg. Med. Chem. Lett., 2003, 13, 3409-14.
-
(2003)
Bioorg. Med. Chem. Lett
, vol.13
, pp. 3409-3414
-
-
Clough, J.1
Chen, S.2
Gordon, E.M.3
Hackbarth, C.4
Lam, S.5
Trias, J.6
White, R.J.7
Candiani, G.8
Donadio, S.9
Romano, G.10
Ciabatti, R.11
Jacobs, J.W.12
-
23
-
-
23744471989
-
Total synthesis of thiostrepton. Retrosynthetic analysis and construction of key building blocks
-
Nicolaou, K.C.; Safina, B.S.; Zak, M.; Lee, S.H.; Nevalainen, M.; Bella, M.; Estrada, A.A.; Funke, C.; Zecri, F.J.; Bulat, S. Total synthesis of thiostrepton. Retrosynthetic analysis and construction of key building blocks. J. Am. Chem. Soc., 2005, 127, 11159-75
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 11159-11175
-
-
Nicolaou, K.C.1
Safina, B.S.2
Zak, M.3
Lee, S.H.4
Nevalainen, M.5
Bella, M.6
Estrada, A.A.7
Funke, C.8
Zecri, F.J.9
Bulat, S.10
-
24
-
-
27644574520
-
Total synthesis of the thiopeptide antibiotic amythiamicin D
-
Hughes, R.A.; Thompson, S.P.; Alcaraz, L.; Moody, C.J. Total synthesis of the thiopeptide antibiotic amythiamicin D. J. Am. Chem. Soc., 2005, 127, 15644-51.
-
(2005)
J. Am. Chem. Soc
, vol.127
, pp. 15644-15651
-
-
Hughes, R.A.1
Thompson, S.P.2
Alcaraz, L.3
Moody, C.J.4
-
25
-
-
53849105812
-
-
Delgado, O.; Muller, H.M.; Bach, T. Concise total synthesis of the thiazolyl peptide antibiotic GE2270 A. Chemistry., 2008, 14, 2322-39.
-
Delgado, O.; Muller, H.M.; Bach, T. Concise total synthesis of the thiazolyl peptide antibiotic GE2270 A. Chemistry., 2008, 14, 2322-39.
-
-
-
-
26
-
-
40149108661
-
Total synthesis of thiopeptide antibiotics GE2270A, GE2270T, and GE2270C1
-
Nicolaou, K.C.; Dethe, D.H.; Leung, G.Y.; Zou, B.; Chen, D. Y. Total synthesis of thiopeptide antibiotics GE2270A, GE2270T, and GE2270C1. Chem. Asian J., 2008, 3, 413-29.
-
(2008)
Chem. Asian J
, vol.3
, pp. 413-429
-
-
Nicolaou, K.C.1
Dethe, D.H.2
Leung, G.Y.3
Zou, B.4
Chen, D.Y.5
-
27
-
-
36549084173
-
Total Syntheses of Lysobactin (Katanosin B)
-
Campagne, J.M. Total Syntheses of Lysobactin (Katanosin B). Angew. Chem. Int. Ed. Engl., 2007, 46, 8548-52.
-
(2007)
Angew. Chem. Int. Ed. Engl
, vol.46
, pp. 8548-8552
-
-
Campagne, J.M.1
-
28
-
-
0024242914
-
-
Bonner, D.P.; O'Sullivan, J.; Tanaka, S.K.; Clark, J.M.; Whitney, R.R. Lysobactin, a novel antibacterial agent produced by Lysobacter sp. II. Biological properties. J. Antibiot., 1988, 41, 1745-51.
-
Bonner, D.P.; O'Sullivan, J.; Tanaka, S.K.; Clark, J.M.; Whitney, R.R. Lysobactin, a novel antibacterial agent produced by Lysobacter sp. II. Biological properties. J. Antibiot., 1988, 41, 1745-51.
-
-
-
-
29
-
-
0024246790
-
-
O'Sullivan, J.; McCullough, J.E.; Tymiak, A.A.; Kirsch, D.R.; Trejo, W.H.; Principe, P.A. Lysobactin, a novel antibacterial agent produced by Lysobacter sp. I. Taxonomy, isolation and partial characterization. J. Antibiot., 1988, 41, 1740-44.
-
O'Sullivan, J.; McCullough, J.E.; Tymiak, A.A.; Kirsch, D.R.; Trejo, W.H.; Principe, P.A. Lysobactin, a novel antibacterial agent produced by Lysobacter sp. I. Taxonomy, isolation and partial characterization. J. Antibiot., 1988, 41, 1740-44.
-
-
-
-
30
-
-
0023952321
-
Isolation and characterization of katanosins A and B
-
Shoji, J.; Hinoo, H.; Matsumoto, K.; Hattori, T.; Yoshida, T.; Matsuura, S.; Kondo, E. Isolation and characterization of katanosins A and B. J. Antibiot., 1988, 41, 713-18.
-
(1988)
J. Antibiot
, vol.41
, pp. 713-718
-
-
Shoji, J.1
Hinoo, H.2
Matsumoto, K.3
Hattori, T.4
Yoshida, T.5
Matsuura, S.6
Kondo, E.7
-
31
-
-
34247606516
-
Structure and total synthesis of lysobactin (katanosin B)
-
von Nussbaum, F.; Anlauf, S.; Benet-Buchholz, J.; Häbich, D.; Köbberling, J.; Musza, L.; Telser, J.; Rübsamen-Waigmann, H.; Brunner, N.A. Structure and total synthesis of lysobactin (katanosin B). Angew. Chem. Int. Ed. Engl., 2007, 46, 2039-42.
-
(2007)
Angew. Chem. Int. Ed. Engl
, vol.46
, pp. 2039-2042
-
-
von Nussbaum, F.1
Anlauf, S.2
Benet-Buchholz, J.3
Häbich, D.4
Köbberling, J.5
Musza, L.6
Telser, J.7
Rübsamen-Waigmann, H.8
Brunner, N.A.9
-
33
-
-
0034999983
-
Katanosin B and plusbacin A(3), inhibitors of peptidoglycan synthesis in methicillin-resistant Staphylococcus aureus
-
Maki, H.; Miura, K.; Yamano, Y. Katanosin B and plusbacin A(3), inhibitors of peptidoglycan synthesis in methicillin-resistant Staphylococcus aureus. Antimicr. Agents Chemoth., 2001, 45, 1823-27.
-
(1823)
Antimicr. Agents Chemoth
, vol.2001
, pp. 45
-
-
Maki, H.1
Miura, K.2
Yamano, Y.3
-
34
-
-
0024559276
-
Structure determination of lysobactin, a macrocyclic peptide lactone antibiotic
-
Tymiak, A.A.; McCormick, T.J.; Unger, S.E. Structure determination of lysobactin, a macrocyclic peptide lactone antibiotic. J. Org. Chem., 1989, 54, 1149-57.
-
(1989)
J. Org. Chem
, vol.54
, pp. 1149-1157
-
-
Tymiak, A.A.1
McCormick, T.J.2
Unger, S.E.3
-
35
-
-
62249191879
-
-
Von Nussbaum, F.; Brunner, N.; Fürstner, C.; Endermann, R.; Ragot, J.; Telser, J.; Schroeder, W.; Anlauf, S.; Schumacher, A.; Hartmann, E. Cyclic nonapeptide amides. WO/2006/048156, 2006.
-
Von Nussbaum, F.; Brunner, N.; Fürstner, C.; Endermann, R.; Ragot, J.; Telser, J.; Schroeder, W.; Anlauf, S.; Schumacher, A.; Hartmann, E. Cyclic nonapeptide amides. WO/2006/048156, 2006.
-
-
-
-
36
-
-
0014219832
-
Methicillin-resistant Staphylococcus aureus. Antimicrobial susceptibility
-
Benner, E.J.; Morthland, V. Methicillin-resistant Staphylococcus aureus. Antimicrobial susceptibility. New Engl. J. Med., 1967, 277, 678-80.
-
(1967)
New Engl. J. Med
, vol.277
, pp. 678-680
-
-
Benner, E.J.1
Morthland, V.2
-
37
-
-
33750988183
-
Antibiotics - past, present, and future
-
Khardori, N. Antibiotics - past, present, and future. Med. Clin. North Am., 2006, 90, 1049-76.
-
(2006)
Med. Clin. North Am
, vol.90
, pp. 1049-1076
-
-
Khardori, N.1
-
38
-
-
33747599631
-
-
McAlpine, J.B.; Yagisawa, M. In Ann. Report. Med. Chem., Doherty, A.M. Ed.; Elsevier: Amsterdam, 2005; 40, pp. 301-21.
-
McAlpine, J.B.; Yagisawa, M. In Ann. Report. Med. Chem., Doherty, A.M. Ed.; Elsevier: Amsterdam, 2005; Vol. 40, pp. 301-21.
-
-
-
-
39
-
-
33747605341
-
Glycopeptides and glycodepsipeptides in clinical development: A comparative review of their antibacterial spectrum, pharmacokinetics and clinical efficacy
-
Van, B.F. Glycopeptides and glycodepsipeptides in clinical development: a comparative review of their antibacterial spectrum, pharmacokinetics and clinical efficacy. Curr. Opin. Investig. Drugs, 2006, 7, 740-49.
-
(2006)
Curr. Opin. Investig. Drugs
, vol.7
, pp. 740-749
-
-
Van, B.F.1
-
40
-
-
0033516914
-
Chemistry, biology, and medicine of the glycopeptide antibiotics
-
Nicolaou, K.C.; Boddy, C.N.; Bräse, S.; Winssinger, N. Chemistry, biology, and medicine of the glycopeptide antibiotics. Angew. Chem. Int. Ed. Engl., 1999, 38, 2096-152.
-
(1999)
Angew. Chem. Int. Ed. Engl
, vol.38
, pp. 2096-2152
-
-
Nicolaou, K.C.1
Boddy, C.N.2
Bräse, S.3
Winssinger, N.4
-
43
-
-
21044456657
-
-
Mercier, R.C.; Hrebickova, L. Oritavancin: A new avenue for resistant gram-positive bacteria. Expert. Rev Anti. Infect. Ther., 2005, 3, 325-32.
-
Mercier, R.C.; Hrebickova, L. Oritavancin: A new avenue for resistant gram-positive bacteria. Expert. Rev Anti. Infect. Ther., 2005, 3, 325-32.
-
-
-
-
47
-
-
39049155534
-
-
Poulakou, G.; Giamarellou, H. Oritavancin: A new promising agent in the treatment of infections due to Gram-positive pathogens. Expert. Opin. Investig. Drugs, 2008, 17, 225-43.
-
Poulakou, G.; Giamarellou, H. Oritavancin: A new promising agent in the treatment of infections due to Gram-positive pathogens. Expert. Opin. Investig. Drugs, 2008, 17, 225-43.
-
-
-
-
48
-
-
15844407157
-
Human pharmacokinetics and rationale for once-weekly dosing of dalbavancin, a semi-synthetic glycopeptide
-
Dorr, M.B.; Jabes, D.; Cavaleri, M.; Dowell, J.; Mosconi, G.; Malabarba, A.; White, R.J.; Henkel, T.J. Human pharmacokinetics and rationale for once-weekly dosing of dalbavancin, a semi-synthetic glycopeptide. J. Antimicrob. Chemother., 2005, 55 Suppl 2, ii25-ii30.
-
(2005)
J. Antimicrob. Chemother
, vol.55
, Issue.SUPPL. 2
-
-
Dorr, M.B.1
Jabes, D.2
Cavaleri, M.3
Dowell, J.4
Mosconi, G.5
Malabarba, A.6
White, R.J.7
Henkel, T.J.8
-
49
-
-
21044448952
-
Daptomycin biosynthesis in Streptomyces roseosporus: Cloning and analysis of the gene cluster and revision of peptide stereochemistry
-
Miao, V.; Coeffet-Legal, M.F.; Brian, P.; Brost, R.; Penn, J.; Whiting, A.; Martin, S.; Ford, R.; Parr, I.; Bouchard, M.; Silva, C.J.; Wrigley, S.K.; Baltz, R.H. Daptomycin biosynthesis in Streptomyces roseosporus: cloning and analysis of the gene cluster and revision of peptide stereochemistry. Microbiology, 2005, 151, 1507-23
-
(2005)
Microbiology
, vol.151
, pp. 1507-1523
-
-
Miao, V.1
Coeffet-Legal, M.F.2
Brian, P.3
Brost, R.4
Penn, J.5
Whiting, A.6
Martin, S.7
Ford, R.8
Parr, I.9
Bouchard, M.10
Silva, C.J.11
Wrigley, S.K.12
Baltz, R.H.13
-
50
-
-
0346958244
-
Daptomycin
-
Raja, A.; LaBonte, J.; Lebbos, J.; Kirkpatrick, P. Daptomycin. Nat. Revs. Drug Disc., 2003, 2, 943-44.
-
(2003)
Nat. Revs. Drug Disc
, vol.2
, pp. 943-944
-
-
Raja, A.1
LaBonte, J.2
Lebbos, J.3
Kirkpatrick, P.4
-
51
-
-
34247641292
-
Daptomycin: A rapidly bactericidal lipopeptide for the treatment of Gram-positive infections
-
Kanafani, Z.A.; Corey, G.R. Daptomycin: A rapidly bactericidal lipopeptide for the treatment of Gram-positive infections. Expert. Rev. Anti. Infect. Ther., 2007, 5, 177-84.
-
(2007)
Expert. Rev. Anti. Infect. Ther
, vol.5
, pp. 177-184
-
-
Kanafani, Z.A.1
Corey, G.R.2
-
52
-
-
11244286128
-
Synthesis and derivatization of daptomycin: A chemoenzymatic route to acidic lipopeptide antibiotics
-
Grunewald, J.; Sieber, S.A.; Mahlert, C.; Linne, U.; Marahiel, M.A. Synthesis and derivatization of daptomycin: A chemoenzymatic route to acidic lipopeptide antibiotics. J. Am. Chem. Soc., 2004, 126, 17025-31.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 17025-17031
-
-
Grunewald, J.1
Sieber, S.A.2
Mahlert, C.3
Linne, U.4
Marahiel, M.A.5
-
53
-
-
33751218042
-
Combinatorial biosynthesis of novel antibiotics related to daptomycin
-
Nguyen, K.T.; Ritz, D.; Gu, J.-Q.; Alexander, D.; Chu, M.; Miao, V.; Brian, P.; Baltz, R.H. Combinatorial biosynthesis of novel antibiotics related to daptomycin. Proc. Natl. Acad. Sci. USA, 2006, 103, 17462-67.
-
(2006)
Proc. Natl. Acad. Sci. USA
, vol.103
, pp. 17462-17467
-
-
Nguyen, K.T.1
Ritz, D.2
Gu, J.-Q.3
Alexander, D.4
Chu, M.5
Miao, V.6
Brian, P.7
Baltz, R.H.8
-
54
-
-
33846018033
-
A topical lipoglycodepsipeptide antibacterial agent
-
Fulco, P.; Wenzel, R.P. Ramoplanin: A topical lipoglycodepsipeptide antibacterial agent. Exp. Rev. Anti. Infect. Ther., 2006, 4, 939-45.
-
(2006)
Exp. Rev. Anti. Infect. Ther
, vol.4
, Issue.939
, pp. 45
-
-
Fulco, P.1
Wenzel2
Ramoplanin, R.P.3
-
55
-
-
2342633291
-
Chemistry and biology of cyclic depsipeptides of medicinal and biological interest
-
Sarabia, F.; Chammaa, S.; Ruiz, A.S.; Ortiz, L.M.; Herrera, F.J. Chemistry and biology of cyclic depsipeptides of medicinal and biological interest. Curr. Med. Chem., 2004, 11, 1309-32.
-
(2004)
Curr. Med. Chem
, vol.11
, pp. 1309-1332
-
-
Sarabia, F.1
Chammaa, S.2
Ruiz, A.S.3
Ortiz, L.M.4
Herrera, F.J.5
-
56
-
-
0021233768
-
-
Cavalleri, B.; Pagani, H.; Volpe, G.; Selva, E.; Parenti, F. A-16686, a new antibiotic from Actinoplanes. I. Fermentation, isolation and preliminary physico-chemical characteristics. J. Antibiot., 1984, 37, 309-17.
-
Cavalleri, B.; Pagani, H.; Volpe, G.; Selva, E.; Parenti, F. A-16686, a new antibiotic from Actinoplanes. I. Fermentation, isolation and preliminary physico-chemical characteristics. J. Antibiot., 1984, 37, 309-17.
-
-
-
-
57
-
-
0029794009
-
3D structure of ramoplanin: A potent inhibitor of bacterial cell wall synthesis
-
Kurz, M.; Guba, W. 3D structure of ramoplanin: A potent inhibitor of bacterial cell wall synthesis. Biochemistry, 1996, 35, 12570-75.
-
(1996)
Biochemistry
, vol.35
, pp. 12570-12575
-
-
Kurz, M.1
Guba, W.2
-
58
-
-
0038298097
-
Ramoplanin inhibits bacterial transglycosylases by binding as a dimer to lipid II
-
Hu, Y.; Helm, J.S.; Chen, L.; Ye, X.Y.; Walker, S. Ramoplanin inhibits bacterial transglycosylases by binding as a dimer to lipid II. J. Am. Chem. Soc., 2003, 125, 8736-37.
-
(2003)
J. Am. Chem. Soc
, vol.125
, pp. 8736-8737
-
-
Hu, Y.1
Helm, J.S.2
Chen, L.3
Ye, X.Y.4
Walker, S.5
-
59
-
-
1442275730
-
Comparative in vitro activities of AC98-6446, a novel semisynthetic glycopeptide derivative of the natural product mannopeptimycin alpha, and other antimicrobial agents against gram-positive clinical isolates
-
Petersen, P.J.; Wang, T.Z.; Dushin, R.G.; Bradford, P.A. Comparative in vitro activities of AC98-6446, a novel semisynthetic glycopeptide derivative of the natural product mannopeptimycin alpha, and other antimicrobial agents against gram-positive clinical isolates. Antimicrobiotic Agents Chemother., 2004, 48, 739-46.
-
(2004)
Antimicrobiotic Agents Chemother
, vol.48
, pp. 739-746
-
-
Petersen, P.J.1
Wang, T.Z.2
Dushin, R.G.3
Bradford, P.A.4
-
60
-
-
0036229133
-
Recent developments in depsipeptide research
-
Ballard, C.E.; Yu, H.; Wang, B. Recent developments in depsipeptide research. Curr. Med. Chem., 2002, 9, 471-98.
-
(2002)
Curr. Med. Chem
, vol.9
, pp. 471-498
-
-
Ballard, C.E.1
Yu, H.2
Wang, B.3
-
61
-
-
0031762638
-
-
Kato, A.; Nakaya, S.; Kokubo, N.; Aiba, Y.; Ohashi, Y.; Hirata, H.; Fujii, K.; Harada, K. A new anti-MRSA antibiotic complex, WAP-8294A. I. Taxonomy, isolation and biological activities. J. Antibiot., 1998, 51, 929-35.
-
Kato, A.; Nakaya, S.; Kokubo, N.; Aiba, Y.; Ohashi, Y.; Hirata, H.; Fujii, K.; Harada, K. A new anti-MRSA antibiotic complex, WAP-8294A. I. Taxonomy, isolation and biological activities. J. Antibiot., 1998, 51, 929-35.
-
-
-
-
62
-
-
0030862876
-
WAP-8294A2, A Novel Anti-MRSA Antibiotic Produced by Lysobacter sp
-
Kato, A.; Nakaya, S.; Ohashi, Y.; Hirata, H.; Fujii, K.; Harada, K. WAP-8294A2, A Novel Anti-MRSA Antibiotic Produced by Lysobacter sp. J. Am. Chem. Soc., 1997, 119, 6680-81.
-
(1997)
J. Am. Chem. Soc
, vol.119
, pp. 6680-6681
-
-
Kato, A.1
Nakaya, S.2
Ohashi, Y.3
Hirata, H.4
Fujii, K.5
Harada, K.6
-
64
-
-
34547931830
-
Antibiotic use: Present and future
-
Zinser, S.H. Antibiotic use: Present and future. New Microbiol., 2008, 30, 321-25.
-
(2008)
New Microbiol
, vol.30
, pp. 321-325
-
-
Zinser, S.H.1
-
65
-
-
0032577606
-
Evaluation of in vitro activity of quinupristin/dalfopristin and comparator antimicrobial agents against worldwide clinical trial and other laboratory isolates
-
Dowzicky, M.; Nadler, H.L.; Feger, C.; Talbot, G.; Bompart, F.; Pease, M. Evaluation of in vitro activity of quinupristin/dalfopristin and comparator antimicrobial agents against worldwide clinical trial and other laboratory isolates. Am. J. Med., 1998, 104, 34S-42S.
-
(1998)
Am. J. Med
, vol.104
-
-
Dowzicky, M.1
Nadler, H.L.2
Feger, C.3
Talbot, G.4
Bompart, F.5
Pease, M.6
-
66
-
-
17444421169
-
Structures of MLSBK antibiotics bound to mutated large ribosomal subunits provide a structural explanation for resistance
-
Tu, D.; Blaha, G.; Moore, P.B.; Steitz, T.A. Structures of MLSBK antibiotics bound to mutated large ribosomal subunits provide a structural explanation for resistance. Cell, 2005, 121, 257-70.
-
(2005)
Cell
, vol.121
, pp. 257-270
-
-
Tu, D.1
Blaha, G.2
Moore, P.B.3
Steitz, T.A.4
-
67
-
-
3242712966
-
Alterations at the peptidyl transferase centre of the ribosome induced by the synergistic action of the streptogramins dalfopristin and quinupristin
-
Harms, J.M.; Schluenzen, F.; Fucini, P.; Bartels, H.; Yonath, A. Alterations at the peptidyl transferase centre of the ribosome induced by the synergistic action of the streptogramins dalfopristin and quinupristin. BMC Biol., 2004, 2, 4.
-
(2004)
BMC Biol
, vol.2
, pp. 4
-
-
Harms, J.M.1
Schluenzen, F.2
Fucini, P.3
Bartels, H.4
Yonath, A.5
-
68
-
-
0022385860
-
-
Ezaki, M.; Iwami, M.; Yamashita, M.; Hashimoto, S.; Komori, T.; Umehara, K.; Mine, Y.; Kohsaka, M.; Aoki, H.; Imanaka, H. Biphenomycins A and B, novel peptide antibiotics. I. Taxonomy, fermentation, isolation and characterization. J. Antibiot., 1985, 38, 1453-61
-
Ezaki, M.; Iwami, M.; Yamashita, M.; Hashimoto, S.; Komori, T.; Umehara, K.; Mine, Y.; Kohsaka, M.; Aoki, H.; Imanaka, H. Biphenomycins A and B, novel peptide antibiotics. I. Taxonomy, fermentation, isolation and characterization. J. Antibiot., 1985, 38, 1453-61
-
-
-
-
69
-
-
0014166168
-
LL-AF283-alpha and LL-AF283-beta, antibacterial antibiotics of unusual biological properties
-
Martin, J.H.; Mitscher, L.A.; Shu, P.; Porter, J.N.; Bohonos, N.; DeVoe, S.E.; Patterson, E.L. LL-AF283-alpha and LL-AF283-beta, antibacterial antibiotics of unusual biological properties. Antimicrob. Agents Chemother., 1967, 7, 422-25.
-
(1967)
Antimicrob. Agents Chemother
, vol.7
, pp. 422-425
-
-
Martin, J.H.1
Mitscher, L.A.2
Shu, P.3
Porter, J.N.4
Bohonos, N.5
DeVoe, S.E.6
Patterson, E.L.7
-
70
-
-
0030024606
-
Effects of ofloxacin on the pharmacokinetics and pharmacodynamics of procainamide
-
Martin, D.E.; Shen, J.; Griener, J.; Raasch, R.; Patterson, J.H.; Cascio, W. Effects of ofloxacin on the pharmacokinetics and pharmacodynamics of procainamide. J. Clin. Pharmacol., 1996, 36, 85-91.
-
(1996)
J. Clin. Pharmacol
, vol.36
, pp. 85-91
-
-
Martin, D.E.1
Shen, J.2
Griener, J.3
Raasch, R.4
Patterson, J.H.5
Cascio, W.6
-
71
-
-
0026089753
-
The synthesis of biphenomycin B
-
Schmidt, U.; Meyer, V.; Leitenberger, A.; Lieberknecht, H.; Griesser, J. The synthesis of biphenomycin B. J. Chem. Soc. Chem. Commun., 1991, 275-77.
-
(1991)
J. Chem. Soc. Chem. Commun
, pp. 275-277
-
-
Schmidt, U.1
Meyer, V.2
Leitenberger, A.3
Lieberknecht, H.4
Griesser, J.5
-
72
-
-
62249115490
-
-
Lampe, T.; Adelt, I.; Beyer, D.; Brunner, N.; Endermann, R.; Ehlert, K.; Kroll, H.P.; Von Nussbaum, F.; Raddatz, S.; Rudolph, J.; Schiffer, G.; Schumacher, A.; Cancho-Grande, Y.; Michels, M.; Weigand, S. Antibacterial amide macrocycles. WO/2005/033129, 2005.
-
Lampe, T.; Adelt, I.; Beyer, D.; Brunner, N.; Endermann, R.; Ehlert, K.; Kroll, H.P.; Von Nussbaum, F.; Raddatz, S.; Rudolph, J.; Schiffer, G.; Schumacher, A.; Cancho-Grande, Y.; Michels, M.; Weigand, S. Antibacterial amide macrocycles. WO/2005/033129, 2005.
-
-
-
-
73
-
-
4644327984
-
Viomycin a new antibiotic active against Mycobacteria
-
Finlay, A.C.; Hobby, G.L.; Hoschstein, F.; Lees, T.M.; Lenert, T.F.; Means, J.A.; P'An, S.Y.; Regna, P.P.; Routien, J.B.; Sobin, B.A.; Tate, K.B.; Kane, J.H. Viomycin a new antibiotic active against Mycobacteria. Am. Rev. Tuberc., 1951, 63, 1-3.
-
(1951)
Am. Rev. Tuberc
, vol.63
, pp. 1-3
-
-
Finlay, A.C.1
Hobby, G.L.2
Hoschstein, F.3
Lees, T.M.4
Lenert, T.F.5
Means, J.A.6
P'An, S.Y.7
Regna, P.P.8
Routien, J.B.9
Sobin, B.A.10
Tate, K.B.11
Kane, J.H.12
-
74
-
-
0015210101
-
Total structure of capreomycin IB, a tuberculostatic peptide antibiotic
-
Bycroft, B.W.; Cameron, D.; Croft, L.R.; Hassanali-Walji, A.; Johnson, A.W.; Webb, T. Total structure of capreomycin IB, a tuberculostatic peptide antibiotic. Nature, 1971, 231, 301.
-
(1971)
Nature
, vol.231
, pp. 301
-
-
Bycroft, B.W.1
Cameron, D.2
Croft, L.R.3
Hassanali-Walji, A.4
Johnson, A.W.5
Webb, T.6
-
75
-
-
0004403924
-
-
Herr Jr., E.B.; Henry, M.E.; Pittenger, G.E.; Higgens, C.E. Proc. Indiana Acad. Sci., 1960, 69, 134.
-
(1960)
Proc. Indiana Acad. Sci
, vol.69
, pp. 134
-
-
Herr Jr., E.B.1
Henry, M.E.2
Pittenger, G.E.3
Higgens, C.E.4
-
76
-
-
0014022779
-
Chemical and physical characterization of capreomycin
-
Herr Jr., E.B.; Redstone, M.O. Chemical and physical characterization of capreomycin. Ann. NY Acad. Sci., 1966, 135, 940-46.
-
(1966)
Ann. NY Acad. Sci
, vol.135
, pp. 940-946
-
-
Herr Jr., E.B.1
Redstone, M.O.2
-
77
-
-
18744422288
-
-
Dirlam, J.P.; Belton, A.M.; Birsner, N.C.; Brooks, R.R.; Chang, S.P.; Chandrasekaran, R.Y.; Clancy, J.; Cronin, B.J.; Dirlam, B.P.; Finegan, S.M.; Froshauer, S.A.; Girard, A.E.; Hayashi, S.F.; Howe, R.J.; Kane, J.C.; Kamicker, B.J.; Kaufman, S.A.; Kolosko, N.L.; LeMay, M.A.; Linde, R.G.; Lyssikatos, J.P.; MacLelland, C.P.; Magee, T.V.; Massa, M.A.; Miller, S.A.; Minich, M.L.; Perry, D.A.; Petitpas, J.W.; Reese, C.P.; Seibel, S.B.; Su, W.G.; Sweeney, K.T.; Whipple, D.A.; Yang, B.V. Cyclic homopentapeptides 1. Analogs of tuberactinomycins and capreomycin with activity against vancomycin-resistant enterococci and Pasteurella. Bioorg. Med. Chem. Lett., 1997, 7, 1139-44.
-
Dirlam, J.P.; Belton, A.M.; Birsner, N.C.; Brooks, R.R.; Chang, S.P.; Chandrasekaran, R.Y.; Clancy, J.; Cronin, B.J.; Dirlam, B.P.; Finegan, S.M.; Froshauer, S.A.; Girard, A.E.; Hayashi, S.F.; Howe, R.J.; Kane, J.C.; Kamicker, B.J.; Kaufman, S.A.; Kolosko, N.L.; LeMay, M.A.; Linde, R.G.; Lyssikatos, J.P.; MacLelland, C.P.; Magee, T.V.; Massa, M.A.; Miller, S.A.; Minich, M.L.; Perry, D.A.; Petitpas, J.W.; Reese, C.P.; Seibel, S.B.; Su, W.G.; Sweeney, K.T.; Whipple, D.A.; Yang, B.V. Cyclic homopentapeptides 1. Analogs of tuberactinomycins and capreomycin with activity against vancomycin-resistant enterococci and Pasteurella. Bioorg. Med. Chem. Lett., 1997, 7, 1139-44.
-
-
-
-
78
-
-
18344411249
-
Cyclic homopentapeptides 3. Synthetic modifications to the capreomycins and tuberactinomycins: Compounds with activity against methicillin-resistant Staphylococcus aureus and vancomycin-resistant enterococci
-
Linde, R.G.; Birsner, N.C.; Chandrasekaran, R.Y.; Clancy, J.; Howe, R.J.; Lyssikatos, J.P.; MacLelland, C.P.; Magee, T.V.; Petitpas, J.W.; Rainville, J.P.; Su, W.G.; Vu, C.B.; Whipple, D.A. Cyclic homopentapeptides 3. Synthetic modifications to the capreomycins and tuberactinomycins: Compounds with activity against methicillin-resistant Staphylococcus aureus and vancomycin-resistant enterococci. Bioorg. Med. Chem. Lett., 1997, 7, 1149-52.
-
(1997)
Bioorg. Med. Chem. Lett
, vol.7
, pp. 1149-1152
-
-
Linde, R.G.1
Birsner, N.C.2
Chandrasekaran, R.Y.3
Clancy, J.4
Howe, R.J.5
Lyssikatos, J.P.6
MacLelland, C.P.7
Magee, T.V.8
Petitpas, J.W.9
Rainville, J.P.10
Su, W.G.11
Vu, C.B.12
Whipple, D.A.13
-
79
-
-
17544398657
-
Cyclic homopentapeptides 2. Synthetic modifications of viomycin
-
Lyssikatos, J.P.; Chang, S.P.; Dirlam, J.P.; Finegan, S.M.; Girard, A.E.; Hayashi, S.F.; Larson, D.P.; Lee, A.S.; Linde Ii, R.G.; McLelland, C.P.; Petipas, J.W.; Seibel, S.B.; Vu, C.B. Cyclic homopentapeptides 2. Synthetic modifications of viomycin. Bioorg. Med. Chem. Lett., 1997, 7, 1145-48.
-
(1997)
Bioorg. Med. Chem. Lett
, vol.7
, pp. 1145-1148
-
-
Lyssikatos, J.P.1
Chang, S.P.2
Dirlam, J.P.3
Finegan, S.M.4
Girard, A.E.5
Hayashi, S.F.6
Larson, D.P.7
Lee, A.S.8
Linde Ii, R.G.9
McLelland, C.P.10
Petipas, J.W.11
Seibel, S.B.12
Vu, C.B.13
-
80
-
-
33845716400
-
A54556 antibiotics and process of production thereof
-
US patent 4,492,650
-
Michel, K.H.; Kastner, R.E. A54556 antibiotics and process of production thereof. US patent 4,492,650, 1985.
-
(1985)
-
-
Michel, K.H.1
Kastner, R.E.2
-
81
-
-
0026351941
-
-
Osada, H.; Yano, T.; Koshino, H.; Isono, K. Enopeptin A, a novel depsipeptide antibiotic with anti-bacteriophage activity. J. Antibiot., 1991, 44, 1463-66.
-
Osada, H.; Yano, T.; Koshino, H.; Isono, K. Enopeptin A, a novel depsipeptide antibiotic with anti-bacteriophage activity. J. Antibiot., 1991, 44, 1463-66.
-
-
-
-
82
-
-
0030750038
-
Synthesis of Enopeptin B from Streptomyces sp RK-1051
-
Schmidt, U.; Neumann, K.; Schumacher, A.; Weinbrenner, S. Synthesis of Enopeptin B from Streptomyces sp RK-1051. Angew. Chem. Int. Ed., 1997, 36, 1110-12.
-
(1997)
Angew. Chem. Int. Ed
, vol.36
, pp. 1110-1112
-
-
Schmidt, U.1
Neumann, K.2
Schumacher, A.3
Weinbrenner, S.4
-
83
-
-
33746604766
-
Medicinal Chemistry Optimization of Acyldepsipeptides of the Enopeptin Class Antibiotics
-
Hinzen, B.; Raddatz, S.; Paulsen, H.; Lampe, T.; Schumacher, A.; Habich, D.; Hellwig, V.; Benet-Buchholz, J.; Endermann, R.; Labischinski, H.; Brötz-Oesterhelt, H. Medicinal Chemistry Optimization of Acyldepsipeptides of the Enopeptin Class Antibiotics. Chem. Med. Chem., 2006, 1, 689-93.
-
(2006)
Chem. Med. Chem
, vol.1
, pp. 689-693
-
-
Hinzen, B.1
Raddatz, S.2
Paulsen, H.3
Lampe, T.4
Schumacher, A.5
Habich, D.6
Hellwig, V.7
Benet-Buchholz, J.8
Endermann, R.9
Labischinski, H.10
Brötz-Oesterhelt, H.11
-
84
-
-
27144460621
-
Dysregulation of bacterial proteolytic machinery by a new class of antibiotics
-
Brötz-Oesterhelt, H.; Beyer, D.; Kroll, H.P.; Endermann, R.; Ladel, C.; Schroeder, W.; Hinzen, B.; Raddatz, S.; Paulsen, H.; Hennenger, K.; Bandow, J.E.; Sahl, H.G.; Labschinski, H. Dysregulation of bacterial proteolytic machinery by a new class of antibiotics. Nat. Med., 2005, 11, 1082-87.
-
(2005)
Nat. Med
, vol.11
, pp. 1082-1087
-
-
Brötz-Oesterhelt, H.1
Beyer, D.2
Kroll, H.P.3
Endermann, R.4
Ladel, C.5
Schroeder, W.6
Hinzen, B.7
Raddatz, S.8
Paulsen, H.9
Hennenger, K.10
Bandow, J.E.11
Sahl, H.G.12
Labschinski, H.13
-
85
-
-
0028030855
-
Solution conformation of enopeptin A, a depsipeptide antibiotic, using 2D NMR and restrained molecular dynamics studies
-
Young, J.J.; Jung, L.J.; Liu, W.T.; Ho, S.N.; Chang, L.R.; Tsai, Y.C.; Bhaskaran, R.; Yu, C. Solution conformation of enopeptin A, a depsipeptide antibiotic, using 2D NMR and restrained molecular dynamics studies. J. Antibiot., 1994, 47, 922-31.
-
(1994)
J. Antibiot
, vol.47
, pp. 922-931
-
-
Young, J.J.1
Jung, L.J.2
Liu, W.T.3
Ho, S.N.4
Chang, L.R.5
Tsai, Y.C.6
Bhaskaran, R.7
Yu, C.8
-
86
-
-
33746604766
-
Medicinal chemistry optimization of acyldepsipeptides of the enopeptin class antibiotics
-
Hinzen, B.; Raddatz, S.; Paulsen, H.; Lampe, T.; Schumacher, A.; Habich, D.; Hellwig, V.; et-Buchholz, J.; Endermann, R.; Labischinski, H.; Brotz-Oesterhelt, H. Medicinal chemistry optimization of acyldepsipeptides of the enopeptin class antibiotics. Chem. Med. Chem., 2006, 1, 689-93.
-
(2006)
Chem. Med. Chem
, vol.1
, pp. 689-693
-
-
Hinzen, B.1
Raddatz, S.2
Paulsen, H.3
Lampe, T.4
Schumacher, A.5
Habich, D.6
Hellwig, V.7
et-Buchholz, J.8
Endermann, R.9
Labischinski, H.10
Brotz-Oesterhelt, H.11
-
87
-
-
0033871574
-
Cationic antimicrobial peptides: Towards clinical applications
-
Hancock, R.E. Cationic antimicrobial peptides: Towards clinical applications. Exp. Opin. Invest. Drugs, 2000, 9, 1723-29.
-
(2000)
Exp. Opin. Invest. Drugs
, vol.9
, pp. 1723-1729
-
-
Hancock, R.E.1
-
88
-
-
33845699790
-
Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies
-
Hancock, R.E.W.; Sahl, H.G. Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies. Nat. Biotech., 2006, 24, 1551-57.
-
(2006)
Nat. Biotech
, vol.24
, pp. 1551-1557
-
-
Hancock, R.E.W.1
Sahl, H.G.2
-
89
-
-
0032007854
-
Cationic peptides: A new source of antibiotics
-
Hancock, R.E.; Lehrer, R. Cationic peptides: A new source of antibiotics. Trends Biotechnol., 1998, 16, 82-88
-
(1998)
Trends Biotechnol
, vol.16
, pp. 82-88
-
-
Hancock, R.E.1
Lehrer, R.2
-
90
-
-
62249209309
-
-
O'Grady, F.; Greenwood D. In Antibiotic and Chemotherapy: Anti-infective agents and their use in therapy, 7th Edition, O'Grady, F.; Lambert, H.P.; Finch, R.G; Greenwood, D., Eds.; Churchill Livingstone Inc.: New York, 1997, pp. 336-43.
-
O'Grady, F.; Greenwood D. In Antibiotic and Chemotherapy: Anti-infective agents and their use in therapy, 7th Edition, O'Grady, F.; Lambert, H.P.; Finch, R.G; Greenwood, D., Eds.; Churchill Livingstone Inc.: New York, 1997, pp. 336-43.
-
-
-
-
91
-
-
84988053681
-
Determination of the major solution conformation of tyrocidine A, using molecular mechanics energy minimization and NMR-derived distance and torsion angle constraints
-
Tonge, A.P.; Murray-Rust, P.; Gibbons, W.A.; McLachlan, L.K. Determination of the major solution conformation of tyrocidine A, using molecular mechanics energy minimization and NMR-derived distance and torsion angle constraints. J. Comp. Chem., 1988, 9, 522-38.
-
(1988)
J. Comp. Chem
, vol.9
, pp. 522-538
-
-
Tonge, A.P.1
Murray-Rust, P.2
Gibbons, W.A.3
McLachlan, L.K.4
-
92
-
-
34548538972
-
Development of tyrocidine A analogues with improved antibacterial activity
-
Marques, M.A.; Citron, D.M.; Wang, C.C. Development of tyrocidine A analogues with improved antibacterial activity. Bioorg. Med. Chem., 2007, 15, 6667-77.
-
(2007)
Bioorg. Med. Chem
, vol.15
, pp. 6667-6677
-
-
Marques, M.A.1
Citron, D.M.2
Wang, C.C.3
-
93
-
-
0037043734
-
Biomimetic synthesis and optimization of cyclic peptide antibiotics
-
Kohli, R.M.; Walsh, C.T.; Burkart, M.D. Biomimetic synthesis and optimization of cyclic peptide antibiotics. Nature, 2002, 418, 658-61.
-
(2002)
Nature
, vol.418
, pp. 658-661
-
-
Kohli, R.M.1
Walsh, C.T.2
Burkart, M.D.3
-
94
-
-
7444226365
-
A chemoenzymatic approach to glycopeptide antibiotics
-
Lin, H.; Walsh, C.T. A chemoenzymatic approach to glycopeptide antibiotics. J. Am. Chem. Soc., 2004, 126, 13998-4003.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 13998-14003
-
-
Lin, H.1
Walsh, C.T.2
-
95
-
-
34347205269
-
High-throughput synthesis and screening of cyclic peptide antibiotics
-
Xiao, Q.; Pei, D. High-throughput synthesis and screening of cyclic peptide antibiotics. J. Med. Chem., 2007, 50, 3132-37.
-
(2007)
J. Med. Chem
, vol.50
, pp. 3132-3137
-
-
Xiao, Q.1
Pei, D.2
-
96
-
-
0000837408
-
-
Koyama, Y.; Kurosasa, A.; Tsuchiya, A.; Takukuta, K. J. Antibiot., 1950, 3, 457-58.
-
(1950)
Antibiot
, vol.3
, pp. 457-458
-
-
Koyama, Y.1
Kurosasa, A.2
Tsuchiya, A.3
Takukuta, K.J.4
-
97
-
-
0017620773
-
Polymyxin and related peptide antibiotics
-
Storm, D.R.; Rosenthal, K.S.; Swanson, P.E. Polymyxin and related peptide antibiotics. Annu. Rev. Biochem., 1977, 46, 723-63.
-
(1977)
Annu. Rev. Biochem
, vol.46
, pp. 723-763
-
-
Storm, D.R.1
Rosenthal, K.S.2
Swanson, P.E.3
-
98
-
-
0014945506
-
Acute renal failure due to overdosage of colistin
-
Brown, J.M.; Dorman, D.C.; Roy, L.P. Acute renal failure due to overdosage of colistin. Med. J. Aust., 1970, 2, 923-24.
-
(1970)
Med. J. Aust
, vol.2
, pp. 923-924
-
-
Brown, J.M.1
Dorman, D.C.2
Roy, L.P.3
-
99
-
-
0014801502
-
Adverse effects of sodium colistimethate. Manifestations and specific reaction rates during 317 courses of therapy
-
Koch-Weser, J.; Sidel, V.W.; Federman, E.B.; Kanarek, P.; Finer, D.C.; Eaton, A.E. Adverse effects of sodium colistimethate. Manifestations and specific reaction rates during 317 courses of therapy. Ann. Intern. Med., 1970, 72, 857-68.
-
(1970)
Ann. Intern. Med
, vol.72
, pp. 857-868
-
-
Koch-Weser, J.1
Sidel, V.W.2
Federman, E.B.3
Kanarek, P.4
Finer, D.C.5
Eaton, A.E.6
-
100
-
-
17644389620
-
Colistin: The revival of polymyxins for the management of multidrug-resistant Gram-negative bacterial infections
-
Falagas, M.E.; Kasiakou, S.K. Colistin: The revival of polymyxins for the management of multidrug-resistant Gram-negative bacterial infections. Clin. Infect. Dis., 2005, 40, 1333-41
-
(2005)
Clin. Infect. Dis
, vol.40
, pp. 1333-1341
-
-
Falagas, M.E.1
Kasiakou, S.K.2
-
101
-
-
0032402376
-
Selective chemical modifications of polymyxin B
-
Weinstein, J.; Afonso, A.; Moss, E., Jr.; Miller, G.H. Selective chemical modifications of polymyxin B. Bioorg. Med. Chem. Lett., 1998, 8, 3391-96.
-
(1998)
Bioorg. Med. Chem. Lett
, vol.8
, pp. 3391-3396
-
-
Weinstein, J.1
Afonso, A.2
Moss Jr., E.3
Miller, G.H.4
-
102
-
-
0030855146
-
Protegrin-1: A broad-spectrum, rapidly microbicidal peptide with in vivo activity
-
Steinberg, D.A.; Hurst, M.A.; Fujii, C.A.; Kung, A.H.; Ho, J.F.; Cheng, F.C.; Loury, D.J.; Fiddes, J.C. Protegrin-1: A broad-spectrum, rapidly microbicidal peptide with in vivo activity. Antimicr. Agents Chemother., 1997, 41, 1738-42.
-
(1738)
Antimicr. Agents Chemother
, vol.1997
, pp. 41
-
-
Steinberg, D.A.1
Hurst, M.A.2
Fujii, C.A.3
Kung, A.H.4
Ho, J.F.5
Cheng, F.C.6
Loury, D.J.7
Fiddes, J.C.8
-
103
-
-
0029886161
-
Synthesis and solution structure of the antimicrobial peptide protegrin-1
-
Aumelas, A.; Mangoni, M.; Roumestand, C.; Chiche, L.; Despaux, E.; Grassy, G.; Calas, B.; Chavanieu, A. Synthesis and solution structure of the antimicrobial peptide protegrin-1. Eur. J. Biochem., 1996, 237, 575-83.
-
(1996)
Eur. J. Biochem
, vol.237
, pp. 575-583
-
-
Aumelas, A.1
Mangoni, M.2
Roumestand, C.3
Chiche, L.4
Despaux, E.5
Grassy, G.6
Calas, B.7
Chavanieu, A.8
-
104
-
-
0030198873
-
Solution structure of protegrin-1, a broad-spectrum antimicrobial peptide from porcine leukocytes
-
Fahrner, R.L.; Dieckmann, T.; Harwig, S.S.L.; Lehrer, R.I.; Eisenberg, D.; Feigon, J. Solution structure of protegrin-1, a broad-spectrum antimicrobial peptide from porcine leukocytes. Chem. Biol., 1996, 3, 543-50.
-
(1996)
Chem. Biol
, vol.3
, pp. 543-550
-
-
Fahrner, R.L.1
Dieckmann, T.2
Harwig, S.S.L.3
Lehrer, R.I.4
Eisenberg, D.5
Feigon, J.6
-
105
-
-
0032536098
-
Oligomerization of protegrin-1 in the presence of DPC micelles. A proton high-resolution NMR study
-
Roumestand, C.; Louis, V.; Aumelas, A.; Grassy, G.; Calas, B.; Chavanieu, A. Oligomerization of protegrin-1 in the presence of DPC micelles. A proton high-resolution NMR study. FEBS Lett., 1998, 421, 263-67.
-
(1998)
FEBS Lett
, vol.421
, pp. 263-267
-
-
Roumestand, C.1
Louis, V.2
Aumelas, A.3
Grassy, G.4
Calas, B.5
Chavanieu, A.6
-
106
-
-
33745855891
-
Membrane-bound dimer structure of a beta-hairpin antimicrobial peptide from rotational-echo double-resonance solid-state NMR
-
Mani, R.; Tang, M.; Wu, X.; Buffy, J.J.; Waring, A.J.; Sherman, M.A.; Hong, M. Membrane-bound dimer structure of a beta-hairpin antimicrobial peptide from rotational-echo double-resonance solid-state NMR. Biochemistry, 2006, 45, 8341-49.
-
(2006)
Biochemistry
, vol.45
, pp. 8341-8349
-
-
Mani, R.1
Tang, M.2
Wu, X.3
Buffy, J.J.4
Waring, A.J.5
Sherman, M.A.6
Hong, M.7
-
107
-
-
45549085024
-
-
Tang, M.; Waring, A.J.; Lehrer, R.L.; Hong, M. Effects of guanidinium-phosphate hydrogen bonding on the membrane-bound structure and activity of an arginine-rich membrane peptide from solid-state NMR spectroscopy. Angew. Chem. Int. Ed., 2008, 47, 3202-05.
-
Tang, M.; Waring, A.J.; Lehrer, R.L.; Hong, M. Effects of guanidinium-phosphate hydrogen bonding on the membrane-bound structure and activity of an arginine-rich membrane peptide from solid-state NMR spectroscopy. Angew. Chem. Int. Ed., 2008, 47, 3202-05.
-
-
-
-
108
-
-
33845903833
-
Drugs for bad bugs: Confronting the challenges of antibacterial discovery
-
Payne, D.J.; Gwynn, M.N.; Holmes, D.J.; Pompliano, D.L. Drugs for bad bugs: Confronting the challenges of antibacterial discovery. Nat. Revs. Drug Disc., 2007, 6, 29-40.
-
(2007)
Nat. Revs. Drug Disc
, vol.6
, pp. 29-40
-
-
Payne, D.J.1
Gwynn, M.N.2
Holmes, D.J.3
Pompliano, D.L.4
-
109
-
-
36749073433
-
The design of drugs for HIV and HCV
-
De, C.E. The design of drugs for HIV and HCV. Nat. Rev. Drug Discov., 2007, 6, 1001-18.
-
(2007)
Nat. Rev. Drug Discov
, vol.6
, pp. 1001-1018
-
-
De, C.E.1
-
110
-
-
0344201903
-
-
Lamarre, D.; Anderson, P.C.; Bailey, M.; Beaulieu, P.; Bolger, G.; Bonneau, P.; Bos, M.; Cameron, D.R.; Cartier, M.; Cordingley, M.G.; Faucher, A.M.; Goudreau, N.; Kawai, S.H.; Kukolj, G.; Lagace, L.; LaPlante, S.R.; Narjes, H.; Poupart, M.A.; Rancourt, J.; Sentjens, R.E.; St, G.R.; Simoneau, B.; Steinmann, G.; Thibeault, D.; Tsantrizos, Y.S.; Weldon, S.M.; Yong, C.L.; Llinas-Brunet, M. An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus. Nature, 2003, 426, 186-89.
-
Lamarre, D.; Anderson, P.C.; Bailey, M.; Beaulieu, P.; Bolger, G.; Bonneau, P.; Bos, M.; Cameron, D.R.; Cartier, M.; Cordingley, M.G.; Faucher, A.M.; Goudreau, N.; Kawai, S.H.; Kukolj, G.; Lagace, L.; LaPlante, S.R.; Narjes, H.; Poupart, M.A.; Rancourt, J.; Sentjens, R.E.; St, G.R.; Simoneau, B.; Steinmann, G.; Thibeault, D.; Tsantrizos, Y.S.; Weldon, S.M.; Yong, C.L.; Llinas-Brunet, M. An NS3 protease inhibitor with antiviral effects in humans infected with hepatitis C virus. Nature, 2003, 426, 186-89.
-
-
-
-
111
-
-
40549101840
-
Relative replication capacity and selective advantage profiles of PI-resistant HCV NS3 protease mutants in the HCV genotype 1b replicon system
-
He, Y.; King, M.S.; Kempf, D.J.; Lu, L.; Lim, H.B.; Krishnan, P.; Kati, W.; Middleton, T.; Molla, A. Relative replication capacity and selective advantage profiles of PI-resistant HCV NS3 protease mutants in the HCV genotype 1b replicon system. Antimicrob. Agents Chemother., 2008, 52, 1101-10.
-
(2008)
Antimicrob. Agents Chemother
, vol.52
, pp. 1101-1110
-
-
He, Y.1
King, M.S.2
Kempf, D.J.3
Lu, L.4
Lim, H.B.5
Krishnan, P.6
Kati, W.7
Middleton, T.8
Molla, A.9
-
112
-
-
34548567684
-
Cyclophilin inhibitors in hepatitis C viral infection
-
Flisiak, R.; Dumont, J.M.; Crabbe, R. Cyclophilin inhibitors in hepatitis C viral infection. Expert. Opin. Invest. Drugs, 2007, 16, 1345-54.
-
(2007)
Expert. Opin. Invest. Drugs
, vol.16
, pp. 1345-1354
-
-
Flisiak, R.1
Dumont, J.M.2
Crabbe, R.3
-
113
-
-
0033989709
-
The CXCR4 antagonist AMD3100 efficiently inhibits cell-surface-expressed human immunodeficiency virus type 1 envelope-induced apoptosis
-
Blanco, J.; Barretina, J.; Henson, G.; Bridger, G.; De, C.E.; Clotet, B.; Este, J.A. The CXCR4 antagonist AMD3100 efficiently inhibits cell-surface-expressed human immunodeficiency virus type 1 envelope-induced apoptosis. Antimicrob. Agents Chemother., 2000, 44, 51-56.
-
(2000)
Antimicrob. Agents Chemother
, vol.44
, pp. 51-56
-
-
Blanco, J.1
Barretina, J.2
Henson, G.3
Bridger, G.4
De, C.E.5
Clotet, B.6
Este, J.A.7
-
114
-
-
23944499800
-
Concise synthesis of all stereoisomers of beta-methoxytyrosine and determination of the absolute configuration of the residue in callipeltin A
-
Zampella, A.; D'Orsi, R.; Sepe, V.; Casapullo, A.; Monti, M.C.; D'Auria, M.V. Concise synthesis of all stereoisomers of beta-methoxytyrosine and determination of the absolute configuration of the residue in callipeltin A. Org. Lett., 2005, 7, 3585-88.
-
(2005)
Org. Lett
, vol.7
, pp. 3585-3588
-
-
Zampella, A.1
D'Orsi, R.2
Sepe, V.3
Casapullo, A.4
Monti, M.C.5
D'Auria, M.V.6
-
115
-
-
0030965148
-
Suppressive effects of destruxin B on hepatitis B virus surface antigen gene expression in human hepatoma cells
-
Chen, H.C.; Chou, C.K.; Sun, C.M.; Yeh, S.F. Suppressive effects of destruxin B on hepatitis B virus surface antigen gene expression in human hepatoma cells. Antivir. Res., 1997, 34, 137-44.
-
(1997)
Antivir. Res
, vol.34
, pp. 137-144
-
-
Chen, H.C.1
Chou, C.K.2
Sun, C.M.3
Yeh, S.F.4
-
116
-
-
24344442462
-
The therapeutic potential of NS3 protease inhibitors in HCV infection
-
Goudreau, N.; Llinas-Brunet, M. The therapeutic potential of NS3 protease inhibitors in HCV infection. Exp. Opin. Invest. Drugs, 2005, 14, 1129-44.
-
(2005)
Exp. Opin. Invest. Drugs
, vol.14
, pp. 1129-1144
-
-
Goudreau, N.1
Llinas-Brunet, M.2
-
117
-
-
10644231764
-
A systematic approach to the optimization of substrate-based inhibitors of the hepatitis C virus NS3 protease: Discovery of potent and specific tripeptide inhibitors
-
Llinas-Brunet, M.; Bailey, M.D.; Ghiro, E.; Gorys, V.; Halmos, T.; Poirier, M.; Rancourt, J.; Goudreau, N. A systematic approach to the optimization of substrate-based inhibitors of the hepatitis C virus NS3 protease: Discovery of potent and specific tripeptide inhibitors. J. Med. Chem., 2004, 47, 6584-94.
-
(2004)
J. Med. Chem
, vol.47
, pp. 6584-6594
-
-
Llinas-Brunet, M.1
Bailey, M.D.2
Ghiro, E.3
Gorys, V.4
Halmos, T.5
Poirier, M.6
Rancourt, J.7
Goudreau, N.8
-
118
-
-
0027207885
-
Human immunodeficiency virus type 1 Gag protein binds to cyclophilins A and B
-
Luban, J.; Bossolt, K.L.; Franke, E.K.; Kalpana, G.V.; Goff, S.P. Human immunodeficiency virus type 1 Gag protein binds to cyclophilins A and B. Cell, 1993, 73, 1067-78.
-
(1993)
Cell
, vol.73
, pp. 1067-1078
-
-
Luban, J.1
Bossolt, K.L.2
Franke, E.K.3
Kalpana, G.V.4
Goff, S.P.5
-
119
-
-
21244433445
-
Cyclophilin B is a functional regulator of hepatitis C virus RNA polymerase
-
Watashi, K.; Ishii, N.; Hijikata, M.; Inoue, D.; Murata, T.; Miyanari, Y.; Shimotohno, K. Cyclophilin B is a functional regulator of hepatitis C virus RNA polymerase. Mol. Cell, 2005, 19, 111-22.
-
(2005)
Mol. Cell
, vol.19
, pp. 111-122
-
-
Watashi, K.1
Ishii, N.2
Hijikata, M.3
Inoue, D.4
Murata, T.5
Miyanari, Y.6
Shimotohno, K.7
-
120
-
-
33646015668
-
The non-immunosuppressive cyclosporin DEBIO-025 is a potent inhibitor of hepatitis C virus replication in vitro
-
Paeshuyse, J.; Kaul, A.; De, C.E.; Rosenwirth, B.; Dumont, J.M.; Scalfaro, P.; Bartenschlager, R.; Neyts, J. The non-immunosuppressive cyclosporin DEBIO-025 is a potent inhibitor of hepatitis C virus replication in vitro. Hepatology, 2006, 4 3, 761-70.
-
(2006)
Hepatology
, vol.4
, Issue.3
, pp. 761-770
-
-
Paeshuyse, J.1
Kaul, A.2
De, C.E.3
Rosenwirth, B.4
Dumont, J.M.5
Scalfaro, P.6
Bartenschlager, R.7
Neyts, J.8
-
121
-
-
35948935297
-
-
Macor J.E, Ed, Elsevier: Amsterdam
-
Kazmierski, W.M.; Gudmundsson, K.S.; Piscitelli, S.C. In Annual Reports in Medicinal Chemistry; Macor J.E., Ed.; Elsevier: Amsterdam, 2007; Vol. 42, pp. 301-20.
-
(2007)
Annual Reports in Medicinal Chemistry
, vol.42
, pp. 301-320
-
-
Kazmierski, W.M.1
Gudmundsson, K.S.2
Piscitelli, S.C.3
-
122
-
-
0038681342
-
The bicyclam AMD3100 story
-
De Clercq, E. The bicyclam AMD3100 story. Nat. Rev. Drug Discov. 2003, 2, 581-87.
-
(2003)
Nat. Rev. Drug Discov
, vol.2
, pp. 581-587
-
-
De Clercq, E.1
-
123
-
-
0034120373
-
Pharmacokinetics and safety of AMD-3100, a novel antagonist of the CXCR-4 chemokine receptor, in human volunteers
-
Hendrix, C.W.; Flexner, C.; Macfarland, R.T.; Giandomenico, C.; Fuchs, E.J.; Redpath, E.; Bridger, G.; Henson, G.W. Pharmacokinetics and safety of AMD-3100, a novel antagonist of the CXCR-4 chemokine receptor, in human volunteers. Antimicrob. Agents Chemoth., 2000, 44, 1667-73.
-
(2000)
Antimicrob. Agents Chemoth
, vol.44
, pp. 1667-1673
-
-
Hendrix, C.W.1
Flexner, C.2
Macfarland, R.T.3
Giandomenico, C.4
Fuchs, E.J.5
Redpath, E.6
Bridger, G.7
Henson, G.W.8
-
124
-
-
0037179166
-
Isolation of callipeltins A-C and of two new open-chain derivatives of callipeltin A from the marine sponge Latrunculia sp. A revision of the stereostructure of callipeltins
-
Zampella, A.; Randazzo, A.; Borbone, N.; Lucani, S.; Travisi, L.; Debitus, C.; D'Auria, M.V. Isolation of callipeltins A-C and of two new open-chain derivatives of callipeltin A from the marine sponge Latrunculia sp. A revision of the stereostructure of callipeltins. Tetrahedron Lett., 2002, 43, 6163-66.
-
(2002)
Tetrahedron Lett
, vol.43
, pp. 6163-6166
-
-
Zampella, A.1
Randazzo, A.2
Borbone, N.3
Lucani, S.4
Travisi, L.5
Debitus, C.6
D'Auria, M.V.7
-
125
-
-
33747384950
-
-
Calimsiz, S.; Morales Ramos, A.I.; Lipton, M.A. Solid-phase synthesis and configurational reassigment of callipeltin E. Implications for the structures of callipeltins A and B. J. Org. Chem., 2006, 71, 6351-56.
-
Calimsiz, S.; Morales Ramos, A.I.; Lipton, M.A. Solid-phase synthesis and configurational reassigment of callipeltin E. Implications for the structures of callipeltins A and B. J. Org. Chem., 2006, 71, 6351-56.
-
-
-
-
126
-
-
0030575413
-
Callipeltins B and C; bioactive peptides from a marine Lithistida sponge Callipelta sp
-
D'Auria, M.V.; Zampella, A.; Palma, L.; Minale, L. Callipeltins B and C; bioactive peptides from a marine Lithistida sponge Callipelta sp. Tetrahedron, 1996, 52, 9589-96.
-
(1996)
Tetrahedron
, vol.52
, pp. 9589-9596
-
-
D'Auria, M.V.1
Zampella, A.2
Palma, L.3
Minale, L.4
-
127
-
-
0032774207
-
Non-cyclic AMP-dependent, positive inotropic cyclodepsipeptides with negative chronotropy
-
Tsunoo, A.; Kamijo, M. Non-cyclic AMP-dependent, positive inotropic cyclodepsipeptides with negative chronotropy. J. Pharmacol. Exp. Ther., 1999, 290, 1006-12.
-
(1999)
J. Pharmacol. Exp. Ther
, vol.290
, pp. 1006-1012
-
-
Tsunoo, A.1
Kamijo, M.2
-
128
-
-
23644457650
-
Complete stereochemistry of neamphamide A and absolute configuration of the methoxytyrosine residue in papuamide B
-
Oku, N.; Krishnamoorthy, R.; Benson, A.G.; Ferguson, R.L.; Lipton, M.A.; Phillips, L.R.; Gustafson, K.R.; McMahon, J.B. Complete stereochemistry of neamphamide A and absolute configuration of the methoxytyrosine residue in papuamide B. J. Org. Chem., 2005, 70, 6842-47.
-
(2005)
J. Org. Chem
, vol.70
, pp. 6842-6847
-
-
Oku, N.1
Krishnamoorthy, R.2
Benson, A.G.3
Ferguson, R.L.4
Lipton, M.A.5
Phillips, L.R.6
Gustafson, K.R.7
McMahon, J.B.8
-
129
-
-
33846348337
-
-
Wood, A. Ed, Elsevier: Amsterdam
-
Di Santo, R. In Annual Reports in Medicinal Chemistry, Wood, A. Ed.; Elsevier: Amsterdam, 2006; Vol. 41, pp. 299-315.
-
(2006)
Annual Reports in Medicinal Chemistry
, vol.41
, pp. 299-315
-
-
Di Santo, R.1
-
131
-
-
33645548610
-
Microbiology of systemic fungal infections
-
Chakrabarti, A. Microbiology of systemic fungal infections. J. Postgrad. Med., 2005, 51 Suppl 1, S16-S20.
-
(2005)
J. Postgrad. Med
, vol.51
, Issue.SUPPL. 1
-
-
Chakrabarti, A.1
-
132
-
-
0037277352
-
Microbial natural products as a source of antifungals
-
Vicente, M.F.; Basilio, A.; Cabello, A.; Pelaez, F. Microbial natural products as a source of antifungals. Clin. Microbiol. Infect., 2003, 9, 15-32.
-
(2003)
Clin. Microbiol. Infect
, vol.9
, pp. 15-32
-
-
Vicente, M.F.1
Basilio, A.2
Cabello, A.3
Pelaez, F.4
-
134
-
-
16644381833
-
Development of antibiotics and the future of marine microorganisms to stem the tide of antibiotic resistance
-
Kasanah, N.; Hamann, M.T. Development of antibiotics and the future of marine microorganisms to stem the tide of antibiotic resistance. Curr. Opin. Invest. Drugs, 2004, 5, 827-37.
-
(2004)
Curr. Opin. Invest. Drugs
, vol.5
, pp. 827-837
-
-
Kasanah, N.1
Hamann, M.T.2
-
135
-
-
0036008192
-
The use of lipid emulsions for the iv administration of a new water soluble polyene antibiotic, SPK-843
-
Mozzi, G.; Benelli, P.; Bruzzese, T.; Galmozzi, M.R.; Bonabello, A. The use of lipid emulsions for the iv administration of a new water soluble polyene antibiotic, SPK-843. J. Antimicrob. Chemother., 2002, 49, 321-25.
-
(2002)
J. Antimicrob. Chemother
, vol.49
, pp. 321-325
-
-
Mozzi, G.1
Benelli, P.2
Bruzzese, T.3
Galmozzi, M.R.4
Bonabello, A.5
-
136
-
-
17844382393
-
Liposomal amphotericin B: Clinical experience and perspectives
-
Gibbs, W.J.; Drew, R.H.; Perfect, J.R. Liposomal amphotericin B: clinical experience and perspectives. Expert. Rev. Anti. Infect. Ther., 2005, 3, 167-81.
-
(2005)
Expert. Rev. Anti. Infect. Ther
, vol.3
, pp. 167-181
-
-
Gibbs, W.J.1
Drew, R.H.2
Perfect, J.R.3
-
137
-
-
0344082207
-
Voriconazole salvage treatment of invasive candidiasis
-
Ostrosky-Zeichner, L.; Oude Lashof, A.M.; Kullberg, B.J.; Rex, J.H. Voriconazole salvage treatment of invasive candidiasis. Eur. J. Clin. Microbiol. Infect. Dis., 2003, 22, 651-55.
-
(2003)
Eur. J. Clin. Microbiol. Infect. Dis
, vol.22
, pp. 651-655
-
-
Ostrosky-Zeichner, L.1
Oude Lashof, A.M.2
Kullberg, B.J.3
Rex, J.H.4
-
138
-
-
17644370312
-
Amphotericin B lipid complex in the management of invasive aspergillosis in immunocompromised patients
-
Chandrasekar, P.H.; Ito, J.I. Amphotericin B lipid complex in the management of invasive aspergillosis in immunocompromised patients. Clin. Infect. Dis., 2005, 40 Suppl 6, S392-S400.
-
(2005)
Clin. Infect. Dis
, vol.40
, Issue.SUPPL. 6
-
-
Chandrasekar, P.H.1
Ito, J.I.2
-
139
-
-
17644405088
-
Successful use of amphotericin B lipid complex in the treatment of cryptococcosis
-
Baddour, L.M.; Perfect, J.R.; Ostrosky-Zeichner, L. Successful use of amphotericin B lipid complex in the treatment of cryptococcosis. Clin. Infect. Dis., 2005, 40 Suppl 6, S409-S13.
-
(2005)
Clin. Infect. Dis
, vol.40
, Issue.SUPPL. 6
-
-
Baddour, L.M.1
Perfect, J.R.2
Ostrosky-Zeichner, L.3
-
140
-
-
0016338169
-
Stoffwechselprodukte von Mikroorganismen 143. Mitteilung. Echinocandin B, ein neuartiges Polypeptid-Antibioticum aus Aspergillus nidulans var. echinulatus: Isolierung und Bausteine.
-
Von Benz, F.; Knusel, F.; Nuesch, J.; Treichler, H.; Voser, W.; Nyfeler, R.; Keller-Schierlein, W. Stoffwechselprodukte von Mikroorganismen 143. Mitteilung. Echinocandin B, ein neuartiges Polypeptid-Antibioticum aus Aspergillus nidulans var. echinulatus: Isolierung und Bausteine. Helv. Chim. Acta, 1974, 57, 2459-77.
-
(1974)
Helv. Chim. Acta
, vol.57
, pp. 2459-2477
-
-
Von Benz, F.1
Knusel, F.2
Nuesch, J.3
Treichler, H.4
Voser, W.5
Nyfeler, R.6
Keller-Schierlein, W.7
-
141
-
-
34047230470
-
Synthesis of the Antifungal -1,3-Glucan Synthase Inhibitor CANCIDAS (Caspofungin Acetate) from Pneumocandin B0
-
Leonard, W.R.; Belyk, K.M.; Conion, D.A.; Bender, D.R.; DiMichele, L.M.; Liu, J.; Hughes, D.L. Synthesis of the Antifungal -1,3-Glucan Synthase Inhibitor CANCIDAS (Caspofungin Acetate) from Pneumocandin B0. J. Org. Chem., 2007, 72, 2335-43.
-
(2007)
J. Org. Chem
, vol.72
, pp. 2335-2343
-
-
Leonard, W.R.1
Belyk, K.M.2
Conion, D.A.3
Bender, D.R.4
DiMichele, L.M.5
Liu, J.6
Hughes, D.L.7
-
142
-
-
0030943354
-
Lipopeptide inhibitors of fungal glucan synthase
-
Kurtz, M.B.; Douglas, C.M. Lipopeptide inhibitors of fungal glucan synthase. J. Med. Vet. Mycol., 1997, 35, 79-86
-
(1997)
J. Med. Vet. Mycol
, vol.35
, pp. 79-86
-
-
Kurtz, M.B.1
Douglas, C.M.2
-
143
-
-
17044455920
-
In vitro preclinical evaluation studies with the echinocandin antifungal MK-0991 (L-743,872)
-
Bartizal, K.; Gill, C.J.; Abruzzo, G.K.; Flattery, A.M.; Kong, L.; Scott, P.M.; Smith, J.G.; Leighton, C.E.; Bouffard, A.; Dropinski, J.F.; Balkovec, J. In vitro preclinical evaluation studies with the echinocandin antifungal MK-0991 (L-743,872). Antimicrob. Agents Chemother., 1997, 41, 2326-32.
-
(1997)
Antimicrob. Agents Chemother
, vol.41
, pp. 2326-2332
-
-
Bartizal, K.1
Gill, C.J.2
Abruzzo, G.K.3
Flattery, A.M.4
Kong, L.5
Scott, P.M.6
Smith, J.G.7
Leighton, C.E.8
Bouffard, A.9
Dropinski, J.F.10
Balkovec, J.11
-
144
-
-
9444248159
-
In-vitro activity of nikkomycin Z alone and in combination with polyenes, triazoles or echinocandins against Aspergillus fumigatus
-
Ganesan, L.T.; Manavathu, E.K.; Cutright, J.L.; Alangaden, G.J.; Chandrasekar, P.H. In-vitro activity of nikkomycin Z alone and in combination with polyenes, triazoles or echinocandins against Aspergillus fumigatus. Clin. Microbiol. Infect., 2004, 10, 961-66.
-
(2004)
Clin. Microbiol. Infect
, vol.10
, pp. 961-966
-
-
Ganesan, L.T.1
Manavathu, E.K.2
Cutright, J.L.3
Alangaden, G.J.4
Chandrasekar, P.H.5
-
145
-
-
0025742968
-
Aureobasidins, new antifungal antibiotics. Taxonomy, fermentation, isolation, and properties
-
Takesako, K.; Ikai, K.; Haruna, F.; Endo, M.; Shimanaka, K.; Sono, E.; Nakamura, T.; Kato, I.; Yamaguchi, H. Aureobasidins, new antifungal antibiotics. Taxonomy, fermentation, isolation, and properties. J. Antibiot., 1991, 44, 919-24.
-
(1991)
J. Antibiot
, vol.44
, pp. 919-924
-
-
Takesako, K.1
Ikai, K.2
Haruna, F.3
Endo, M.4
Shimanaka, K.5
Sono, E.6
Nakamura, T.7
Kato, I.8
Yamaguchi, H.9
-
146
-
-
0031923118
-
Syntheses of antifungal aureobasidin A analogs with alkyl chains for structure-activity relationship
-
Kurome, T.; Inoue, T.; Takesako, K.; Kato, I. Syntheses of antifungal aureobasidin A analogs with alkyl chains for structure-activity relationship. J. Antibiot., 1998, 51, 359-67.
-
(1998)
J. Antibiot
, vol.51
, pp. 359-367
-
-
Kurome, T.1
Inoue, T.2
Takesako, K.3
Kato, I.4
-
147
-
-
0031967494
-
Role of ABC transporters in aureobasidin A resistance
-
Ogawa, A.; Hashida-Okado, T.; Endo, M.; Yoshioka, H.; Tsuruo, T.; Takesako, K.; Kato, I. Role of ABC transporters in aureobasidin A resistance. Antimicrob. Agents Chemother., 1998, 42, 755-61.
-
(1998)
Antimicrob. Agents Chemother
, vol.42
, pp. 755-761
-
-
Ogawa, A.1
Hashida-Okado, T.2
Endo, M.3
Yoshioka, H.4
Tsuruo, T.5
Takesako, K.6
Kato, I.7
-
148
-
-
0030464228
-
UK-2A, B, C and D, novel antifungal antibiotics from Streptomyces sp. 517-02. II. Structural elucidation
-
Hanafi, M.; Shibata, K.; Ueki, M.; Taniguchi, M. UK-2A, B, C and D, novel antifungal antibiotics from Streptomyces sp. 517-02. II. Structural elucidation. J. Antibiot., 1996, 49, 1226-31.
-
(1996)
J. Antibiot
, vol.49
, pp. 1226-1231
-
-
Hanafi, M.1
Shibata, K.2
Ueki, M.3
Taniguchi, M.4
-
149
-
-
0029784909
-
-
Ueki, M.; Abe, K.; Hanafi, M.; Shibata, K.; Tanaka, T.; Taniguchi, M. UK-2A, B, C and D, novel antifungal antibiotics from Streptomyces sp. 517-02. I. Fermentation, isolation, and biological properties. J. Antibiot., 1996, 49, 639-43.
-
Ueki, M.; Abe, K.; Hanafi, M.; Shibata, K.; Tanaka, T.; Taniguchi, M. UK-2A, B, C and D, novel antifungal antibiotics from Streptomyces sp. 517-02. I. Fermentation, isolation, and biological properties. J. Antibiot., 1996, 49, 639-43.
-
-
-
-
150
-
-
0030777755
-
UK-3A, a novel antifungal antibiotic from Streptomyces sp. 517-02: Fermentation, isolation, structural elucidation and biological properties
-
Ueki, M.; Kusumoto, A.; Hanafi, M.; Shibata, K.; Tanaka, T.; Taniguchi, M. UK-3A, a novel antifungal antibiotic from Streptomyces sp. 517-02: fermentation, isolation, structural elucidation and biological properties. J. Antibiot., 1997, 50, 551-55.
-
(1997)
J. Antibiot
, vol.50
, pp. 551-555
-
-
Ueki, M.1
Kusumoto, A.2
Hanafi, M.3
Shibata, K.4
Tanaka, T.5
Taniguchi, M.6
-
151
-
-
0032971831
-
UK-2A, B, C and D, Novel Antifungal Antibiotics from Streptomyces sp. 517-02. IV. Comparative Studies of UK-2A with Antimycin A3 on Cytotoxic Activity and Reactive Oxygen Species Generation in LLC-PK1 Cells
-
Takimoto, H.; Machida, K.; Ueki, M.; Tanaka, T.; Taniguchi, M. UK-2A, B, C and D, Novel Antifungal Antibiotics from Streptomyces sp. 517-02. IV. Comparative Studies of UK-2A with Antimycin A3 on Cytotoxic Activity and Reactive Oxygen Species Generation in LLC-PK1 Cells. J. Antibiot., 1999, 52, 480-84.
-
(1999)
J. Antibiot
, vol.52
, pp. 480-484
-
-
Takimoto, H.1
Machida, K.2
Ueki, M.3
Tanaka, T.4
Taniguchi, M.5
-
152
-
-
0022645010
-
-
Maehr, H.; Liu, C.M.; Palleroni, N.J.; Smallheer, J.; Todaro, L.; Williams, T.H.; Blount, J.F. Microbial products. VIII. Azinothricin, a novel hexadepsipeptide antibiotic. J. Antibiot., 1986, 39, 17-25.
-
Maehr, H.; Liu, C.M.; Palleroni, N.J.; Smallheer, J.; Todaro, L.; Williams, T.H.; Blount, J.F. Microbial products. VIII. Azinothricin, a novel hexadepsipeptide antibiotic. J. Antibiot., 1986, 39, 17-25.
-
-
-
-
153
-
-
0023918003
-
A83586C, a new depsipeptide antibiotic
-
Smitka, T.A.; Deeter, J.B.; Hunt, A.H.; Mertz, F.P.; Ellis, R.M.; Boeck, L.D.; Yao, R.C. A83586C, a new depsipeptide antibiotic. J. Antibiot., 1988, 41, 726-33.
-
(1988)
J. Antibiot
, vol.41
, pp. 726-733
-
-
Smitka, T.A.1
Deeter, J.B.2
Hunt, A.H.3
Mertz, F.P.4
Ellis, R.M.5
Boeck, L.D.6
Yao, R.C.7
-
154
-
-
0026320088
-
-
Harrison, L.; Teplow, D.B.; Rinaldi, M.; Strobel, G. Pseudomycins, a family of novel peptides from Pseudomonas syringae possessing broad-spectrum antifungal activity. J. Gen. Microbiol., 1991, 137, 2857-65.
-
Harrison, L.; Teplow, D.B.; Rinaldi, M.; Strobel, G. Pseudomycins, a family of novel peptides from Pseudomonas syringae possessing broad-spectrum antifungal activity. J. Gen. Microbiol., 1991, 137, 2857-65.
-
-
-
-
155
-
-
0026683249
-
A new anthelmintic cyclodepsipeptide, PF1022A
-
Sasaki, T.; Takagi, M.; Yaguchi, T.; Miyadoh, S.; Okada, T.; Koyama, M. A new anthelmintic cyclodepsipeptide, PF1022A. J. Antibiot., 1992, 45, 692-97.
-
(1992)
J. Antibiot
, vol.45
, pp. 692-697
-
-
Sasaki, T.1
Takagi, M.2
Yaguchi, T.3
Miyadoh, S.4
Okada, T.5
Koyama, M.6
-
156
-
-
0029089287
-
Anthelmintic profile of the cyclodepsipeptide PF1022A in in vitro and in vivo models
-
Conder, G.A.; Johnson, S.S.; Nowakowski, D.S.; Blake, T.E.; Dutton, F.E.; Nelson, S.J.; Thomas, E.M.; Davis, J.P.; Thompson, D.P. Anthelmintic profile of the cyclodepsipeptide PF1022A in in vitro and in vivo models. J. Antibiot., 1995, 48, 820-23.
-
(1995)
J. Antibiot
, vol.48
, pp. 820-823
-
-
Conder, G.A.1
Johnson, S.S.2
Nowakowski, D.S.3
Blake, T.E.4
Dutton, F.E.5
Nelson, S.J.6
Thomas, E.M.7
Davis, J.P.8
Thompson, D.P.9
-
157
-
-
0030952646
-
Target sites of anthelmintics
-
Martin, R.J.; Robertson, A.P.; Bjorn, H. Target sites of anthelmintics. Parasitology, 1997, 114 Suppl, S111-S24.
-
(1997)
Parasitology
, vol.114
, Issue.SUPPL.
-
-
Martin, R.J.1
Robertson, A.P.2
Bjorn, H.3
-
158
-
-
18744394963
-
Synthesis of anthelmintically active N-methylated amidoxime analogues of the cyclic octadepsipeptide PF1022A
-
Jeschke, P.; Harder, A.; von Samson-Himmelstjerna, G.; Etzel, W.; Gau, W.; Thielking, G.; Bonse, G. Synthesis of anthelmintically active N-methylated amidoxime analogues of the cyclic octadepsipeptide PF1022A. Pest. Manag. Sci., 2002, 58, 1205-15.
-
(2002)
Pest. Manag. Sci
, vol.58
, pp. 1205-1215
-
-
Jeschke, P.1
Harder, A.2
von Samson-Himmelstjerna, G.3
Etzel, W.4
Gau, W.5
Thielking, G.6
Bonse, G.7
-
159
-
-
0035452083
-
Effects of Bay 44-4400, a new cyclodepsipeptide, on developing stages of filariae (Acanthocheilonema viteae, Brugia malayi, Litomosoides sigmodontis) in the rodent Mastomys coucha
-
Zahner, H.; Taubert, A.; Harder, A.; von Samson-Himmelstjerna, G. Effects of Bay 44-4400, a new cyclodepsipeptide, on developing stages of filariae (Acanthocheilonema viteae, Brugia malayi, Litomosoides sigmodontis) in the rodent Mastomys coucha. Acta Trop., 2001, 80, 19-28.
-
(2001)
Acta Trop
, vol.80
, pp. 19-28
-
-
Zahner, H.1
Taubert, A.2
Harder, A.3
von Samson-Himmelstjerna, G.4
-
160
-
-
3042776646
-
Structural mimicry of retroviral tat proteins by constrained beta-hairpin peptidomimetics: Ligands with high affinity and selectivity for viral TAR RNA regulatory elements
-
Athanassiou, Z.; Dias, R.L.; Moehle, K.; Dobson, N.; Varani, G.; Robinson, J.A. Structural mimicry of retroviral tat proteins by constrained beta-hairpin peptidomimetics: Ligands with high affinity and selectivity for viral TAR RNA regulatory elements. J. Am. Chem. Soc., 2004, 126, 6906-13.
-
(2004)
J. Am. Chem. Soc
, vol.126
, pp. 6906-6913
-
-
Athanassiou, Z.1
Dias, R.L.2
Moehle, K.3
Dobson, N.4
Varani, G.5
Robinson, J.A.6
-
161
-
-
33846391016
-
Structure-guided peptidomimetic design leads to nanomolar beta-hairpin inhibitors of the Tat-TAR interaction of bovine immunodeficiency Virus
-
Athanassiou, Z.; Patora, K.; Dias, R.L.A.; Moehle, K.; Robinson, J.A.; Varani, G. Structure-guided peptidomimetic design leads to nanomolar beta-hairpin inhibitors of the Tat-TAR interaction of bovine immunodeficiency Virus. Biochemistry, 2007, 46, 741-51.
-
(2007)
Biochemistry
, vol.46
, pp. 741-751
-
-
Athanassiou, Z.1
Patora, K.2
Dias, R.L.A.3
Moehle, K.4
Robinson, J.A.5
Varani, G.6
-
162
-
-
24944500398
-
-
Leeper, T.C.; Athanassiou, Z.; Dias, R.L.A.; Robinson, J.A.; Varani, G. TAR RNA recognition by a cyclic peptidomimetic of Tat protein. Biochemistry, 2005, 44, 12362-72.
-
Leeper, T.C.; Athanassiou, Z.; Dias, R.L.A.; Robinson, J.A.; Varani, G. TAR RNA recognition by a cyclic peptidomimetic of Tat protein. Biochemistry, 2005, 44, 12362-72.
-
-
-
-
163
-
-
85047698934
-
A new family of beta-hairpin mimetics based on a trypsin inhibitor from sunflower seeds
-
Descours, A.; Moehle, K.; Renard, A.; Robinson, J.A. A new family of beta-hairpin mimetics based on a trypsin inhibitor from sunflower seeds. Chembiochem, 2002, 3, 318-23.
-
(2002)
Chembiochem
, vol.3
, pp. 318-323
-
-
Descours, A.1
Moehle, K.2
Renard, A.3
Robinson, J.A.4
-
164
-
-
33644647749
-
Protein ligand design: From phage display to synthetic protein epitope mimetics in human antibody Fc-binding peptidomimetics
-
Dias, R.L.; Fasan, R.; Moehle, K.; Renard, A.; Obrecht, D.; Robinson, J.A. Protein ligand design: From phage display to synthetic protein epitope mimetics in human antibody Fc-binding peptidomimetics. J. Am. Chem. Soc., 2006, 128, 2726-32.
-
(2006)
J. Am. Chem. Soc
, vol.128
, pp. 2726-2732
-
-
Dias, R.L.1
Fasan, R.2
Moehle, K.3
Renard, A.4
Obrecht, D.5
Robinson, J.A.6
-
165
-
-
33644896783
-
Structure-activity studies in a family of beta-hairpin protein epitope mimetic inhibitors of the p53-HDM2 protein-protein interaction
-
Fasan, R.; Dias, R.L.; Moehle, K.; Zerbe, O.; Obrecht, D.; Mittl, P.R.; Grutter, M.G.; Robinson, J.A. Structure-activity studies in a family of beta-hairpin protein epitope mimetic inhibitors of the p53-HDM2 protein-protein interaction. Chembiochem, 2006, 7, 515-26.
-
(2006)
Chembiochem
, vol.7
, pp. 515-526
-
-
Fasan, R.1
Dias, R.L.2
Moehle, K.3
Zerbe, O.4
Obrecht, D.5
Mittl, P.R.6
Grutter, M.G.7
Robinson, J.A.8
-
166
-
-
4544342753
-
Using a beta-hairpin to mimic an alpha-helix: Cyclic peptidomimetic inhibitors of the p53-HDM2 protein-protein interaction
-
Fasan, R.; Dias, R.L.; Moehle, K.; Zerbe, O.; Vrijbloed, J.W.; Obrecht, D.; Robinson, J.A. Using a beta-hairpin to mimic an alpha-helix: Cyclic peptidomimetic inhibitors of the p53-HDM2 protein-protein interaction. Angew. Chem. Int. Ed. Engl., 2004, 43, 2109-12.
-
(2004)
Angew. Chem. Int. Ed. Engl
, vol.43
, pp. 2109-2112
-
-
Fasan, R.1
Dias, R.L.2
Moehle, K.3
Zerbe, O.4
Vrijbloed, J.W.5
Obrecht, D.6
Robinson, J.A.7
-
167
-
-
0033620414
-
Structural mimicry of canonical conformations in antibody hypervariable loops using cyclic peptides containing a heterochiral diproline template
-
Favre, M.; Moehle, K.; Jiang, L.; Pfeiffer, B.; Robinson, J.A. Structural mimicry of canonical conformations in antibody hypervariable loops using cyclic peptides containing a heterochiral diproline template. J. Am. Chem. Soc., 1999, 121, 2679-85
-
(1999)
J. Am. Chem. Soc
, vol.121
, pp. 2679-2685
-
-
Favre, M.1
Moehle, K.2
Jiang, L.3
Pfeiffer, B.4
Robinson, J.A.5
-
168
-
-
0042168659
-
A family of macrocyclic antibiotics with a mixed peptide-peptoid beta-hairpin backbone conformation
-
Shankaramma, S.C.; Moehle, K.; James, S.; Vrijbloed, J.W.; Obrecht, D.; Robinson, J.A. A family of macrocyclic antibiotics with a mixed peptide-peptoid beta-hairpin backbone conformation. Chem. Commun. (Camb.), 2003, 1842-43.
-
(2003)
Chem. Commun. (Camb.)
, pp. 1842-1843
-
-
Shankaramma, S.C.1
Moehle, K.2
James, S.3
Vrijbloed, J.W.4
Obrecht, D.5
Robinson, J.A.6
-
169
-
-
0342716088
-
Stabilization of a β-hairpin conformation in a cyclic peptide using the templating effect of a heterochiral diproline unit
-
Späth, J.; Stuart, F.; Jiang, L.; Robinson, J.A. Stabilization of a β-hairpin conformation in a cyclic peptide using the templating effect of a heterochiral diproline unit. Helv. Chim. Acta, 1998, 81, 1726-38.
-
(1726)
Helv. Chim. Acta
, vol.81
, pp. 38
-
-
Späth, J.1
Stuart, F.2
Jiang, L.3
Robinson, J.A.4
-
170
-
-
0037165196
-
Antimicrobial peptides of multicellular organisms
-
Zasloff, M. Antimicrobial peptides of multicellular organisms. Nature, 2002, 415, 389-95.
-
(2002)
Nature
, vol.415
, pp. 389-395
-
-
Zasloff, M.1
-
171
-
-
0027094178
-
A novel anti-HIV synthetic peptide, T-22 (Tyr5,12,Lys7-polyphemusin II)
-
Masuda, M.; Nakashima, H.; Ueda, T.; Naba, H.; Ikoma, R.; Otaka, A.; Terakawa, Y.; Tamamura, H.; Ibuka, T.; Murakami, T. A novel anti-HIV synthetic peptide, T-22 (Tyr5,12,Lys7-polyphemusin II). Biochem. Biophys. Res. Commun., 1992, 189, 845-50.
-
(1992)
Biochem. Biophys. Res. Commun
, vol.189
, pp. 845-850
-
-
Masuda, M.1
Nakashima, H.2
Ueda, T.3
Naba, H.4
Ikoma, R.5
Otaka, A.6
Terakawa, Y.7
Tamamura, H.8
Ibuka, T.9
Murakami, T.10
-
172
-
-
0024741960
-
Antimicrobial peptides, isolated from horseshoe crab hemocytes, tachyplesin II, and polyphemusins I and II: Chemical structures and biological activity
-
Miyata, T.; Tokunaga, F.; Yoneya, T.; Yoshikawa, K.; Iwanaga, S.; Niwa, M.; Takao, T.; Shimonishi, Y. Antimicrobial peptides, isolated from horseshoe crab hemocytes, tachyplesin II, and polyphemusins I and II: chemical structures and biological activity. J. Biochem., 1989, 106, 663-68.
-
(1989)
J. Biochem
, vol.106
, pp. 663-668
-
-
Miyata, T.1
Tokunaga, F.2
Yoneya, T.3
Yoshikawa, K.4
Iwanaga, S.5
Niwa, M.6
Takao, T.7
Shimonishi, Y.8
-
173
-
-
0023700978
-
-
Nakamura, T.; Furunaka, H.; Miyata, T.; Tokunaga, F.; Muta, T.; Iwanaga, S.; Niwa, M.; Takao, T.; Shimonishi, Y. Tachyplesin, a class of antimicrobial peptide from the hemocytes of the horseshoe crab ( Tachypleus tridentatus). Isolation and chemical structure. J. Biol. Chem., 1988, 263, 16709-13.
-
Nakamura, T.; Furunaka, H.; Miyata, T.; Tokunaga, F.; Muta, T.; Iwanaga, S.; Niwa, M.; Takao, T.; Shimonishi, Y. Tachyplesin, a class of antimicrobial peptide from the hemocytes of the horseshoe crab ( Tachypleus tridentatus). Isolation and chemical structure. J. Biol. Chem., 1988, 263, 16709-13.
-
-
-
-
174
-
-
0033569410
-
A cyclic antimicrobial peptide produced in primate leukocytes by the ligation of two truncated alpha-defensins
-
Tang, Y.Q.; Yuan, J.; Osapay, G.; Osapay, K.; Tran, D.; Miller, C.J.; Ouellette, A.J.; Selsted, M.E. A cyclic antimicrobial peptide produced in primate leukocytes by the ligation of two truncated alpha-defensins. Science, 1999, 286, 498-502.
-
(1999)
Science
, vol.286
, pp. 498-502
-
-
Tang, Y.Q.1
Yuan, J.2
Osapay, G.3
Osapay, K.4
Tran, D.5
Miller, C.J.6
Ouellette, A.J.7
Selsted, M.E.8
-
175
-
-
14544282377
-
Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria?
-
Brogden, K.A. Antimicrobial peptides: Pore formers or metabolic inhibitors in bacteria? Nat. Rev. Microbiol., 2005, 3, 238-50.
-
(2005)
Nat. Rev. Microbiol
, vol.3
, pp. 238-250
-
-
Brogden, K.A.1
-
176
-
-
13944259333
-
Properties and structure-activity studies of cyclic beta-hairpin peptidomimetics based on the cationic antimicrobial peptide protegrin I
-
Robinson, J.A.; Shankaramma, S.C.; Jetter, P.; Kienzl, U.; Schwendener, R.A.; Vrijbloed, J.W.; Obrecht, D. Properties and structure-activity studies of cyclic beta-hairpin peptidomimetics based on the cationic antimicrobial peptide protegrin I. Bioorg. Med. Chem., 2005, 13, 2055-64.
-
(2005)
Bioorg. Med. Chem
, vol.13
, pp. 2055-2064
-
-
Robinson, J.A.1
Shankaramma, S.C.2
Jetter, P.3
Kienzl, U.4
Schwendener, R.A.5
Vrijbloed, J.W.6
Obrecht, D.7
-
177
-
-
33746075554
-
QSAR analysis of antimicrobial and haemolytic effects of cyclic cationic antimicrobial peptides derived from protegrin-1
-
Frecer, V. QSAR analysis of antimicrobial and haemolytic effects of cyclic cationic antimicrobial peptides derived from protegrin-1. Bioorgan. Med. Chem., 2006, 14, 6065-74.
-
(2006)
Bioorgan. Med. Chem
, vol.14
, pp. 6065-6074
-
-
Frecer, V.1
-
178
-
-
34548785508
-
Biaryl amino acid templates in place of D-Pro-L-Pro in cyclic β-hairpin cationic antimicrobial peptidomimetics
-
Srinivas, N.; Moehle, K.; Abou-Hadeed, K.; Obrecht, D.; Robinson, J.A. Biaryl amino acid templates in place of D-Pro-L-Pro in cyclic β-hairpin cationic antimicrobial peptidomimetics. Org. Biomol. Chem., 2007, 5, 3100-05.
-
(2007)
Org. Biomol. Chem
, vol.5
, pp. 3100-3105
-
-
Srinivas, N.1
Moehle, K.2
Abou-Hadeed, K.3
Obrecht, D.4
Robinson, J.A.5
-
179
-
-
0034604628
-
Substitutions in a homologous region of extracellular loop 2 of CXCR4 and CCR5 alter coreceptor activities for HIV-1 membrane fusion and virus entry
-
Chabot, D.J.; Broder, C.C. Substitutions in a homologous region of extracellular loop 2 of CXCR4 and CCR5 alter coreceptor activities for HIV-1 membrane fusion and virus entry. J. Biol. Chem., 2000, 275, 23774-82.
-
(2000)
J. Biol. Chem
, vol.275
, pp. 23774-23782
-
-
Chabot, D.J.1
Broder, C.C.2
-
180
-
-
0030002637
-
HIV-1 entry cofactor: Functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor
-
Feng, Y.; Broder, C.C.; Kennedy, P.E.; Berger, E.A. HIV-1 entry cofactor: Functional cDNA cloning of a seven-transmembrane, G protein-coupled receptor. Science, 1996, 272, 872-77.
-
(1996)
Science
, vol.272
, pp. 872-877
-
-
Feng, Y.1
Broder, C.C.2
Kennedy, P.E.3
Berger, E.A.4
-
181
-
-
0026625277
-
Anti-human immunodeficiency virus activity of a novel synthetic peptide, T22 ([Tyr-5,12, Lys-7]polyphemusin II): A possible inhibitor of virus-cell fusion
-
Nakashima, H.; Masuda, M.; Murakami, T.; Koyanagi, Y.; Matsumoto, A.; Fujii, N.; Yamamoto, N. Anti-human immunodeficiency virus activity of a novel synthetic peptide, T22 ([Tyr-5,12, Lys-7]polyphemusin II): A possible inhibitor of virus-cell fusion. Antimicrob. Agents Chemother., 1992, 36, 1249-55.
-
(1992)
Antimicrob. Agents Chemother
, vol.36
, pp. 1249-1255
-
-
Nakashima, H.1
Masuda, M.2
Murakami, T.3
Koyanagi, Y.4
Matsumoto, A.5
Fujii, N.6
Yamamoto, N.7
-
182
-
-
0027273475
-
A comparative study of the solution structures of tachyplesin I and a novel anti-HIV synthetic peptide, T22 ([Tyr5,12, Lys7]-polyphemusin II), determined by nuclear magnetic resonance
-
Tamamura, H.; Kuroda, M.; Masuda, M.; Otaka, A.; Funakoshi, S.; Nakashima, H.; Yamamoto, N.; Waki, M.; Matsumoto, A.; Lancelin, J.M. A comparative study of the solution structures of tachyplesin I and a novel anti-HIV synthetic peptide, T22 ([Tyr5,12, Lys7]-polyphemusin II), determined by nuclear magnetic resonance. Biochim. Biophys. Acta, 1993, 1163, 209-16.
-
(1993)
Biochim. Biophys. Acta
, vol.1163
, pp. 209-216
-
-
Tamamura, H.1
Kuroda, M.2
Masuda, M.3
Otaka, A.4
Funakoshi, S.5
Nakashima, H.6
Yamamoto, N.7
Waki, M.8
Matsumoto, A.9
Lancelin, J.M.10
-
183
-
-
41149151814
-
Anti-HIV Activity and Resistance Profile of the CXC Chemokine Receptor 4 Antagonist POL3026
-
Moncunill, G.; rmand-Ugon, M.; Clotet-Codina, I.; Pauls, E.; Ballana, E.; Llano, A.; Romagnoli, B.; Vrijbloed, J.W.; Gombert, F.O.; Clotet, B.; De Marco, S.; Este, J.A. Anti-HIV Activity and Resistance Profile of the CXC Chemokine Receptor 4 Antagonist POL3026. Mol. Pharmacol., 2008, 73, 1264-73.
-
(2008)
Mol. Pharmacol
, vol.73
, pp. 1264-1273
-
-
Moncunill, G.1
rmand-Ugon, M.2
Clotet-Codina, I.3
Pauls, E.4
Ballana, E.5
Llano, A.6
Romagnoli, B.7
Vrijbloed, J.W.8
Gombert, F.O.9
Clotet, B.10
De Marco, S.11
Este, J.A.12
-
184
-
-
0030589727
-
Crystal structure of vancomycin
-
Schafer, M.; Schneider, T.R.; Sheldrake, G.M. Crystal structure of vancomycin. Structure, 1996, 4, 1509-15.
-
(1996)
Structure
, vol.4
, pp. 1509-1515
-
-
Schafer, M.1
Schneider, T.R.2
Sheldrake, G.M.3
-
185
-
-
3142746827
-
NMR structure determination and calcium binding effects of lipopeptide antibiotic daptomycin
-
Ball, L.J.; Goult, C.M.; Donarski, J.A.; Micklefield, J.; Ramesh, V. NMR structure determination and calcium binding effects of lipopeptide antibiotic daptomycin. Org. Biomol. Chem., 2004, 2, 1872-78.
-
(2004)
Org. Biomol. Chem
, vol.2
, pp. 1872-1878
-
-
Ball, L.J.1
Goult, C.M.2
Donarski, J.A.3
Micklefield, J.4
Ramesh, V.5
-
186
-
-
0032761523
-
In vitro microbiological characterization of novel cyclic homopentapeptides, CP-101680 and CP-163,234 for animal health use
-
Norcia, L.J.L.; Silvia, A.M.; Dirlam, J.P.; Schnur, R.C.; Bergeron, J.M.; Retsema, J.A.; Hayashi, S.F. In vitro microbiological characterization of novel cyclic homopentapeptides, CP-101680 and CP-163,234 for animal health use. J. Antibiot. 1999, 52, 1007-16.
-
(1999)
J. Antibiot
, vol.52
, pp. 1007-1016
-
-
Norcia, L.J.L.1
Silvia, A.M.2
Dirlam, J.P.3
Schnur, R.C.4
Bergeron, J.M.5
Retsema, J.A.6
Hayashi, S.F.7
-
187
-
-
0033524028
-
Solution structure of polymyxins B and E and effect of binding to lipopolysaccharide: An NMR and molecular modeling study
-
Pristovsek, P.; Kidric, J. Solution structure of polymyxins B and E and effect of binding to lipopolysaccharide: An NMR and molecular modeling study. J. Med. Chem., 1999, 42, 4604-13.
-
(1999)
J. Med. Chem
, vol.42
, pp. 4604-4613
-
-
Pristovsek, P.1
Kidric, J.2
-
188
-
-
0043167790
-
Structural basis for the quinone reduction in the bc(1) complex: A comparative analysis of crystal structures of mitochondrial cytochrome bc(1) with bound substrate and inhibitors at the Q(i) site
-
Gao, X.; Wen, X.; Esser, L.; Quinn, B.; Yu, L.; Yu, C.-A.; Xia, D. Structural basis for the quinone reduction in the bc(1) complex: A comparative analysis of crystal structures of mitochondrial cytochrome bc(1) with bound substrate and inhibitors at the Q(i) site. Biochemistry, 2003, 42, 9067-80.
-
(2003)
Biochemistry
, vol.42
, pp. 9067-9080
-
-
Gao, X.1
Wen, X.2
Esser, L.3
Quinn, B.4
Yu, L.5
Yu, C.-A.6
Xia, D.7
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