-
1
-
-
85011311161
-
Mechanisms of Antibiotic Resistance
-
Munita, J. M.; Arias, C. A. Mechanisms of Antibiotic Resistance. Microbiol. Spectr. 2016, 4, 42 10.1128/microbiolspec.VMBF-0016-2015
-
(2016)
Microbiol. Spectr.
, vol.4
, pp. 42
-
-
Munita, J.M.1
Arias, C.A.2
-
2
-
-
0035992370
-
Molecular analysis of beta-lactamase structure and function
-
Majiduddin, F. K.; Materon, I. C.; Palzkill, T. G. Molecular analysis of beta-lactamase structure and function. Int. J. Med. Microbiol. 2002, 292, 127-137, 10.1078/1438-4221-00198
-
(2002)
Int. J. Med. Microbiol.
, vol.292
, pp. 127-137
-
-
Majiduddin, F.K.1
Materon, I.C.2
Palzkill, T.G.3
-
3
-
-
0019498660
-
Augmentin (amoxycillin and clavulanic acid) therapy in complicated infections due to beta-lactamase producing bacteria
-
Leigh, D. A.; Bradnock, K.; Marriner, J. M. Augmentin (amoxycillin and clavulanic acid) therapy in complicated infections due to beta-lactamase producing bacteria. J. Antimicrob. Chemother. 1981, 7, 229-236, 10.1093/jac/7.3.229
-
(1981)
J. Antimicrob. Chemother.
, vol.7
, pp. 229-236
-
-
Leigh, D.A.1
Bradnock, K.2
Marriner, J.M.3
-
4
-
-
0017727925
-
Clavulanic acid: A beta-lactamase-inhiting beta-lactam from Streptomyces clavuligerus
-
Reading, C.; Cole, M. Clavulanic acid: a beta-lactamase-inhiting beta-lactam from Streptomyces clavuligerus. Antimicrob. Agents Chemother. 1977, 11, 852-857, 10.1128/AAC.11.5.852
-
(1977)
Antimicrob. Agents Chemother.
, vol.11
, pp. 852-857
-
-
Reading, C.1
Cole, M.2
-
5
-
-
0023677044
-
Sulbactam/ampicillin, a new beta-lactamase inhibitor/beta-lactam antibiotic combination
-
Benson, J. M.; Nahata, M. C. Sulbactam/ampicillin, a new beta-lactamase inhibitor/beta-lactam antibiotic combination. Drug Intell. Clin. Pharm. 1988, 22, 534-541, 10.1177/106002808802200702
-
(1988)
Drug Intell. Clin. Pharm.
, vol.22
, pp. 534-541
-
-
Benson, J.M.1
Nahata, M.C.2
-
6
-
-
0022625994
-
Comparative evaluation of a new beta-lactamase inhibitor, YTR 830, combined with different beta-lactam antibiotics against bacteria harboring known beta-lactamases
-
Gutmann, L.; Kitzis, M. D.; Yamabe, S.; Acar, J. F. Comparative evaluation of a new beta-lactamase inhibitor, YTR 830, combined with different beta-lactam antibiotics against bacteria harboring known beta-lactamases. Antimicrob. Agents Chemother. 1986, 29, 955-957, 10.1128/AAC.29.5.955
-
(1986)
Antimicrob. Agents Chemother.
, vol.29
, pp. 955-957
-
-
Gutmann, L.1
Kitzis, M.D.2
Yamabe, S.3
Acar, J.F.4
-
7
-
-
80054693925
-
Carbapenems: Past, present, and future
-
Papp-Wallace, K. M.; Endimiani, A.; Taracila, M. A.; Bonomo, R. A. Carbapenems: past, present, and future. Antimicrob. Agents Chemother. 2011, 55, 4943-4960, 10.1128/AAC.00296-11
-
(2011)
Antimicrob. Agents Chemother.
, vol.55
, pp. 4943-4960
-
-
Papp-Wallace, K.M.1
Endimiani, A.2
Taracila, M.A.3
Bonomo, R.A.4
-
8
-
-
85062617281
-
Interplay between beta-lactamases and new beta-lactamase inhibitors
-
Bush, K.; Bradford, P. A. Interplay between beta-lactamases and new beta-lactamase inhibitors. Nat. Rev. Microbiol. 2019, 17, 295-306, 10.1038/s41579-019-0159-8
-
(2019)
Nat. Rev. Microbiol.
, vol.17
, pp. 295-306
-
-
Bush, K.1
Bradford, P.A.2
-
9
-
-
84872871981
-
Metallo-beta-lactamase structure and function
-
Palzkill, T. Metallo-beta-lactamase structure and function. Ann. N. Y. Acad. Sci. 2013, 1277, 91-104, 10.1111/j.1749-6632.2012.06796.x
-
(2013)
Ann. N. Y. Acad. Sci.
, vol.1277
, pp. 91-104
-
-
Palzkill, T.1
-
10
-
-
78649697323
-
Emerging carbapenemases: A global perspective
-
Walsh, T. R. Emerging carbapenemases: a global perspective. Int. J. Antimicrob. Agents 2010, 36, S8-S14, 10.1016/S0924-8579(10)70004-2
-
(2010)
Int. J. Antimicrob. Agents
, vol.36
, pp. S8-S14
-
-
Walsh, T.R.1
-
11
-
-
84872732888
-
Ceftazidime-avibactam: A novel cephalosporin/beta-lactamase inhibitor combination
-
Zhanel, G. G.; Lawson, C. D.; Adam, H.; Schweizer, F.; Zelenitsky, S.; Lagace-Wiens, P. R.; Denisuik, A.; Rubinstein, E.; Gin, A. S.; Hoban, D. J.; Lynch, J. P., 3rd; Karlowsky, J. A. Ceftazidime-avibactam: a novel cephalosporin/beta-lactamase inhibitor combination. Drugs 2013, 73, 159-177, 10.1007/s40265-013-0013-7
-
(2013)
Drugs
, vol.73
, pp. 159-177
-
-
Zhanel, G.G.1
Lawson, C.D.2
Adam, H.3
Schweizer, F.4
Zelenitsky, S.5
Lagace-Wiens, P.R.6
Denisuik, A.7
Rubinstein, E.8
Gin, A.S.9
Hoban, D.J.10
Lynch, J.P.11
Karlowsky, J.A.12
-
12
-
-
84863905057
-
Avibactam is a covalent, reversible, non-beta-lactam beta-lactamase inhibitor
-
Ehmann, D. E.; Jahic, H.; Ross, P. L.; Gu, R. F.; Hu, J.; Kern, G.; Walkup, G. K.; Fisher, S. L. Avibactam is a covalent, reversible, non-beta-lactam beta-lactamase inhibitor. Proc. Natl. Acad. Sci. U.S.A. 2012, 109, 11663-11668, 10.1073/pnas.1205073109
-
(2012)
Proc. Natl. Acad. Sci. U.S.A.
, vol.109
, pp. 11663-11668
-
-
Ehmann, D.E.1
Jahic, H.2
Ross, P.L.3
Gu, R.F.4
Hu, J.5
Kern, G.6
Walkup, G.K.7
Fisher, S.L.8
-
13
-
-
84992579923
-
Interaction of Avibactam with Class B Metallo-β-Lactamases
-
Abboud, M. I.; Damblon, C.; Brem, J.; Smargiasso, N.; Mercuri, P.; Gilbert, B.; Rydzik, A. M.; Claridge, T. D. W.; Schofield, C. J.; Frère, J.-M. Interaction of Avibactam with Class B Metallo-β-Lactamases. Antimicrob. Agents Chemother. 2016, 60, 5655-5662, 10.1128/AAC.00897-16
-
(2016)
Antimicrob. Agents Chemother.
, vol.60
, pp. 5655-5662
-
-
Abboud, M.I.1
Damblon, C.2
Brem, J.3
Smargiasso, N.4
Mercuri, P.5
Gilbert, B.6
Rydzik, A.M.7
Claridge, T.D.W.8
Schofield, C.J.9
Frère, J.-M.10
-
14
-
-
85034739279
-
New Delhi Metallo-β-Lactamase 1 Catalyzes Avibactam and Aztreonam Hydrolysis
-
Lohans, C. T.; Brem, J.; Schofield, C. J. New Delhi Metallo-β-Lactamase 1 Catalyzes Avibactam and Aztreonam Hydrolysis. Antimicrob. Agents Chemother. 2017, 61, e01224-e01217, 10.1128/AAC.01224-17
-
(2017)
Antimicrob. Agents Chemother.
, vol.61
, pp. e01224-e01217
-
-
Lohans, C.T.1
Brem, J.2
Schofield, C.J.3
-
15
-
-
85066453493
-
Profiling Interactions of Vaborbactam with Metallo-β-Lactamases
-
Gareth, W.; Langley, R. C.; Tyrrell, J. M.; Hinchliffe, P.; Calvopiña, K.; Tooke, C.; Widlake, E.; Dowson, C. G.; Spencer, J.; Walsh, T. R.; Schofield, C. J.; Brem, J. Profiling Interactions of Vaborbactam with Metallo-β-Lactamases. Bioorg. Med. Chem. Lett. 2019, 29, 1981-1984, 10.1016/j.bmcl.2019.05.031
-
(2019)
Bioorg. Med. Chem. Lett.
, vol.29
, pp. 1981-1984
-
-
Gareth, W.1
Langley, R.C.2
Tyrrell, J.M.3
Hinchliffe, P.4
Calvopiña, K.5
Tooke, C.6
Widlake, E.7
Dowson, C.G.8
Spencer, J.9
Walsh, T.R.10
Schofield, C.J.11
Brem, J.12
-
16
-
-
33748443001
-
Bortezomib (Velcade trade mark) in the Treatment of Multiple Myeloma
-
Field-Smith, A.; Morgan, G. J.; Davies, F. E. Bortezomib (Velcade trade mark) in the Treatment of Multiple Myeloma. Ther. Clin. Risk Manage. 2006, 2, 271-279, 10.2147/tcrm.2006.2.3.271
-
(2006)
Ther. Clin. Risk Manage.
, vol.2
, pp. 271-279
-
-
Field-Smith, A.1
Morgan, G.J.2
Davies, F.E.3
-
17
-
-
0037460187
-
Nanomolar inhibitors of AmpC beta-lactamase
-
Morandi, F.; Caselli, E.; Morandi, S.; Focia, P. J.; Blazquez, J.; Shoichet, B. K.; Prati, F. Nanomolar inhibitors of AmpC beta-lactamase. J. Am. Chem. Soc. 2003, 125, 685-695, 10.1021/ja0288338
-
(2003)
J. Am. Chem. Soc.
, vol.125
, pp. 685-695
-
-
Morandi, F.1
Caselli, E.2
Morandi, S.3
Focia, P.J.4
Blazquez, J.5
Shoichet, B.K.6
Prati, F.7
-
18
-
-
85013654812
-
Exploring the potential of boronic acids as inhibitors of OXA-24/40 beta-lactamase
-
Werner, J. P.; Mitchell, J. M.; Taracila, M. A.; Bonomo, R. A.; Powers, R. A. Exploring the potential of boronic acids as inhibitors of OXA-24/40 beta-lactamase. Protein Sci. 2017, 26, 515-526, 10.1002/pro.3100
-
(2017)
Protein Sci.
, vol.26
, pp. 515-526
-
-
Werner, J.P.1
Mitchell, J.M.2
Taracila, M.A.3
Bonomo, R.A.4
Powers, R.A.5
-
19
-
-
84960153171
-
Boronic Acid Transition State Inhibitors Active against KPC and Other Class A beta-Lactamases: Structure-Activity Relationships as a Guide to Inhibitor Design
-
Rojas, L. J.; Taracila, M. A.; Papp-Wallace, K. M.; Bethel, C. R.; Caselli, E.; Romagnoli, C.; Winkler, M. L.; Spellberg, B.; Prati, F.; Bonomo, R. A. Boronic Acid Transition State Inhibitors Active against KPC and Other Class A beta-Lactamases: Structure-Activity Relationships as a Guide to Inhibitor Design. Antimicrob. Agents Chemother. 2016, 60, 1751-1759, 10.1128/AAC.02641-15
-
(2016)
Antimicrob. Agents Chemother.
, vol.60
, pp. 1751-1759
-
-
Rojas, L.J.1
Taracila, M.A.2
Papp-Wallace, K.M.3
Bethel, C.R.4
Caselli, E.5
Romagnoli, C.6
Winkler, M.L.7
Spellberg, B.8
Prati, F.9
Bonomo, R.A.10
-
20
-
-
0029760859
-
Structure-based design of a potent transition state analogue for TEM-1 beta-lactamase
-
Strynadka, N. C.; Martin, R.; Jensen, S. E.; Gold, M.; Jones, J. B. Structure-based design of a potent transition state analogue for TEM-1 beta-lactamase. Nat. Struct. Mol. Biol. 1996, 3, 688-695, 10.1038/nsb0896-688
-
(1996)
Nat. Struct. Mol. Biol.
, vol.3
, pp. 688-695
-
-
Strynadka, N.C.1
Martin, R.2
Jensen, S.E.3
Gold, M.4
Jones, J.B.5
-
21
-
-
0034625157
-
Structure-based design guides the improved efficacy of deacylation transition state analogue inhibitors of TEM-1 beta-Lactamase
-
Ness, S.; Martin, R.; Kindler, A. M.; Paetzel, M.; Gold, M.; Jensen, S. E.; Jones, J. B.; Strynadka, N. C. Structure-based design guides the improved efficacy of deacylation transition state analogue inhibitors of TEM-1 beta-Lactamase. Biochemistry 2000, 39, 5312-5321, 10.1021/bi992505b
-
(2000)
Biochemistry
, vol.39
, pp. 5312-5321
-
-
Ness, S.1
Martin, R.2
Kindler, A.M.3
Paetzel, M.4
Gold, M.5
Jensen, S.E.6
Jones, J.B.7
Strynadka, N.C.8
-
22
-
-
85026356593
-
The versatility of boron in biological target engagement
-
Diaz, D. B.; Yudin, A. K. The versatility of boron in biological target engagement. Nat. Chem. 2017, 9, 731-742, 10.1038/nchem.2814
-
(2017)
Nat. Chem.
, vol.9
, pp. 731-742
-
-
Diaz, D.B.1
Yudin, A.K.2
-
23
-
-
85064319209
-
Will morphing boron-based inhibitors beat the beta-lactamases?
-
Krajnc, A.; Lang, P. A.; Panduwawala, T. D.; Brem, J.; Schofield, C. J. Will morphing boron-based inhibitors beat the beta-lactamases?. Curr. Opin. Chem. Biol. 2019, 50, 101-110, 10.1016/j.cbpa.2019.03.001
-
(2019)
Curr. Opin. Chem. Biol.
, vol.50
, pp. 101-110
-
-
Krajnc, A.1
Lang, P.A.2
Panduwawala, T.D.3
Brem, J.4
Schofield, C.J.5
-
24
-
-
84929340109
-
Discovery of a Cyclic Boronic Acid beta-Lactamase Inhibitor (RPX7009) with Utility vs Class A Serine Carbapenemases
-
Hecker, S. J.; Reddy, K. R.; Totrov, M.; Hirst, G. C.; Lomovskaya, O.; Griffith, D. C.; King, P.; Tsivkovski, R.; Sun, D.; Sabet, M.; Tarazi, Z.; Clifton, M. C.; Atkins, K.; Raymond, A.; Potts, K. T.; Abendroth, J.; Boyer, S. H.; Loutit, J. S.; Morgan, E. E.; Durso, S.; Dudley, M. N. Discovery of a Cyclic Boronic Acid beta-Lactamase Inhibitor (RPX7009) with Utility vs Class A Serine Carbapenemases. J. Med. Chem. 2015, 58, 3682-3692, 10.1021/acs.jmedchem.5b00127
-
(2015)
J. Med. Chem.
, vol.58
, pp. 3682-3692
-
-
Hecker, S.J.1
Reddy, K.R.2
Totrov, M.3
Hirst, G.C.4
Lomovskaya, O.5
Griffith, D.C.6
King, P.7
Tsivkovski, R.8
Sun, D.9
Sabet, M.10
Tarazi, Z.11
Clifton, M.C.12
Atkins, K.13
Raymond, A.14
Potts, K.T.15
Abendroth, J.16
Boyer, S.H.17
Loutit, J.S.18
Morgan, E.E.19
Durso, S.20
Dudley, M.N.21
more..
-
25
-
-
85052318433
-
Meropenem/Vaborbactam: A Review in Complicated Urinary Tract Infections
-
Dhillon, S. Meropenem/Vaborbactam: A Review in Complicated Urinary Tract Infections. Drugs 2018, 78, 1259-1270, 10.1007/s40265-018-0966-7
-
(2018)
Drugs
, vol.78
, pp. 1259-1270
-
-
Dhillon, S.1
-
26
-
-
85032476113
-
Vaborbactam: Spectrum of Beta-Lactamase Inhibition and Impact of Resistance Mechanisms on Activity in Enterobacteriaceae
-
Lomovskaya, O.; Sun, D.; Rubio-Aparicio, D.; Nelson, K.; Tsivkovski, R.; Griffith, D. C.; Dudley, M. N. Vaborbactam: Spectrum of Beta-Lactamase Inhibition and Impact of Resistance Mechanisms on Activity in Enterobacteriaceae. Antimicrob. Agents Chemother. 2017, 61, e01443-e01417, 10.1128/AAC.01443-17
-
(2017)
Antimicrob. Agents Chemother.
, vol.61
, pp. e01443-e01417
-
-
Lomovskaya, O.1
Sun, D.2
Rubio-Aparicio, D.3
Nelson, K.4
Tsivkovski, R.5
Griffith, D.C.6
Dudley, M.N.7
-
27
-
-
84981356473
-
Structural basis of metallo-β-lactamase, serine-β-lactamase and penicillin-binding protein inhibition by cyclic boronates
-
Brem, J.; Cain, R.; Cahill, S.; McDonough, M. A.; Clifton, I. J.; Jiménez-Castellanos, J.-C.; Avison, M. B.; Spencer, J.; Fishwick, C. W. G.; Schofield, C. J. Structural basis of metallo-β-lactamase, serine-β-lactamase and penicillin-binding protein inhibition by cyclic boronates. Nat. Commun. 2016, 7, 12406 10.1038/ncomms12406
-
(2016)
Nat. Commun.
, vol.7
, pp. 12406
-
-
Brem, J.1
Cain, R.2
Cahill, S.3
McDonough, M.A.4
Clifton, I.J.5
Jiménez-Castellanos, J.-C.6
Avison, M.B.7
Spencer, J.8
Fishwick, C.W.G.9
Schofield, C.J.10
-
28
-
-
85016467068
-
Cyclic Boronates Inhibit All Classes of β-Lactamases
-
Cahill, S. T.; Cain, R.; Wang, D. Y.; Lohans, C. T.; Wareham, D. W.; Oswin, H. P.; Mohammed, J.; Spencer, J.; Fishwick, C. W. G.; McDonough, M. A.; Schofield, C. J.; Brem, J. Cyclic Boronates Inhibit All Classes of β-Lactamases. Antimicrob. Agents Chemother. 2017, 61, e02260-e02216, 10.1128/AAC.02260-16
-
(2017)
Antimicrob. Agents Chemother.
, vol.61
, pp. e02260-e02216
-
-
Cahill, S.T.1
Cain, R.2
Wang, D.Y.3
Lohans, C.T.4
Wareham, D.W.5
Oswin, H.P.6
Mohammed, J.7
Spencer, J.8
Fishwick, C.W.G.9
McDonough, M.A.10
Schofield, C.J.11
Brem, J.12
-
29
-
-
85061339455
-
Studies on the inhibition of AmpC and other beta-lactamases by cyclic boronates
-
Cahill, S. T.; Tyrrell, J. M.; Navratilova, I. H.; Calvopina, K.; Robinson, S. W.; Lohans, C. T.; McDonough, M. A.; Cain, R.; Fishwick, C. W. G.; Avison, M. B.; Walsh, T. R.; Schofield, C. J.; Brem, J. Studies on the inhibition of AmpC and other beta-lactamases by cyclic boronates. Biochim. Biophys. Acta, Gen. Subj. 2019, 1863, 742-748, 10.1016/j.bbagen.2019.02.004
-
(2019)
Biochim. Biophys. Acta, Gen. Subj.
, vol.1863
, pp. 742-748
-
-
Cahill, S.T.1
Tyrrell, J.M.2
Navratilova, I.H.3
Calvopina, K.4
Robinson, S.W.5
Lohans, C.T.6
McDonough, M.A.7
Cain, R.8
Fishwick, C.W.G.9
Avison, M.B.10
Walsh, T.R.11
Schofield, C.J.12
Brem, J.13
-
30
-
-
84858306615
-
-
WO Patent WO 2014/089365 A1
-
Burns, C. J.; Daigle, D.; Liu, B.; McGarry, D.; Pevear, D. C.; Trout, R. E. L. Beta-Lactamase Inhibitors. WO Patent WO 2014/089365 A1.
-
Beta-Lactamase Inhibitors
-
-
Burns, C.J.1
Daigle, D.2
Liu, B.3
McGarry, D.4
Pevear, D.C.5
Trout, R.E.L.6
-
33
-
-
85073124869
-
-
European Congress of Clinical Microbiology and Infectious Diseases (ECCMID) in Madrid: Spain
-
Hamrick, J. C.; Chatwin, C. L.; John, K. J.; Pevear, D. C.; Burns, C. J.; Xerri, L. The Ability of Broad-spectrum β-Lactamase Inhibitor Vnrx-5133 to Restore Bactericidal Activity of Cefepime in Enterobacteriaceae and P. aeruginosa-Expressing Ambler Class A, B, C and D Enzymes is Demonstrated Using Time-Kill Kinetics; European Congress of Clinical Microbiology and Infectious Diseases (ECCMID) in Madrid: Spain, 2018.
-
(2018)
The Ability of Broad-spectrum β-Lactamase Inhibitor Vnrx-5133 to Restore Bactericidal Activity of Cefepime in Enterobacteriaceae and P. Aeruginosa-Expressing Ambler Class A, B, C and D Enzymes Is Demonstrated Using Time-Kill Kinetics
-
-
Hamrick, J.C.1
Chatwin, C.L.2
John, K.J.3
Pevear, D.C.4
Burns, C.J.5
Xerri, L.6
-
34
-
-
84886380675
-
Boronic esters in asymmetric synthesis
-
Matteson, D. S. Boronic esters in asymmetric synthesis. J. Org. Chem. 2013, 78, 10009-10023, 10.1021/jo4013942
-
(2013)
J. Org. Chem.
, vol.78
, pp. 10009-10023
-
-
Matteson, D.S.1
-
35
-
-
0000962353
-
Homologation of Boronic Esters to Alpha-Chloro Boronic Esters
-
Matteson, D. S.; Majumdar, D. Homologation of Boronic Esters to Alpha-Chloro Boronic Esters. Organometallics 1983, 2, 1529-1535, 10.1021/om50005a008
-
(1983)
Organometallics
, vol.2
, pp. 1529-1535
-
-
Matteson, D.S.1
Majumdar, D.2
-
36
-
-
33847087715
-
Directed Chiral Synthesis with Pinanediol Boronic Esters
-
Matteson, D. S.; Ray, R. Directed Chiral Synthesis with Pinanediol Boronic Esters. J. Am. Chem. Soc. 1980, 102, 7590-7591, 10.1021/ja00545a046
-
(1980)
J. Am. Chem. Soc.
, vol.102
, pp. 7590-7591
-
-
Matteson, D.S.1
Ray, R.2
-
37
-
-
0025014627
-
PyBOP: A new peptide coupling reagent devoid of toxic by-product
-
Coste, J.; Le-Nguyen, D.; Castro, B. PyBOP: A new peptide coupling reagent devoid of toxic by-product. Tetrahedron Lett. 1990, 31, 205-208, 10.1016/S0040-4039(00)94371-5
-
(1990)
Tetrahedron Lett.
, vol.31
, pp. 205-208
-
-
Coste, J.1
Le-Nguyen, D.2
Castro, B.3
-
38
-
-
84884245033
-
Assay platform for clinically relevant metallo-beta-lactamases
-
van Berkel, S. S.; Brem, J.; Rydzik, A. M.; Salimraj, R.; Cain, R.; Verma, A.; Owens, R. J.; Fishwick, C. W.; Spencer, J.; Schofield, C. J. Assay platform for clinically relevant metallo-beta-lactamases. J. Med. Chem. 2013, 56, 6945-6953, 10.1021/jm400769b
-
(2013)
J. Med. Chem.
, vol.56
, pp. 6945-6953
-
-
Van Berkel, S.S.1
Brem, J.2
Rydzik, A.M.3
Salimraj, R.4
Cain, R.5
Verma, A.6
Owens, R.J.7
Fishwick, C.W.8
Spencer, J.9
Schofield, C.J.10
-
39
-
-
85063115624
-
1370. Cefepime/VNRX-5133 Broad-Spectrum Activity Is Maintained against Emerging KPC- And PDC-Variants in Multidrug-Resistant K. pneumoniae and P. aeruginosa
-
Daigle, D.; Hamrick, J.; Chatwin, C.; Kurepina, N.; Kreiswirth, B. N.; Shields, R. K.; Oliver, A.; Clancy, C. J.; Nguyen, M.-H.; Pevear, D.; Xerri, L. 1370. Cefepime/VNRX-5133 Broad-Spectrum Activity Is Maintained Against Emerging KPC-and PDC-Variants in Multidrug-Resistant K. pneumoniae and P. aeruginosa. Open Forum Infect. Dis. 2018, 5, S419-S420, 10.1093/ofid/ofy210.1201
-
(2018)
Open Forum Infect. Dis.
, vol.5
, pp. S419-S420
-
-
Daigle, D.1
Hamrick, J.2
Chatwin, C.3
Kurepina, N.4
Kreiswirth, B.N.5
Shields, R.K.6
Oliver, A.7
Clancy, C.J.8
Nguyen, M.-H.9
Pevear, D.10
Xerri, L.11
-
40
-
-
85045042380
-
Exploring Additional Dimensions of Complexity in Inhibitor Design for Serine β-Lactamases: Mechanistic and Intra- And Inter-molecular Chemistry Approaches
-
van den Akker, F.; Bonomo, R. A. Exploring Additional Dimensions of Complexity in Inhibitor Design for Serine β-Lactamases: Mechanistic and Intra-and Inter-molecular Chemistry Approaches. Front. Microbiol. 2018, 9, 1-622, 10.3389/fmicb.2018.00622
-
(2018)
Front. Microbiol.
, vol.9
, pp. 1-622
-
-
Van Den Akker, F.1
Bonomo, R.A.2
-
41
-
-
85032861340
-
Structural/mechanistic insights into the efficacy of nonclassical beta-lactamase inhibitors against extensively drug resistant Stenotrophomonas maltophilia clinical isolates
-
Calvopiña, K.; Hinchliffe, P.; Brem, J.; Heesom, K. J.; Johnson, S.; Cain, R.; Lohans, C. T.; Fishwick, C. W. G.; Schofield, C. J.; Spencer, J.; Avison, M. B. Structural/mechanistic insights into the efficacy of nonclassical beta-lactamase inhibitors against extensively drug resistant Stenotrophomonas maltophilia clinical isolates. Mol. Microbiol. 2017, 106, 492-504, 10.1111/mmi.13831
-
(2017)
Mol. Microbiol.
, vol.106
, pp. 492-504
-
-
Calvopiña, K.1
Hinchliffe, P.2
Brem, J.3
Heesom, K.J.4
Johnson, S.5
Cain, R.6
Lohans, C.T.7
Fishwick, C.W.G.8
Schofield, C.J.9
Spencer, J.10
Avison, M.B.11
-
42
-
-
75349104493
-
Observations on the Deprotection of Pinanediol and Pinacol Boronate Esters via Fluorinated Intermediates
-
Inglis, S. R.; Woon, E. C. Y.; Thompson, A. L.; Schofield, C. J. Observations on the Deprotection of Pinanediol and Pinacol Boronate Esters via Fluorinated Intermediates. J. Org. Chem. 2010, 75, 468-471, 10.1021/jo901930v
-
(2010)
J. Org. Chem.
, vol.75
, pp. 468-471
-
-
Inglis, S.R.1
Woon, E.C.Y.2
Thompson, A.L.3
Schofield, C.J.4
-
43
-
-
85055603894
-
Active-Site Conformational Fluctuations Promote the Enzymatic Activity of NDM-1
-
Zhang, H.; Ma, G.; Zhu, Y.; Zeng, L.; Ahmad, A.; Wang, C.; Pang, B.; Fang, H.; Zhao, L.; Hao, Q. Active-Site Conformational Fluctuations Promote the Enzymatic Activity of NDM-1. Antimicrob. Agents Chemother. 2018, 62, e01579-e01518, 10.1128/AAC.01579-18
-
(2018)
Antimicrob. Agents Chemother.
, vol.62
, pp. e01579-e01518
-
-
Zhang, H.1
Ma, G.2
Zhu, Y.3
Zeng, L.4
Ahmad, A.5
Wang, C.6
Pang, B.7
Fang, H.8
Zhao, L.9
Hao, Q.10
-
44
-
-
0032553559
-
The crystal structure of the L1 metallo-β-lactamase from Stenotrophomonas maltophilia at 1.7 å resolution11 Edited by K. Nagai
-
Ullah, J. H.; Walsh, T. R.; Taylor, I. A.; Emery, D. C.; Verma, C. S.; Gamblin, S. J.; Spencer, J. The crystal structure of the L1 metallo-β-lactamase from Stenotrophomonas maltophilia at 1.7 å resolution11 Edited by K. Nagai. J. Mol. Biol. 1998, 284, 125-136, 10.1006/jmbi.1998.2148
-
(1998)
J. Mol. Biol.
, vol.284
, pp. 125-136
-
-
Ullah, J.H.1
Walsh, T.R.2
Taylor, I.A.3
Emery, D.C.4
Verma, C.S.5
Gamblin, S.J.6
Spencer, J.7
-
45
-
-
84880016971
-
5-Carboxy-8-hydroxyquinoline is a Broad Spectrum 2-Oxoglutarate Oxygenase Inhibitor which Causes Iron Translocation
-
Hopkinson, R. J.; Tumber, A.; Yapp, C.; Chowdhury, R.; Aik, W.; Che, K. H.; Li, X. S.; Kristensen, J. B. L.; King, O. N. F.; Chan, M. C.; Yeoh, K. K.; Choi, H.; Walport, L. J.; Thinnes, C. C.; Bush, J. T.; Lejeune, C.; Rydzik, A. M.; Rose, N. R.; Bagg, E. A.; McDonough, M. A.; Krojer, T.; Yue, W. W.; Ng, S. S.; Olsen, L.; Brennan, P. E.; Oppermann, U.; Muller-Knapp, S.; Klose, R. J.; Ratcliffe, P. J.; Schofield, C. J.; Kawamura, A. 5-Carboxy-8-hydroxyquinoline is a Broad Spectrum 2-Oxoglutarate Oxygenase Inhibitor which Causes Iron Translocation. Chem. Sci. 2013, 4, 3110-3117, 10.1039/c3sc51122g
-
(2013)
Chem. Sci.
, vol.4
, pp. 3110-3117
-
-
Hopkinson, R.J.1
Tumber, A.2
Yapp, C.3
Chowdhury, R.4
Aik, W.5
Che, K.H.6
Li, X.S.7
Kristensen, J.B.L.8
King, O.N.F.9
Chan, M.C.10
Yeoh, K.K.11
Choi, H.12
Walport, L.J.13
Thinnes, C.C.14
Bush, J.T.15
Lejeune, C.16
Rydzik, A.M.17
Rose, N.R.18
Bagg, E.A.19
McDonough, M.A.20
Krojer, T.21
Yue, W.W.22
Ng, S.S.23
Olsen, L.24
Brennan, P.E.25
Oppermann, U.26
Muller-Knapp, S.27
Klose, R.J.28
Ratcliffe, P.J.29
Schofield, C.J.30
Kawamura, A.31
more..
-
46
-
-
84909619197
-
X-ray absorption spectroscopy of dinuclear metallohydrolases
-
Tierney, D. L.; Schenk, G. X-ray absorption spectroscopy of dinuclear metallohydrolases. Biophys. J. 2014, 107, 1263-1272, 10.1016/j.bpj.2014.07.066
-
(2014)
Biophys. J.
, vol.107
, pp. 1263-1272
-
-
Tierney, D.L.1
Schenk, G.2
-
47
-
-
84955303871
-
Probing substrate binding to the metal binding sites in metallo-β-lactamase L1 during catalysis
-
Aitha, M.; Al-Adbul-Wahid, S.; Tierney, D. L.; Crowder, M. W. Probing substrate binding to the metal binding sites in metallo-β-lactamase L1 during catalysis. MedChemComm 2016, 7, 194-201, 10.1039/C5MD00358J
-
(2016)
MedChemComm
, vol.7
, pp. 194-201
-
-
Aitha, M.1
Al-Adbul-Wahid, S.2
Tierney, D.L.3
Crowder, M.W.4
-
48
-
-
84969261451
-
Bisthiazolidines: A Substrate-Mimicking Scaffold as an Inhibitor of the NDM-1 Carbapenemase
-
Gonzalez, M. M.; Kosmopoulou, M.; Mojica, M. F.; Castillo, V.; Hinchliffe, P.; Pettinati, I.; Brem, J.; Schofield, C. J.; Mahler, G.; Bonomo, R. A.; Llarrull, L. I.; Spencer, J.; Vila, A. J. Bisthiazolidines: A Substrate-Mimicking Scaffold as an Inhibitor of the NDM-1 Carbapenemase. ACS Infect. Dis. 2015, 1, 544-554, 10.1021/acsinfecdis.5b00046
-
(2015)
ACS Infect. Dis.
, vol.1
, pp. 544-554
-
-
Gonzalez, M.M.1
Kosmopoulou, M.2
Mojica, M.F.3
Castillo, V.4
Hinchliffe, P.5
Pettinati, I.6
Brem, J.7
Schofield, C.J.8
Mahler, G.9
Bonomo, R.A.10
Llarrull, L.I.11
Spencer, J.12
Vila, A.J.13
-
49
-
-
10044225894
-
A Metallo-β-lactamase Enzyme in Action: Crystal Structures of the Monozinc Carbapenemase CphA and its Complex with Biapenem
-
Garau, G.; Bebrone, C.; Anne, C.; Galleni, M.; Frère, J.-M.; Dideberg, O. A Metallo-β-lactamase Enzyme in Action: Crystal Structures of the Monozinc Carbapenemase CphA and its Complex with Biapenem. J. Mol. Biol. 2005, 345, 785-795, 10.1016/j.jmb.2004.10.070
-
(2005)
J. Mol. Biol.
, vol.345
, pp. 785-795
-
-
Garau, G.1
Bebrone, C.2
Anne, C.3
Galleni, M.4
Frère, J.-M.5
Dideberg, O.6
-
50
-
-
78650620354
-
QM/MM Studies of Monozinc β-Lactamase CphA Suggest That the Crystal Structure of an Enzyme-Intermediate Complex Represents a Minor Pathway
-
Wu, S.; Xu, D.; Guo, H. QM/MM Studies of Monozinc β-Lactamase CphA Suggest That the Crystal Structure of an Enzyme-Intermediate Complex Represents a Minor Pathway. J. Am. Chem. Soc. 2010, 132, 17986-17988, 10.1021/ja104241g
-
(2010)
J. Am. Chem. Soc.
, vol.132
, pp. 17986-17988
-
-
Wu, S.1
Xu, D.2
Guo, H.3
-
51
-
-
78649835464
-
Three factors that modulate the activity of class D β-lactamases and interfere with the post-translational carboxylation of Lys70
-
Vercheval, L.; Bauvois, C.; di Paolo, A.; Borel, F.; Ferrer, J.-L.; Sauvage, E.; Matagne, A.; Frère, J.-M.; Charlier, P.; Galleni, M.; Kerff, F. Three factors that modulate the activity of class D β-lactamases and interfere with the post-translational carboxylation of Lys70. Biochem. J. 2010, 432, 495-506, 10.1042/BJ20101122
-
(2010)
Biochem. J.
, vol.432
, pp. 495-506
-
-
Vercheval, L.1
Bauvois, C.2
Di Paolo, A.3
Borel, F.4
Ferrer, J.-L.5
Sauvage, E.6
Matagne, A.7
Frère, J.-M.8
Charlier, P.9
Galleni, M.10
Kerff, F.11
-
52
-
-
85074117382
-
1405. Efficacy of the Human-Simulated Regimen (HSR) of Cefepime (FEP)/VNRX-5133 Combination against Serine β-Lactamase-Producing Gram-negative Bacteria in the Neutropenic Murine Thigh Infection Model
-
Abdelraouf, K.; Abuhussain, S. A.; Nicolau, D. P. 1405. Efficacy of the Human-Simulated Regimen (HSR) of Cefepime (FEP)/VNRX-5133 Combination Against Serine β-Lactamase-Producing Gram-negative Bacteria in the Neutropenic Murine Thigh Infection Model. Open Forum Infect. Dis. 2018, 5, S432-S433, 10.1093/ofid/ofy210.1236
-
(2018)
Open Forum Infect. Dis.
, vol.5
, pp. S432-S433
-
-
Abdelraouf, K.1
Abuhussain, S.A.2
Nicolau, D.P.3
-
53
-
-
85074117213
-
1401. A Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Pharmacokinetics of Single and Repeat Doses of VNRX-5133 in Healthy Subjects
-
Geibel, B.; Dowell, J.; Dickerson, D.; Henkel, T. 1401. A Randomized, Double-Blind, Placebo-Controlled Study of the Safety and Pharmacokinetics of Single and Repeat Doses of VNRX-5133 in Healthy Subjects. Open Forum Infect. Dis. 2018, 5, S431, 10.1093/ofid/ofy210.1232
-
(2018)
Open Forum Infect. Dis.
, vol.5
, pp. S431
-
-
Geibel, B.1
Dowell, J.2
Dickerson, D.3
Henkel, T.4
-
54
-
-
85074117201
-
1360. Antimicrobial Activity of Cefepime in Combination with VNRX-5133 against a Global Collection of Enterobacteriaceae including Resistant Phenotypes
-
Hackel, M.; Sahm, D. 1360. Antimicrobial Activity of Cefepime in Combination with VNRX-5133 Against a Global Collection of Enterobacteriaceae Including Resistant Phenotypes. Open Forum Infect. Dis. 2018, 5, S416-S417, 10.1093/ofid/ofy210.1191
-
(2018)
Open Forum Infect. Dis.
, vol.5
, pp. S416-S417
-
-
Hackel, M.1
Sahm, D.2
-
55
-
-
84863208034
-
Dynamic combinatorial chemistry employing boronic acids/boronate esters leads to potent oxygenase inhibitors
-
Demetriades, M.; Leung, I. K.; Chowdhury, R.; Chan, M. C.; McDonough, M. A.; Yeoh, K. K.; Tian, Y. M.; Claridge, T. D.; Ratcliffe, P. J.; Woon, E. C.; Schofield, C. J. Dynamic combinatorial chemistry employing boronic acids/boronate esters leads to potent oxygenase inhibitors. Angew. Chem., Int. Ed. 2012, 51, 6672-6675, 10.1002/anie.201202000
-
(2012)
Angew. Chem., Int. Ed.
, vol.51
, pp. 6672-6675
-
-
Demetriades, M.1
Leung, I.K.2
Chowdhury, R.3
Chan, M.C.4
McDonough, M.A.5
Yeoh, K.K.6
Tian, Y.M.7
Claridge, T.D.8
Ratcliffe, P.J.9
Woon, E.C.10
Schofield, C.J.11
-
56
-
-
79960260060
-
Unexpected tricovalent binding mode of boronic acids within the active site of a penicillin-binding protein
-
Zervosen, A.; Herman, R.; Kerff, F.; Herman, A.; Bouillez, A.; Prati, F.; Pratt, R. F.; Frere, J. M.; Joris, B.; Luxen, A.; Charlier, P.; Sauvage, E. Unexpected tricovalent binding mode of boronic acids within the active site of a penicillin-binding protein. J. Am. Chem. Soc. 2011, 133, 10839-10848, 10.1021/ja200696y
-
(2011)
J. Am. Chem. Soc.
, vol.133
, pp. 10839-10848
-
-
Zervosen, A.1
Herman, R.2
Kerff, F.3
Herman, A.4
Bouillez, A.5
Prati, F.6
Pratt, R.F.7
Frere, J.M.8
Joris, B.9
Luxen, A.10
Charlier, P.11
Sauvage, E.12
-
58
-
-
84860389616
-
Crystal structure of New Delhi metallo-beta-lactamase reveals molecular basis for antibiotic resistance
-
King, D.; Strynadka, N. Crystal structure of New Delhi metallo-beta-lactamase reveals molecular basis for antibiotic resistance. Protein Sci. 2011, 20, 1484-1491, 10.1002/pro.697
-
(2011)
Protein Sci.
, vol.20
, pp. 1484-1491
-
-
King, D.1
Strynadka, N.2
-
59
-
-
14244272868
-
PHENIX: Building new software for automated crystallographic structure determination
-
Adams, P. D.; Grosse-Kunstleve, R. W.; Hung, L.-W.; Ioerger, T. R.; McCoy, A. J.; Moriarty, N. W.; Read, R. J.; Sacchettini, J. C.; Sauter, N. K.; Terwilliger, T. C. PHENIX: building new software for automated crystallographic structure determination. Acta Crystallogr., Sect. D: Biol. Crystallogr. 2002, 58, 1948-1954, 10.1107/S0907444902016657
-
(2002)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.58
, pp. 1948-1954
-
-
Adams, P.D.1
Grosse-Kunstleve, R.W.2
Hung, L.-W.3
Ioerger, T.R.4
McCoy, A.J.5
Moriarty, N.W.6
Read, R.J.7
Sacchettini, J.C.8
Sauter, N.K.9
Terwilliger, T.C.10
-
60
-
-
77949535720
-
Features and development of Coot
-
Emsley, P.; Lohkamp, B.; Scott, W. G.; Cowtan, K. Features and development of Coot. Acta Crystallogr., Sect. D: Biol. Crystallogr. 2010, 66, 486-501, 10.1107/S0907444910007493
-
(2010)
Acta Crystallogr., Sect. D: Biol. Crystallogr.
, vol.66
, pp. 486-501
-
-
Emsley, P.1
Lohkamp, B.2
Scott, W.G.3
Cowtan, K.4
|