-
1
-
-
84934286719
-
A β-lactamase inhibitor revival provides new hope for old antibiotics
-
Garber, K., A β-lactamase inhibitor revival provides new hope for old antibiotics. Nat. Rev. Drug Discov. 14 (2015), 445–447.
-
(2015)
Nat. Rev. Drug Discov.
, vol.14
, pp. 445-447
-
-
Garber, K.1
-
2
-
-
84948709890
-
Antibiotic resistance breakers: can repurposed drugs fill the antibiotic discovery void?
-
Brown, D., Antibiotic resistance breakers: can repurposed drugs fill the antibiotic discovery void?. Nat. Rev. Drug Discov. 14 (2015), 821–832.
-
(2015)
Nat. Rev. Drug Discov.
, vol.14
, pp. 821-832
-
-
Brown, D.1
-
3
-
-
79955453026
-
Metallo-β-lactamases: a last frontier for β-lactams?
-
Cornaglia, G., Giamarellou, H., Rossolini, G.M., Metallo-β-lactamases: a last frontier for β-lactams?. Lancet Infect. Dis. 11 (2011), 381–393.
-
(2011)
Lancet Infect. Dis.
, vol.11
, pp. 381-393
-
-
Cornaglia, G.1
Giamarellou, H.2
Rossolini, G.M.3
-
4
-
-
77149165713
-
Updated functional classification of β-lactamases
-
Bush, K., Jacoby, G.A., Updated functional classification of β-lactamases. Antimicrob. Agents Chemother. 54 (2010), 969–976.
-
(2010)
Antimicrob. Agents Chemother.
, vol.54
, pp. 969-976
-
-
Bush, K.1
Jacoby, G.A.2
-
5
-
-
33750624074
-
Metallo-beta-lactamases: novel weaponry for antibiotic resistance in bacteria
-
Crowder, M.W., Spencer, J., Vila, A.J., Metallo-beta-lactamases: novel weaponry for antibiotic resistance in bacteria. Acc. Chem. Res. 39 (2006), 721–728.
-
(2006)
Acc. Chem. Res.
, vol.39
, pp. 721-728
-
-
Crowder, M.W.1
Spencer, J.2
Vila, A.J.3
-
6
-
-
74249108028
-
Three decades of β-lactamase inhibitors
-
Drawz, S.M., Bonomo, R.A., Three decades of β-lactamase inhibitors. Clin. Microbiol. Rev. 23 (2010), 160–201.
-
(2010)
Clin. Microbiol. Rev.
, vol.23
, pp. 160-201
-
-
Drawz, S.M.1
Bonomo, R.A.2
-
7
-
-
84977073918
-
The road to avibactam: the first clinically useful non-beta-lactam working somewhat like a beta-lactam
-
Wang, D.Y., Abboud, M.I., Markoulides, M.S., Brem, J., Schofield, C.J., The road to avibactam: the first clinically useful non-beta-lactam working somewhat like a beta-lactam. Future Med. Chem. 8 (2016), 1063–1084.
-
(2016)
Future Med. Chem.
, vol.8
, pp. 1063-1084
-
-
Wang, D.Y.1
Abboud, M.I.2
Markoulides, M.S.3
Brem, J.4
Schofield, C.J.5
-
8
-
-
85014230238
-
19F-NMR reveals the role of mobile loops in product and inhibitor binding by the são paulo metallo-β-lactamase
-
Abboud, M.I., Hinchliffe, P., Brem, J., Macsics, R., Pfeffer, I., Makena, A., Umland, K.-D., Rydzik, A.M., Li, G.-B., Spencer, J., Claridge, T.D.W., Schofield, C.J., 19F-NMR reveals the role of mobile loops in product and inhibitor binding by the são paulo metallo-β-lactamase. Angew. Chem. Int. Ed. 56 (2017), 3862–3866.
-
(2017)
Angew. Chem. Int. Ed.
, vol.56
, pp. 3862-3866
-
-
Abboud, M.I.1
Hinchliffe, P.2
Brem, J.3
Macsics, R.4
Pfeffer, I.5
Makena, A.6
Umland, K.-D.7
Rydzik, A.M.8
Li, G.-B.9
Spencer, J.10
Claridge, T.D.W.11
Schofield, C.J.12
-
9
-
-
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. 56 (2013), 6945–6953.
-
(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
-
10
-
-
84893391938
-
Targeting metallo-β-lactamase enzymes in antibiotic resistance
-
King, D.T., Strynadka, N.C., Targeting metallo-β-lactamase enzymes in antibiotic resistance. Future Med. Chem. 5 (2013), 1243–1263.
-
(2013)
Future Med. Chem.
, vol.5
, pp. 1243-1263
-
-
King, D.T.1
Strynadka, N.C.2
-
11
-
-
84911489666
-
Rhodanine hydrolysis leads to potent thioenolate mediated metallo-β-lactamase inhibition
-
Brem, J., van Berkel, S.S., Aik, W., Rydzik, A.M., Avison, M.B., Pettinati, I., Umland, K.-D., Kawamura, A., Spencer, J., Claridge, T.D., McDonough, M.A., Schofield, C.J., Rhodanine hydrolysis leads to potent thioenolate mediated metallo-β-lactamase inhibition. Nat. Chem. 6 (2014), 1084–1090.
-
(2014)
Nat. Chem.
, vol.6
, pp. 1084-1090
-
-
Brem, J.1
van Berkel, S.S.2
Aik, W.3
Rydzik, A.M.4
Avison, M.B.5
Pettinati, I.6
Umland, K.-D.7
Kawamura, A.8
Spencer, J.9
Claridge, T.D.10
McDonough, M.A.11
Schofield, C.J.12
-
12
-
-
74549179120
-
The emerging threat of acquired carbapenemases in Gram-negative bacteria
-
Cornaglia, G., Rossolini, G.M., The emerging threat of acquired carbapenemases in Gram-negative bacteria. Clin. Microbiol. Infect. 16 (2010), 99–101.
-
(2010)
Clin. Microbiol. Infect.
, vol.16
, pp. 99-101
-
-
Cornaglia, G.1
Rossolini, G.M.2
-
13
-
-
84946567642
-
A resurgence of beta-lactamase inhibitor combinations effective against multidrug-resistant Gram-negative pathogens
-
Bush, K., A resurgence of beta-lactamase inhibitor combinations effective against multidrug-resistant Gram-negative pathogens. Int. J. Antimicrob. Agents 46 (2015), 483–493.
-
(2015)
Int. J. Antimicrob. Agents
, vol.46
, pp. 483-493
-
-
Bush, K.1
-
14
-
-
62949166438
-
Metallo-beta-lactamases in Gram-negative bacteria: introducing the era of pan-resistance?
-
e401-407
-
Maltezou, H.C., Metallo-beta-lactamases in Gram-negative bacteria: introducing the era of pan-resistance?. Int. J. Antimicrob. Agents, 33, 2009, 405 e401-407.
-
(2009)
Int. J. Antimicrob. Agents
, vol.33
, pp. 405
-
-
Maltezou, H.C.1
-
15
-
-
85041586950
-
Evolution of β-lactamases: past, present, and future
-
T. Dougherty M. Pucci Springer Boston, MA
-
Bush, K., Evolution of β-lactamases: past, present, and future. Dougherty, T., Pucci, M., (eds.) Antibiotic Discovery and Development, 2012, Springer, Boston, MA.
-
(2012)
Antibiotic Discovery and Development
-
-
Bush, K.1
-
16
-
-
84953208647
-
Promiscuous metallo-beta-lactamases: MIM-1 and MIM-2 may play an essential role in quorum sensing networks
-
Miraula, M., Schenk, G., Mitic, N., Promiscuous metallo-beta-lactamases: MIM-1 and MIM-2 may play an essential role in quorum sensing networks. J. Inorg. Biochem. 162 (2016), 366–375.
-
(2016)
J. Inorg. Biochem.
, vol.162
, pp. 366-375
-
-
Miraula, M.1
Schenk, G.2
Mitic, N.3
-
17
-
-
85027469306
-
Characterization of a highly efficient antibiotic-degrading metallo-beta-lactamase obtained from an uncultured member of a permafrost community
-
Pedroso, M.M., Selleck, C., Enculescu, C., Harmer, J.R., Mitic, N., Craig, W.R., Helweh, W., Hugenholtz, P., Tyson, G.W., Tierney, D.L., Larrabee, J.A., Schenk, G., Characterization of a highly efficient antibiotic-degrading metallo-beta-lactamase obtained from an uncultured member of a permafrost community. Metallomics 9 (2017), 1157–1168.
-
(2017)
Metallomics
, vol.9
, pp. 1157-1168
-
-
Pedroso, M.M.1
Selleck, C.2
Enculescu, C.3
Harmer, J.R.4
Mitic, N.5
Craig, W.R.6
Helweh, W.7
Hugenholtz, P.8
Tyson, G.W.9
Tierney, D.L.10
Larrabee, J.A.11
Schenk, G.12
-
18
-
-
85019738771
-
Progress toward inhibitors of metallo-β-lactamases
-
McGeary, R.P., Tan, D.T.C., Schenk, G., Progress toward inhibitors of metallo-β-lactamases. Future Med. Chem. 9 (2017), 673–691.
-
(2017)
Future Med. Chem.
, vol.9
, pp. 673-691
-
-
McGeary, R.P.1
Tan, D.T.C.2
Schenk, G.3
-
19
-
-
85041630798
-
N.a. Miti?, Unusual metallo-β-lactamases may constitute a new subgroup in this family of enzymes
-
Hou, C.-F.D., Phelan, E.K., Miraula, M., Ollis, D.L., Schenk, G., N.a. Miti?, Unusual metallo-β-lactamases may constitute a new subgroup in this family of enzymes. Am. J. Mol. Biol., 4, 2014, 5.
-
(2014)
Am. J. Mol. Biol.
, vol.4
, pp. 5
-
-
Hou, C.-F.D.1
Phelan, E.K.2
Miraula, M.3
Ollis, D.L.4
Schenk, G.5
-
20
-
-
84885650988
-
Identification and characterization of an unusual metallo-beta-lactamase from Serratia proteamaculans
-
Vella, P., Miraula, M., Phelan, E., Leung, E.W., Ely, F., Ollis, D.L., McGeary, R.P., Schenk, G., Mitic, N., Identification and characterization of an unusual metallo-beta-lactamase from Serratia proteamaculans. J. Biol. Inorg. Chem. 18 (2013), 855–863.
-
(2013)
J. Biol. Inorg. Chem.
, vol.18
, pp. 855-863
-
-
Vella, P.1
Miraula, M.2
Phelan, E.3
Leung, E.W.4
Ely, F.5
Ollis, D.L.6
McGeary, R.P.7
Schenk, G.8
Mitic, N.9
-
21
-
-
84928208370
-
-
C.Z. Christov Elsevier Oxford
-
Mitic, et al. Christov, C.Z., (eds.) Advances in Protein Chemistry and Structural Biology: Metal-containing Enzymes, vol. 97, 2014, Elsevier, Oxford, 49.
-
(2014)
Advances in Protein Chemistry and Structural Biology: Metal-containing Enzymes
, vol.97
, pp. 49
-
-
Mitic1
-
22
-
-
84976477345
-
Cross-class metallo-β-lactamase inhibition by bisthiazolidines reveals multiple binding modes
-
Hinchliffe, P., Gonzalez, M.M., Mojica, M.F., Gonzalez, J.M., Castillo, V., Saiz, C., Kosmopoulou, M., Tooke, C.L., Llarrull, L.I., Mahler, G., Bonomo, R.A., Vila, A.J., Spencer, J., Cross-class metallo-β-lactamase inhibition by bisthiazolidines reveals multiple binding modes. Proc. Natl. Acad. Sci. U. S. A 113 (2016), E3745–E3754.
-
(2016)
Proc. Natl. Acad. Sci. U. S. A
, vol.113
, pp. E3745-E3754
-
-
Hinchliffe, P.1
Gonzalez, M.M.2
Mojica, M.F.3
Gonzalez, J.M.4
Castillo, V.5
Saiz, C.6
Kosmopoulou, M.7
Tooke, C.L.8
Llarrull, L.I.9
Mahler, G.10
Bonomo, R.A.11
Vila, A.J.12
Spencer, J.13
-
23
-
-
84957867042
-
Structural basis of metallo-β-lactamase inhibition by captopril stereoisomers
-
Brem, J., van Berkel, S.S., Zollman, D., Lee, S.Y., Gileadi, O., McHugh, P.J., Walsh, T.R., McDonough, M.A., Schofield, C.J., Structural basis of metallo-β-lactamase inhibition by captopril stereoisomers. Antimicrob. Agents Chemother. 60 (2016), 142–150.
-
(2016)
Antimicrob. Agents Chemother.
, vol.60
, pp. 142-150
-
-
Brem, J.1
van Berkel, S.S.2
Zollman, D.3
Lee, S.Y.4
Gileadi, O.5
McHugh, P.J.6
Walsh, T.R.7
McDonough, M.A.8
Schofield, C.J.9
-
24
-
-
85018471501
-
Metallo-β-lactamase inhibitors by bioisosteric replacement: preparation, activity and binding
-
Skagseth, S., Akhter, S., Paulsen, M.H., Muhammad, Z., Lauksund, S., Samuelsen, Ø., Leiros, H.-K.S., Bayer, A., Metallo-β-lactamase inhibitors by bioisosteric replacement: preparation, activity and binding. Eur. J. Med. Chem. 135 (2017), 159–173.
-
(2017)
Eur. J. Med. Chem.
, vol.135
, pp. 159-173
-
-
Skagseth, S.1
Akhter, S.2
Paulsen, M.H.3
Muhammad, Z.4
Lauksund, S.5
Samuelsen, Ø.6
Leiros, H.-K.S.7
Bayer, A.8
-
25
-
-
84962239845
-
Design, synthesis, and in vitro and biological evaluation of potent amino acid-derived thiol inhibitors of the metallo-β-lactamase IMP-1
-
Arjomandi, O.K., Hussein, W.M., Vella, P., Yusof, Y., Sidjabat, H.E., Schenk, G., McGeary, R.P., Design, synthesis, and in vitro and biological evaluation of potent amino acid-derived thiol inhibitors of the metallo-β-lactamase IMP-1. Eur. J. Med. Chem. 114 (2016), 318–327.
-
(2016)
Eur. J. Med. Chem.
, vol.114
, pp. 318-327
-
-
Arjomandi, O.K.1
Hussein, W.M.2
Vella, P.3
Yusof, Y.4
Sidjabat, H.E.5
Schenk, G.6
McGeary, R.P.7
-
26
-
-
84903457328
-
Aspergillomarasmine A overcomes metallo-beta-lactamase antibiotic resistance
-
King, A.M., Reid-Yu, S.A., Wang, W., King, D.T., De Pascale, G., Strynadka, N.C., Walsh, T.R., Coombes, B.K., Wright, G.D., Aspergillomarasmine A overcomes metallo-beta-lactamase antibiotic resistance. Nature 510 (2014), 503–506.
-
(2014)
Nature
, vol.510
, pp. 503-506
-
-
King, A.M.1
Reid-Yu, S.A.2
Wang, W.3
King, D.T.4
De Pascale, G.5
Strynadka, N.C.6
Walsh, T.R.7
Coombes, B.K.8
Wright, G.D.9
-
27
-
-
84947213893
-
Discovery of novel inhibitor scaffolds against the metallo-β-lactamase VIM-2 by surface plasmon resonance (SPR) based fragment screening
-
Christopeit, T., Carlsen, T.J.O., Helland, R., Leiros, H.-K.S., Discovery of novel inhibitor scaffolds against the metallo-β-lactamase VIM-2 by surface plasmon resonance (SPR) based fragment screening. J. Med. Chem. 58 (2015), 8671–8682.
-
(2015)
J. Med. Chem.
, vol.58
, pp. 8671-8682
-
-
Christopeit, T.1
Carlsen, T.J.O.2
Helland, R.3
Leiros, H.-K.S.4
-
28
-
-
84965002978
-
Triazolylthioacetamide: a valid scaffold for the development of New Delhi metallo-beta-lactmase-1 (NDM-1) inhibitors
-
Zhai, L., Zhang, Y.L., Kang, J.S., Oelschlaeger, P., Xiao, L., Nie, S.S., Yang, K.W., Triazolylthioacetamide: a valid scaffold for the development of New Delhi metallo-beta-lactmase-1 (NDM-1) inhibitors. ACS Med. Chem. Lett. 7 (2016), 413–417.
-
(2016)
ACS Med. Chem. Lett.
, vol.7
, pp. 413-417
-
-
Zhai, L.1
Zhang, Y.L.2
Kang, J.S.3
Oelschlaeger, P.4
Xiao, L.5
Nie, S.S.6
Yang, K.W.7
-
29
-
-
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. 7 (2016), 12406–12413.
-
(2016)
Nat. Commun.
, vol.7
, pp. 12406-12413
-
-
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
-
30
-
-
85016467068
-
Cyclic boronates inhibit all classes of β-lactamase
-
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-lactamase. Antimicrob. Agents Chemother., 61, 2017, e02260-02216.
-
(2017)
Antimicrob. Agents Chemother.
, vol.61
-
-
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
-
31
-
-
85020462323
-
Structure-activity relationship study and optimisation of 2-aminopyrrole-1-benzyl-4,5-diphenyl-1H-pyrrole-3-carbonitrile as a broad spectrum metallo-β-lactamase inhibitor
-
McGeary, R.P., Tan, D.T.C., Selleck, C., Monteiro Pedroso, M., Sidjabat, H.E., Schenk, G., Structure-activity relationship study and optimisation of 2-aminopyrrole-1-benzyl-4,5-diphenyl-1H-pyrrole-3-carbonitrile as a broad spectrum metallo-β-lactamase inhibitor. Eur. J. Med. Chem. 137 (2017), 351–364.
-
(2017)
Eur. J. Med. Chem.
, vol.137
, pp. 351-364
-
-
McGeary, R.P.1
Tan, D.T.C.2
Selleck, C.3
Monteiro Pedroso, M.4
Sidjabat, H.E.5
Schenk, G.6
-
32
-
-
79956140677
-
The identification of new metallo-β-lactamase inhibitor leads from fragment-based screening
-
Vella, P., Hussein, W.M., Leung, E.W., Clayton, D., Ollis, D.L., Mitić, N., Schenk, G., McGeary, R.P., The identification of new metallo-β-lactamase inhibitor leads from fragment-based screening. Bioorg. Med. Chem. Lett. 21 (2011), 3282–3285.
-
(2011)
Bioorg. Med. Chem. Lett.
, vol.21
, pp. 3282-3285
-
-
Vella, P.1
Hussein, W.M.2
Leung, E.W.3
Clayton, D.4
Ollis, D.L.5
Mitić, N.6
Schenk, G.7
McGeary, R.P.8
-
33
-
-
80955151611
-
Synthesis and kinetic testing of new inhibitors for a metallo-β-lactamase from Klebsiella pneumonia and Pseudomonas aeruginosa
-
Mohamed, M.S., Hussein, W.M., McGeary, R.P., Vella, P., Schenk, G., Abd El-Hameed, R.H., Synthesis and kinetic testing of new inhibitors for a metallo-β-lactamase from Klebsiella pneumonia and Pseudomonas aeruginosa. Eur. J. Med. Chem. 46 (2011), 6075–6082.
-
(2011)
Eur. J. Med. Chem.
, vol.46
, pp. 6075-6082
-
-
Mohamed, M.S.1
Hussein, W.M.2
McGeary, R.P.3
Vella, P.4
Schenk, G.5
Abd El-Hameed, R.H.6
-
34
-
-
84655167173
-
McGeary, 3-mercapto-1,2,4-triazoles and N-acylated thiosemicarbazides as metallo-beta-lactamase inhibitors
-
Faridoon, W.M., Hussein, P., Vella, N.U., Islam, D.L., Ollis, G., Schenk, R.P., McGeary, 3-mercapto-1,2,4-triazoles and N-acylated thiosemicarbazides as metallo-beta-lactamase inhibitors. Bioorg. Med. Chem. Lett 22 (2012), 380–386.
-
(2012)
Bioorg. Med. Chem. Lett
, vol.22
, pp. 380-386
-
-
Faridoon, W.M.1
Hussein, P.2
Vella, N.U.3
Islam, D.L.4
Ollis, G.5
Schenk, R.P.6
-
35
-
-
84866631880
-
Synthesis and kinetic testing of tetrahydropyrimidine-2-thione and pyrrole derivatives as inhibitors of the metallo-β-lactamase from Klebsiella pneumonia and Pseudomonas aeruginosa
-
Hussein, W.M., Fatahala, S.S., Mohamed, Z.M., McGeary, R.P., Schenk, G., Ollis, D.L., Mohamed, M.S., Synthesis and kinetic testing of tetrahydropyrimidine-2-thione and pyrrole derivatives as inhibitors of the metallo-β-lactamase from Klebsiella pneumonia and Pseudomonas aeruginosa. Chem. Biol. Drug Des. 80 (2012), 500–515.
-
(2012)
Chem. Biol. Drug Des.
, vol.80
, pp. 500-515
-
-
Hussein, W.M.1
Fatahala, S.S.2
Mohamed, Z.M.3
McGeary, R.P.4
Schenk, G.5
Ollis, D.L.6
Mohamed, M.S.7
-
36
-
-
85020428257
-
1,2,4-Triazole-3-thione compounds as inhibitors of di-zinc metallo-beta-lactamases
-
Sevaille, L., Gavara, L., Bebrone, C., De Luca, F., Nauton, L., Achard, M., Mercuri, P., Tanfoni, S., Borgianni, L., Guyon, C., Lonjon, P., Turan-Zitouni, G., Dzieciolowski, J., Becker, K., Benard, L., Condon, C., Maillard, L., Martinez, J., Frere, J.M., Dideberg, O., Galleni, M., Docquier, J.D., Hernandez, J.F., 1,2,4-Triazole-3-thione compounds as inhibitors of di-zinc metallo-beta-lactamases. ChemMedChem 12 (2017), 972–985.
-
(2017)
ChemMedChem
, vol.12
, pp. 972-985
-
-
Sevaille, L.1
Gavara, L.2
Bebrone, C.3
De Luca, F.4
Nauton, L.5
Achard, M.6
Mercuri, P.7
Tanfoni, S.8
Borgianni, L.9
Guyon, C.10
Lonjon, P.11
Turan-Zitouni, G.12
Dzieciolowski, J.13
Becker, K.14
Benard, L.15
Condon, C.16
Maillard, L.17
Martinez, J.18
Frere, J.M.19
Dideberg, O.20
Galleni, M.21
Docquier, J.D.22
Hernandez, J.F.23
more..
-
37
-
-
85011000691
-
NMR-filtered virtual screening leads to non-metal chelating metallo-β-lactamase inhibitors
-
Li, G.-B., Abboud, M.I., Brem, J., Someya, H., Lohans, C.T., Yang, S.-Y., Spencer, J., Wareham, D.W., McDonough, M.A., Schofield, C.J., NMR-filtered virtual screening leads to non-metal chelating metallo-β-lactamase inhibitors. Chem. Sci. 8 (2017), 928–937.
-
(2017)
Chem. Sci.
, vol.8
, pp. 928-937
-
-
Li, G.-B.1
Abboud, M.I.2
Brem, J.3
Someya, H.4
Lohans, C.T.5
Yang, S.-Y.6
Spencer, J.7
Wareham, D.W.8
McDonough, M.A.9
Schofield, C.J.10
-
38
-
-
85021770905
-
Crystallographic analyses of isoquinoline complexes reveal a new mode of metallo-β-lactamase inhibition
-
Li, G.-B., Brem, J., Lesniak, R., Abboud, M.I., Lohans, C.T., Clifton, I.J., Yang, S.-Y., Jimenez-Castellanos, J.-C., Avison, M.B., Spencer, J., McDonough, M.A., Schofield, C.J., Crystallographic analyses of isoquinoline complexes reveal a new mode of metallo-β-lactamase inhibition. Chem. Commun. 53 (2017), 5806–5809.
-
(2017)
Chem. Commun.
, vol.53
, pp. 5806-5809
-
-
Li, G.-B.1
Brem, J.2
Lesniak, R.3
Abboud, M.I.4
Lohans, C.T.5
Clifton, I.J.6
Yang, S.-Y.7
Jimenez-Castellanos, J.-C.8
Avison, M.B.9
Spencer, J.10
McDonough, M.A.11
Schofield, C.J.12
-
39
-
-
84979026616
-
Captopril analogues as metallo-beta-lactamase inhibitors
-
Yusof, Y., Tan, D.T.C., Arjomandi, O.K., Schenk, G., McGeary, R.P., Captopril analogues as metallo-beta-lactamase inhibitors. Bioorg. Med. Chem. Lett 26 (2016), 1589–1593.
-
(2016)
Bioorg. Med. Chem. Lett
, vol.26
, pp. 1589-1593
-
-
Yusof, Y.1
Tan, D.T.C.2
Arjomandi, O.K.3
Schenk, G.4
McGeary, R.P.5
-
40
-
-
84923933405
-
LEADOPT: an automatic tool for structure-based lead optimization, and its application in structural optimizations of VEGFR2 and SYK inhibitors
-
Li, G.-B., Ji, S., Yang, L.-L., Zhang, R.-J., Chen, K., Zhong, L., Ma, S., Yang, S.-Y., LEADOPT: an automatic tool for structure-based lead optimization, and its application in structural optimizations of VEGFR2 and SYK inhibitors. Eur. J. Med. Chem. 93 (2015), 523–538.
-
(2015)
Eur. J. Med. Chem.
, vol.93
, pp. 523-538
-
-
Li, G.-B.1
Ji, S.2
Yang, L.-L.3
Zhang, R.-J.4
Chen, K.5
Zhong, L.6
Ma, S.7
Yang, S.-Y.8
-
41
-
-
27344459398
-
Virtual computational chemistry laboratory–design and description
-
Tetko, I.V., Gasteiger, J., Todeschini, R., Mauri, A., Livingstone, D., Ertl, P., Palyulin, V.A., Radchenko, E.V., Zefirov, N.S., Makarenko, A.S., Tanchuk, V.Y., Prokopenko, V.V., Virtual computational chemistry laboratory–design and description. J. Comput. Aided Mol. Des. 19 (2005), 453–463.
-
(2005)
J. Comput. Aided Mol. Des.
, vol.19
, pp. 453-463
-
-
Tetko, I.V.1
Gasteiger, J.2
Todeschini, R.3
Mauri, A.4
Livingstone, D.5
Ertl, P.6
Palyulin, V.A.7
Radchenko, E.V.8
Zefirov, N.S.9
Makarenko, A.S.10
Tanchuk, V.Y.11
Prokopenko, V.V.12
-
42
-
-
84975796082
-
Are the physicochemical properties of antibacterial compounds really different from other drugs?
-
Ebejer, J.P., Charlton, M.H., Finn, P.W., Are the physicochemical properties of antibacterial compounds really different from other drugs?. J. Cheminf., 8, 2016, 30.
-
(2016)
J. Cheminf.
, vol.8
, pp. 30
-
-
Ebejer, J.P.1
Charlton, M.H.2
Finn, P.W.3
-
43
-
-
84918539871
-
Trends and exceptions of physical properties on antibacterial activity for gram-positive and gram-negative pathogens
-
Brown, D.G., May-Dracka, T.L., Gagnon, M.M., Tommasi, R., Trends and exceptions of physical properties on antibacterial activity for gram-positive and gram-negative pathogens. J. Med. Chem. 57 (2014), 10144–10161.
-
(2014)
J. Med. Chem.
, vol.57
, pp. 10144-10161
-
-
Brown, D.G.1
May-Dracka, T.L.2
Gagnon, M.M.3
Tommasi, R.4
-
44
-
-
33845491449
-
Interpreting steep dose-response curves in early inhibitor discovery
-
Shoichet, B.K., Interpreting steep dose-response curves in early inhibitor discovery. J. Med. Chem. 49 (2006), 7274–7277.
-
(2006)
J. Med. Chem.
, vol.49
, pp. 7274-7277
-
-
Shoichet, B.K.1
-
45
-
-
23944514165
-
Evaluation of Enzyme Inhibitors in Drug Discovery
-
Wiley
-
Copeland, R.A., Evaluation of Enzyme Inhibitors in Drug Discovery. 2013, Wiley.
-
(2013)
-
-
Copeland, R.A.1
-
46
-
-
84863976350
-
New Delhi metallo-β-lactamase: structural insights into β-lactam recognition and inhibition
-
King, D.T., Worrall, L.J., Gruninger, R., Strynadka, N.C.J., New Delhi metallo-β-lactamase: structural insights into β-lactam recognition and inhibition. J. Am. Chem. Soc. 134 (2012), 11362–11365.
-
(2012)
J. Am. Chem. Soc.
, vol.134
, pp. 11362-11365
-
-
King, D.T.1
Worrall, L.J.2
Gruninger, R.3
Strynadka, N.C.J.4
-
47
-
-
84908461884
-
Structural and mechanistic insights into NDM-1 catalyzed hydrolysis of cephalosporins
-
Feng, H., Ding, J., Zhu, D., Liu, X., Xu, X., Zhang, Y., Zang, S., Wang, D.C., Liu, W., Structural and mechanistic insights into NDM-1 catalyzed hydrolysis of cephalosporins. J. Am. Chem. Soc. 136 (2014), 14694–14697.
-
(2014)
J. Am. Chem. Soc.
, vol.136
, pp. 14694-14697
-
-
Feng, H.1
Ding, J.2
Zhu, D.3
Liu, X.4
Xu, X.5
Zhang, Y.6
Zang, S.7
Wang, D.C.8
Liu, W.9
-
48
-
-
76449098262
-
PHENIX: a comprehensive Python-based system for macromolecular structure solution
-
Adams, P.D., Afonine, P.V., Bunkoczi, G., Chen, V.B., Davis, I.W., Echols, N., Headd, J.J., Hung, L.W., Kapral, G.J., Grosse-Kunstleve, R.W., McCoy, A.J., Moriarty, N.W., Oeffner, R., Read, R.J., Richardson, D.C., Richardson, J.S., Terwilliger, T.C., Zwart, P.H., PHENIX: a comprehensive Python-based system for macromolecular structure solution. Acta Crystallogr. D Biol. Crystallogr 66 (2010), 213–221.
-
(2010)
Acta Crystallogr. D Biol. Crystallogr
, vol.66
, pp. 213-221
-
-
Adams, P.D.1
Afonine, P.V.2
Bunkoczi, G.3
Chen, V.B.4
Davis, I.W.5
Echols, N.6
Headd, J.J.7
Hung, L.W.8
Kapral, G.J.9
Grosse-Kunstleve, R.W.10
McCoy, A.J.11
Moriarty, N.W.12
Oeffner, R.13
Read, R.J.14
Richardson, D.C.15
Richardson, J.S.16
Terwilliger, T.C.17
Zwart, P.H.18
-
50
-
-
76149120388
-
AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading
-
Trott, O., Olson, A.J., AutoDock Vina: improving the speed and accuracy of docking with a new scoring function, efficient optimization, and multithreading. J. Comput. Chem. 31 (2010), 455–461.
-
(2010)
J. Comput. Chem.
, vol.31
, pp. 455-461
-
-
Trott, O.1
Olson, A.J.2
-
51
-
-
85025681024
-
IFPTarget: a customized virtual target identification method based on protein–ligand interaction fingerprinting analyses
-
Li, G.-B., Yu, Z.-J., Liu, S., Huang, L.-Y., Yang, L.-L., Lohans, C.T., Yang, S.-Y., IFPTarget: a customized virtual target identification method based on protein–ligand interaction fingerprinting analyses. J. Chem. Inf. Model. 57 (2017), 1640–1651.
-
(2017)
J. Chem. Inf. Model.
, vol.57
, pp. 1640-1651
-
-
Li, G.-B.1
Yu, Z.-J.2
Liu, S.3
Huang, L.-Y.4
Yang, L.-L.5
Lohans, C.T.6
Yang, S.-Y.7
-
52
-
-
84875428269
-
ID-score: a new empirical scoring function based on a comprehensive set of descriptors related to protein–ligand interactions
-
Li, G.-B., Yang, L.-L., Wang, W.-J., Li, L.-L., Yang, S.-Y., ID-score: a new empirical scoring function based on a comprehensive set of descriptors related to protein–ligand interactions. J. Chem. Inf. Model. 53 (2013), 592–600.
-
(2013)
J. Chem. Inf. Model.
, vol.53
, pp. 592-600
-
-
Li, G.-B.1
Yang, L.-L.2
Wang, W.-J.3
Li, L.-L.4
Yang, S.-Y.5
-
53
-
-
85026370818
-
Interactions between sirtuins and fluorogenic small-molecule substrates offer insights into inhibitor design
-
Wang, H.-L., Liu, S., Yu, Z.-J., Wu, C., Cheng, L., Wang, Y., Chen, K., Zhou, S., Chen, Q., Yu, Y., Li, G.-B., Interactions between sirtuins and fluorogenic small-molecule substrates offer insights into inhibitor design. RSC Adv. 7 (2017), 36214–36222.
-
(2017)
RSC Adv.
, vol.7
, pp. 36214-36222
-
-
Wang, H.-L.1
Liu, S.2
Yu, Z.-J.3
Wu, C.4
Cheng, L.5
Wang, Y.6
Chen, K.7
Zhou, S.8
Chen, Q.9
Yu, Y.10
Li, G.-B.11
-
54
-
-
85041598218
-
-
2 ed., Clinical and Laboratory Standards Institute, Wayne, PA, U.S., Vol. 35.
-
CLSI M07-A10, 2 ed., Clinical and Laboratory Standards Institute, Wayne, PA, U.S., 2015, Vol. 35.
-
(2015)
-
-
M07-A10, C.L.S.I.1
-
55
-
-
84935855840
-
Amino acid thioester derivatives: a highly promising scaffold for the development of metallo-β-lactamase L1 inhibitors
-
Liu, X.-L., Shi, Y., Kang, J.S., Oelschlaeger, P., Yang, K.-W., Amino acid thioester derivatives: a highly promising scaffold for the development of metallo-β-lactamase L1 inhibitors. ACS Med. Chem. Lett. 6 (2015), 660–664.
-
(2015)
ACS Med. Chem. Lett.
, vol.6
, pp. 660-664
-
-
Liu, X.-L.1
Shi, Y.2
Kang, J.S.3
Oelschlaeger, P.4
Yang, K.-W.5
-
56
-
-
84874643132
-
Structure–activity relationship studies of pyrazolo [3, 4-d] pyrimidine derivatives leading to the discovery of a novel multikinase inhibitor that potently inhibits FLT3 and VEGFR2 and evaluation of its activity against acute myeloid leukemia in vitro and in vivo
-
Yang, L.-L., Li, G.-B., Ma, S., Zou, C., Zhou, S., Sun, Q.-Z., Cheng, C., Chen, X., Wang, L.-J., Feng, S., Li, L.-L., Yang, S.-Y., Structure–activity relationship studies of pyrazolo [3, 4-d] pyrimidine derivatives leading to the discovery of a novel multikinase inhibitor that potently inhibits FLT3 and VEGFR2 and evaluation of its activity against acute myeloid leukemia in vitro and in vivo. J. Med. Chem. 56 (2013), 1641–1655.
-
(2013)
J. Med. Chem.
, vol.56
, pp. 1641-1655
-
-
Yang, L.-L.1
Li, G.-B.2
Ma, S.3
Zou, C.4
Zhou, S.5
Sun, Q.-Z.6
Cheng, C.7
Chen, X.8
Wang, L.-J.9
Feng, S.10
Li, L.-L.11
Yang, S.-Y.12
-
57
-
-
84880184008
-
SC-535, a novel oral multikinase inhibitor, showed potent antitumor activity in human melanoma models
-
Chen, X., Ji, P., Yang, H.-W., Yang, L.-L., Zhou, S., Zhong, L., Ma, S., Fu, X.-Y., Zhou, C., Li, G.-B., Zheng, M.-W., Wei, Y.-Q., Yang, S.-Y., SC-535, a novel oral multikinase inhibitor, showed potent antitumor activity in human melanoma models. Cell. Physiol. Biochem. 32 (2013), 138–153.
-
(2013)
Cell. Physiol. Biochem.
, vol.32
, pp. 138-153
-
-
Chen, X.1
Ji, P.2
Yang, H.-W.3
Yang, L.-L.4
Zhou, S.5
Zhong, L.6
Ma, S.7
Fu, X.-Y.8
Zhou, C.9
Li, G.-B.10
Zheng, M.-W.11
Wei, Y.-Q.12
Yang, S.-Y.13
|