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Items: 1 to 20 of 110

1.

Potent and selective inhibitors of class A β-lactamase: 7-prenyloxy coumarins.

Safdari H, Neshani A, Sadeghian A, Ebrahimi M, Iranshahi M, Sadeghian H.

J Antibiot (Tokyo). 2014 May;67(5):373-7. doi: 10.1038/ja.2014.9. Epub 2014 Feb 12.

PMID:
24517922
2.

Structure-based enhancement of boronic acid-based inhibitors of AmpC beta-lactamase.

Weston GS, Blázquez J, Baquero F, Shoichet BK.

J Med Chem. 1998 Nov 5;41(23):4577-86.

PMID:
9804697
3.

Galbanic acid from Ferula szowitsiana enhanced the antibacterial activity of penicillin G and cephalexin against Staphylococcus aureus.

Shahverdi AR, Fakhimi A, Zarrini G, Dehghan G, Iranshahi M.

Biol Pharm Bull. 2007 Sep;30(9):1805-7.

4.

Sesquiterpene coumarins from Ferula szowitsiana and in vitro antileishmanial activity of 7-prenyloxycoumarins against promastigotes.

Iranshahi M, Arfa P, Ramezani M, Jaafari MR, Sadeghian H, Bassarello C, Piacente S, Pizza C.

Phytochemistry. 2007 Feb;68(4):554-61. Epub 2006 Dec 29.

PMID:
17196626
6.

Structure-based design of beta-lactamase inhibitors. 1. Synthesis and evaluation of bridged monobactams.

Heinze-Krauss I, Angehrn P, Charnas RL, Gubernator K, Gutknecht EM, Hubschwerlen C, Kania M, Oefner C, Page MG, Sogabe S, Specklin JL, Winkler F.

J Med Chem. 1998 Oct 8;41(21):3961-71.

PMID:
9767633
7.

N-heterocyclic dicarboxylic acids: broad-spectrum inhibitors of metallo-β-lactamases with co-antibacterial effect against antibiotic-resistant bacteria.

Feng L, Yang KW, Zhou LS, Xiao JM, Yang X, Zhai L, Zhang YL, Crowder MW.

Bioorg Med Chem Lett. 2012 Aug 15;22(16):5185-9. doi: 10.1016/j.bmcl.2012.06.074. Epub 2012 Jul 1.

PMID:
22796180
8.

In vitro effects of beta-lactams combined with beta-lactamase inhibitors against methicillin-resistant Staphylococcus aureus.

Kobayashi S, Arai S, Hayashi S, Sakaguchi T.

Antimicrob Agents Chemother. 1989 Mar;33(3):331-5.

9.

The synthesis and evaluation of 6-alkylidene-2'beta-substituted penam sulfones as beta-lactamase inhibitors.

Buynak JD, Rao AS, Doppalapudi VR, Adam G, Petersen PJ, Nidamarthy SD.

Bioorg Med Chem Lett. 1999 Jul 19;9(14):1997-2002.

PMID:
10450969
10.

Synthesis and antimicrobial evaluation of 2 beta-chloromethyl-6 beta-carbamoylmethyl-penam-1,1-dioxide-3-carboxylic acid.

Gaviraghi G, Perboni A, Tamburini B, Xerri L, Salvatori A, Spadoni G, Tarzia G.

Farmaco. 1996 Jul;51(7):535-8.

PMID:
8765676
11.

Effect of beta-lactamase inhibitors on minimum inhibitory concentration of ampicillin and amoxicillin for Staphylococcus aureus strains.

Paniagua GL, Monroy E, García O, Vaca S.

Rev Latinoam Microbiol. 1998 Jul-Dec;40(3-4):128-34.

PMID:
10932741
12.
13.

Thiophenyl oxime-derived phosphonates as nano-molar class C beta-lactamase inhibitors reducing MIC of imipenem against Pseudomonas aeruginosa and Acinetobacter baumannii.

Tan Q, Ogawa AM, Raghoobar SL, Wisniewski D, Colwell L, Park YW, Young K, Hermes JD, Dininno FP, Hammond ML.

Bioorg Med Chem Lett. 2011 Jul 15;21(14):4363-5. doi: 10.1016/j.bmcl.2011.04.122. Epub 2011 May 13.

PMID:
21664132
14.

Role of beta-lactamase in expression of resistance by methicillin-resistant Staphylococcus aureus.

Boyce JM, Medeiros AA.

Antimicrob Agents Chemother. 1987 Sep;31(9):1426-8.

15.

Synthesis and biological evaluation of penam sulfones as inhibitors of beta-lactamases.

Phillips OA, Reddy AV, Setti EL, Spevak P, Czajkowski DP, Atwal H, Salama S, Micetich RG, Maiti SN.

Bioorg Med Chem. 2005 Apr 15;13(8):2847-58. Erratum in: Bioorg Med Chem. 2005 Nov 15;13(22):6276.

PMID:
15781395
16.
17.
18.

The synthesis and evaluation of 3-substituted-7-(alkylidene)cephalosporin sulfones as beta-lactamase inhibitors.

Buynak JD, Doppalapudi VR, Adam G.

Bioorg Med Chem Lett. 2000 May 1;10(9):853-7.

PMID:
10853646
19.

Nanomolar inhibitors of AmpC beta-lactamase.

Morandi F, Caselli E, Morandi S, Focia PJ, Blázquez J, Shoichet BK, Prati F.

J Am Chem Soc. 2003 Jan 22;125(3):685-95.

PMID:
12526668
20.

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