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Volumn 21, Issue 28, 2015, Pages 4106-4111

Repurposing non-antimicrobial drugs and clinical molecules to treat bacterial infections

Author keywords

Antibiotics; Antimicrobial; MRSA; Repositioning; Repurposing

Indexed keywords

EBSELEN; FLOXURIDINE; ANTIINFECTIVE AGENT;

EID: 84941925231     PISSN: 13816128     EISSN: 18734286     Source Type: Journal    
DOI: 10.2174/1381612821666150506154434     Document Type: Article
Times cited : (76)

References (15)
  • 1
    • 34547770279 scopus 로고    scopus 로고
    • New uses for old drugs
    • Chong CR, Sullivan DJ. New uses for old drugs. Nature 2007; 448: 645-6.
    • (2007) Nature , vol.448 , pp. 645-646
    • Chong, C.R.1    Sullivan, D.J.2
  • 2
    • 84862015314 scopus 로고    scopus 로고
    • A high-throughput drug screen for Entamoeba histolytica identifies a new lead and target
    • Debnath A, Parsonage D, Andrade RM, et al. A high-throughput drug screen for Entamoeba histolytica identifies a new lead and target. Nat Med 2012; 18: 956-60.
    • (2012) Nat Med , vol.18 , pp. 956-960
    • Debnath, A.1    Parsonage, D.2    Andrade, R.M.3
  • 5
    • 0029114721 scopus 로고
    • Molecular actions of ebselen--an antiinflammatory antioxidant
    • Schewe T. Molecular actions of ebselen--an antiinflammatory antioxidant. Gen Pharmacol 1995; 26: 1153-69.
    • (1995) Gen Pharmacol , vol.26 , pp. 1153-1169
    • Schewe, T.1
  • 6
    • 0024316299 scopus 로고
    • Susceptibility of methicillinresistant Staphylococcus aureus to the selenium-containing compound 2-phenyl-1,2-benzoisoselenazol-3(2H)-one (PZ51)
    • Nozawa R, Yokota T, Fujimoto T. Susceptibility of methicillinresistant Staphylococcus aureus to the selenium-containing compound 2-phenyl-1,2-benzoisoselenazol-3(2H)-one (PZ51). Antimicrob Agents Chemother 1989; 33: 1388-90.
    • (1989) Antimicrob Agents Chemother , vol.33 , pp. 1388-1390
    • Nozawa, R.1    Yokota, T.2    Fujimoto, T.3
  • 7
    • 84875701168 scopus 로고    scopus 로고
    • Inhibition of bacterial thioredoxin reductase: An antibiotic mechanism targeting bacteria lacking glutathione
    • Lu J, Vlamis-Gardikas A, Kandasamy K, et al. Inhibition of bacterial thioredoxin reductase: an antibiotic mechanism targeting bacteria lacking glutathione. FASEB J 2013; 27: 1394-403.
    • (2013) FASEB J , vol.27 , pp. 1394-1403
    • Lu, J.1    Vlamis-Gardikas, A.2    Kandasamy, K.3
  • 8
    • 84889248820 scopus 로고    scopus 로고
    • Mechanism of inhibition of Mycobacterium tuberculosis antigen 85 by ebselen
    • Favrot L, Grzegorzewicz AE, Lajiness DH, et al. Mechanism of inhibition of Mycobacterium tuberculosis antigen 85 by ebselen. Nat Commun 2013; 4: 2748.
    • (2013) Nat Commun , vol.4 , pp. 2748
    • Favrot, L.1    Grzegorzewicz, A.E.2    Lajiness, D.H.3
  • 9
    • 0034821411 scopus 로고    scopus 로고
    • Ebselen protects both gray and white matter in a rodent model of focal cerebral ischemia
    • Imai H, Masayasu H, Dewar D, Graham DI, Macrae IM. Ebselen protects both gray and white matter in a rodent model of focal cerebral ischemia. Stroke 2001; 32: 2149-54.
    • (2001) Stroke , vol.32 , pp. 2149-2154
    • Imai, H.1    Masayasu, H.2    Dewar, D.3    Graham, D.I.4    Macrae, I.M.5
  • 10
    • 0029760529 scopus 로고    scopus 로고
    • Therapeutic efficacy of fluoropyrimidines depends on the duration of thymidylate synthase inhibition in the murine colon 26-B carcinoma tumor model
    • van Laar JA, van der Wilt CL, Rustum YM, et al. Therapeutic efficacy of fluoropyrimidines depends on the duration of thymidylate synthase inhibition in the murine colon 26-B carcinoma tumor model. Clin Cancer Res 1996; 2: 1327-33.
    • (1996) Clin Cancer Res , vol.2 , pp. 1327-1333
    • van Laar, J.A.1    van der Wilt, C.L.2    Rustum, Y.M.3
  • 12
    • 0036057596 scopus 로고    scopus 로고
    • Clinical studies of three oral prodrugs of 5-fluorouracil (capecitabine, UFT, S-1): A review
    • Malet-Martino M, Martino R. Clinical studies of three oral prodrugs of 5-fluorouracil (capecitabine, UFT, S-1): a review. Oncologist 2002; 7: 288-323.
    • (2002) Oncologist , vol.7 , pp. 288-323
    • Malet-Martino, M.1    Martino, R.2
  • 13
    • 0028853499 scopus 로고
    • Intraperitoneal 5-fluoro-2'- deoxyuridine (FUDR) and (S)-leucovorin for disease predominantly confined to the peritoneal cavity: A pharmacokinetic and toxicity study
    • Israel VK, Jiang C, Muggia FM, et al. Intraperitoneal 5-fluoro-2'- deoxyuridine (FUDR) and (S)-leucovorin for disease predominantly confined to the peritoneal cavity: a pharmacokinetic and toxicity study. Cancer Chemother Pharmacol 1995; 37: 32-8.
    • (1995) Cancer Chemother Pharmacol , vol.37 , pp. 32-38
    • Israel, V.K.1    Jiang, C.2    Muggia, F.M.3
  • 14
    • 0025767056 scopus 로고
    • Phase I and pharmacologic evaluation of intraperitoneal 5-fluoro-2'-deoxyuridine
    • Muggia FM, Chan KK, Russell C, et al. Phase I and pharmacologic evaluation of intraperitoneal 5-fluoro-2'-deoxyuridine. Cancer Chemother Pharmacol 1991; 28: 241-50.
    • (1991) Cancer Chemother Pharmacol , vol.28 , pp. 241-250
    • Muggia, F.M.1    Chan, K.K.2    Russell, C.3
  • 15
    • 0028044223 scopus 로고
    • Intraperitoneal 5-fluoro- 2'-deoxyuridine with escalating doses of leucovorin: Pharmacology and clinical tolerance
    • Muggia FM, Tulpule A, Retzios A, et al. Intraperitoneal 5-fluoro- 2'-deoxyuridine with escalating doses of leucovorin: pharmacology and clinical tolerance. Invest New Drugs 1994; 12: 197-206.
    • (1994) Invest New Drugs , vol.12 , pp. 197-206
    • Muggia, F.M.1    Tulpule, A.2    Retzios, A.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.