Fosfomicina (Portuguese Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fosfomicina" in Portuguese language version.

refsWebsite

Global rank Portuguese rank

19doi.org

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17nih.gov

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3drugs.com

399^th place

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1books.google.com

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1harvard.edu

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1archive.org

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1ercros.es

low place

1worldcat.org

5^th place

archive.org

«Fosfomycin resistance proteins: a nexus of glutathione transferases and epoxide hydrolases in a metalloenzyme superfamily». Gluthione Transferases and Gamma-Glutamyl Transpeptidases. Col: Methods in Enzymology. 401. [S.l.: s.n.] 2005. pp. 367–379. ISBN 9780121828066. PMID 16399398. doi:10.1016/S0076-6879(05)01023-2

books.google.com

Antibiotic and Chemotherapy E-Book (em inglês). [S.l.]: Elsevier Health Sciences. 2010. ISBN 9780702047657

doi.org

dx.doi.org

Patel SS, Balfour JA, Bryson HM (abril de 1997). «Fosfomycin tromethamine. A review of its antibacterial activity, pharmacokinetic properties and therapeutic efficacy as a single-dose oral treatment for acute uncomplicated lower urinary tract infections». Drugs. 53 (4): 637–56. PMID 9098664. doi:10.2165/00003495-199753040-00007
Falagas ME, Giannopoulou KP, Kokolakis GN, Rafailidis PI (abril de 2008). «Fosfomycin: use beyond urinary tract and gastrointestinal infections». Clinical Infectious Diseases. 46 (7): 1069–77. PMID 18444827. doi:10.1086/527442
Falagas ME, Grammatikos AP, Michalopoulos A (outubro de 2008). «Potential of old-generation antibiotics to address current need for new antibiotics». Expert Review of Anti-Infective Therapy. 6 (5): 593–600. PMID 18847400. doi:10.1586/14787210.6.5.593
Zhanel GG, Zhanel MA, Karlowsky JA (28 de março de 2020). «Oral and Intravenous Fosfomycin for the Treatment of Complicated Urinary Tract Infections». Hindawi Limited. The Canadian Journal of Infectious Diseases & Medical Microbiology. 2020. 8513405 páginas. PMC 7142339. PMID 32300381. doi:10.1155/2020/8513405
Antonello RM, Principe L, Maraolo AE, Viaggi V, Pol R, Fabbiani M, et al. (agosto de 2020). «Fosfomycin as Partner Drug for Systemic Infection Management. A Systematic Review of Its Synergistic Properties from In Vitro and In Vivo Studies». Antibiotics. 9 (8). 500 páginas. PMC 7460049. PMID 32785114. doi:10.3390/antibiotics9080500
Navas J, León J, Arroyo M, García Lobo JM (outubro de 1990). «Nucleotide sequence and intracellular location of the product of the fosfomycin resistance gene from transposon Tn2921». Antimicrobial Agents and Chemotherapy. 34 (10): 2016–8. PMC 171982. PMID 1963292. doi:10.1128/AAC.34.10.2016
Kahan FM, Kahan JS, Cassidy PJ, Kropp H (maio de 1974). «The mechanism of action of fosfomycin (phosphonomycin)». Annals of the New York Academy of Sciences. 235 (1): 364–86. Bibcode:1974NYASA.235..364K. PMID 4605290. doi:10.1111/j.1749-6632.1974.tb43277.x
Castañeda-García A, Blázquez J, Rodríguez-Rojas A (abril de 2013). «Molecular Mechanisms and Clinical Impact of Acquired and Intrinsic Fosfomycin Resistance». Antibiotics. 2 (2): 217–36. PMC 4790336. PMID 27029300. doi:10.3390/antibiotics2020217
«Fosfomycin resistance proteins: a nexus of glutathione transferases and epoxide hydrolases in a metalloenzyme superfamily». Gluthione Transferases and Gamma-Glutamyl Transpeptidases. Col: Methods in Enzymology. 401. [S.l.: s.n.] 2005. pp. 367–379. ISBN 9780121828066. PMID 16399398. doi:10.1016/S0076-6879(05)01023-2
Sharma SV, Jothivasan VK, Newton GL, Upton H, Wakabayashi JI, Kane MG, et al. (julho de 2011). «Chemical and Chemoenzymatic syntheses of bacillithiol: a unique low-molecular-weight thiol amongst low G + C Gram-positive bacteria». Angewandte Chemie. 50 (31): 7101–4. PMID 21751306. doi:10.1002/anie.201100196
Roberts AA, Sharma SV, Strankman AW, Duran SR, Rawat M, Hamilton CJ (abril de 2013). «Mechanistic studies of FosB: a divalent-metal-dependent bacillithiol-S-transferase that mediates fosfomycin resistance in Staphylococcus aureus». The Biochemical Journal. 451 (1): 69–79. PMC 3960972. PMID 23256780. doi:10.1042/BJ20121541
García P, Arca P, Evaristo Suárez J (julho de 1995). «Product of fosC, a gene from Pseudomonas syringae, mediates fosfomycin resistance by using ATP as cosubstrate». Antimicrobial Agents and Chemotherapy. 39 (7): 1569–73. PMC 162783. PMID 7492106. doi:10.1128/aac.39.7.1569
Brown ED, Vivas EI, Walsh CT, Kolter R (julho de 1995). «MurA (MurZ), the enzyme that catalyzes the first committed step in peptidoglycan biosynthesis, is essential in Escherichia coli». Journal of Bacteriology. 177 (14): 4194–7. PMC 177162. PMID 7608103. doi:10.1128/jb.177.14.4194-4197.1995
Zhu JY, Yang Y, Han H, Betzi S, Olesen SH, Marsilio F, Schönbrunn E (abril de 2012). «Functional consequence of covalent reaction of phosphoenolpyruvate with UDP-N-acetylglucosamine 1-carboxyvinyltransferase (MurA)». The Journal of Biological Chemistry. 287 (16): 12657–67. PMC 3339971. PMID 22378791. doi:10.1074/jbc.M112.342725
Krekel F, Samland AK, Macheroux P, Amrhein N, Evans JN (outubro de 2000). «Determination of the pKa value of C115 in MurA (UDP-N-acetylglucosamine enolpyruvyltransferase) from Enterobacter cloacae». Biochemistry. 39 (41): 12671–7. PMID 11027147. doi:10.1021/bi001310x
Santoro A, Cappello AR, Madeo M, Martello E, Iacopetta D, Dolce V (dezembro de 2011). «Interaction of fosfomycin with the glycerol 3-phosphate transporter of Escherichia coli». Biochimica et Biophysica Acta (BBA) - General Subjects. 1810 (12): 1323–9. PMID 21791237. doi:10.1016/j.bbagen.2011.07.006
«Chapter 2, Rational approaches to antibiotic discovery: pre-genomic directed and phenotypic screening». Antibiotic Discovery and Development. [S.l.]: Springer. 2011. 46 páginas. ISBN 978-1-4614-1400-1. doi:10.1007/978-1-4614-1400-1_2
Woodyer RD, Shao Z, Thomas PM, Kelleher NL, Blodgett JA, Metcalf WW, et al. (novembro de 2006). «Heterologous production of fosfomycin and identification of the minimal biosynthetic gene cluster». Chemistry & Biology. 13 (11): 1171–82. PMID 17113999. doi:10.1016/j.chembiol.2006.09.007
Marocco CP, Davis EV, Finnell JE, Nguyen PH, Mateer SC, Ghiviriga I, et al. (2011). «Asymmetric synthesis of (−)-fosfomycin and its trans-(1S,2S)-diastereomer using a biocatalytic reduction as the key step». Elsevier BV. Tetrahedron: Asymmetry. 22 (18–19): 1784–1789. ISSN 0957-4166. doi:10.1016/j.tetasy.2011.10.009

drugs.com

«Fosfomycin Tromethamine Monograph for Professionals». Drugs.com (em inglês). Consultado em 29 de outubro de 2019
«Fosfomycin (Monurol) Use During Pregnancy». Drugs.com (em inglês). Consultado em 29 de outubro de 2019
«MONURIL SACHETS 3G». Consultado em 26 de maio de 2014

ercros.es

Encros About us: Our history.

harvard.edu

ui.adsabs.harvard.edu

Kahan FM, Kahan JS, Cassidy PJ, Kropp H (maio de 1974). «The mechanism of action of fosfomycin (phosphonomycin)». Annals of the New York Academy of Sciences. 235 (1): 364–86. Bibcode:1974NYASA.235..364K. PMID 4605290. doi:10.1111/j.1749-6632.1974.tb43277.x

nih.gov

ncbi.nlm.nih.gov

Patel SS, Balfour JA, Bryson HM (abril de 1997). «Fosfomycin tromethamine. A review of its antibacterial activity, pharmacokinetic properties and therapeutic efficacy as a single-dose oral treatment for acute uncomplicated lower urinary tract infections». Drugs. 53 (4): 637–56. PMID 9098664. doi:10.2165/00003495-199753040-00007
Falagas ME, Giannopoulou KP, Kokolakis GN, Rafailidis PI (abril de 2008). «Fosfomycin: use beyond urinary tract and gastrointestinal infections». Clinical Infectious Diseases. 46 (7): 1069–77. PMID 18444827. doi:10.1086/527442
Falagas ME, Grammatikos AP, Michalopoulos A (outubro de 2008). «Potential of old-generation antibiotics to address current need for new antibiotics». Expert Review of Anti-Infective Therapy. 6 (5): 593–600. PMID 18847400. doi:10.1586/14787210.6.5.593
Zhanel GG, Zhanel MA, Karlowsky JA (28 de março de 2020). «Oral and Intravenous Fosfomycin for the Treatment of Complicated Urinary Tract Infections». Hindawi Limited. The Canadian Journal of Infectious Diseases & Medical Microbiology. 2020. 8513405 páginas. PMC 7142339. PMID 32300381. doi:10.1155/2020/8513405
Antonello RM, Principe L, Maraolo AE, Viaggi V, Pol R, Fabbiani M, et al. (agosto de 2020). «Fosfomycin as Partner Drug for Systemic Infection Management. A Systematic Review of Its Synergistic Properties from In Vitro and In Vivo Studies». Antibiotics. 9 (8). 500 páginas. PMC 7460049. PMID 32785114. doi:10.3390/antibiotics9080500
Navas J, León J, Arroyo M, García Lobo JM (outubro de 1990). «Nucleotide sequence and intracellular location of the product of the fosfomycin resistance gene from transposon Tn2921». Antimicrobial Agents and Chemotherapy. 34 (10): 2016–8. PMC 171982. PMID 1963292. doi:10.1128/AAC.34.10.2016
Kahan FM, Kahan JS, Cassidy PJ, Kropp H (maio de 1974). «The mechanism of action of fosfomycin (phosphonomycin)». Annals of the New York Academy of Sciences. 235 (1): 364–86. Bibcode:1974NYASA.235..364K. PMID 4605290. doi:10.1111/j.1749-6632.1974.tb43277.x
Castañeda-García A, Blázquez J, Rodríguez-Rojas A (abril de 2013). «Molecular Mechanisms and Clinical Impact of Acquired and Intrinsic Fosfomycin Resistance». Antibiotics. 2 (2): 217–36. PMC 4790336. PMID 27029300. doi:10.3390/antibiotics2020217
«Fosfomycin resistance proteins: a nexus of glutathione transferases and epoxide hydrolases in a metalloenzyme superfamily». Gluthione Transferases and Gamma-Glutamyl Transpeptidases. Col: Methods in Enzymology. 401. [S.l.: s.n.] 2005. pp. 367–379. ISBN 9780121828066. PMID 16399398. doi:10.1016/S0076-6879(05)01023-2
Sharma SV, Jothivasan VK, Newton GL, Upton H, Wakabayashi JI, Kane MG, et al. (julho de 2011). «Chemical and Chemoenzymatic syntheses of bacillithiol: a unique low-molecular-weight thiol amongst low G + C Gram-positive bacteria». Angewandte Chemie. 50 (31): 7101–4. PMID 21751306. doi:10.1002/anie.201100196
Roberts AA, Sharma SV, Strankman AW, Duran SR, Rawat M, Hamilton CJ (abril de 2013). «Mechanistic studies of FosB: a divalent-metal-dependent bacillithiol-S-transferase that mediates fosfomycin resistance in Staphylococcus aureus». The Biochemical Journal. 451 (1): 69–79. PMC 3960972. PMID 23256780. doi:10.1042/BJ20121541
García P, Arca P, Evaristo Suárez J (julho de 1995). «Product of fosC, a gene from Pseudomonas syringae, mediates fosfomycin resistance by using ATP as cosubstrate». Antimicrobial Agents and Chemotherapy. 39 (7): 1569–73. PMC 162783. PMID 7492106. doi:10.1128/aac.39.7.1569
Brown ED, Vivas EI, Walsh CT, Kolter R (julho de 1995). «MurA (MurZ), the enzyme that catalyzes the first committed step in peptidoglycan biosynthesis, is essential in Escherichia coli». Journal of Bacteriology. 177 (14): 4194–7. PMC 177162. PMID 7608103. doi:10.1128/jb.177.14.4194-4197.1995
Zhu JY, Yang Y, Han H, Betzi S, Olesen SH, Marsilio F, Schönbrunn E (abril de 2012). «Functional consequence of covalent reaction of phosphoenolpyruvate with UDP-N-acetylglucosamine 1-carboxyvinyltransferase (MurA)». The Journal of Biological Chemistry. 287 (16): 12657–67. PMC 3339971. PMID 22378791. doi:10.1074/jbc.M112.342725
Krekel F, Samland AK, Macheroux P, Amrhein N, Evans JN (outubro de 2000). «Determination of the pKa value of C115 in MurA (UDP-N-acetylglucosamine enolpyruvyltransferase) from Enterobacter cloacae». Biochemistry. 39 (41): 12671–7. PMID 11027147. doi:10.1021/bi001310x
Santoro A, Cappello AR, Madeo M, Martello E, Iacopetta D, Dolce V (dezembro de 2011). «Interaction of fosfomycin with the glycerol 3-phosphate transporter of Escherichia coli». Biochimica et Biophysica Acta (BBA) - General Subjects. 1810 (12): 1323–9. PMID 21791237. doi:10.1016/j.bbagen.2011.07.006
Woodyer RD, Shao Z, Thomas PM, Kelleher NL, Blodgett JA, Metcalf WW, et al. (novembro de 2006). «Heterologous production of fosfomycin and identification of the minimal biosynthetic gene cluster». Chemistry & Biology. 13 (11): 1171–82. PMID 17113999. doi:10.1016/j.chembiol.2006.09.007

worldcat.org

Marocco CP, Davis EV, Finnell JE, Nguyen PH, Mateer SC, Ghiviriga I, et al. (2011). «Asymmetric synthesis of (−)-fosfomycin and its trans-(1S,2S)-diastereomer using a biocatalytic reduction as the key step». Elsevier BV. Tetrahedron: Asymmetry. 22 (18–19): 1784–1789. ISSN 0957-4166. doi:10.1016/j.tetasy.2011.10.009