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Barbiturate (German Wikipedia)

Analysis of information sources in references of the Wikipedia article "Barbiturate" in German language version.

Last modified:

Ref.Un. Ref.Website
Global rank German rank
88doi.org
2nd place
3rd place
77nih.gov
5th place
7th place
21thieme.de
2,800th place
167th place
11web.archive.org
1st place
1st place
11redirecter.toolforge.org
29th place
2nd place

doi.org (Global: 2nd place; German: 3rd place)

  • Adolf Baeyer: Untersuchungen über die Harnsäuregruppe. In: Justus Liebigs Annalen der Chemie, Band 131, Nr. 3, 1864, S. 291–302. doi:10.1002/jlac.18641310306
  • A. M. Qureshi, S. Mumtaz, A. Rauf, M. Ashraf, R. Nasar, Z. H. Chohan: New barbiturates and thiobarbiturates as potential enzyme inhibitors. In: J Enzyme Inhib Med Chem. Band 30, Nr. 1, 2015, S. 119–125, doi:10.3109/14756366.2014.895717, PMID 24666295.
  • J. Figueiredo, J. L. Serrano, E. Cavalheiro, L. Keurulainen, J. Yli-Kauhaluoma, V. M. Moreira, S. Ferreira, F. C. Domingues, S. Silvestre, P. Almeida: Trisubstituted barbiturates and thiobarbiturates: Synthesis and biological evaluation as xanthine oxidase inhibitors, antioxidants, antibacterial and anti-proliferative agents. In: Eur J Med Chem. Band 143, 2018, S. 829–842, doi:10.1016/j.ejmech.2017.11.070, PMID 29223098.
  • K. M. Moon, B. Lee, J. W. Jeong, D. H. Kim, Y. J. Park, H. R. Kim, J. Y. Park, M. J. Kim, H. J. An, E. K. Lee, Y. M. Ha, E. Im, P. Chun, J. Y. Ma, W. K. Cho, H. R. Moon, H. Y. Chung: Thio-barbiturate-derived compounds are novel antioxidants to prevent LPS-induced inflammation in the liver. In: Oncotarget. Band 8, Nr. 53, 2017, S. 91662–91673, doi:10.18632/oncotarget.21714, PMID 29207675, PMC 5710955 (freier Volltext).
  • S. S. Jayakar, X. Zhou, P. Y. Savechenkov, D. C. Chiara, R. Desai, K. S. Bruzik, K. W. Miller, J. B. Cohen: Positive and Negative Allosteric Modulation of an α1β3γ2 γ-Aminobutyric Acid Type A (GABAA) Receptor by Binding to a Site in the Transmembrane Domain at the γ+-β- Interface. In: J. Biol. Chem. Band 290, Nr. 38, 2015, S. 23432–23446, doi:10.1074/jbc.M115.672006, PMID 26229099, PMC 4645599 (freier Volltext).
  • A. M. Ziemba, S. A. Forman: Correction for Inhibition Leads to an Allosteric Co-Agonist Model for Pentobarbital Modulation and Activation of α1β3γ2L GABAA Receptors. In: PLoS ONE. Band 11, Nr. 4, 2016, Artikel e0154031, doi:10.1371/journal.pone.0154031, PMID 27110714, PMC 4844112 (freier Volltext).
  • R. Desai, P. Y. Savechenkov, D. Zolkowska, R. L. Ge, M. A. Rogawski, K. S. Bruzik, S. A. Forman, D. E. Raines, K. W. Miller: Contrasting actions of a convulsant barbiturate and its anticonvulsant enantiomer on the α1 β3 γ2L GABAA receptor account for their in vivo effects. In: J. Physiol. (Lond.). Band 593, Nr. 22, 2015, S. 4943–4961, doi:10.1113/JP270971, PMID 26378885, PMC 4650410 (freier Volltext).
  • A. K. Hamouda, D. S. Stewart, D. C. Chiara, P. Y. Savechenkov, K. S. Bruzik, J. B. Cohen: Identifying barbiturate binding sites in a nicotinic acetylcholine receptor with [3H]allyl m-trifluoromethyldiazirine mephobarbital, a photoreactive barbiturate. In: Mol. Pharmacol. Band 85, Nr. 5, 2014, S. 735–746, doi:10.1124/mol.113.090985, PMID 24563544, PMC 3990015 (freier Volltext).

nih.gov (Global: 5th place; German: 7th place)

ncbi.nlm.nih.gov

  • A. M. Qureshi, S. Mumtaz, A. Rauf, M. Ashraf, R. Nasar, Z. H. Chohan: New barbiturates and thiobarbiturates as potential enzyme inhibitors. In: J Enzyme Inhib Med Chem. Band 30, Nr. 1, 2015, S. 119–125, doi:10.3109/14756366.2014.895717, PMID 24666295.
  • J. Figueiredo, J. L. Serrano, E. Cavalheiro, L. Keurulainen, J. Yli-Kauhaluoma, V. M. Moreira, S. Ferreira, F. C. Domingues, S. Silvestre, P. Almeida: Trisubstituted barbiturates and thiobarbiturates: Synthesis and biological evaluation as xanthine oxidase inhibitors, antioxidants, antibacterial and anti-proliferative agents. In: Eur J Med Chem. Band 143, 2018, S. 829–842, doi:10.1016/j.ejmech.2017.11.070, PMID 29223098.
  • K. M. Moon, B. Lee, J. W. Jeong, D. H. Kim, Y. J. Park, H. R. Kim, J. Y. Park, M. J. Kim, H. J. An, E. K. Lee, Y. M. Ha, E. Im, P. Chun, J. Y. Ma, W. K. Cho, H. R. Moon, H. Y. Chung: Thio-barbiturate-derived compounds are novel antioxidants to prevent LPS-induced inflammation in the liver. In: Oncotarget. Band 8, Nr. 53, 2017, S. 91662–91673, doi:10.18632/oncotarget.21714, PMID 29207675, PMC 5710955 (freier Volltext).
  • S. S. Jayakar, X. Zhou, P. Y. Savechenkov, D. C. Chiara, R. Desai, K. S. Bruzik, K. W. Miller, J. B. Cohen: Positive and Negative Allosteric Modulation of an α1β3γ2 γ-Aminobutyric Acid Type A (GABAA) Receptor by Binding to a Site in the Transmembrane Domain at the γ+-β- Interface. In: J. Biol. Chem. Band 290, Nr. 38, 2015, S. 23432–23446, doi:10.1074/jbc.M115.672006, PMID 26229099, PMC 4645599 (freier Volltext).
  • A. M. Ziemba, S. A. Forman: Correction for Inhibition Leads to an Allosteric Co-Agonist Model for Pentobarbital Modulation and Activation of α1β3γ2L GABAA Receptors. In: PLoS ONE. Band 11, Nr. 4, 2016, Artikel e0154031, doi:10.1371/journal.pone.0154031, PMID 27110714, PMC 4844112 (freier Volltext).
  • R. Desai, P. Y. Savechenkov, D. Zolkowska, R. L. Ge, M. A. Rogawski, K. S. Bruzik, S. A. Forman, D. E. Raines, K. W. Miller: Contrasting actions of a convulsant barbiturate and its anticonvulsant enantiomer on the α1 β3 γ2L GABAA receptor account for their in vivo effects. In: J. Physiol. (Lond.). Band 593, Nr. 22, 2015, S. 4943–4961, doi:10.1113/JP270971, PMID 26378885, PMC 4650410 (freier Volltext).
  • A. K. Hamouda, D. S. Stewart, D. C. Chiara, P. Y. Savechenkov, K. S. Bruzik, J. B. Cohen: Identifying barbiturate binding sites in a nicotinic acetylcholine receptor with [3H]allyl m-trifluoromethyldiazirine mephobarbital, a photoreactive barbiturate. In: Mol. Pharmacol. Band 85, Nr. 5, 2014, S. 735–746, doi:10.1124/mol.113.090985, PMID 24563544, PMC 3990015 (freier Volltext).

redirecter.toolforge.org (Global: 29th place; German: 2nd place)

thieme.de (Global: 2,800th place; German: 167th place)

roempp.thieme.de

web.archive.org (Global: 1st place; German: 1st place)