Fenothiazin (Czech Wikipedia)

Analysis of information sources in references of the Wikipedia article "Fenothiazin" in Czech language version.

refsWebsite

Global rank Czech rank

8doi.org

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5nih.gov

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1if-pan.krakow.pl

low place

1patient.info

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1clemson.edu

5,952^nd place

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1europa.eu

68^th place

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1web.archive.org

1^st place

1apvma.gov.au

low place

apvma.gov.au

Australian Pesticides and Veterinary Medicine Authority Phenothiazine Chemical Review Page accessed July 26, 2015

clemson.edu

http://www.clemson.edu/extension/pest_ed/histor.html History of Insecticides and Control Equipment] Clemson University Pesticide Information Program.

doi.org

Gérard Taurand, "Phenothiazine and Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005 doi:10.1002/14356007.a19_387
M. J. Ohlow; B. Moosmann. Phenothiazine: the seven lives of pharmacology's first lead structure. Drug Discovery Today. 2011, s. 119–131. doi:10.1016/j.drudis.2011.01.001. PMID 21237283.
Chemical structure of phenothiazines and their biological activity. Pharmacol Rep.. 2012, s. 16–23. Dostupné online. doi:10.1016/s1734-1140(12)70726-0. PMID 21237283.
Qijin Chi; Shaojun Dong. Electrocatalytic oxidation of reduced nicotinamide coenzymes at Methylene Green-modified electrodes and fabrication of amperometric alcohol biosensors. Analytica Chimica Acta. 1994-01-20, s. 125–133. doi:10.1016/0003-2670(94)85016-X.
Arkady A. Karyakin; Elena E. Karyakina; Wolfgang Schuhmann; Hanns-Ludwig Schmidt. Electropolymerized Azines: Part II. In a Search of the Best Electrocatalyst of NADH Oxidation. Electroanalysis. 1999, s. 553–557. doi:10.1002/(SICI)1521-4109(199906)11:8<553::AID-ELAN553>3.0.CO;2-6.
Daria Sokic-Lazic; Shelley D. Minteer. Citric acid cycle biomimic on a carbon electrode. Biosensors and Bioelectronics. 2008, s. 939–944. doi:10.1016/j.bios.2008.07.043. PMID 18774285.
Leon B. Levy. Inhibition of acrylic acid polymerization by phenothiazine and p‐methoxyphenol. II. Catalytic inhibition by phenothiazine. Journal of Polymer Science Part A: Polymer Chemistry. 1992-03-30, s. 569–576. doi:10.1002/pola.1992.080300407.
Anthelmintic resistance in equine parasites--current evidence and knowledge gaps. Veterinary Parasitology. 2014, s. 55–63. doi:10.1016/j.vetpar.2013.11.030. PMID 24433852.

europa.eu

apps.echa.europa.eu

ECHA phenothiazine at the European Chemicals Authority Archivováno 23. 1. 2019 na Wayback Machine.

if-pan.krakow.pl

Chemical structure of phenothiazines and their biological activity. Pharmacol Rep.. 2012, s. 16–23. Dostupné online. doi:10.1016/s1734-1140(12)70726-0. PMID 21237283.

nih.gov

ncbi.nlm.nih.gov

M. J. Ohlow; B. Moosmann. Phenothiazine: the seven lives of pharmacology's first lead structure. Drug Discovery Today. 2011, s. 119–131. doi:10.1016/j.drudis.2011.01.001. PMID 21237283.
Chemical structure of phenothiazines and their biological activity. Pharmacol Rep.. 2012, s. 16–23. Dostupné online. doi:10.1016/s1734-1140(12)70726-0. PMID 21237283.
Daria Sokic-Lazic; Shelley D. Minteer. Citric acid cycle biomimic on a carbon electrode. Biosensors and Bioelectronics. 2008, s. 939–944. doi:10.1016/j.bios.2008.07.043. PMID 18774285.
Anthelmintic resistance in equine parasites--current evidence and knowledge gaps. Veterinary Parasitology. 2014, s. 55–63. doi:10.1016/j.vetpar.2013.11.030. PMID 24433852.

pubchem.ncbi.nlm.nih.gov

Phenothiazine. pubchem.ncbi.nlm.nih.gov [online]. PubChem [cit. 2021-05-24]. Dostupné online. (anglicky)

patient.info

Antiphospholipid Syndrome - Doctor's Information [online]. [cit. 2015-07-25]. Dostupné online.

web.archive.org

ECHA phenothiazine at the European Chemicals Authority Archivováno 23. 1. 2019 na Wayback Machine.