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DFMDA (English Wikipedia)

Analysis of information sources in references of the Wikipedia article "DFMDA" in English language version.

refsWebsite
Global rank English rank
8nih.gov
4th place
4th place
7doi.org
2nd place
2nd place
4semanticscholar.org
11th place
8th place
2psu.edu
207th place
136th place

doi.org

  • Trachsel D, Hadorn M, Baumberger F (March 2006). "Synthesis of fluoro analogues of 3,4-(methylenedioxy)amphetamine (MDA) and its derivatives". Chemistry & Biodiversity. 3 (3): 326–36. CiteSeerX 10.1.1.688.5803. doi:10.1002/cbdv.200690035. PMID 17193269. S2CID 23036634.
  • Meanwell NA (March 2011). "Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design". Journal of Medicinal Chemistry. 54 (8): 2529–91. doi:10.1021/jm1013693. PMID 21413808.
  • Takač MJ, Magina JD, Takač T (December 2019). "Evaluation of phenylethylamine type entactogens and their metabolites relevant to ecotoxicology - a QSAR study". Acta Pharmaceutica. 69 (4). Zagreb, Croatia: 563–584. doi:10.2478/acph-2019-0038. PMID 31639096. S2CID 204850967.
  • Walline CC, Nichols DE, Carroll FI, Barker EL (June 2008). "Comparative molecular field analysis using selectivity fields reveals residues in the third transmembrane helix of the serotonin transporter associated with substrate and antagonist recognition". The Journal of Pharmacology and Experimental Therapeutics. 325 (3): 791–800. doi:10.1124/jpet.108.136200. PMC 2637348. PMID 18354055.
  • Capela JP, Carmo H, Remião F, Bastos ML, Meisel A, Carvalho F (June 2009). "Molecular and cellular mechanisms of ecstasy-induced neurotoxicity: an overview". Molecular Neurobiology. 39 (3): 210–71. CiteSeerX 10.1.1.670.6897. doi:10.1007/s12035-009-8064-1. PMID 19373443. S2CID 21190104.
  • Sarkar S, Schmued L (August 2010). "Neurotoxicity of ecstasy (MDMA): an overview". Current Pharmaceutical Biotechnology. 11 (5): 460–9. doi:10.2174/138920110791591490. PMID 20420572.
  • Escubedo E, Abad S, Torres I, Camarasa J, Pubill D (January 2011). "Comparative neurochemical profile of 3,4-methylenedioxymethamphetamine and its metabolite alpha-methyldopamine on key targets of MDMA neurotoxicity". Neurochemistry International. 58 (1): 92–101. doi:10.1016/j.neuint.2010.11.001. PMID 21074589. S2CID 2853533.

nih.gov

pubmed.ncbi.nlm.nih.gov

  • Trachsel D, Hadorn M, Baumberger F (March 2006). "Synthesis of fluoro analogues of 3,4-(methylenedioxy)amphetamine (MDA) and its derivatives". Chemistry & Biodiversity. 3 (3): 326–36. CiteSeerX 10.1.1.688.5803. doi:10.1002/cbdv.200690035. PMID 17193269. S2CID 23036634.
  • Meanwell NA (March 2011). "Synopsis of Some Recent Tactical Application of Bioisosteres in Drug Design". Journal of Medicinal Chemistry. 54 (8): 2529–91. doi:10.1021/jm1013693. PMID 21413808.
  • Takač MJ, Magina JD, Takač T (December 2019). "Evaluation of phenylethylamine type entactogens and their metabolites relevant to ecotoxicology - a QSAR study". Acta Pharmaceutica. 69 (4). Zagreb, Croatia: 563–584. doi:10.2478/acph-2019-0038. PMID 31639096. S2CID 204850967.
  • Walline CC, Nichols DE, Carroll FI, Barker EL (June 2008). "Comparative molecular field analysis using selectivity fields reveals residues in the third transmembrane helix of the serotonin transporter associated with substrate and antagonist recognition". The Journal of Pharmacology and Experimental Therapeutics. 325 (3): 791–800. doi:10.1124/jpet.108.136200. PMC 2637348. PMID 18354055.
  • Capela JP, Carmo H, Remião F, Bastos ML, Meisel A, Carvalho F (June 2009). "Molecular and cellular mechanisms of ecstasy-induced neurotoxicity: an overview". Molecular Neurobiology. 39 (3): 210–71. CiteSeerX 10.1.1.670.6897. doi:10.1007/s12035-009-8064-1. PMID 19373443. S2CID 21190104.
  • Sarkar S, Schmued L (August 2010). "Neurotoxicity of ecstasy (MDMA): an overview". Current Pharmaceutical Biotechnology. 11 (5): 460–9. doi:10.2174/138920110791591490. PMID 20420572.
  • Escubedo E, Abad S, Torres I, Camarasa J, Pubill D (January 2011). "Comparative neurochemical profile of 3,4-methylenedioxymethamphetamine and its metabolite alpha-methyldopamine on key targets of MDMA neurotoxicity". Neurochemistry International. 58 (1): 92–101. doi:10.1016/j.neuint.2010.11.001. PMID 21074589. S2CID 2853533.

ncbi.nlm.nih.gov

psu.edu

citeseerx.ist.psu.edu

  • Trachsel D, Hadorn M, Baumberger F (March 2006). "Synthesis of fluoro analogues of 3,4-(methylenedioxy)amphetamine (MDA) and its derivatives". Chemistry & Biodiversity. 3 (3): 326–36. CiteSeerX 10.1.1.688.5803. doi:10.1002/cbdv.200690035. PMID 17193269. S2CID 23036634.
  • Capela JP, Carmo H, Remião F, Bastos ML, Meisel A, Carvalho F (June 2009). "Molecular and cellular mechanisms of ecstasy-induced neurotoxicity: an overview". Molecular Neurobiology. 39 (3): 210–71. CiteSeerX 10.1.1.670.6897. doi:10.1007/s12035-009-8064-1. PMID 19373443. S2CID 21190104.

semanticscholar.org

api.semanticscholar.org

  • Trachsel D, Hadorn M, Baumberger F (March 2006). "Synthesis of fluoro analogues of 3,4-(methylenedioxy)amphetamine (MDA) and its derivatives". Chemistry & Biodiversity. 3 (3): 326–36. CiteSeerX 10.1.1.688.5803. doi:10.1002/cbdv.200690035. PMID 17193269. S2CID 23036634.
  • Takač MJ, Magina JD, Takač T (December 2019). "Evaluation of phenylethylamine type entactogens and their metabolites relevant to ecotoxicology - a QSAR study". Acta Pharmaceutica. 69 (4). Zagreb, Croatia: 563–584. doi:10.2478/acph-2019-0038. PMID 31639096. S2CID 204850967.
  • Capela JP, Carmo H, Remião F, Bastos ML, Meisel A, Carvalho F (June 2009). "Molecular and cellular mechanisms of ecstasy-induced neurotoxicity: an overview". Molecular Neurobiology. 39 (3): 210–71. CiteSeerX 10.1.1.670.6897. doi:10.1007/s12035-009-8064-1. PMID 19373443. S2CID 21190104.
  • Escubedo E, Abad S, Torres I, Camarasa J, Pubill D (January 2011). "Comparative neurochemical profile of 3,4-methylenedioxymethamphetamine and its metabolite alpha-methyldopamine on key targets of MDMA neurotoxicity". Neurochemistry International. 58 (1): 92–101. doi:10.1016/j.neuint.2010.11.001. PMID 21074589. S2CID 2853533.