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1.Affinity and stoichiometry of calcium binding by arsenazo III
Analytical Biochemistry, Volume 110, Issue 1, 1 January 1981, Pages 61-72
Paul J. Bauer

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 http://dx.doi.org/10.1016/0003-2697(81)90112-3 

2.Intracellular free Ca and Mg of human red blood cell ghosts measured with entrapped arsenazo III
Analytical Biochemistry, Volume 132, Issue 2, 15 July 1983, Pages 431-448
Douglas R. Yingst and Joseph F. Hoffman

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http://dx.doi.org/10.1016/0003-2697(83)90031-3

3.Kinetics and mechanism of Ca2+ binding to arsenazo III and antipyrylazo III
Biochimica et Biophysica Acta (BBA) - General Subjects, Volume 799, Issue 1, 25 May 1984, Pages 9-19
Peter L. Dorogi

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 http://dx.doi.org/10.1016/0304-4165(84)90321-0

4.The binding of arsenazo III to cell components
Biochimica et Biophysica Acta (BBA) - General Subjects, Volume 629, Issue 2, 7 May 1980, Pages 317-327
Troy J. Beeler, Angelo Schibeci and A. Martonosi

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http://dx.doi.org/10.1016/0304-4165(80)90104-X

5.Increase in intracellular free calcium concentration of limulus photoreceptors caused by a metabolic inhibitor
Vision Research, Volume 20, Issue 6, 1980, Pages 539-544
Mei-Ven C. Lo, Fulton Wong and William L. Pak

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http://dx.doi.org/10.1016/0042-6989(80)90129-7 

6.Residues in the Fifth Membrane-Spanning Segment of the Dopamine D2 Receptor Exposed in the Binding-Site Crevice
Jonathan A. Javitch, Dingyi Fu, and Jiayun Chen
Biochemistry; 1995; 34(50) pp 16433 - 16439

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http://dx.doi.org/10.1021/bi00050a026

7.A Cluster of Aromatic Residues in the Sixth Membrane-Spanning Segment of the Dopamine D2 Receptor Is Accessible in the Binding-Site Crevice
Jonathan A. Javitch,Juan A. Ballesteros, Harel Weinstein, and Jiayun Chen
Biochemistry, 1998, 37 (4), pp 998–1006

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http://dx.doi.org/10.1021/bi972241y

8.Conformational analysis of dopamine D-2 receptor antagonists of the benzamide series in relation to a recently proposed D-2 receptor-interaction model
Ingrid Pettersson and Tommy Liljefors
J. Med. Chem.; 1992; 35(13) pp 2355 - 2363

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http://dx.doi.org/10.1021/jm00091a002

9.pH Dependence of Ligand Binding to D2 Dopamine Receptors
Ursula M. D'Souza and Philip G. Strange
Biochemistry; 1995; 34(41) pp 13635 - 13641

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http://dx.doi.org/10.1021/bi00041a044

10.1-Naphthylpiperazine derivatives as potential atypical antipsychotic agents
John A. Lowe, III, Thomas F. Seeger, Arthur A. Nagel, Harry R. Howard, Patricia A. Seymour, James H. Heym, Frank E. Ewing, Michael E. Newman, Anne W. Schmidt, and et al.
J. Med. Chem.; 1991; 34(6) pp 1860 - 1866

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http://dx.doi.org/10.1021/jm00110a016

11.Synthesis and dopamine receptor affinity of (R)-(-)-2-fluoro-N-n-propylnorapomorphine: a highly potent and selective dopamine D2 agonist
John L. Neumeyer, Yigong Gao, Nora S. Kula, and Ross J. Baldessarini
J. Med. Chem.; 1990; 33(12) pp 3122 - 3124

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http://dx.doi.org/10.1021/jm00174a002

12.Structure−Activity Relationships for a Novel Series of Dopamine D2-like Receptor Ligands Based on N-Substituted 3-Aryl-8-azabicyclo[3.2.1]octan-3-ol
Noel M. Paul, Michelle Taylor, Rakesh Kumar.J. Med. Chem., 2008, 51 (19), pp 6095–6109

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http://dx.doi.org/10.1021/jm800532x

13.Synthesis, Binding Affinity, and Molecular Docking Analysis of New Benzofuranone Derivatives as Potential Antipsychotics
Reyes Aranda, Karen Villalba, Enrique Raviña, Christian F. Masaguer
J. Med. Chem., 2008, 51 (19), pp 6085–6094

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http://dx.doi.org/10.1021/jm800602w

14.Residues in the Seventh Membrane-Spanning Segment of the Dopamine D2 Receptor Accessible in the Binding-Site Crevice
Dingyi Fu, Juan A. Ballesteros,Harel Weinstein
Biochemistry, 1996, 35 (35), pp 11278–11285

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http://dx.doi.org/10.1021/bi960928x

15.4-(1,2,5,6-Tetrahydro-1-alkyl-3-pyridinyl)-2-thiazolamines: a novel class of compounds with central dopamine agonist properties
Juan C. Jaen, Lawrence D. Wise, Bradley W. Caprathe, Haile Tecle, Stephen Bergmeier, Christine C. Humblet, Thomas G. Heffner, Leonard T. Meltzer, Thomas A. Pugsley
J. Med. Chem., 1990, 33 (1), pp 311–317

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http://dx.doi.org/10.1021/jm00163a051

16.Locating Biologically Active Compounds in Medium-Sized Heterogeneous Datasets by Topological Autocorrelation Vectors: Dopamine and Benzodiazepine Agonists
Henri Bauknecht,Andreas Zell, Harald Bayer, Paul Levi
J. Chem. Inf. Comput. Sci., 1996, 36 (6), pp 1205–1213

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http://dx.doi.org/10.1021/ci960346m

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