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1. Analogs of Ac-CCK-7 incorporating dipeptide mimics in place of Met28-Gly29
Jefferson W. Tilley, Waleed Danho, Shian Jan Shiuey, Irina Kulesha, Joseph Swistok, Raymond Makofske
J. Med. Chem., 1992, 35 (21), pp 3774–3783

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http://dx.doi.org/10.1021/jm00099a005

2. Structure−Activity Relationships of a Series of Substituted Benzamides: Potent D2/5-HT2 Antagonists and 5-HT1a Agonists as Neuroleptic Agents
Mark H. Norman,*† Greg C. Rigdon,‡ William R. Hall,† and Frank Navas
J. Med. Chem., 1996, 39 (5), pp 1172–1188

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http://dx.doi.org/10.1021/jm950551d

3. (3R)-N-(1-(tert-Butylcarbonylmethyl)-2,3-dihydro-2-oxo-5-(2-pyridyl)-1H- 1,4-benzodiazepin-3-yl)-N‘-(3-(methylamino)phenyl)urea (YF476): A Potent and Orally Active Gastrin/CCK-B Antagonist
Graeme Semple,*† Hamish Ryder,† David P. Rooker,† Andrzej R. Batt,† David A. Kendrick,† Michael Szelke,† Mitsuaki Ohta,‡ Masato Satoh
J. Med. Chem., 1997, 40 (3), pp 331–341

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http://dx.doi.org/10.1021/jm960669+

4. Toward the antibody-catalyzed chemiluminescence. Design and synthesis of hapten
Masaaki Sawaa, Yasuhiro Imaedaa, Jun Hiratakea, Ryota Fujiia, Ritsuko Umeshitab, Mitsuo Watanabeb, Hitoshi Kondo
Bioorganic & Medicinal Chemistry Letters Volume 8, Issue 6, 17 March 1998, Pages 647-652

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http://dx.doi.org/10.1016/S0960-894X(98)00080-8

5. Anion transport in liposomes responds to variations in the anchor chains and the fourth amino acid of heptapeptide ion channels.
Riccardo Ferdani, Robert Pajewski, Natasha Djedovi, Jolanta Pajewska, Paul H. Schlesinger and George W. Gokel
New J. Chem., 2005, 29, 673 - 680

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http://dx.doi.org/10.1039/b417808b

6. Design, Synthesis, and Biological Evaluation of a Series of Lavendustin A Analogues That Inhibit EGFR and Syk Tyrosine Kinases, as Well as Tubulin Polymerization
Fanrong Mu,† Stephanie L. Coffing,† David J. Riese II,† Robert L. Geahlen,† Pascal Verdier-Pinard,‡ Ernest Hamel,‡ Jill Johnson,§ and Mark Cushman
J. Med. Chem., 2001, 44 (3), pp 441–452

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http://dx.doi.org/10.1021/jm000387g

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