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C Tucci

Showing results (61-70 of 82) with videos related to

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Bioorganic & Medicinal Chemistry Letters|January 15, 2011
Influence of pKa on the biotransformation of indene H1-antihistamines by CYP2D6Charles Huang, Wilna J Moree, Said Zamani-Kord, et al.
Bioorganic & Medicinal Chemistry Letters|July 11, 2006
Propionylpiperazines as human melanocortin-4 receptor ligandsCaroline W Chen, Joe A Tran, Wanlong Jiang, et al.
Bioorganic & Medicinal Chemistry Letters|June 17, 2006
Arylpropionylpiperazines as antagonists of the human melanocortin-4 receptorWanlong Jiang, Fabio C Tucci, Caroline W Chen, et al.
Bioorganic & Medicinal Chemistry Letters|May 3, 2005
A potent and selective nonpeptide antagonist of the melanocortin-4 receptor induces food intake in satiated miceJoseph Pontillo, Joseph A Tran, Stacy Markison, et al.
Bioorganic & Medicinal Chemistry Letters|September 8, 2007
Pyrrolidinones as potent functional antagonists of the human melanocortin-4 receptorWanlong Jiang, Fabio C Tucci, Joe A Tran, et al.
Bioorganic & Medicinal Chemistry Letters|November 23, 2007
Identification and characterization of pyrrolidine diastereoisomers as potent functional agonists and antagonists of the human melanocortin-4 receptorChen Chen, Wanlong Jiang, Joe A Tran, et al.
Bioorganic & Medicinal Chemistry Letters|December 14, 2011
Lead optimization of 2-(piperidin-3-yl)-1H-benzimidazoles: identification of 2-morpholin- and 2-thiomorpholin-2-yl-1H-benzimidazoles as selective and CNS penetrating H₁-antihistamines for insomniaSatheesh Babu Ravula, Jinghua Yu, Joe A Tran, et al.
Bioorganic & Medicinal Chemistry Letters|September 3, 2004
Synthesis and structure-activity relationships of uracil derived human GnRH receptor antagonists: (R)-3-[2-(2-amino)phenethyl]-1-(2,6-difluorobenzyl)-6-methyluracils containing a substituted thiophene or thiazole at C-5Martin W Rowbottom, Fabio C Tucci, Patrick J Connors, et al.
Bioorganic & Medicinal Chemistry Letters|September 11, 2004
Structure-activity relationships of piperazinebenzylamines as potent and selective agonists of the human melanocortin-4 receptorJoseph Pontillo, Joseph A Tran, Melissa Arellano, et al.
Bioorganic & Medicinal Chemistry Letters|April 30, 2008
Potent and orally bioavailable zwitterion GnRH antagonists with low CYP3A4 inhibitory activityChen Chen, Yongsheng Chen, Joseph Pontillo, et al.
Pageof 9

Showing results (61-70 of 82) with videos related to

Sort By:
Pageof 9
Bioorganic & Medicinal Chemistry Letters|January 15, 2011
Influence of pKa on the biotransformation of indene H1-antihistamines by CYP2D6Charles Huang, Wilna J Moree, Said Zamani-Kord, et al.
Bioorganic & Medicinal Chemistry Letters|July 11, 2006
Propionylpiperazines as human melanocortin-4 receptor ligandsCaroline W Chen, Joe A Tran, Wanlong Jiang, et al.
Bioorganic & Medicinal Chemistry Letters|June 17, 2006
Arylpropionylpiperazines as antagonists of the human melanocortin-4 receptorWanlong Jiang, Fabio C Tucci, Caroline W Chen, et al.
Bioorganic & Medicinal Chemistry Letters|May 3, 2005
A potent and selective nonpeptide antagonist of the melanocortin-4 receptor induces food intake in satiated miceJoseph Pontillo, Joseph A Tran, Stacy Markison, et al.
Bioorganic & Medicinal Chemistry Letters|September 8, 2007
Pyrrolidinones as potent functional antagonists of the human melanocortin-4 receptorWanlong Jiang, Fabio C Tucci, Joe A Tran, et al.
Bioorganic & Medicinal Chemistry Letters|November 23, 2007
Identification and characterization of pyrrolidine diastereoisomers as potent functional agonists and antagonists of the human melanocortin-4 receptorChen Chen, Wanlong Jiang, Joe A Tran, et al.
Bioorganic & Medicinal Chemistry Letters|December 14, 2011
Lead optimization of 2-(piperidin-3-yl)-1H-benzimidazoles: identification of 2-morpholin- and 2-thiomorpholin-2-yl-1H-benzimidazoles as selective and CNS penetrating H₁-antihistamines for insomniaSatheesh Babu Ravula, Jinghua Yu, Joe A Tran, et al.
Bioorganic & Medicinal Chemistry Letters|September 3, 2004
Synthesis and structure-activity relationships of uracil derived human GnRH receptor antagonists: (R)-3-[2-(2-amino)phenethyl]-1-(2,6-difluorobenzyl)-6-methyluracils containing a substituted thiophene or thiazole at C-5Martin W Rowbottom, Fabio C Tucci, Patrick J Connors, et al.
Bioorganic & Medicinal Chemistry Letters|September 11, 2004
Structure-activity relationships of piperazinebenzylamines as potent and selective agonists of the human melanocortin-4 receptorJoseph Pontillo, Joseph A Tran, Melissa Arellano, et al.
Bioorganic & Medicinal Chemistry Letters|April 30, 2008
Potent and orally bioavailable zwitterion GnRH antagonists with low CYP3A4 inhibitory activityChen Chen, Yongsheng Chen, Joseph Pontillo, et al.
Pageof 9