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C Tucci

Showing results (41-50 of 82) with videos related to

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Bioorganic & Medicinal Chemistry Letters|February 26, 2008
Design and synthesis of 3-arylpyrrolidine-2-carboxamide derivatives as melanocortin-4 receptor ligandsJoe A Tran, Fabio C Tucci, Melissa Arellano, et al.
Bioorganic & Medicinal Chemistry Letters|September 3, 2003
Synthesis and structure-activity relationships of 1-arylmethyl-3-(2-aminopropyl)-5-aryl-6-methyluracils as potent GnRH receptor antagonistsZhiqiang Guo, Yun-Fei Zhu, Fabio C Tucci, et al.
Bioorganic & Medicinal Chemistry Letters|June 14, 2005
Structure-activity relationship of a series of cyclohexylpiperidines bearing an amide side chain as antagonists of the human melanocortin-4 receptorJoseph A Tran, Joseph Pontillo, Melissa Arellano, et al.
Bioorganic & Medicinal Chemistry Letters|August 18, 2005
Optimization of piperazinebenzylamines with a N-(1-methoxy-2-propyl) side chain as potent and selective antagonists of the human melanocortin-4 receptorJoseph Pontillo, Dragan Marinkovic, Joe A Tran, et al.
The New England Journal of Medicine|September 6, 1990
Lung cancer and exposure to tobacco smoke in the householdD T Janerich, W D Thompson, L R Varela, et al.
Bioorganic & Medicinal Chemistry Letters|November 7, 2002
A novel synthesis of 7-aryl-8-fluoro-pyrrolo[1,2-a]pyrimid-4-ones as potent, stable GnRH receptor antagonistsFabio C Tucci, Yun-Fei Zhu, Zhiqiang Guo, et al.
Bioorganic & Medicinal Chemistry Letters|April 15, 2004
Synthesis and structure-activity relationships of (R)-1-alkyl-3-[2-(2-amino)phenethyl]-5-(2-fluorophenyl)-6-methyluracils as human GnRH receptor antagonistsMartin W Rowbottom, Fabio C Tucci, Yun-Fei Zhu, et al.
Chirality|October 1, 2005
Atropisomeric property of 1-(2,6-difluorobenzyl)-3-[(2R)-amino-2-phenethyl]-5-(2-fluoro-3-methoxyphenyl)-6-methyluracilFabio C Tucci, Tao Hu, Michael F Mesleh, et al.
Brain, Behavior, and Immunity|April 6, 2016
Systemic TAK-242 prevents intrathecal LPS evoked hyperalgesia in male, but not female mice and prevents delayed allodynia following intraplantar formalin in both male and female mice: The role of TLR4 in the evolution of a persistent pain stateSarah A Woller, Satheesh B Ravula, Fabio C Tucci, et al.
Brain, Behavior, and Immunity|January 3, 2018
Corrigendum to "Systemic TAK-242 prevents intrathecal LPS evoked hyperalgesia in male, but not female mice and prevents delayed allodynia following intraplantar formalin in both male and female mice: The role of TLR4 in the evolution of a persistent pain state" [Brain Behav. Immun. 56 (2016) 271-280]S A Woller, S B Ravula, F C Tucci, et al.
Pageof 9

Showing results (41-50 of 82) with videos related to

Sort By:
Pageof 9
Bioorganic & Medicinal Chemistry Letters|February 26, 2008
Design and synthesis of 3-arylpyrrolidine-2-carboxamide derivatives as melanocortin-4 receptor ligandsJoe A Tran, Fabio C Tucci, Melissa Arellano, et al.
Bioorganic & Medicinal Chemistry Letters|September 3, 2003
Synthesis and structure-activity relationships of 1-arylmethyl-3-(2-aminopropyl)-5-aryl-6-methyluracils as potent GnRH receptor antagonistsZhiqiang Guo, Yun-Fei Zhu, Fabio C Tucci, et al.
Bioorganic & Medicinal Chemistry Letters|June 14, 2005
Structure-activity relationship of a series of cyclohexylpiperidines bearing an amide side chain as antagonists of the human melanocortin-4 receptorJoseph A Tran, Joseph Pontillo, Melissa Arellano, et al.
Bioorganic & Medicinal Chemistry Letters|August 18, 2005
Optimization of piperazinebenzylamines with a N-(1-methoxy-2-propyl) side chain as potent and selective antagonists of the human melanocortin-4 receptorJoseph Pontillo, Dragan Marinkovic, Joe A Tran, et al.
The New England Journal of Medicine|September 6, 1990
Lung cancer and exposure to tobacco smoke in the householdD T Janerich, W D Thompson, L R Varela, et al.
Bioorganic & Medicinal Chemistry Letters|November 7, 2002
A novel synthesis of 7-aryl-8-fluoro-pyrrolo[1,2-a]pyrimid-4-ones as potent, stable GnRH receptor antagonistsFabio C Tucci, Yun-Fei Zhu, Zhiqiang Guo, et al.
Bioorganic & Medicinal Chemistry Letters|April 15, 2004
Synthesis and structure-activity relationships of (R)-1-alkyl-3-[2-(2-amino)phenethyl]-5-(2-fluorophenyl)-6-methyluracils as human GnRH receptor antagonistsMartin W Rowbottom, Fabio C Tucci, Yun-Fei Zhu, et al.
Chirality|October 1, 2005
Atropisomeric property of 1-(2,6-difluorobenzyl)-3-[(2R)-amino-2-phenethyl]-5-(2-fluoro-3-methoxyphenyl)-6-methyluracilFabio C Tucci, Tao Hu, Michael F Mesleh, et al.
Brain, Behavior, and Immunity|April 6, 2016
Systemic TAK-242 prevents intrathecal LPS evoked hyperalgesia in male, but not female mice and prevents delayed allodynia following intraplantar formalin in both male and female mice: The role of TLR4 in the evolution of a persistent pain stateSarah A Woller, Satheesh B Ravula, Fabio C Tucci, et al.
Brain, Behavior, and Immunity|January 3, 2018
Corrigendum to "Systemic TAK-242 prevents intrathecal LPS evoked hyperalgesia in male, but not female mice and prevents delayed allodynia following intraplantar formalin in both male and female mice: The role of TLR4 in the evolution of a persistent pain state" [Brain Behav. Immun. 56 (2016) 271-280]S A Woller, S B Ravula, F C Tucci, et al.
Pageof 9