M. Albanese

发表

The synthesis and structure-activity relationship of 4-benzimidazolyl-piperidinylcarbonyl-piperidine analogs as histamine H3 antagonists.

Walter A. Korfmacher, M. Corboz, J. Hey, 2010, Bioorganic & medicinal chemistry letters.

Dual antagonists of platelet activating factor and histamine. 3. Synthesis, biological activity and conformational implications of substituted N-acyl-bis-arylcycloheptapiperazines.

M. Billah, F. Colizzo, M. Green, 1998, Bioorganic & medicinal chemistry letters.

Synthesis and structure-activity relationships of oxime neurokinin antagonists: discovery of potent arylamides.

Cheryl A. Grice, N. Carruthers, N. Shih, 2002, Bioorganic & medicinal chemistry letters.

The synthesis of substituted fluorenes as novel non-imidazole histamine h(3) inhibitors.

R. Aslanian, N. Shih, R. West, 2002, Bioorganic & medicinal chemistry letters.

Tricyclic farnesyl protein transferase inhibitors: crystallographic and calorimetric studies of structure-activity relationships.

P. Weber, R. Doll, W. Windsor, 1999, Journal of medicinal chemistry.

Discovery of novel nonpeptide tricyclic inhibitors of Ras farnesyl protein transferase.

W. R. Bishop, N. Carruthers, P. Kirschmeier, 1997, Bioorganic & medicinal chemistry.

Identification of a novel, orally bioavailable histamine H(3) receptor antagonist based on the 4-benzyl-(1H-imidazol-4-yl) template.

Xiaohong Zhu, Matthew Bryant, Xiaohong Zhu, 2002, Bioorganic & medicinal chemistry letters.

Reduction of CYP450 inhibition in the 4-[(1H-imidazol-4-yl)methyl]piperidine series of histamine H3 receptor antagonists.

Walter A. Korfmacher, M. Corboz, J. Hey, 2006, Bioorganic & medicinal chemistry letters.

The synthesis and structure-activity relationship of 4-benzimidazolyl-piperidinylcarbonyl-piperidine analogs as histamine H3 antagonists.

Walter A. Korfmacher, M. Corboz, J. Hey, 2010, Bioorganic & medicinal chemistry letters.