Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Chennagiri R. Pandit"'
Autor:
Ann J. Barbier, Steven B Sands, Lilian Y Li, Anthony Ndifor, Chandra R. Shah, Kirsten L. Morton, Michael A. Letavic, Timothy W. Lovenberg, Anne Bonneville, Heather McAllister, Neelakandha S. Mani, Ian Fraser, Kiev S. Ly, Richard Apodaca, Nicholas I. Carruthers, Manoj Bajpai, Swanson Devin M, Michelle Kramer, Christine Dugovic, Sandra S Snook, Chennagiri R. Pandit, Jonathan Shelton, Wei Xiao, Leah Aluisio, Pascal Bonaventure, Brian Lord, S Diane Nepomuceno
Publikováno v:
ACS Medicinal Chemistry Letters. 6:450-454
The preclinical characterization of novel phenyl(piperazin-1-yl)methanones that are histamine H3 receptor antagonists is described. The compounds described are high affinity histamine H3 antagonists. Optimization of the physical properties of these h
Autor:
Frank J. Villani, Neelakandha S. Mani, Lana K. Young, Pippel Daniel J, Hua M. Zhong, John E. Mills, Chennagiri R. Pandit
Publikováno v:
Organic Process Research & Development. 15:638-648
Our teams have recently completed scale-up campaigns for two structurally similar H3 receptor antagonists. The first and second generation processes were developed for the synthesis of 107 and 125 ...
Autor:
Christopher M. Mapes, Shirin Shinde, Kelly J. McClure, Laurent Gomez, J. Guy Breitenbucher, Todd K. Jones, Clark A. Sehon, Neelakandha S. Mani, Marna C. W. Pippel, Xiaohu Deng, Chennagiri R. Pandit
Publikováno v:
The Journal of Organic Chemistry. 75:7950-7953
We describe a practical and scalable route to compound (Z)-1, a selective CCK1 receptor antagonist. Notable features of this concise route are (1) a regioselective construction of the pyrazole core through the reaction of an aryl hydrazine and an ela
Publikováno v:
Synthesis. 2009:4032-4036
A novel, one-pot protocol for the direct reductive amination of aldehyde bisulfite adducts is reported. Bisulfite adducts of aliphatic and aromatic aldehydes, on treatment with an organic base under non-aqueous conditions liberate the aldehyde in sit
Checkpoint Kinase Inhibitors: SAR and Radioprotective Properties of a Series of 2-Arylbenzimidazoles
Autor:
Anders Brunmark, Danielle K. Neff, Shelby Crawford, Lars Karlsson, Kelly J. McClure, Alice Lee, J. Guy Breitenbucher, Chennagiri R. Pandit, Frank U. Axe, Kristen L. Arienti, Jon Blevitt, Liming Huang
Publikováno v:
Journal of Medicinal Chemistry. 48:1873-1885
The discovery of a series of novel, potent, and highly selective inhibitors of the DNA damage control kinase chk2 is disclosed. Here we report the first SAR study around inhibitors of this kinase. High-throughput screening of purified human chk2 led
Autor:
Derek J. Norris, Rulin Zhao, Katerina Leftheris, John Hynes, Ping Chen, Bang-Chi Chen, Chennagiri R. Pandit, Lori A. Turk, Hong Wu, Vina Patil-Koota, Kathleen M. Gillooly, Peter A. Kiener, David J. Shuster, Xiaorong Chen, Kim W. McIntyre
Publikováno v:
Bioorganic & Medicinal Chemistry Letters. 12:2399-2402
C-3 Amido-indoles were found to selectively bind to the CB2 receptor. SAR studies led to optimized compounds with excellent in vivo potency against LPS induced TNF-alpha release in murine models of cytokine production.
Publikováno v:
Synthetic Communications. 32:2427-2432
A simple and economical method for 2-substituted oxazole synthesis and its scope are described.
Publikováno v:
The Journal of Organic Chemistry. 58:3407-3410
Methylisothiazoles undergo phototransposition in neutral solution to methylthiazoles by a single permutation process. Methylisothiazole→methylisothiazole transpositions, previously reported to occur, were not detected in these reactions. In trifluo
Publikováno v:
ChemInform. 28
Autor:
Hong Wu, Joseph E. Sundeen, Chennagiri R. Pandit, Amanda P. Skoumbourdis, Katerina Leftheris, Bang-Chi Chen, John Hynes, Rulin Zhao
Publikováno v:
ChemInform. 32