Synthesis of azaspirocycles and their evaluation in drug discovery
JA Burkhard, B Wagner, H Fischer…
Index: Burkhard, Johannes A.; Wagner, Bjoern; Fischer, Holger; Schuler, Franz; Mueller, Klaus; Carreira, Erick M. Angewandte Chemie - International Edition, 2010 , vol. 49, # 20 p. 3524 - 3527
Full Text: HTML
Citation Number: 78
Abstract
In modern drug discovery, high-throughput screening may generate promising lead compounds that are less than ideal with respect to important parameters such as absorption, distribution, metabolism, and excretion (ADME). In the process of lead optimization, various structural features are fine-tuned and physicochemical properties such as the basicity (pKa [1]), lipophilicity (logD), solubility (Solint), and clearance rates (CLint) are improved.[2] ...
Related Articles:
Reusable supported ruthenium catalysts for the alkylation of amines by using primary alcohols
[Peishan, Siah; Dang, Tuan Thanh; Seayad, Abdul Majeed; Ramalingam, Balamurugan ChemCatChem, 2014 , vol. 6, # 3 p. 808 - 814]