This is the companion web site for publication: Statistical Validation of Structure-Selectivity Relationship Using NCI Cancer Database Jing Li 1,2 , Chris Benner 2 , Tao Jia
A novel series of optically active 2,6-disubstituted alkylphenols with improved anesthetic profiles compared to widely used propofol were synthesized. The incorporation of the cyclopropyl group not on
Muscarinic acetylcholine receptors (MRs), comprising five subtypes (M1R–M5R) in humans, exhibit a high degree of structural similarity. Therefore, subtype-selective MR agonists and antagonists are lac
