Sign Up to like & get
recommendations!
0
Published in 2019 at "Biochemistry"
DOI: 10.1021/acs.biochem.9b00156
Abstract: In a continuing effort to identify structural attributes required for strong binding and potent inhibition of human drug-metabolizing CYP3A4, we designed ten ritonavir-like analogues differing in the side-group stereochemistry, backbone atomic composition, and headgroup spacing.…
read more here.
Keywords:
group stereochemistry;
side group;
group;
ritonavir ... See more keywords