TY - JOUR
T1 - Design, synthesis, and biological evaluation of a biyouyanagin compound library
AU - Nicolaou, K. C.
AU - Sanchini, Silvano
AU - Sarlah, David
AU - Lu, Gang
AU - Wu, T. Robert
AU - Nomura, Daniel K.
AU - Cravatt, Benjamin F.
AU - Cubitt, Beatrice
AU - De La Torre, Juan C.
AU - Hessell, Ann J.
AU - Burton, Dennis R.
PY - 2011/4/26
Y1 - 2011/4/26
N2 - Modern drug discovery efforts rely, to a large extent, on lead compounds from two classes of small organic molecules; namely, natural products (i.e., secondary metabolites) and designed compounds (i.e., synthetic molecules). In this article, we demonstrate how these two domains of lead compounds can be merged through total synthesis and molecular design of analogs patterned after the targeted natural products, whose promising biological properties provide the motivation. Specifically, the present study targeted the naturally occurring biyouyanagins A and B and their analogs throughmodular chemical synthesis and led to the discovery of small organic molecules possessing anti-HIV and anti-arenavirus properties.
AB - Modern drug discovery efforts rely, to a large extent, on lead compounds from two classes of small organic molecules; namely, natural products (i.e., secondary metabolites) and designed compounds (i.e., synthetic molecules). In this article, we demonstrate how these two domains of lead compounds can be merged through total synthesis and molecular design of analogs patterned after the targeted natural products, whose promising biological properties provide the motivation. Specifically, the present study targeted the naturally occurring biyouyanagins A and B and their analogs throughmodular chemical synthesis and led to the discovery of small organic molecules possessing anti-HIV and anti-arenavirus properties.
KW - Anti-inflammatory agents
KW - Antiviral agents
KW - [2 + 2] photocycloaddition
UR - http://www.scopus.com/inward/record.url?scp=79955551140&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=79955551140&partnerID=8YFLogxK
U2 - 10.1073/pnas.1015258108
DO - 10.1073/pnas.1015258108
M3 - Article
C2 - 21245351
AN - SCOPUS:79955551140
SN - 0027-8424
VL - 108
SP - 6715
EP - 6720
JO - Proceedings of the National Academy of Sciences of the United States of America
JF - Proceedings of the National Academy of Sciences of the United States of America
IS - 17
ER -