TY - JOUR
T1 - Human microbial metabolite mimicry as a strategy to expand the chemical space of potential drugs
AU - Li, Hao
AU - Ranhotra, Harmit S.
AU - Mani, Sridhar
AU - Dvořák, Zdeněk
AU - Sokol, Harry
AU - Müller, Rolf
N1 - Funding Information:
Supported, in part, by The Peer Reviewed Medical Research Program – Investigator Initiated Research Award under Award No. W81XWH-17-1-0479; NIH grants ( ES030197 ; CA 222469 ); and Czech Science Foundation ( 20-00449S ).
Publisher Copyright:
© 2020 Elsevier Ltd
PY - 2020/9
Y1 - 2020/9
N2 - The concept of small-molecule mimicry even of weak microbial metabolites present in rodents and humans, as a means to expand drug repertoires, is new. Hitherto, there are few proof-of-concept papers demonstrating utility of this concept. More recently, papers demonstrating mimicry of intestinal microbial metabolites could expand the drug repertoire for diseases such as inflammatory bowel disease (IBD). We opine that, as more functional metabolite–receptor pairings are discovered, small-molecule metabolite mimicry could be a significant effort in drug discovery.
AB - The concept of small-molecule mimicry even of weak microbial metabolites present in rodents and humans, as a means to expand drug repertoires, is new. Hitherto, there are few proof-of-concept papers demonstrating utility of this concept. More recently, papers demonstrating mimicry of intestinal microbial metabolites could expand the drug repertoire for diseases such as inflammatory bowel disease (IBD). We opine that, as more functional metabolite–receptor pairings are discovered, small-molecule metabolite mimicry could be a significant effort in drug discovery.
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U2 - 10.1016/j.drudis.2020.06.007
DO - 10.1016/j.drudis.2020.06.007
M3 - Short survey
C2 - 32562605
AN - SCOPUS:85086777427
SN - 1359-6446
VL - 25
SP - 1575
EP - 1579
JO - Drug Discovery Today
JF - Drug Discovery Today
IS - 9
ER -