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Human microbial metabolite mimicry as a strategy to expand the chemical space of potential drugs
H. Li, HS. Ranhotra, S. Mani, Z. Dvořák, H. Sokol, R. Müller
Jazyk angličtina Země Velká Británie
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, práce podpořená grantem
Grantová podpora
R01 CA222469
NCI NIH HHS - United States
R01 ES030197
NIEHS NIH HHS - United States
- MeSH
- lidé MeSH
- mikrobiota * MeSH
- molekulární mimikry * MeSH
- objevování léků * MeSH
- zvířata MeSH
- Check Tag
- lidé MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
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.
Department of Cell Biology and Genetics Palacký University Olomouc 78371 Czech Republic
Department of Genetics Albert Einstein College of Medicine Bronx NY 10461 USA
Department of Medicine Albert Einstein College of Medicine Bronx NY 10461 USA
Department of Molecular Pharmacology Albert Einstein College of Medicine Bronx NY 10461 USA
German Center for Infection Research Partner Site Hannover Braunschweig Germany
Helmholtz Center for Infection Research GmbH Inhoffenstrasse 738124 Braunschweig Germany
INRA UMR1319 Micalis and AgroParisTech Jouy en Josas 78352 France
Paris Centre for Microbiome Medicine FHU Paris France
St Edmund's College Shillong Old Jowai Road Shillong Meghalaya 793003 India
Citace poskytuje Crossref.org
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- $a Li, Hao $u Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA
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- $a 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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- $a Ranhotra, Harmit S $u St Edmund's College, Shillong, Old Jowai Road, Shillong, Meghalaya 793003, India
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- $a Mani, Sridhar $u Department of Molecular Pharmacology, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Genetics, Albert Einstein College of Medicine, Bronx, NY 10461, USA; Department of Medicine, Albert Einstein College of Medicine, Bronx, NY 10461, USA. Electronic address: sridhar.mani@einsteinmed.org
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