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Carleton R Sage

Showing results (1-10 of 16) with videos related to

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Journal of Chemical Information and Modeling|June 23, 2009
Elucidating molecular overlays from pairwise alignments using a genetic algorithmGareth Jones, Yinghong Gao, Carleton R Sage
Pharmaceuticals (Basel, Switzerland)|February 27, 2026
OPLE: Drug Discovery Platform Combining 2D Similarity with AI to Predict Off-Target LiabilitiesSarah E Biehn, Juerg Lehmann, Christoph Mueller, et al.
Future Medicinal Chemistry|February 19, 2024
BioPrint meets the AI age: development of artificial intelligence-based ADMET models for the drug-discovery platform SAFIRESarah E Biehn, Luis Miguel Goncalves, Juerg Lehmann, et al.
Journal of Medicinal Chemistry|February 17, 2006
1-Alkyl-benzotriazole-5-carboxylic acids are highly selective agonists of the human orphan G-protein-coupled receptor GPR109bGraeme Semple, Philip J Skinner, Martin C Cherrier, et al.
Bioorganic & Medicinal Chemistry Letters|June 16, 2009
5-N,N-Disubstituted 5-aminopyrazole-3-carboxylic acids are highly potent agonists of GPR109bPhilip J Skinner, Peter J Webb, Carleton R Sage, et al.
Journal of Medicinal Chemistry|March 16, 2007
Analogues of acifran: agonists of the high and low affinity niacin receptors, GPR109a and GPR109bJae-Kyu Jung, Benjamin R Johnson, Tracy Duong, et al.
Bioorganic & Medicinal Chemistry Letters|October 13, 2007
3-Nitro-4-amino benzoic acids and 6-amino nicotinic acids are highly selective agonists of GPR109bPhilip J Skinner, Martin C Cherrier, Peter J Webb, et al.
Bioorganic & Medicinal Chemistry Letters|January 19, 2020
Discovery of a lead series of potent benzodiazepine 5-HT<sub>2C</sub> receptor agonists with high selectivity in functional and binding assaysAlbert Ren, Xiuwen Zhu, Konrad Feichtinger, et al.
Journal of Medicinal Chemistry|May 14, 2025
Diazepine Agonists of the 5-HT<sub>2C</sub> Receptor with Unprecedented Selectivity: Discovery of Bexicaserin (LP352)Albert Ren, Xiuwen Zhu, Juerg Lehmann, et al.
Bioorganic & Medicinal Chemistry Letters|April 6, 2010
Potent tricyclic pyrazole tetrazole agonists of the nicotinic acid receptor (GPR109a)P Douglas Boatman, Thomas O Schrader, Michelle Kasem, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
Journal of Chemical Information and Modeling|June 23, 2009
Elucidating molecular overlays from pairwise alignments using a genetic algorithmGareth Jones, Yinghong Gao, Carleton R Sage
Pharmaceuticals (Basel, Switzerland)|February 27, 2026
OPLE: Drug Discovery Platform Combining 2D Similarity with AI to Predict Off-Target LiabilitiesSarah E Biehn, Juerg Lehmann, Christoph Mueller, et al.
Future Medicinal Chemistry|February 19, 2024
BioPrint meets the AI age: development of artificial intelligence-based ADMET models for the drug-discovery platform SAFIRESarah E Biehn, Luis Miguel Goncalves, Juerg Lehmann, et al.
Journal of Medicinal Chemistry|February 17, 2006
1-Alkyl-benzotriazole-5-carboxylic acids are highly selective agonists of the human orphan G-protein-coupled receptor GPR109bGraeme Semple, Philip J Skinner, Martin C Cherrier, et al.
Bioorganic & Medicinal Chemistry Letters|June 16, 2009
5-N,N-Disubstituted 5-aminopyrazole-3-carboxylic acids are highly potent agonists of GPR109bPhilip J Skinner, Peter J Webb, Carleton R Sage, et al.
Journal of Medicinal Chemistry|March 16, 2007
Analogues of acifran: agonists of the high and low affinity niacin receptors, GPR109a and GPR109bJae-Kyu Jung, Benjamin R Johnson, Tracy Duong, et al.
Bioorganic & Medicinal Chemistry Letters|October 13, 2007
3-Nitro-4-amino benzoic acids and 6-amino nicotinic acids are highly selective agonists of GPR109bPhilip J Skinner, Martin C Cherrier, Peter J Webb, et al.
Bioorganic & Medicinal Chemistry Letters|January 19, 2020
Discovery of a lead series of potent benzodiazepine 5-HT<sub>2C</sub> receptor agonists with high selectivity in functional and binding assaysAlbert Ren, Xiuwen Zhu, Konrad Feichtinger, et al.
Journal of Medicinal Chemistry|May 14, 2025
Diazepine Agonists of the 5-HT<sub>2C</sub> Receptor with Unprecedented Selectivity: Discovery of Bexicaserin (LP352)Albert Ren, Xiuwen Zhu, Juerg Lehmann, et al.
Bioorganic & Medicinal Chemistry Letters|April 6, 2010
Potent tricyclic pyrazole tetrazole agonists of the nicotinic acid receptor (GPR109a)P Douglas Boatman, Thomas O Schrader, Michelle Kasem, et al.
Pageof 2