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David R Witty

Showing results (11-20 of 17) with videos related to

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Bioorganic & Medicinal Chemistry Letters|July 15, 2006
SAR of biphenyl carboxamide ligands of the human melanin-concentrating hormone receptor 1 (MCH R1): discovery of antagonist SB-568849David R Witty, John H Bateson, Guillaume J Hervieu, et al.
ACS Medicinal Chemistry Letters|September 18, 2020
Discovery of Vixotrigine: A Novel Use-Dependent Sodium Channel Blocker for the Treatment of Trigeminal NeuralgiaDavid R Witty, Giuseppe Alvaro, Dominique Derjean, et al.
Bioorganic & Medicinal Chemistry Letters|July 15, 2006
Discovery of potent and stable conformationally constrained analogues of the MCH R1 antagonist SB-568849David R Witty, John Bateson, Guillaume J Hervieu, et al.
Bioorganic & Medicinal Chemistry Letters|July 1, 2004
Definition of the heterocyclic pharmacophore of bacterial methionyl tRNA synthetase inhibitors: potent antibacterially active non-quinolone analoguesRichard L Jarvest, Sula A Armstrong, John M Berge, et al.
Bioorganic & Medicinal Chemistry Letters|October 10, 2002
The antimicrobial natural product chuangxinmycin and some synthetic analogues are potent and selective inhibitors of bacterial tryptophanyl tRNA synthetaseMurray J Brown, Paul S Carter, Ashley S Fenwick, et al.
Bioorganic & Medicinal Chemistry Letters|September 17, 2008
Tricyclic azepine derivatives as selective brain penetrant 5-HT6 receptor antagonistsGiancarlo Trani, Stuart M Baddeley, Michael A Briggs, et al.
Bioorganic & Medicinal Chemistry Letters|September 7, 2005
Bicyclic heteroarylpiperazines as selective brain penetrant 5-HT6 receptor antagonistsMahmood Ahmed, Michael A Briggs, Steven M Bromidge, et al.
Pageof 2

Showing results (11-20 of 17) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 17 results.
Bioorganic & Medicinal Chemistry Letters|July 15, 2006
SAR of biphenyl carboxamide ligands of the human melanin-concentrating hormone receptor 1 (MCH R1): discovery of antagonist SB-568849David R Witty, John H Bateson, Guillaume J Hervieu, et al.
ACS Medicinal Chemistry Letters|September 18, 2020
Discovery of Vixotrigine: A Novel Use-Dependent Sodium Channel Blocker for the Treatment of Trigeminal NeuralgiaDavid R Witty, Giuseppe Alvaro, Dominique Derjean, et al.
Bioorganic & Medicinal Chemistry Letters|July 15, 2006
Discovery of potent and stable conformationally constrained analogues of the MCH R1 antagonist SB-568849David R Witty, John Bateson, Guillaume J Hervieu, et al.
Bioorganic & Medicinal Chemistry Letters|July 1, 2004
Definition of the heterocyclic pharmacophore of bacterial methionyl tRNA synthetase inhibitors: potent antibacterially active non-quinolone analoguesRichard L Jarvest, Sula A Armstrong, John M Berge, et al.
Bioorganic & Medicinal Chemistry Letters|October 10, 2002
The antimicrobial natural product chuangxinmycin and some synthetic analogues are potent and selective inhibitors of bacterial tryptophanyl tRNA synthetaseMurray J Brown, Paul S Carter, Ashley S Fenwick, et al.
Bioorganic & Medicinal Chemistry Letters|September 17, 2008
Tricyclic azepine derivatives as selective brain penetrant 5-HT6 receptor antagonistsGiancarlo Trani, Stuart M Baddeley, Michael A Briggs, et al.
Bioorganic & Medicinal Chemistry Letters|September 7, 2005
Bicyclic heteroarylpiperazines as selective brain penetrant 5-HT6 receptor antagonistsMahmood Ahmed, Michael A Briggs, Steven M Bromidge, et al.
Pageof 2