[BOOK][B] The Functions of the Vibrissae in the Behavior of the White Rat...

SB Vincent - 1912 - books.google.com
Any psychological merit which this paper may possess is due entirely to the teaching and
inspiration of Professor James R. Angell under whom I have worked. I am glad also here to …

Metabolism and excretion of the dipeptidyl peptidase 4 inhibitor [14C] sitagliptin in humans

SH Vincent, JR Reed, AJ Bergman, CS Elmore… - Drug metabolism and …, 2007 - ASPET
The metabolism and excretion of [ 14 C]sitagliptin, an orally active, potent and selective
dipeptidyl peptidase 4 inhibitor, were investigated in humans after a single oral dose of 83 mg/…

Discovery of a Novel Glucagon Receptor Antagonist N-[(4-{(1S)-1-[3-(3, 5-Dichlorophenyl)-5-(6-methoxynaphthalen-2-yl)-1H-pyrazol-1-yl]ethyl}phenyl)carbonyl]-β …

…, X Tong, SS Xu, J Shang, SH Vincent… - Journal of medicinal …, 2012 - ACS Publications
A potent, selective glucagon receptor antagonist 9m, N-[(4-{(1S)-1-[3-(3,5-dichlorophenyl)-5-(6-methoxynaphthalen-2-yl)-1H-pyrazol-1-yl]ethyl}phenyl)carbonyl]-β-alanine,
was …

Disposition of the dipeptidyl peptidase 4 inhibitor sitagliptin in rats and dogs

…, S Ciccotto, DF Hora, RA Stearns, SH Vincent - Drug Metabolism and …, 2007 - ASPET
The pharmacokinetics, metabolism, and excretion of sitagliptin [MK-0431; (2R)-4-oxo-4-[3-(trifluoromethyl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazin-7(8H)-yl]-1-(2,4,5-trifluorophenyl)butan…

Correolide and derivatives are novel immunosuppressants blocking the lymphocyte Kv1. 3 potassium channels

…, WH Parsons, XC Tong, IE Ita, J Pivnichny, S Vincent… - Cellular …, 1999 - Elsevier
The voltage-gated potassium channel, Kv1.3, is specifically expressed on human lymphocytes,
where it controls membrane potential and calcium influx. Blockade of Kv1.3 channels by …

Characterization of 1′-hydroxymidazolam glucuronidation in human liver microsomes

B Zhu, D Bush, GA Doss, S Vincent, RB Franklin… - Drug metabolism and …, 2008 - ASPET
Midazolam is a potent benzodiazepine derivative with sedative, hypnotic, anticonvulsant,
muscle-relaxant, and anxiolytic activities. It undergoes oxidative metabolism catalyzed almost …

Oxetane promise delivered: discovery of long-acting IDO1 inhibitors suitable for Q3W oral or parenteral dosing

…, J Zhai, I Knemeyer, KM Otte, S Vincent… - Journal of Medicinal …, 2022 - ACS Publications
3,3-Disubstituted oxetanes have been utilized as bioisosteres for gem-dimethyl and cyclobutane
functionalities. We report the discovery of a novel class of oxetane indole-amine 2,3-…

Carbamate and N-Pyrimidine Mitigate Amide Hydrolysis: Structure-Based Drug Design of Tetrahydroquinoline IDO1 Inhibitors

…, JR Miller, I Knemeyer, KM Otte, S Vincent… - ACS medicinal …, 2021 - ACS Publications
Stella Vincent Stella Vincent … More by Stella Vincent

Orally bioavailable, indole-based nonpeptide GnRH receptor antagonists with high potency and functional activity

…, AH Mao, JR Carlin, BV Karanam, SH Vincent… - Bioorganic & medicinal …, 2001 - Elsevier
Stereospecific introduction of a methyl group to the indole-3-side chain enhanced activity in
our tryptamine-derived series of GnRH receptor antagonists. Further improvements were …

The discovery of sulfonylated dipeptides as potent VLA-4 antagonists

…, LA Egger, U Kidambi, K Lyons, S Vincent… - Bioorganic & medicinal …, 2001 - Elsevier
Directed screening of a carboxylic acid-containing combinatorial library led to the discovery
of potent inhibitors of the integrin VLA-4. Subsequent optimization by solid-phase synthesis …