Disposition of posaconazole following single-dose oral administration in healthy subjects
P Krieter, B Flannery, T Musick, M Gohdes… - Antimicrobial agents …, 2004 - Am Soc Microbiol
Posaconazole is a potent, broad-spectrum triazole antifungal agent currently in clinical
development for the treatment of refractory invasive fungal infections. Eight healthy male subjects …
development for the treatment of refractory invasive fungal infections. Eight healthy male subjects …
Pharmacokinetic properties and human use characteristics of an FDA‐approved intranasal naloxone product for the treatment of opioid overdose
P Krieter, N Chiang, S Gyaw, P Skolnick… - The Journal of …, 2016 - Wiley Online Library
Parenteral naloxone has been approved to treat opiate overdose for over 4 decades. Intranasal
naloxone, administered “off label” using improvised devices, has been widely used by …
naloxone, administered “off label” using improvised devices, has been widely used by …
Preclinical and clinical pharmacology of DOV 216,303, a “triple” reuptake inhibitor
P Skolnick, P Krieter, J Tizzano, A Basile… - CNS drug …, 2006 - Wiley Online Library
DOV 216,303 [(±)‐1‐(3,4‐dichlorophenyl)‐3‐azabicyclo‐[3.1.0]hexane hydrochloride] is the
prototype of a class of compounds referred to as “triple” reuptake inhibitors. Such …
prototype of a class of compounds referred to as “triple” reuptake inhibitors. Such …
Fighting fire with fire: development of intranasal nalmefene to treat synthetic opioid overdose
P Krieter, S Gyaw, R Crystal, P Skolnick - Journal of pharmacology and …, 2019 - ASPET
The dramatic rise in overdose deaths linked to synthetic opioids (eg, fentanyl, carfentanil)
may require more potent, longer-duration opiate antagonists than naloxone. Both the high …
may require more potent, longer-duration opiate antagonists than naloxone. Both the high …
Characterization of the antinociceptive actions of bicifadine in models of acute, persistent, and chronic pain
…, A Nikiforuk, M Krawczyk, G Nowak, PA Krieter… - … of Pharmacology and …, 2007 - ASPET
Bicifadine (1-p-tolyl-3-azabicyclo[3.1.0]hexane) inhibits monoamine neurotransmitter uptake
by recombinant human transporters in vitro with a relative potency of norepinephrine > …
by recombinant human transporters in vitro with a relative potency of norepinephrine > …
Comparison of the pharmacokinetic properties of naloxone following the use of FDA‐approved intranasal and intramuscular devices versus a common improvised …
PA Krieter, CN Chiang, S Gyaw… - The Journal of Clinical …, 2019 - Wiley Online Library
For more than a decade, first responders and the general public have been able to treat
suspected opioid overdoses using an improvised nasal naloxone device (INND) constructed …
suspected opioid overdoses using an improvised nasal naloxone device (INND) constructed …
Metabolism of 6-chlorotryptophan to 4-chloro-3-hydroxyanthranilic acid: a potent inhibitor of 3-hydroxyanthranilic acid oxidase
CJ Parli, P Krieter, B Schmidt - Archives of Biochemistry and Biophysics, 1980 - Elsevier
Rats and guinea pigs dosed with dl-6-chlorotryptophan or d-6-chlorotryptophan excrete
significantly greater amounts of 3-hydroxyanthranilic acid in the urine than do animals treated …
significantly greater amounts of 3-hydroxyanthranilic acid in the urine than do animals treated …
Inhibition of Stromelysin-1 (MMP-3) by P1'-Biphenylylethyl Carboxyalkyl Dipeptides
…, DM Visco, F Shen, A Colletti, PA Krieter… - Journal of medicinal …, 1997 - ACS Publications
Carboxyalkyl peptides containing a biphenylylethyl group at the P 1 ‘ position were found to
be potent inhibitors of stromelysin-1 (MMP-3) and gelatinase A (MMP-2), in the range of 10−…
be potent inhibitors of stromelysin-1 (MMP-3) and gelatinase A (MMP-2), in the range of 10−…
DOV 216,303, a “triple” reuptake inhibitor: safety, tolerability, and pharmacokinetic profile
B Beer, J Stark, P Krieter, P Czobor… - The Journal of …, 2004 - Wiley Online Library
This report describes the first evaluation in humans of DOV 216,303, a putative antidepressive
that inhibits the reuptake of norepinephrine, serotonin, and dopamine. Subjects received …
that inhibits the reuptake of norepinephrine, serotonin, and dopamine. Subjects received …
Highly potent, orally active diester macrocyclic human renin inhibitors
AE Weber, MG Steiner, PA Krieter… - Journal of medicinal …, 1992 - ACS Publications
Replacing one amide bond in macrocyclic renin inhibitors of the general structure 1 and 2
with an ester linkage gave glutamate-derived inhibitors 3 and serine-derived inhibitors 4. …
with an ester linkage gave glutamate-derived inhibitors 3 and serine-derived inhibitors 4. …