A. Deese

发表

NMR of biofluids and pattern recognition: assessing the impact of NMR parameters on the principal component analysis of urine from rat and mouse.

M. Reily, D. Robertson, B. Potts, 2001, Journal of pharmaceutical and biomedical analysis.

The Application of Metabonomics as an Early In Vivo Toxicity Screen

Gregory J. Stevens, A. Deese, 2005 .

Significant Species Difference in Amide Hydrolysis of GDC-0834, a Novel Potent and Selective Bruton's Tyrosine Kinase Inhibitor

John C. Davis, P. Kuebler, J. Lubach, 2011, Drug Metabolism and Disposition.

Elucidating the structure and cytochrome P450-mediated mechanism for novel metabolites of GDC-0575 in rats

Yuan Chen, C. Han, J. Napolitano, 2022, Xenobiotica; the fate of foreign compounds in biological systems.

Novel mechanism for dehalogenation and glutathione conjugation of dihalogenated anilines in human liver microsomes: evidence for ipso glutathione addition.

Kevin A Ford, J. Driscoll, C. Hop, 2011, Chemical research in toxicology.

Proton, carbon-13, and phosphorus-31 NMR methods for the investigation of rhodopsin--lipid interactions in retinal rod outer segment membranes.

E. Dratz, M. F. Brown, A. Deese, 1982, Methods in enzymology.

IN VITRO METABOLIC ACTIVATION OF THIABENDAZOLE VIA 5-HYDROXYTHIABENDAZOLE: IDENTIFICATION OF A GLUTATHIONE CONJUGATE OF 5-HYDROXYTHIABENDAZOLE

D. Dalvie, A. Deese, Steve Bowlin, 2006, Drug Metabolism and Disposition.

CHAPTER 16 – THE ROLE OF DOCOSAHEXAENOIC ACID (22:6ω3) IN BIOLOGICAL MEMBRANES: EXAMPLES FROM PHOTORECEPTORS AND MODEL MEMBRANE BILAYERS1

E. Dratz, A. Deese, 1986 .

Retinal rod outer segment lipids form bilayers in the presence and absence of rhodopsin: a 31P NMR study

E. Dratz, M. F. Brown, A. Deese, 1981, FEBS letters.

An isolable acyclic hemiacetal of ansamitocin P‐3

A. Deese, Nathaniel L. Segraves, D. Yazzie, 2012, Magnetic resonance in chemistry : MRC.

Simultaneous observation of order and dynamics at several defined positions in a single acyl chain using 2H NMR of single acyl chain perdeuterated phosphatidylcholines.

F. Dahlquist, E. Dratz, M. Paddy, 1985, Biochemistry.

Novel Potent and Selective Bruton's Tyrosine Kinase (BTK) Inhibitor

P. Kuebler, J. Lubach, H. Wong, 2011 .

Absorption, metabolism and excretion of pictilisib, a potent pan-class I phosphatidylinositol-3-Kinase (PI3K) inhibitor, in rats, dogs, and humans

J. Ware, L. Salphati, Shuguang Ma, 2021, Xenobiotica; the fate of foreign compounds in biological systems.

Interaction of rhodopsin with two unsaturated phosphatidylcholines: a deuterium nuclear magnetic resonance study.

F. Dahlquist, E. Dratz, M. Paddy, 1981, Biochemistry.

Absorption, Distribution, Metabolism, and Excretion of [14C]GDC-0449 (Vismodegib), an Orally Active Hedgehog Pathway Inhibitor, in Rats and Dogs: A Unique Metabolic Pathway via Pyridine Ring Opening

H. Wong, C. Hop, M. Reynolds, 2011, Drug Metabolism and Disposition.

Pharmacokinetics, Metabolism, and Excretion of [14C]Axitinib, a Vascular Endothelial Growth Factor Receptor Tyrosine Kinase Inhibitor, in Humans

D. Dalvie, Y. Pithavala, B. Hee, 2014, Drug Metabolism and Disposition.

Microsoft Word-49502143-file00.docx

D. Dalvie, W. Pool, A. Deese, 2014 .

Degradation of a pharmaceutical in HPLC grade methanol containing trace level formaldehyde

Ke Zhang, A. Deese, K. Ngim, 2013, Pharmaceutical development and technology.

Strategies for the analysis of highly reactive pinacolboronate esters.

A. Deese, K. Ngim, Nik P. Chetwyn, 2012, Journal of chromatography. A.

Synthesis of Akt Inhibitor Ipatasertib. Part 2. Total Synthesis and First Kilogram Scale-up

M. W. Dong, J. Stults, D. Askin, 2014 .

Chemoselective sp2-sp3 cross-couplings: iron-catalyzed alkyl transfer to dihaloaromatics.

Kevin A Ford, Kevin A. Ford, Sushant Malhotra, 2013, Organic letters.

Development of an Expedient Process for the Multi-Kilogram Synthesis of Chk1 Inhibitor GDC-0425

M. Reynolds, L. Gazzard, A. Deese, 2015 .

Isotropic solutions of phospholipid bicelles: A new membrane mimetic for high-resolution NMR studies of polypeptides

R. Prosser, A. Deese, R. R. Vold, 1997, Journal of biomolecular NMR.

Bioactivation of Flutamide Metabolites by Human Liver Microsomes

J. Nieman, D. Dalvie, A. Deese, 2008, Drug Metabolism and Disposition.

Identification of a Novel Glutathione Conjugate of Flutamide in Incubations with Human Liver Microsomes

D. Dalvie, A. Deese, Ping Kang, 2007, Drug Metabolism and Disposition.

Solid-State Characterization of Novel Propylene Glycol Ester Solvates Isolated from Lipid Formulations.

J. Lubach, S. Kothari, A. Deese, 2015, Molecular pharmaceutics.

HUMAN IN VITRO GLUTATHIONYL AND PROTEIN ADDUCTS OF CARBAMAZEPINE-10,11-EPOXIDE, A STABLE AND PHARMACOLOGICALLY ACTIVE METABOLITE OF CARBAMAZEPINE

Ping Zhao, P. Zhao, Ping Kang, 2005, Drug Metabolism and Disposition.

Characterizing the in vitro species differences in N-glucuronidation of a potent pan-PIM inhibitor GNE-924 containing a 3,5-substituted 6-azaindazole

Sarah J. Robinson, J. Ly, Susan D. Wong, 2018, Xenobiotica; the fate of foreign compounds in biological systems.

Elucidating the Mechanism of Cytochrome P450–Mediated Pyrimidine Ring Conversion to Pyrazole Metabolites with the BACE1 Inhibitor GNE-892 in Rats

Xingrong Liu, C. Hop, Shuguang Ma, 2014, Drug Metabolism and Disposition.

Microsoft Word-93038660-file00

C. Hop, S. C. Khojasteh, A. Deese, 2014 .

Chemoselective sp2-sp3 cross-couplings: iron-catalyzed alkyl transfer to dihaloaromatics.

Kevin A. Ford, S. Koenig, A. Deese, 2013, Organic letters.

Characterizing the in vitro species differences in N-glucuronidation of a potent pan-PIM inhibitor GNE-924 containing a 3,5-substituted 6-azaindazole

Sarah J. Robinson, J. Ly, Susan D. Wong, 2018, Xenobiotica; the fate of foreign compounds in biological systems.

Bioactivation of Flutamide Metabolites by Human Liver Microsomes

J. Nieman, D. Dalvie, A. Deese, 2008, Drug Metabolism and Disposition.