Deepak Dalvie
Deepak Dalvie has a total of 36 co-authors. Here are the top co-authors by number of shared publications:
- Amit S. Kalgutkar
Medicine Design, Pfizer Worldwide Research, Development and Medical, Cambridge, MA, USA
9 shared publications - R. Scott Obach
Pfizer Inc., Groton, Connecticut
9 shared publications - Dennis A. Smith
Pfizer Inc., IPC475, Ramsgate Road, Sandwich, Kent CT13 9NJ, United Kingdom
8 shared publications Cathie Xiang
4 shared publicationsPing Kang
4 shared publicationsR. Scott Obach
4 shared publications
Latest Publications
- 11 July 2016
- Published by Wiley
- p. 261-273
DEALING WITH REALITY
- 24 October 2012
- Published by Wiley
- p. 93-129
Pathways of Reactive Metabolite Formation with Toxicophores/‐Structural Alerts
- 24 October 2012
- Published by Wiley
- p. 93-129
Pathways of Reactive Metabolite Formation with Toxicophores/‐Structural Alerts
- 24 October 2012
- Published by Wiley
- p. 357-375
Managing IADRs - a Risk-Benefit Analysis
- 24 October 2012
- Published by Wiley
- p. 13-42
Role of Reactive Metabolites in Genotoxicity
- 24 October 2012
- Published by Wiley
- p. 313-334
Mitigating Toxicity Risks with Affinity Labeling Drug Candidates
- 24 October 2012
- Published by Wiley
- p. 313-334
Mitigating Toxicity Risks with Affinity Labeling Drug Candidates
- 24 October 2012
- Published by Wiley
- p. 185-202
Retrospective Analysis of Structure-Toxicity Relationships of Drugs
- 24 October 2012
- Published by Wiley
- p. 185-202
Retrospective Analysis of Structure-Toxicity Relationships of Drugs
- 24 October 2012
- Published by Wiley
- p. 335-355
Dealing with Reactive Metabolite-Positive Compounds in Drug Discovery
- 24 October 2012
- Published by Wiley
- p. 335-355
Dealing with Reactive Metabolite-Positive Compounds in Drug Discovery
- 10 October 2012
- Published by Taylor & Francis in Xenobiotica
- Vol. 43 (5) , 399-408
Interspecies variation in the metabolism of zoniporide by aldehyde oxidase
1. Aldehyde oxidase (AO) is a cytosolic enzyme that contributes to the Phase I metabolism of xenobiotics in human and preclinical species. 2. Current studies explored in vitro metabolism of zoniporide in various animal species and humans using S9 fractions. The animal species included commonly used pharmacology and toxicology models and domestic animals such as the cat, cow or bull, pig and horse. 3. In addition, gender and strain differences in some species were also explored. 4. All animals except the dog and cat converted zoniporide to 2-oxozoniporide (M1). 5. Michael-Menten kinetic studies were conducted in species that turned over zoniporide to M1. 6. Marked differences in KM, Vmax and Clint were observed in the oxidation of zoniporide. 7. Although the KM and Vmax of zoniporide oxidation in male and female human S9 was similar, some gender difference was observed in animals especially, in Vmax. 8. The domestic animals also showed marked species differences in the AO activity and affinity toward zoniporide.
- 10 October 2012
- Published by Taylor & Francis in Xenobiotica
- Vol. 43 (5) , 399-408
Interspecies variation in the metabolism of zoniporide by aldehyde oxidase
1. Aldehyde oxidase (AO) is a cytosolic enzyme that contributes to the Phase I metabolism of xenobiotics in human and preclinical species. 2. Current studies explored in vitro metabolism of zoniporide in various animal species and humans using S9 fractions. The animal species included commonly used pharmacology and toxicology models and domestic animals such as the cat, cow or bull, pig and horse. 3. In addition, gender and strain differences in some species were also explored. 4. All animals except the dog and cat converted zoniporide to 2-oxozoniporide (M1). 5. Michael-Menten kinetic studies were conducted in species that turned over zoniporide to M1. 6. Marked differences in KM, Vmax and Clint were observed in the oxidation of zoniporide. 7. Although the KM and Vmax of zoniporide oxidation in male and female human S9 was similar, some gender difference was observed in animals especially, in Vmax. 8. The domestic animals also showed marked species differences in the AO activity and affinity toward zoniporide.