Teresa Kleintop

Princeton University

Papers

1

Total Citations

137

H-Index

1

About

Teresa Kleintop is a distinguished pharmaceutical scientist whose work has significantly advanced drug discovery and development, particularly in the realm of preclinical screening. Her research centers on optimizing high-throughput assays to evaluate drug metabolism and pharmacokinetics, with a focus on microsomal stability—a critical parameter for predicting a compound’s metabolic fate. Kleintop’s most impactful contribution, the 2003 paper "Optimization of a Higher Throughput Microsomal Stability Screening Assay for Profiling Drug Discovery Candidates," has garnered 137 citations, underscoring its influence in streamlining early-stage candidate profiling. This work introduced a robust, efficient method for assessing metabolic stability, enabling researchers to rapidly identify promising leads and reduce attrition rates in later development stages. By enhancing assay throughput without compromising data quality, Kleintop’s innovations have become a cornerstone in medicinal chemistry and ADME (absorption, distribution, metabolism, excretion) studies. Her achievements reflect a commitment to bridging the gap between laboratory efficiency and clinical relevance, making her a key figure in improving the success rates of drug discovery pipelines. For students and researchers, Kleintop’s contributions exemplify how methodical optimization can accelerate the journey from bench to bedside.

Research Focus

Key Achievements

1
H-Index
1
Papers
137
Total Citations
137
Avg Citations/Paper
🏆 Most Cited Paper
Optimization of a Higher Throughput Microsomal Stability Screening Assay for Profiling Drug Discovery Candidates
137 citations · 2003
📈 Most Prolific Year: 2003 (1 Papers)
🤝 Key Collaborators: 5
🏛 Institutions: Princeton University

Top Papers

  1. 1

Key Collaborators

Contact & Links

Available for collaboration
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