Drug Candidate Optimization
Drug Candidate Optimization is a systematic medicinal chemistry and pharmacokinetic refinement process that distinguishes itself by enhancing the metabolic stability, bioavailability, and safety profile of investigational compounds through iterative structural modification and in vitro microsomal stability assessment.
668
Publications
33.6K
Citations
6.6K
Authors
1.1K
Institutions
Publications per year
2017–2026
337
Parents
668
Travis T. Wager, Xinjun Hou, Patrick R. Verhoest et al. · ACS Chemical Neuroscience · 2010 · 1K citations
Lipophilicity in drug discovery
Michael J. Waring · Expert Opinion on Drug Discovery · 2010 · 844 citations
Synthesis and Antibacterial Evaluation of Certain Quinolone Derivatives
Yeh‐Long Chen, Kuo‐Chang Fang, Shu‐Lin Hsu et al. · Journal of Medicinal Chemistry · 2001 · 550 citations
1–5 of 668
6.6K
7
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6
h-index
5
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4
h-index
1–5 of 6.6K
1.1K
Pfizer (United States)
New York, United States
22 h-index
378 publications
31.9K citations
Bristol-Myers Squibb (United States)
New York, United States
15 h-index
198 publications
15.5K citations

Chinese Academy of Sciences
Beijing, China
15 h-index
86 publications
3.1K citations
AstraZeneca (United Kingdom)
Cambridge, United Kingdom
13 h-index
127 publications
7.2K citations

China Pharmaceutical University
Nanjing, China
11 h-index
82 publications
2.4K citations
Amgen (United States)
Thousand Oaks, United States
11 h-index
125 publications
5.3K citations
Merck & Co., Inc., Rahway, NJ, USA (United States)
Rahway, United States
10 h-index
187 publications
7.3K citations
AstraZeneca (Sweden)
Södertälje, Sweden
10 h-index
103 publications
6.3K citations
1–8 of 1.1K
180 publications · 10.8K citations
61
h-index
27 publications · 1.3K citations
19
h-index
16 publications · 317 citations
12
h-index
15 publications · 400 citations
12
h-index
12 publications · 359 citations
11
h-index
1–5