Structure-based virtual screening of chemical libraries for drug discovery
S Ghosh, A Nie, J An, Z Huang - Current opinion in chemical biology, 2006 - Elsevier
One of the main goals in drug discovery is to identify new chemical entities that have a high
likelihood of binding to the target protein to elicit the desired biological response. To this …
likelihood of binding to the target protein to elicit the desired biological response. To this …
[引用][C] Structure-based virtual screening of chemical libraries for drug discovery
S GHOSH, A NIE, J AN, Z HUANG - Current Opinion in Chemical Biology, 2006 - cir.nii.ac.jp
Structure-based virtual screening of chemical libraries for drug discovery | CiNii Research
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CiNii 国立情報学研究所 学術情報ナビゲータ[サイニィ] 詳細へ移動 検索フォームへ移動 論文・データを …
Structure-based virtual screening of chemical libraries for drug discovery
S Ghosh, A Nie, J An, Z Huang - Current Opinion in Chemical Biology, 2006 - infona.pl
One of the main goals in drug discovery is to identify new chemical entities that have a high
likelihood of binding to the target protein to elicit the desired biological response. To this …
likelihood of binding to the target protein to elicit the desired biological response. To this …
Structure-based virtual screening of chemical libraries for drug discovery
S Ghosh, A Nie, J An, Z Huang - Current opinion in …, 2006 - pubmed.ncbi.nlm.nih.gov
One of the main goals in drug discovery is to identify new chemical entities that have a high
likelihood of binding to the target protein to elicit the desired biological response. To this …
likelihood of binding to the target protein to elicit the desired biological response. To this …
[PDF][PDF] Structure-based virtual screening of chemical libraries for drug discovery
S Ghosh, A Nie, J An, Z Huang - Current Opinion in Chemical Biology, 2006 - academia.edu
Introduction The identification of a proper lead compound for a given molecular target is a
critical step in the process of drug discovery. Traditionally high-throughput screening (HTS) …
critical step in the process of drug discovery. Traditionally high-throughput screening (HTS) …
Structure-based virtual screening of chemical libraries for drug discovery.
S Ghosh, A Nie, J An, Z Huang - Current Opinion in Chemical …, 2006 - europepmc.org
One of the main goals in drug discovery is to identify new chemical entities that have a high
likelihood of binding to the target protein to elicit the desired biological response. To this …
likelihood of binding to the target protein to elicit the desired biological response. To this …