2010年2月28日
創薬バリューチェインのインシリコ技術を活用した阻害剤開発の試み
日本結晶学会誌
- 巻
- 52
- 号
- 1
- 開始ページ
- 89
- 終了ページ
- 94
- 記述言語
- 日本語
- 掲載種別
- DOI
- 10.5940/jcrsj.52.89
- 出版者・発行元
- 日本結晶学会
We have recently established Pharmaceutical Innovation Value Chain collaborated by The SOSHO project (http://www.so-sho.jp) and The BioGrid Project (http://www.biogrid.jp/) to accelerate new drug development. The in-silico group calculated the matrices on the interaction between the proteins and chemical compounds, and developed the novel in-silico screening methods, Multiple Target Screening (MTS) and Docking score index (DSI), improving the hit rate of screening a lead compound.<br>We have applied these methods for the two target enzymes; human hematopoietic prostaglandin D synthase (H-PGDS) and orotidine 5’-monophosphate decarboxylase from human malaria parasite plasmodium falciparum (PfOMPDC). The optimizing of HQL-79, one of the known inhibitors for human H-PGDS and the screening of lead compounds for both enzymes are in study.
- リンク情報
- ID情報
-
- DOI : 10.5940/jcrsj.52.89
- ISSN : 0369-4585
- J-Global ID : 201002204178366251
- CiNii Articles ID : 10026107997
- CiNii Books ID : AN00188364
- identifiers.cinii_nr_id : 9000004567427