| pubmed-article:19362479 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C1175743 | lld:lifeskim |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C0033382 | lld:lifeskim |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C0220825 | lld:lifeskim |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C1527148 | lld:lifeskim |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C0243077 | lld:lifeskim |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C1707689 | lld:lifeskim |
| pubmed-article:19362479 | lifeskim:mentions | umls-concept:C0205460 | lld:lifeskim |
| pubmed-article:19362479 | pubmed:issue | 10 | lld:pubmed |
| pubmed-article:19362479 | pubmed:dateCreated | 2009-5-4 | lld:pubmed |
| pubmed-article:19362479 | pubmed:abstractText | A series of trifluoromethyl, benzothiazolyl or thiazolyl ketone-containing peptidic compounds as SARS-CoV 3CL protease inhibitors were developed and their potency was evaluated by in vitro protease inhibitory assays. Three candidates had encouraging results for the development of new anti-SARS compounds. | lld:pubmed |
| pubmed-article:19362479 | pubmed:grant | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:19362479 | pubmed:language | eng | lld:pubmed |
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| pubmed-article:19362479 | pubmed:citationSubset | IM | lld:pubmed |
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| pubmed-article:19362479 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:19362479 | pubmed:month | May | lld:pubmed |
| pubmed-article:19362479 | pubmed:issn | 1464-3405 | lld:pubmed |
| pubmed-article:19362479 | pubmed:author | pubmed-author:FreireErnesto... | lld:pubmed |
| pubmed-article:19362479 | pubmed:author | pubmed-author:KisoYoshiakiY | lld:pubmed |
| pubmed-article:19362479 | pubmed:author | pubmed-author:HayashiYoshio... | lld:pubmed |
| pubmed-article:19362479 | pubmed:author | pubmed-author:HidakaKoushiK | lld:pubmed |
| pubmed-article:19362479 | pubmed:author | pubmed-author:BachaUsmanU | lld:pubmed |
| pubmed-article:19362479 | pubmed:author | pubmed-author:SarmaDigantaD | lld:pubmed |
| pubmed-article:19362479 | pubmed:author | pubmed-author:RegnierThomas... | lld:pubmed |
| pubmed-article:19362479 | pubmed:issnType | Electronic | lld:pubmed |
| pubmed-article:19362479 | pubmed:day | 15 | lld:pubmed |
| pubmed-article:19362479 | pubmed:volume | 19 | lld:pubmed |
| pubmed-article:19362479 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:19362479 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:19362479 | pubmed:pagination | 2722-7 | lld:pubmed |
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| pubmed-article:19362479 | pubmed:meshHeading | pubmed-meshheading:19362479... | lld:pubmed |
| pubmed-article:19362479 | pubmed:year | 2009 | lld:pubmed |
| pubmed-article:19362479 | pubmed:articleTitle | New developments for the design, synthesis and biological evaluation of potent SARS-CoV 3CL(pro) inhibitors. | lld:pubmed |
| pubmed-article:19362479 | pubmed:affiliation | Department of Medicinal Chemistry, Center for Frontier Research in Medicinal Science, Kyoto Pharmaceutical University, Japan. | lld:pubmed |
| pubmed-article:19362479 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:19362479 | pubmed:publicationType | Research Support, Non-U.S. Gov't | lld:pubmed |
| pubmed-article:19362479 | pubmed:publicationType | Research Support, N.I.H., Extramural | lld:pubmed |
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| http://linkedlifedata.com/r... | http://linkedlifedata.com/r... | pubmed-article:19362479 | lld:pdb |
