pubmed-article:17490879 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C0034242 | lld:lifeskim |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C0201734 | lld:lifeskim |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C1260969 | lld:lifeskim |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C0243077 | lld:lifeskim |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C1706204 | lld:lifeskim |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C1555721 | lld:lifeskim |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C0439611 | lld:lifeskim |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C0231449 | lld:lifeskim |
pubmed-article:17490879 | lifeskim:mentions | umls-concept:C0216510 | lld:lifeskim |
pubmed-article:17490879 | pubmed:issue | 13 | lld:pubmed |
pubmed-article:17490879 | pubmed:dateCreated | 2007-6-18 | lld:pubmed |
pubmed-article:17490879 | pubmed:abstractText | A study on substitutions at the four open positions on the phenyl ring of the 1,4-dihydroindeno[1,2-c]pyrazoles as potent CHK-1 inhibitors is described. Bis-substitution at both the 6- and 7-positions led to inhibitors with IC(50) values below 0.3nM. The compound with the best overall activities (36) was able to potentiate the anti-proliferative effect of doxorubicin in HeLa cells by at least 47-fold. Physicochemical, metabolic, and pharmacokinetic properties of selected inhibitors are also disclosed. | lld:pubmed |
pubmed-article:17490879 | pubmed:language | eng | lld:pubmed |
pubmed-article:17490879 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17490879 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:17490879 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17490879 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17490879 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17490879 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:17490879 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:17490879 | pubmed:month | Jul | lld:pubmed |
pubmed-article:17490879 | pubmed:issn | 0960-894X | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:WuJianJ | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:ClaiborneAkiy... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:KovarPeterP | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:ShamHing LHL | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:TaoZhi-FuZF | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:RosenbergSaul... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:StewartKent... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:SowinThomas... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:ZhangHaiyingH | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:ChenZehanZ | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:TongYunsongY | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:BouskaJennife... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:GuanRanR | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:MertaPhilip... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:EverittElizab... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:HickmanDeanD | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:CredoRobert... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:PyzytulinskaM... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:MurryBernard... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:StrattonTim... | lld:pubmed |
pubmed-article:17490879 | pubmed:author | pubmed-author:LinNan-horngN... | lld:pubmed |
pubmed-article:17490879 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:17490879 | pubmed:day | 1 | lld:pubmed |
pubmed-article:17490879 | pubmed:volume | 17 | lld:pubmed |
pubmed-article:17490879 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:17490879 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:17490879 | pubmed:pagination | 3618-23 | lld:pubmed |
pubmed-article:17490879 | pubmed:dateRevised | 2011-11-2 | lld:pubmed |
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pubmed-article:17490879 | pubmed:meshHeading | pubmed-meshheading:17490879... | lld:pubmed |
pubmed-article:17490879 | pubmed:year | 2007 | lld:pubmed |
pubmed-article:17490879 | pubmed:articleTitle | 1,4-Dihydroindeno[1,2-c]pyrazoles as potent checkpoint kinase 1 inhibitors: extended exploration on phenyl ring substitutions and preliminary ADME/PK studies. | lld:pubmed |
pubmed-article:17490879 | pubmed:affiliation | Cancer Research, Global Pharmaceutical R&D, R47S, AP10, Abbott Laboratories, 100 Abbott Park Road, Abbott Park, IL 60064, USA. yunsong.tong@abbott.com <yunsong.tong@abbott.com> | lld:pubmed |
pubmed-article:17490879 | pubmed:publicationType | Journal Article | lld:pubmed |
http://linkedlifedata.com/r... | http://linkedlifedata.com/r... | pubmed-article:17490879 | lld:chembl |