| pubmed-article:9871521 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0023544 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0268563 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0220781 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0034423 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0231491 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0456387 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0679622 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0205314 | lld:lifeskim |
| pubmed-article:9871521 | lifeskim:mentions | umls-concept:C0205352 | lld:lifeskim |
| pubmed-article:9871521 | pubmed:issue | 8 | lld:pubmed |
| pubmed-article:9871521 | pubmed:dateCreated | 1999-1-26 | lld:pubmed |
| pubmed-article:9871521 | pubmed:abstractText | The two geminal ethyl groups in the succinic acid moiety of CGP57698 (4-[3-(7-fluoro-2-quinolinyl-methoxy)phenyl-amino]-2,2-diethyl-4-oxo- butanoic acid) are responsible for the high in vitro and in vivo potency of this peptidoleukotriene antagonist of the quinoline type. The synthesis and structure activity relationships of CGP57698 and its analogs are described. | lld:pubmed |
| pubmed-article:9871521 | pubmed:language | eng | lld:pubmed |
| pubmed-article:9871521 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9871521 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:9871521 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9871521 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9871521 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9871521 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9871521 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9871521 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9871521 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:9871521 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:9871521 | pubmed:month | Apr | lld:pubmed |
| pubmed-article:9871521 | pubmed:issn | 0960-894X | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:BrayM AMA | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:SubramanianNN | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:NiederhauserU... | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:BeckAA | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:AndersonG PGP | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:KimmelSS | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:von... | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:GerspacherMM | lld:pubmed |
| pubmed-article:9871521 | pubmed:author | pubmed-author:WiestnerHH | lld:pubmed |
| pubmed-article:9871521 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:9871521 | pubmed:day | 21 | lld:pubmed |
| pubmed-article:9871521 | pubmed:volume | 8 | lld:pubmed |
| pubmed-article:9871521 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:9871521 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:9871521 | pubmed:pagination | 965-70 | lld:pubmed |
| pubmed-article:9871521 | pubmed:dateRevised | 2003-11-14 | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:meshHeading | pubmed-meshheading:9871521-... | lld:pubmed |
| pubmed-article:9871521 | pubmed:year | 1998 | lld:pubmed |
| pubmed-article:9871521 | pubmed:articleTitle | Synthesis and SAR of a novel, potent and structurally simple LTD4 antagonist of the quinoline class. | lld:pubmed |
| pubmed-article:9871521 | pubmed:affiliation | Research Department, Novartis Pharma AG, Basel, Switzerland. andreas.von_sprecher@pharma.novartis.com | lld:pubmed |
| pubmed-article:9871521 | pubmed:publicationType | Journal Article | lld:pubmed |
| http://linkedlifedata.com/r... | http://linkedlifedata.com/r... | pubmed-article:9871521 | lld:chembl |
