| pubmed-article:6553561 | rdf:type | pubmed:Citation | lld:pubmed |
| pubmed-article:6553561 | lifeskim:mentions | umls-concept:C0009546 | lld:lifeskim |
| pubmed-article:6553561 | lifeskim:mentions | umls-concept:C1999216 | lld:lifeskim |
| pubmed-article:6553561 | lifeskim:mentions | umls-concept:C1883254 | lld:lifeskim |
| pubmed-article:6553561 | pubmed:issue | 4 | lld:pubmed |
| pubmed-article:6553561 | pubmed:dateCreated | 1983-9-20 | lld:pubmed |
| pubmed-article:6553561 | pubmed:abstractText | The inhibitory effects of 6-amidino-2-naphthyl 4-guanidinobenzoate (FUT-175) on the activities of factor B, factor D and cobra venom factor (CVF) X Bb were examined. FUT-175 bound specifically to the Bb fragment of factor B or CVF X Bb. FUT-175 was a non-competitive inhibitor of the esterolysis of L-leucyl-L-alanyl-L-arginine naphthylester by factor B and CVF X Bb. FUT-175 also inhibited the haemolytic activity of factor B, the C3 convertase activity of CVF X Bb and the factor B-cleaving activity of factor D. The concentration of FUT-175 causing 50% inhibition of these activities was 10(-5) - 10(-4)M. | lld:pubmed |
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| pubmed-article:6553561 | pubmed:language | eng | lld:pubmed |
| pubmed-article:6553561 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
| pubmed-article:6553561 | pubmed:citationSubset | IM | lld:pubmed |
| pubmed-article:6553561 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:6553561 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:6553561 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
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| pubmed-article:6553561 | pubmed:status | MEDLINE | lld:pubmed |
| pubmed-article:6553561 | pubmed:month | Aug | lld:pubmed |
| pubmed-article:6553561 | pubmed:issn | 0019-2805 | lld:pubmed |
| pubmed-article:6553561 | pubmed:author | pubmed-author:FujiiSS | lld:pubmed |
| pubmed-article:6553561 | pubmed:author | pubmed-author:SakaiYY | lld:pubmed |
| pubmed-article:6553561 | pubmed:author | pubmed-author:IkariNN | lld:pubmed |
| pubmed-article:6553561 | pubmed:author | pubmed-author:HitomiYY | lld:pubmed |
| pubmed-article:6553561 | pubmed:issnType | Print | lld:pubmed |
| pubmed-article:6553561 | pubmed:volume | 49 | lld:pubmed |
| pubmed-article:6553561 | pubmed:owner | NLM | lld:pubmed |
| pubmed-article:6553561 | pubmed:authorsComplete | Y | lld:pubmed |
| pubmed-article:6553561 | pubmed:pagination | 685-91 | lld:pubmed |
| pubmed-article:6553561 | pubmed:dateRevised | 2009-11-18 | lld:pubmed |
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| pubmed-article:6553561 | pubmed:year | 1983 | lld:pubmed |
| pubmed-article:6553561 | pubmed:articleTitle | New synthetic inhibitor to the alternative complement pathway. | lld:pubmed |
| pubmed-article:6553561 | pubmed:publicationType | Journal Article | lld:pubmed |
| pubmed-article:6553561 | pubmed:publicationType | In Vitro | lld:pubmed |
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