pubmed-article:11312679 | rdf:type | pubmed:Citation | lld:pubmed |
pubmed-article:11312679 | lifeskim:mentions | umls-concept:C0007996 | lld:lifeskim |
pubmed-article:11312679 | lifeskim:mentions | umls-concept:C0301869 | lld:lifeskim |
pubmed-article:11312679 | pubmed:issue | 2 | lld:pubmed |
pubmed-article:11312679 | pubmed:dateCreated | 2001-4-23 | lld:pubmed |
pubmed-article:11312679 | pubmed:abstractText | Commercially-available sulforhodamine sulfonyl chlorides contain two isomeric monosulfonyl chlorides. Conjugates of these isomers with amines have different properties because the sulfonamide formed from one isomer can undergo ring-closure to a colorless sultam. This chemistry has been examined for a model conjugate with methylamine and for a bioconjugate with 2'(3')-O-[N-(2-aminoethyl)carbamoyl]ATP. The interaction of each isomer of the latter conjugates with myosin subfragment 1 has been characterized. Significant differences between the two isomers are observed in these interactions. | lld:pubmed |
pubmed-article:11312679 | pubmed:language | eng | lld:pubmed |
pubmed-article:11312679 | pubmed:journal | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11312679 | pubmed:citationSubset | IM | lld:pubmed |
pubmed-article:11312679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11312679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11312679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11312679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11312679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11312679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11312679 | pubmed:chemical | http://linkedlifedata.com/r... | lld:pubmed |
pubmed-article:11312679 | pubmed:status | MEDLINE | lld:pubmed |
pubmed-article:11312679 | pubmed:issn | 1043-1802 | lld:pubmed |
pubmed-article:11312679 | pubmed:author | pubmed-author:EcclestonJ... | lld:pubmed |
pubmed-article:11312679 | pubmed:author | pubmed-author:CorrieJ EJE | lld:pubmed |
pubmed-article:11312679 | pubmed:author | pubmed-author:DavisC TCT | lld:pubmed |
pubmed-article:11312679 | pubmed:issnType | Print | lld:pubmed |
pubmed-article:11312679 | pubmed:volume | 12 | lld:pubmed |
pubmed-article:11312679 | pubmed:owner | NLM | lld:pubmed |
pubmed-article:11312679 | pubmed:authorsComplete | Y | lld:pubmed |
pubmed-article:11312679 | pubmed:pagination | 186-94 | lld:pubmed |
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pubmed-article:11312679 | pubmed:articleTitle | Chemistry of sulforhodamine--amine conjugates. | lld:pubmed |
pubmed-article:11312679 | pubmed:affiliation | National Institute for Medical Research, The Ridgeway, Mill Hill, London NW7 1AA, UK. jcorrie@nimr.mrc.ac.uk | lld:pubmed |
pubmed-article:11312679 | pubmed:publicationType | Journal Article | lld:pubmed |