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rdf:type |
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lifeskim:mentions |
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pubmed:issue |
5
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pubmed:dateCreated |
1999-1-14
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pubmed:abstractText |
Modifications of 4,4' residues of Biphalin have resulted in greater binding selectivity and biological potency for the mu opioid receptor. A higher partition coefficient across the phospholipid bilayer membrane has been achieved by using a beta-branched unusual amino acids.
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pubmed:grant |
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pubmed:language |
eng
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pubmed:journal |
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pubmed:citationSubset |
IM
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pubmed:chemical |
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pubmed:status |
MEDLINE
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pubmed:month |
Mar
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pubmed:issn |
0960-894X
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pubmed:author |
pubmed-author:DavisPP,
pubmed-author:DavisT PTP,
pubmed-author:De LeonI AIA,
pubmed-author:GOHK OKO,
pubmed-author:GillespieT JTJ,
pubmed-author:HaoYY,
pubmed-author:HrubyV JVJ,
pubmed-author:HughesRR,
pubmed-author:LipkowskiA WAW,
pubmed-author:LogB ABA,
pubmed-author:MisickaAA,
pubmed-author:O'BrienD FDF,
pubmed-author:PorrecaFF,
pubmed-author:RomanowskaEE,
pubmed-author:XiangLL,
pubmed-author:YamamuraH IHI,
pubmed-author:ZiaMM
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pubmed:issnType |
Print
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pubmed:day |
3
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pubmed:volume |
8
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
555-60
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pubmed:dateRevised |
2007-11-14
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pubmed:meshHeading |
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pubmed:year |
1998
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pubmed:articleTitle |
Modifications of the 4,4'-residues and SAR studies of Biphalin, a highly potent opioid receptor active peptide.
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pubmed:affiliation |
Department of Chemistry, University of Arizona, Tucson 85721, USA.
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pubmed:publicationType |
Journal Article,
In Vitro,
Research Support, U.S. Gov't, P.H.S.,
Research Support, Non-U.S. Gov't
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