|
rdf:type |
|
|
lifeskim:mentions |
umls-concept:C0139071,
umls-concept:C0185023,
umls-concept:C0237497,
umls-concept:C0337112,
umls-concept:C0392747,
umls-concept:C0439851,
umls-concept:C0441833,
umls-concept:C0772162,
umls-concept:C1314972,
umls-concept:C1511539,
umls-concept:C1524075,
umls-concept:C1552596,
umls-concept:C1554963,
umls-concept:C1947904,
umls-concept:C1947931,
umls-concept:C1999228,
umls-concept:C2825781
|
|
pubmed:issue |
2
|
|
pubmed:dateCreated |
1989-3-22
|
|
pubmed:abstractText |
PRP-hexapeptide possessing the azo-bridge between Tyr1 and Phe5 residues, called azo-PRP-hexapeptide: (formula; see text), was synthesized and tested for immunoregulatory activity. High biological activity of the synthesized azo-PRP-hexapeptide suggests that the biologically active conformation of PRP-hexapeptide must be such that both aromatic rings (Tyr and Phe) are apparently close to each other.
|
|
pubmed:language |
eng
|
|
pubmed:journal |
|
|
pubmed:citationSubset |
IM
|
|
pubmed:chemical |
|
|
pubmed:status |
MEDLINE
|
|
pubmed:month |
Aug
|
|
pubmed:issn |
0367-8377
|
|
pubmed:author |
|
|
pubmed:issnType |
Print
|
|
pubmed:volume |
32
|
|
pubmed:owner |
NLM
|
|
pubmed:authorsComplete |
Y
|
|
pubmed:pagination |
98-103
|
|
pubmed:dateRevised |
2006-11-15
|
|
pubmed:meshHeading |
|
|
pubmed:year |
1988
|
|
pubmed:articleTitle |
Conformational modification of the PRP-hexapeptide by a direct covalent attachment of aromatic side chain groups.
|
|
pubmed:affiliation |
Institute of Chemistry, University of Wroclaw, Poland.
|
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|
