rdf:type |
|
lifeskim:mentions |
|
pubmed:issue |
29
|
pubmed:dateCreated |
2010-7-15
|
pubmed:abstractText |
By a stepwise synthesis strategy biofunctionalized Pyrrolopyrrole Cyanines (PPCy) with an asymmetric substitution pattern were obtained. These exhibit extremely strong and narrowband NIR absorption and fluorescence. Internalization of a peptide bound PPCy is demonstrated using live cell microscopy.
|
pubmed:language |
eng
|
pubmed:journal |
|
pubmed:citationSubset |
IM
|
pubmed:chemical |
|
pubmed:status |
MEDLINE
|
pubmed:month |
Aug
|
pubmed:issn |
1364-548X
|
pubmed:author |
|
pubmed:issnType |
Electronic
|
pubmed:day |
7
|
pubmed:volume |
46
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
5289-91
|
pubmed:meshHeading |
pubmed-meshheading:20539898-Carbocyanines,
pubmed-meshheading:20539898-Electrons,
pubmed-meshheading:20539898-Fluorescent Dyes,
pubmed-meshheading:20539898-HeLa Cells,
pubmed-meshheading:20539898-Humans,
pubmed-meshheading:20539898-Microscopy, Fluorescence,
pubmed-meshheading:20539898-Molecular Structure,
pubmed-meshheading:20539898-Pyrroles,
pubmed-meshheading:20539898-Spectroscopy, Near-Infrared,
pubmed-meshheading:20539898-Stereoisomerism
|
pubmed:year |
2010
|
pubmed:articleTitle |
Asymmetric PPCys: strongly fluorescing NIR labels.
|
pubmed:affiliation |
Fachbereich Chemie and Center of Applied Photonics, Universität Konstanz, 78457 Konstanz, Germany.
|
pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
|