reference/984018

http://rdf.ncbi.nlm.nih.gov/pubchem/reference/984018

Outgoing Links

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endingPage	136
issn	1520-4812 1043-1802
issueIdentifier	1
pageRange	128-136
publicationName	Bioconjugate Chemistry
startingPage	128
bibliographicCitation	Stephenson KA, Zubieta J, Banerjee SR, Levadala MK, Taggart L, Ryan L, McFarlane N, Boreham DR, Maresca KP, Babich JW, Valliant JF. A New Strategy for the Preparation of Peptide-Targeted Radiopharmaceuticals Based on an Fmoc-Lysine-Derived Single Amino Acid Chelate (SAAC). Automated Solid-Phase Synthesis, NMR Characterization, and in Vitro Screening of fMLF(SAAC)G and fMLF[(SAAC−Re(CO)₃)⁺]G. Bioconjugate Chem. 2003 Nov 22;15(1):128–36. doi: 10.1021/bc034128s.
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date	2003-11-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
identifier	https://pubmed.ncbi.nlm.nih.gov/14733592 https://doi.org/10.1021/bc034128s
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language	English
source	https://pubmed.ncbi.nlm.nih.gov/ https://www.crossref.org/
title	A New Strategy for the Preparation of Peptide-Targeted Radiopharmaceuticals Based on an Fmoc-Lysine-Derived Single Amino Acid Chelate (SAAC). Automated Solid-Phase Synthesis, NMR Characterization, and in Vitro Screening of fMLF(SAAC)G and fMLF[(SAAC−Re(CO)3)+]G
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Total number of triples: 62.