4-(2-Aminooxyethoxy)-2-(ethylureido)quinoline-oligonucleotide conjugates: Synthesis, binding interactions, and derivatization with peptides

Bioconjugate Chemistry

Volumn 14, Issue 2, 2003, Pages 320-330

  Hamma, Tomoko ^a,b   Miller, Paul S ^a  

^a JOHNS HOPKINS BLOOMBERG SCHOOL OF PUBLIC HEALTH   (United States)

^b USA   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

ALDEHYDES; AMINO ACIDS; BINDING ENERGY; DISSOCIATION; ELECTROPHORESIS; KETONES; OLIGOMERS; OLIGONUCLEOTIDES; RNA;

AMINOOXY GROUPS; BINDING AFFINITIES; BINDING INTERACTION; C-TERMINUS; CONJUGATED OLIGOMER; CONTROLLED PORE GLASS; DERIVATIZATIONS; OLIGONUCLEOTIDE CONJUGATES; PHOSPHORAMIDITES; QUINOLINE RINGS;

PEPTIDES;

4 (2 AMINOOXYETHOXY) 2 (ETHYLUREIDO)QUINOLINE OLIGO 2' O METHYLRIBONUCLEOTIDE CONJUGATE; 4 ETHOXY 2 (ETHYLUREIDO)QUINOLINE OLIGO 2' O METHYLRIBONUCLEOTIDE CONJUGATE; ACETONE; ALDEHYDE; COMPLEMENTARY RNA; CYSTEINE; FUNCTIONAL GROUP; GLASS; KETONE; LEUPEPTIN; OLIGOMER; OLIGONUCLEOTIDE; OXIME DERIVATIVE; PEPTIDE DERIVATIVE; QUINOLINE DERIVATIVE; TRANSACTIVATOR PROTEIN; UNCLASSIFIED DRUG; VIRUS RNA;

ARTICLE; BINDING AFFINITY; COMPLEX FORMATION; CONCENTRATION (PARAMETERS); CONJUGATE; DEPROTECTION REACTION; DERIVATIZATION; DISSOCIATION CONSTANT; HUMAN IMMUNODEFICIENCY VIRUS; MOLECULAR STABILITY; NUCLEIC ACID SYNTHESIS;

HUMAN IMMUNODEFICIENCY VIRUS; RNA VIRUSES;

EID: 0037347154     PISSN: 10431802     EISSN: None     Source Type: Journal    
DOI: 10.1021/bc025638+     Document Type: Article

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