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Journal of the American Chemical Society

Volumn 124, Issue 13, 2002, Pages 3254-3262

Substituted 1,8-naphthyridin-2(1H)-ones are superior to thymine in the recognition of adenine in duplex as well as triplex structures

(4) Eldrup, Anne B a,b Christensen, Caspar a Haaima, Gerald a,c Nielsen, Peter E a,d

a UNIVERSITY OF COPENHAGEN (Denmark)

b ISIS PHARMACEUTICALS (United States)

c CISRO (Australia)

d UNIVERSITY OF COPENHAGEN (Denmark)

Author keywords

[No Author keywords available]

Indexed keywords

RECOGNITION SYSTEMS;

BIOSYNTHESIS; DNA; ENTHALPY; THERMODYNAMIC STABILITY;

NUCLEIC ACID SEQUENCES;

1,8 NAPHTHYRIDIN 2(1H) ONE DERIVATIVE; 7 CHLORO 1,8 NAPHTHYRIDIN 2(1H) ONE; ADENINE; OLIGONUCLEOTIDE; PEPTIDE NUCLEIC ACID; THYMINE DERIVATIVE; UNCLASSIFIED DRUG;

ARTICLE; BASE PAIRING; BINDING AFFINITY; COMPLEX FORMATION; DRUG DESIGN; DRUG DNA BINDING; DRUG DNA INTERACTION; DRUG STABILITY; DRUG STRUCTURE; DRUG SYNTHESIS; ENTHALPY; TEMPERATURE DEPENDENCE; THERMOSTABILITY;

ADENINE; BASE PAIRING; DNA; NAPHTHYRIDINES; NUCLEIC ACID CONFORMATION; PEPTIDE NUCLEIC ACIDS; RNA; THERMODYNAMICS; THYMINE;

EID: 0037012360 PISSN: 00027863 EISSN: None Source Type: Journal
DOI: 10.1021/ja0117027 Document Type: Article

Times cited : (46)

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