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Volumn 74, Issue 3, 2009, Pages 1070-1081

Functionalized 2̀-amino-α-L-LNA: Directed positioning of intercalators for DNA targeting

Author keywords

[No Author keywords available]

Indexed keywords

[CARBONYL; AMINO ALCOHOLS; BIOPHYSICAL CHARACTERIZATIONS; BUILDING BLOCKS; CHEMICALLY MODIFIED; CHEMO-SELECTIVE; CIRCULAR DICHROISM SIGNALS; DETRIMENTAL EFFECTS; DIAGNOSTIC APPLICATIONS; DIASTEREOMER; DNA TARGETS; DUPLEX FORMATIONS; ENTROPIC CONTRIBUTIONS; ENZYMATIC STABILITIES; FUNCTIONALIZATION; FUNCTIONALIZED; INTERCALATORS; LOCKED NUCLEIC ACIDS; MOLECULAR MODELING STUDIES; PHOSPHITYLATION; PHOSPHORAMIDITES; POSITIONAL CONTROLS; PRECISE POSITIONING; PYRENE ABSORPTIONS;

EID: 60649099809     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo802037v     Document Type: Article
Times cited : (42)

References (99)
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    • We define LNA, a-L-LNA, 2́-amino-LNA, and 2́-amino-α-L- LNA as a oligonucleotide containing one or more 2́-O,4́-C-methylene- β-D-ribofuranosyl monomer(s), 2́-O,4́-C- methylene-α-L-ribofuranosyl monomer(s), 2́-amino-2́-deoxy- 2́-N,4́-C-methylene-β-D-ribofuranosyl monomer(s), or 2́-amino-2́-deoxy-2́-A,4́-C-methylene-α-L- ribofuranosyl monomer(s), respectively. Similar definitions are used for N2́-functionalized α-L-LNA derivatives.
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    • The following definitions of torsion angles are used: χ (O4′-C1′-N1-C2 or O4′-C1′-N9-C4 for pyrimidines or purines, respectively, The pseu-dorotation phase angle P is given as tan P, v4, v1-v3, v 0, 2v2(sin 36°, sin 72°, where V0 (C4′-O4′-C1′-C2′, V 1 (O4′-C1′-C2′-C3′, V2 (C1′-C2′-C3′-C4′, v3 (C2′-C3′-C4′-O4′, and v4 C3′-C4′-O4′-C1′, For further information see: Saenger, W. Principles of Nucleic Acid Structure; Springer-Verlag: Berlin, 1984
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    • The integral of the H1′ signal of the least predominant rotamer (termed B) is set to 1.0.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.