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Volumn , Issue 6, 2008, Pages 706-708

Chimeric (α-amino acid + nucleoside-β-amino acid)n peptide oligomers show sequence specific DNA/RNA recognition

Author keywords

[No Author keywords available]

Indexed keywords

ALPHA AMINO ACID; BETA AMINO ACID; METHIONINE; NUCLEOSIDE DERIVATIVE; OLIGOMER; OLIGONUCLEOTIDE; PROLINE; SARCOSINE; THYMIDINE;

EID: 38649140147     PISSN: 13597345     EISSN: None     Source Type: Journal    
DOI: 10.1039/b716835g     Document Type: Article
Times cited : (30)

References (45)
  • 39
    • 0026527978 scopus 로고
    • Stereoelectronically benign β-alanine was used as a spacer from the support during the synthesis of sequences 12, 13, and 15 for exerting a uniform steric effect at the C-terminus where amino acids were uncharged. In sequence 14, positively charged l-lysine was preferred at the C-terminus because l-lysine at the C-terminus of peptide nucleic acids is known to have stabilizing effects on complexes with DNA and RNA due to electronic contributions (see reference 4)
    • A. K. Singh R. S. Varma Tetrahedron Lett. 1992 33 2307 2310
    • (1992) Tetrahedron Lett. , vol.33 , pp. 2307-2310
    • Singh, A.K.1    Varma, R.S.2
  • 41
    • 0003546549 scopus 로고    scopus 로고
    • N. Berova, K. Nakanishi and R. W. Woody, Wiley-VCH, New York, pp. 703-736
    • Circular Dichroism: Principles and Applications, ed., N. Berova,,, K. Nakanishi, and, R. W. Woody,, Wiley-VCH, New York, pp. 703-736
    • Circular Dichroism: Principles and Applications, Ed.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.