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Volumn 56, Issue 26, 2000, Pages 4427-4435

A novel synthesis of oligonucleotide-peptide conjugates with a base- labile phosphate linker between the two components according to the allyl- protected phosphoramidite strategy

Author keywords

Nucleic acid analogs; Peptide analogs; Phosphoramidites; Solid phase synthesis

Indexed keywords

OLIGONUCLEOTIDE; PEPTIDE;

EID: 0034705563     PISSN: 00404020     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4020(00)00376-8     Document Type: Article
Times cited : (23)

References (34)
  • 21
    • 85037964167 scopus 로고    scopus 로고
    • note
    • Conjugates of type A might be more attractive as chemotherapeutical substances than conjugates of type B, because the digestion produces only biological substances including nucleosides, nucleotides, amino acids, and peptides in the former conjugates, but produces the undesired, non-biological linker or its fragments in the latter conjugates.
  • 34
    • 85037962024 scopus 로고    scopus 로고
    • note
    • Structures of degradation products resulting from the peptide components were not determined.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.