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Volumn 131, Issue 45, 2009, Pages 16555-16567

New strategies for the design of folded peptoids revealed by a survey of noncovalent interactions in model systems

Author keywords

[No Author keywords available]

Indexed keywords

BACKBONE INTERACTIONS; CHEMICAL FUNCTIONALITY; DESIGN TOOL; FULLY COMPATIBLE; HYDROGEN BONDING INTERACTIONS; MODEL SYSTEM; MODULAR DESIGNS; NEW STRATEGY; NON-COVALENT INTERACTION; PEPTOIDS; ROTAMERS; SIDE CHAINS; SYNTHESIS TECHNIQUES;

EID: 70450177277     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja907184g     Document Type: Article
Times cited : (175)

References (67)
  • 35
    • 0004757060 scopus 로고    scopus 로고
    • v. 3.110; University of California, San Francisco
    • Goddard, T. D., Kneller, D. G. SPARKY, v. 3.110; University of California, San Francisco.
    • SPARKY
    • Goddard, T.D.1    Kneller, D.G.2
  • 66
    • 70450142386 scopus 로고    scopus 로고
    • note
    • We note that the ammonium groups at the N-termini of the analogous, unacylated peptoids (see ref 37) would also be expected to form strong hydrogen bonds that could account for the similar overall Kcis/trans values observed for these systems.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.