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Volumn , Issue 5, 2000, Pages 695-699

Rationally designed bicyclic lactams control different turn motifs and folding patterns in hexapeptide mimics

Author keywords

Peptides; Reverse turn mimics; Hairpins; Turns; Turns

Indexed keywords

HEXAPEPTIDE; LACTAM DERIVATIVE;

EID: 0034005654     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/(SICI)1099-0690(200003)2000:5<695::AID-EJOC695>3.0.CO;2-V     Document Type: Article
Times cited : (24)

References (45)
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    • [2a] A. Giannis, T. Kolter, Angew. Chem. 1993, 105, 1303-1326; Angew. Chem. Int. Ed. Engl. 1993, 32, 1244-1267. -
    • (1993) Angew. Chem. , vol.105 , pp. 1303-1326
    • Giannis, A.1    Kolter, T.2
  • 4
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    • [2a] A. Giannis, T. Kolter, Angew. Chem. 1993, 105, 1303-1326; Angew. Chem. Int. Ed. Engl. 1993, 32, 1244-1267. -
    • (1993) Angew. Chem. Int. Ed. Engl. , vol.32 , pp. 1244-1267
  • 30
    • 0343658656 scopus 로고    scopus 로고
    • note
    • 1H-NMR spectra for determining temperature coefficients were obtained at 240-300 K with increments of 10 K. Complete proton resonance assignments were made with the aid of COSY experiments.
  • 31
    • 0343658655 scopus 로고    scopus 로고
    • note
    • [11]
  • 41
    • 0343222998 scopus 로고    scopus 로고
    • [3b,3e])
    • [3b,3e]).
  • 42
    • 0342788416 scopus 로고    scopus 로고
    • [11], it was assumed that a hydrogen bond is formed when the distance between the hydrqgen of the donor and the acceptor is smaller than 2.5 A (NH⋯O distance), the N-H⋯O bond angle is greater than 120°, and the H C=O angle is greater than 90°
    • [11], it was assumed that a hydrogen bond is formed when the distance between the hydrqgen of the donor and the acceptor is smaller than 2.5 A (NH⋯O distance), the N-H⋯O bond angle is greater than 120°, and the H C=O angle is greater than 90°.
  • 44
    • 0342788418 scopus 로고    scopus 로고
    • [16])
    • [16]).
  • 45
    • 0342353512 scopus 로고    scopus 로고
    • It should be noted that calculations tend to overestimate the relative stability of γ-turn conformations relative to other turn types
    • It should be noted that calculations tend to overestimate the relative stability of γ-turn conformations relative to other turn types.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.