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Volumn 2, Issue 3, 2004, Pages 281-283

Synthesis and bio-assay of RCM-derived Bowman-Birk inhibitor analogues

Author keywords

[No Author keywords available]

Indexed keywords

BIOASSAY; CARBON; MICROWAVES; PROTEINS; RESINS; STEREOCHEMISTRY; SULFUR COMPOUNDS; SYNTHESIS (CHEMICAL);

EID: 1342282240     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b312908j     Document Type: Article
Times cited : (25)

References (30)
  • 16
    • 1342276903 scopus 로고    scopus 로고
    • A known strategy for simpler peptides, see ref. 2h above
    • A known strategy for simpler peptides, see ref. 2h above.
  • 17
    • 1342340496 scopus 로고    scopus 로고
    • note
    • Linear peptide precursors for the RCM reaction such as 2a were fully side-chain protected using the following standard protecting groups: Ser(tBu), Thr(tBu) and Gln(Trt).
  • 18
    • 1342297975 scopus 로고    scopus 로고
    • note
    • +, 100%). ALl other RCM-derived peptides were synthesised similarly, with characterisation by FAB-MS and HPLC purity > 90%, and with olefins assumed to be a mixture of E and Z isomers (ratios not determined).
  • 24
    • 1342276902 scopus 로고    scopus 로고
    • note
    • 8
  • 26
    • 1342276904 scopus 로고    scopus 로고
    • note
    • i values quoted in Table 1 are the mean of two closely agreeing assays, except in the case of entries 1 and 7 when a single assay was performed. In the case of peptide 3a, hydrolysis assays were also performed to demonstrate the stability of the peptide under the assay conditions. Thus, peptide 3a was incubated with chymotrypsin (I : E ratio of 550 : 1) at 25°C and pH 7.8. Analytical HPLC of an aliquot after 30 min showed no detectable hydrolysis of 3a had occurred.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.