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Volumn 69, Issue 24, 2004, Pages 8394-8402

Solid-phase synthesis of arginine-containing peptides and fluorogenic substrates using a side-chain anchoring approach

Author keywords

[No Author keywords available]

Indexed keywords

AMMONIUM COMPOUNDS; ENZYMES; SUBSTITUTION REACTIONS; SULFUR COMPOUNDS; SYNTHESIS (CHEMICAL); UREA;

EID: 9344265209     PISSN: 00223263     EISSN: None     Source Type: Journal    
DOI: 10.1021/jo048792t     Document Type: Article
Times cited : (14)

References (84)
  • 46
    • 9344249898 scopus 로고    scopus 로고
    • note
    • 2, derived from the substrate of Pfgp76, a Plasmodium falciparum protease. See ref 31.
  • 49
    • 9344248790 scopus 로고    scopus 로고
    • note
    • R(C) = 14.02 min. See conditions and chromatograms in the Supporting Information).
  • 62
    • 9344222583 scopus 로고    scopus 로고
    • note
    • The commercial substrates are blocked at their N-terminus by a protecting group (Boc, Z, or benzoyl). For convenience, we replaced it with an acetyl group.
  • 70
    • 0035804501 scopus 로고    scopus 로고
    • Among others, a convenient method of Met(O) reduction effected during resin cleavage was reported by: Taboada, L.; Nicolas, E.; Giralt, E. Tetrahedron Lett. 2001, 42, 1891-1893.
    • (2001) Tetrahedron Lett. , vol.42 , pp. 1891-1893
    • Taboada, L.1    Nicolas, E.2    Giralt, E.3
  • 78
    • 0030773013 scopus 로고    scopus 로고
    • For instance, dipeptides containing arginine or thiocitrulline analogues were shown to be selective for one of the three NOS isoforms. See: (a) Silverman, R. B.; Huang, H.; Marietta, M. A.; Martasek, P. J. Med. Chem. 1997, 40, 2813-2817.
    • (1997) J. Med. Chem. , vol.40 , pp. 2813-2817
    • Silverman, R.B.1    Huang, H.2    Marietta, M.A.3    Martasek, P.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.