메뉴 건너뛰기




Volumn 48, Issue 15, 2007, Pages 2683-2686

Synthesis of an azacrown template for phosphatidylinositol-4,5-bis(phosphate) recognition

Author keywords

[No Author keywords available]

Indexed keywords

HETEROCYCLIC COMPOUND; MACROCYCLIC COMPOUND; METACYCLOPHANE DERIVATIVE; PHOSPHATIDYLINOSITOL 4,5 BISPHOSPHATE;

EID: 33947186787     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2007.02.073     Document Type: Article
Times cited : (7)

References (39)
  • 16
    • 0029121937 scopus 로고
    • Preliminary molecular modeling studies (Spartan: molecular mechanics/MMFF) indicate H-1 and H-3 can adopt a position atop the aromatic ring as depicted in Figure 1. Such an interaction has precedence in nature, where the PI-specific phospholipase from B. cereus places a tyrosine ring directly beneath the three axial hydrogens of inositol:
    • Preliminary molecular modeling studies (Spartan: molecular mechanics/MMFF) indicate H-1 and H-3 can adopt a position atop the aromatic ring as depicted in Figure 1. Such an interaction has precedence in nature, where the PI-specific phospholipase from B. cereus places a tyrosine ring directly beneath the three axial hydrogens of inositol:. Heinz D.W., Ryan M., Bullock T.L., and Griffith O.H. EMBO J. 14 (1995) 3855
    • (1995) EMBO J. , vol.14 , pp. 3855
    • Heinz, D.W.1    Ryan, M.2    Bullock, T.L.3    Griffith, O.H.4
  • 30
    • 4243140363 scopus 로고    scopus 로고
    • For example a bis(guanidine)boronate receptor for citrate has improved binding affinity for citrate over a corresponding tris(guanidine). See:
    • For example a bis(guanidine)boronate receptor for citrate has improved binding affinity for citrate over a corresponding tris(guanidine). See:. Wiskur S.L., Lavigne J.J., Metzger A., Tobey S.L., and Anslyn E.V. Chem. Eur. J. 10 (2004) 3792
    • (2004) Chem. Eur. J. , vol.10 , pp. 3792
    • Wiskur, S.L.1    Lavigne, J.J.2    Metzger, A.3    Tobey, S.L.4    Anslyn, E.V.5
  • 33
    • 33947163346 scopus 로고    scopus 로고
    • +, calculated: 910.2, found: 910.3.
  • 39
    • 33947179916 scopus 로고    scopus 로고
    • 6) δ 7.69 (s, 1H), 7.37-07.11 (m, 3H), 3.92 (s, 4H), 2.71 (m, 8H), 2.65 (s, 4H).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.