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Volumn 7, Issue 10, 1997, Pages 1311-1316

Piperidine carboxylic acid derivatives as sialyl Lewis X mimetics

Author keywords

[No Author keywords available]

Indexed keywords

CD4 ANTIGEN; ENDOTHELIAL LEUKOCYTE ADHESION MOLECULE 1; HYBRID PROTEIN; PADGEM PROTEIN; PIPERIDINE DERIVATIVE; SIALOGLYCOPROTEIN;

EID: 0031579965     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(97)00213-8     Document Type: Article
Times cited : (16)

References (41)
  • 2
    • 0025283118 scopus 로고
    • b) Osborn, L., Cell, 1990, 62, 3.
    • (1990) Cell , vol.62 , pp. 3
    • Osborn, L.1
  • 3
    • 0029056695 scopus 로고
    • and references cited therein
    • Huang H., Wong C.-H. J., Org. Chem. 60:1995;3100. and references cited therein.
    • (1995) J., Org. Chem. , vol.60 , pp. 3100
    • Huang, H.1    Wong, C.-H.2
  • 34
    • 0011229843 scopus 로고    scopus 로고
    • 1H NMR (D2O): 7A: δ = 1.05 (d, 3 H, 6-Hfuc), 1.56 (m, 2 H, CH2), 1.78 (m, 3 H, 12 CH2), 2.00 (m, 1 H, 12 CH2), 2.45 (m, 1 H, CHCOOH), 2.80 (m, 2 H, CH2), 4.50 (m, 1 H, 2-Hcyclohex), 4.87 (bs, 1 H, 1-Hfuc).
    • 1H NMR (D2O): 7A: δ = 1.05 (d, 3 H, 6-Hfuc), 1.56 (m, 2 H, CH2), 1.78 (m, 3 H, 1 1 2 CH2), 2.00 (m, 1 H, 1 2 CH2), 2.45 (m, 1 H, C H COOH), 2.80 (m, 2 H, CH2), 4.50 (m, 1 H, 2-Hcyclohex), 4.87 (bs, 1 H, 1-Hfuc).
  • 35
    • 0011205060 scopus 로고    scopus 로고
    • 1H NMR (D2O): 10: δ = 1.18-1.48 (m, 6 H, 3 CH2), 1.62 (m, 2 H, CH2), 1.72-2.03 (m, 4 H, 2 CH2), 2.28 (m, 1 H, CHCOOH), 2.83 (m, 2 H, CH2), 3.50-3.82 (m, 7 H), 3.98 (m, 2 H), 4.47 (m, 1 H, 2-Hcyclo-hex), 4.94 (d, 1 H, 1-Hman).
    • 1H NMR (D2O): 10: δ = 1.18-1.48 (m, 6 H, 3 CH2), 1.62 (m, 2 H, CH2), 1.72-2.03 (m, 4 H, 2 CH2), 2.28 (m, 1 H, C H COOH), 2.83 (m, 2 H, CH2), 3.50-3.82 (m, 7 H), 3.98 (m, 2 H), 4.47 (m, 1 H, 2-Hcyclo-hex), 4.94 (d, 1 H, 1-Hman).
  • 36
    • 0011254964 scopus 로고    scopus 로고
    • 1H NMR (D2O): 13: δ = 1.10-1.50 (m, 6 H, 3 CH2), 1.63 (m, 2 H, CH2), 1.71-1.92 (m, 3 H, 112 CH2), 2.10 (m, 1 H, 12 CH2), 2.24 (m, 1 H, CHCOOH), 2.82 (m, 2 H, CH2), 3.50-3.80 (m, 7 H), 3.96 (m, 2 H), 4.53 (m, 1 H, 2-Hcyclohex), 4.91 (d, 1 H, 1-Hman)
    • 1H NMR (D2O): 13: δ = 1.10-1.50 (m, 6 H, 3 CH2), 1.63 (m, 2 H, CH2), 1.71-1.92 (m, 3 H, 1 1 2 CH2), 2.10 (m, 1 H, 1 2 CH2), 2.24 (m, 1 H, C H COOH), 2.82 (m, 2 H, CH2), 3.50-3.80 (m, 7 H), 3.96 (m, 2 H), 4.53 (m, 1 H, 2-Hcyclohex), 4.91 (d, 1 H, 1-Hman).
  • 37
    • 0001783413 scopus 로고
    • The synthesis of a N-carbethoxy substituted 4,4 dicarboxylated piperidine was described in
    • The synthesis of a N-carbethoxy substituted 4,4 dicarboxylated piperidine was described in: Huybrechts, S.; Hoornaert, G.J., Synthetic Communications, 1981, 11, 17-23;
    • (1981) Synthetic Communications , vol.11 , pp. 17-23
    • Huybrechts, S.1    Hoornaert, G.J.2
  • 39
    • 0011255698 scopus 로고    scopus 로고
    • 1H NMR (D2O): 7B: δ = 0.95 (d, 3 H, 6-Hfuc), 1.46 (m, 2 H, CH2), 1.74 (m, 4 H, 2 CH2), 1.90 (m, 1 H, 12 CH2), 3.69 (q, 1 H, 5-Hfuc), 4.41 (m, 1 H, 2-Hcyclohex), 4.78 (bs, 1 H, 1-Hfuc); ESI-MS: m/e = 460.2 [M-H]-
    • -.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.