메뉴 건너뛰기




Volumn 13, Issue 2, 2003, Pages 229-236

Synthesis of non-competitive inhibitors of sphingomyelinases with significant activity

Author keywords

[No Author keywords available]

Indexed keywords

N PALMITOYLSPHINGOSINE 1 PHOSPHATE; SCHYPHOSTATIN; SPHINGOMYELIN PHOSPHODIESTERASE; SPHINGOMYELIN PHOSPHODIESTERASE INHIBITOR; SPHINGOSINE DERIVATIVE; UNCLASSIFIED DRUG; CERAMIDE; DYES, REAGENTS, INDICATORS, MARKERS AND BUFFERS; ENZYME INHIBITOR; PHOSPHOLIPID;

EID: 0037212776     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(02)00888-0     Document Type: Article
Times cited : (70)

References (30)
  • 8
    • 0030762064 scopus 로고    scopus 로고
    • Recent studies of synthesis of inhibitors for SMases (a) Murakami M., Iwama S., Fujii S., Ikeda K., Katsumura S. Bioorg. Med. Chem. Lett. 7:1997;1725. (b) Hakogi T., Monden Y., Iwama S., Katsumura S. Org. Lett. 2:2000;2627. (c) Arenz C., Giannis A. Angew. Chem. Int. Ed. 39:2000;1440. (d) Hakogi T., Monden Y., Taichi M., Iwama S., Fujii S., Ikeda K., Katsumura S. J. Org. Chem. 67:2002;4839.
    • (1997) Bioorg. Med. Chem. Lett. , vol.7 , pp. 1725
    • Murakami, M.1    Iwama, S.2    Fujii, S.3    Ikeda, K.4    Katsumura, S.5
  • 9
    • 0034710487 scopus 로고    scopus 로고
    • Recent studies of synthesis of inhibitors for SMases (a) Murakami M., Iwama S., Fujii S., Ikeda K., Katsumura S. Bioorg. Med. Chem. Lett. 7:1997;1725. (b) Hakogi T., Monden Y., Iwama S., Katsumura S. Org. Lett. 2:2000;2627. (c) Arenz C., Giannis A. Angew. Chem. Int. Ed. 39:2000;1440. (d) Hakogi T., Monden Y., Taichi M., Iwama S., Fujii S., Ikeda K., Katsumura S. J. Org. Chem. 67:2002;4839.
    • (2000) Org. Lett. , vol.2 , pp. 2627
    • Hakogi, T.1    Monden, Y.2    Iwama, S.3    Katsumura, S.4
  • 10
    • 0034678911 scopus 로고    scopus 로고
    • Recent studies of synthesis of inhibitors for SMases (a) Murakami M., Iwama S., Fujii S., Ikeda K., Katsumura S. Bioorg. Med. Chem. Lett. 7:1997;1725. (b) Hakogi T., Monden Y., Iwama S., Katsumura S. Org. Lett. 2:2000;2627. (c) Arenz C., Giannis A. Angew. Chem. Int. Ed. 39:2000;1440. (d) Hakogi T., Monden Y., Taichi M., Iwama S., Fujii S., Ikeda K., Katsumura S. J. Org. Chem. 67:2002;4839.
    • (2000) Angew. Chem. Int. Ed. , vol.39 , pp. 1440
    • Arenz, C.1    Giannis, A.2
  • 11
    • 0037067332 scopus 로고    scopus 로고
    • Recent studies of synthesis of inhibitors for SMases (a) Murakami M., Iwama S., Fujii S., Ikeda K., Katsumura S. Bioorg. Med. Chem. Lett. 7:1997;1725. (b) Hakogi T., Monden Y., Iwama S., Katsumura S. Org. Lett. 2:2000;2627. (c) Arenz C., Giannis A. Angew. Chem. Int. Ed. 39:2000;1440. (d) Hakogi T., Monden Y., Taichi M., Iwama S., Fujii S., Ikeda K., Katsumura S. J. Org. Chem. 67:2002;4839.
    • (2002) J. Org. Chem. , vol.67 , pp. 4839
    • Hakogi, T.1    Monden, Y.2    Taichi, M.3    Iwama, S.4    Fujii, S.5    Ikeda, K.6    Katsumura, S.7
  • 15
    • 0028026762 scopus 로고
    • A similar replacement strategy has been also applied to synthesis of a hydrolytically stable analogue of phospholipids as an inhibitor of phospholipase C from Bacillus cereus:
    • A similar replacement strategy has been also applied to synthesis of a hydrolytically stable analogue of phospholipids as an inhibitor of phospholipase C from Bacillus cereus: Martin S.F., Wong Y.-L., Wagman A.S. J. Org. Chem. 59:1994;4821.
    • (1994) J. Org. Chem. , vol.59 , pp. 4821
    • Martin, S.F.1    Wong, Y.-L.2    Wagman, A.S.3
  • 17
    • 1842663065 scopus 로고    scopus 로고
    • and the references cited therein
    • (b) O'Hagan D., Rzepa H.S. Chem. Commun. 1997;645. and the references cited therein.
    • (1997) Chem. Commun. , pp. 645
    • O'Hagan, D.1    Rzepa, H.S.2
  • 19
    • 0011994206 scopus 로고    scopus 로고
    • 35.
  • 25
    • 0011935028 scopus 로고    scopus 로고
    • The stereochemistry of 15 was also ascertained in a similar manner to that for 8.
  • 27
    • 0011935428 scopus 로고    scopus 로고
    • Partial N→O acyl migration was also observed with the erythro isomers (3, 12, ent-3 and ent-12). However, the rate of the migration was estimated to be slow in comparison to that of the threo isomers.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.