메뉴 건너뛰기




Volumn 42, Issue 43, 2003, Pages 5361-5364

Total Synthesis and Reassessment of the Phosphatase-Inhibitory Activity of the Antitumor Agent TMC-69-6H

Author keywords

Heterocycles; Natural products; Palladium; Phosphatases; Structure activity relationships

Indexed keywords

CATALYSIS; CHEMICAL BONDS; SYNTHESIS (CHEMICAL); TUMORS;

EID: 0345306825     PISSN: 14337851     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.200352268     Document Type: Article
Times cited : (41)

References (61)
  • 14
    • 0344871176 scopus 로고    scopus 로고
    • c) see also: K. Sugawara, J. Kohno, N. Nakanishi, T. Hashiyama, Tennen Yuki Kagobutsu Toronkai Koen Yoshishu 2000, 42, 661-666 [Chem. Abstr. 2001, 134, 340370].
    • (2001) Chem. Abstr. , vol.134 , pp. 340370
  • 32
    • 0345302357 scopus 로고    scopus 로고
    • note
    • 10,H11eq = 2.6 Hz.
  • 37
    • 0345302356 scopus 로고    scopus 로고
    • note
    • 20 = + 88.6 (c = 0.50, MeOH).
  • 47
    • 0037165320 scopus 로고    scopus 로고
    • While several other bioactive natural products that contain an N-hydroxy-2-pyridone motif are known in the literature, it appears that none have been checked for phosphatase inhibition; see: a) militarinone A: K. Schmidt, W. Günther, S. Stoyanova, B. Schubert, Z. Li, M. Hamburger, Org. Lett. 2002, 4, 197-199;
    • (2002) Org. Lett. , vol.4 , pp. 197-199
    • Schmidtnther, W.1    Stoyanova, S.2    Schubert, B.3    Li, Z.4    Hamburger, M.5
  • 61
    • 0032491228 scopus 로고    scopus 로고
    • For a structurally different synthetic 2-pyridone derivative that bears an N-methylphosphonate moiety, which exhibits phosphatase-inhibiting properties, see: J.-M. Fu, A. L. Castelhano, Bioorg. Med. Chem. Lett. 1998, 8, 2813-2816.
    • (1998) Bioorg. Med. Chem. Lett. , vol.8 , pp. 2813-2816
    • Fu, J.-M.1    Castelhano, A.L.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.