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Volumn 68, Issue 10, 2004, Pages 2178-2182

Structure-activity relationship for FR901464: A versatile method for the conversion and preparation of biologically active biotinylated probes

Author keywords

Biotin; Cell cycle inhibitor; Conversion; FR901464

Indexed keywords

BIOLOGICAL MATERIALS; CELLS; ENZYME INHIBITION; PROTEINS; SYNTHESIS (CHEMICAL);

EID: 9244219683     PISSN: 09168451     EISSN: None     Source Type: Journal    
DOI: 10.1271/bbb.68.2178     Document Type: Article
Times cited : (46)

References (11)
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    • Nakajima, H., Sato, B., Fujita, T., Takase, S., Terano, H., and Okuhara, M., New antitumor substances, FR901463, FR901464 and FR901465. I. Taxonomy, fermentation, isolation, physico-chemical properties and biological activities. J. Antibiot., 49, 1196-1203 (1996).
    • (1996) J. Antibiot. , vol.49 , pp. 1196-1203
    • Nakajima, H.1    Sato, B.2    Fujita, T.3    Takase, S.4    Terano, H.5    Okuhara, M.6
  • 2
    • 0030466895 scopus 로고    scopus 로고
    • New antitumor substances, FR901463, FR901464 and FR901465. II. Activities against experimental tumors in mice and mechanism of action
    • Nakajima, H., Hori, Y., Terano, H., Okuhara, M., Manda, T., Matsumoto, S., and Shimomura, K., New antitumor substances, FR901463, FR901464 and FR901465. II. Activities against experimental tumors in mice and mechanism of action. J. Antibiot., 49, 1204-1211 (1996).
    • (1996) J. Antibiot. , vol.49 , pp. 1204-1211
    • Nakajima, H.1    Hori, Y.2    Terano, H.3    Okuhara, M.4    Manda, T.5    Matsumoto, S.6    Shimomura, K.7
  • 3
    • 0031054453 scopus 로고    scopus 로고
    • New antitumor substances, FR901463, FR901464 and FR901465. III. Structures of FR901463, FR901464 and FR901465
    • Nakajima, H., Takase, S., Terano, H., and Tanaka, H., New antitumor substances, FR901463, FR901464 and FR901465. III. Structures of FR901463, FR901464 and FR901465. J. Antibiot., 50, 96-99 (1997).
    • (1997) J. Antibiot. , vol.50 , pp. 96-99
    • Nakajima, H.1    Takase, S.2    Terano, H.3    Tanaka, H.4
  • 4
    • 0344431240 scopus 로고    scopus 로고
    • FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor
    • Nakajima, H., Kim, Y. B., Terano, H., Yoshida, M., and Horinouchi, S., FR901228, a potent antitumor antibiotic, is a novel histone deacetylase inhibitor. Exp. Cell Res., 241, 126-133 (1998).
    • (1998) Exp. Cell Res. , vol.241 , pp. 126-133
    • Nakajima, H.1    Kim, Y.B.2    Terano, H.3    Yoshida, M.4    Horinouchi, S.5
  • 7
    • 0034715459 scopus 로고    scopus 로고
    • Total synthesis of FR901464. Convergent assembly of chiral components prepared by asymmetric catalysis
    • Thompson, C. F., Jamison, T. F., and Jacobsen, E. N., Total synthesis of FR901464. Convergent assembly of chiral components prepared by asymmetric catalysis. J. Am. Chem. Soc., 122, 10482-10483 (2000).
    • (2000) J. Am. Chem. Soc. , vol.122 , pp. 10482-10483
    • Thompson, C.F.1    Jamison, T.F.2    Jacobsen, E.N.3
  • 8
    • 0035904404 scopus 로고    scopus 로고
    • FR901464: Total synthesis, proof of structure, and evaluation of synthetic analogues
    • Thompson, C. F., Jamison, T. F., and Jacobsen, E. N., FR901464: Total synthesis, proof of structure, and evaluation of synthetic analogues. J. Am. Chem. Soc., 123, 9974-9983 (2001).
    • (2001) J. Am. Chem. Soc. , vol.123 , pp. 9974-9983
    • Thompson, C.F.1    Jamison, T.F.2    Jacobsen, E.N.3
  • 11
    • 0000650928 scopus 로고
    • The use of ω-iodo azides as primary protected electrophilic reagents. Alkylation of some carbanions derived from active methylene compounds and N,H-dimethylhydrazones
    • Khoukhi, M., Vaultier, M., and Carrié, R., The use of ω-iodo azides as primary protected electrophilic reagents. Alkylation of some carbanions derived from active methylene compounds and N,H-dimethylhydrazones. Tetrahedron Lett., 27, 1031-1034 (1986).
    • (1986) Tetrahedron Lett. , vol.27 , pp. 1031-1034
    • Khoukhi, M.1    Vaultier, M.2    Carrié, R.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.