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Volumn 129, Issue 16, 2007, Pages 4898-4899

Evidence for the rapid conversion of stephacidin B into the electrophilic monomer avrainvillamide in cell culture

Author keywords

[No Author keywords available]

Indexed keywords

ALKALOID DERIVATIVE; AVRAINVILLAMIDE; MONOMER; STEPHACIDIN B; UNCLASSIFIED DRUG;

EID: 34247540356     PISSN: 00027863     EISSN: None     Source Type: Journal    
DOI: 10.1021/ja0690971     Document Type: Article
Times cited : (50)

References (22)
  • 3
    • 33846306493 scopus 로고    scopus 로고
    • Avrainvillamide, a Cytotoxic Marine Natural Product, and Derivatives Thereof
    • U.S. Patent 6,066,635, -Avrainvillamide (2) was independently isolated under the name CJ-17,665
    • (a) Fenical, W.; Jensen, P. R.; Cheng, X. C. Avrainvillamide, a Cytotoxic Marine Natural Product, and Derivatives Thereof. U.S. Patent 6,066,635, 2000. (+)-Avrainvillamide (2) was independently isolated under the name CJ-17,665:
    • (2000)
    • Fenical, W.1    Jensen, P.R.2    Cheng, X.C.3
  • 9
    • 0014211424 scopus 로고    scopus 로고
    • Roswell Park Memorial Institute culture medium, series 1640, was purchased from ATCC. For formulation, see: Moore, G. E.; Gerner, R. E.; Franklin, H. A. J. Am. Med. Assoc. 1967, 199, 519-524.
    • Roswell Park Memorial Institute culture medium, series 1640, was purchased from ATCC. For formulation, see: Moore, G. E.; Gerner, R. E.; Franklin, H. A. J. Am. Med. Assoc. 1967, 199, 519-524.
  • 10
    • 34247531642 scopus 로고    scopus 로고
    • This experiment employed the unnatural enantiomers, )-1 and, -2, which we had synthesized first
    • This experiment employed the unnatural enantiomers ((+)-1 and (-)-2), which we had synthesized first.
  • 12
    • 34247536925 scopus 로고    scopus 로고
    • Structural analogues were evaluated using a slightly different method than that used for the data in Table 1 (see Supporting Information, In this assay, the GI50 for, )-2 was 330 nM vs. LNCaP and 420 nM vs. T-47D
    • 50 for (+)-2 was 330 nM vs. LNCaP and 420 nM vs. T-47D.
  • 13
    • 34247473182 scopus 로고    scopus 로고
    • Bogyo, M.; Baruch, A.; Jeffery, D. A.; Greenbaum, D.; Borodovsky, A.; Ovaa, H.; Kessler, B. Curr. Protoc. Protein Sci. 2004, 21, 17.1.
    • Bogyo, M.; Baruch, A.; Jeffery, D. A.; Greenbaum, D.; Borodovsky, A.; Ovaa, H.; Kessler, B. Curr. Protoc. Protein Sci. 2004, 21, 17.1.
  • 22
    • 34247517984 scopus 로고    scopus 로고
    • Control experiments (lanes 6-8 of Figure 2) with compounds lacking either the biotin moiety (2 or 3) or the 3-alkylidene-3H-indole 1-oxide function (6) did not afford detectable quantities of protein in subsequent Western-blot analyses.
    • Control experiments (lanes 6-8 of Figure 2) with compounds lacking either the biotin moiety (2 or 3) or the 3-alkylidene-3H-indole 1-oxide function (6) did not afford detectable quantities of protein in subsequent Western-blot analyses.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.