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Volumn 14, Issue 5, 2012, Pages 1290-1293

Design, synthesis, and biological evaluations of aplyronine A-mycalolide B hybrid compound

Author keywords

[No Author keywords available]

Indexed keywords

APLYRONINE A; MACROLIDE; MYCALOLIDE B; OXAZOLE DERIVATIVE;

EID: 84857829022     PISSN: 15237060     EISSN: 15237052     Source Type: Journal    
DOI: 10.1021/ol300182r     Document Type: Article
Times cited : (30)

References (30)
  • 25
    • 27644464046 scopus 로고    scopus 로고
    • Namba and Kishi reported a catalytic intramolecular NHK reaction without the use of high-dilution techniques
    • Namba and Kishi reported a catalytic intramolecular NHK reaction without the use of high-dilution techniques: Namba, K.; Kishi, Y. J. Am. Chem. Soc. 2005, 127, 15382
    • (2005) J. Am. Chem. Soc. , vol.127 , pp. 15382
    • Namba, K.1    Kishi, Y.2
  • 29
    • 0345059373 scopus 로고    scopus 로고
    • Kabiramide C (20) is a cytotoxic marine macrolide, which binds to actin at the 1,3-cleft, as well as aplyronine A (1), and shows actin-depolymerizing activity
    • Kabiramide C (20) is a cytotoxic marine macrolide, which binds to actin at the 1,3-cleft, as well as aplyronine A (1), and shows actin-depolymerizing activity: Klenchin, V. A.; Allingham, J. S.; King, R.; Tanaka, J.; Maririott, G.; Rayment, I. Nat. Struct. Mol. Biol. 2003, 10, 1058
    • (2003) Nat. Struct. Mol. Biol. , vol.10 , pp. 1058
    • Klenchin, V.A.1    Allingham, J.S.2    King, R.3    Tanaka, J.4    Maririott, G.5    Rayment, I.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.