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Volumn 13, Issue 22, 2003, Pages 4055-4057

Spectrophotometric and ESI-MS/HPLC studies reveal a common mechanism for the reaction of various artemisinin analogues with hemin

Author keywords

[No Author keywords available]

Indexed keywords

ARTEMETHER; ARTEMISININ DERIVATIVE; ARTESUNATE; DIHYDROARTEMISININ; HEMIN; PORPHYRIN;

EID: 0242317284     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2003.08.032     Document Type: Article
Times cited : (19)

References (18)
  • 4
    • 0035005885 scopus 로고    scopus 로고
    • Olliaro P.L., Haynes R.K., Meunier B., Yuthavong Y. Trends. Parasitol. 17:2001;122 Posner G.P., Meshnick S.R. Trends. Parasitol. 17:2001;266.
    • (2001) Trends. Parasitol. , vol.17 , pp. 266
    • Posner, G.P.1    Meshnick, S.R.2
  • 15
    • 85030966432 scopus 로고    scopus 로고
    • -1, 20 μL of samples were injected. UV-Vis spectra were recorded in the range 200-450 nm. The HPLC system was interfaced with a HP 1100 MSD API-electrospray (Hewlett & Packard, Palo Alto, CA, USA). MS spectra were registered in positive ion mode. Capillary temperature was 220 °C, capillary voltage 3.0 V, source voltage 4.2 kV, tube lens voltage 30 V and collision energy 35%.
  • 16
    • 85030953671 scopus 로고    scopus 로고
    • 3COOH moiety a fragment of 115 m/z, most likely due to the loss of 4-oxo-pentanoic-acid; and the latter further lacks a fragment of 18 m/z, thus a molecule of water.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.