The circular dichroism (CD) spectra of the powerful antimalarian active principle artemisinin (ART; 1) from Artemisia annua, and of epiartemisinin (EPI, 2), its C(7) epimer, were studied in solution in the presence and absence of ?-cyclodextrin (?-cd). A significant inversion of sign in the region of the second electronic transition was detected. The rotational strengths were successfully calculated within the time-dependent density functional theory (DFT), which enabled us to establish a correlation between the molecular recognition and the biological acitivities of the two isomers.

Circular Dichroism studies on Artemisinin and Epiartemisinin in solution and in beta-cyclodextrin Complexes in Solution

Marconi G;Monti S;Manoli F;Degli Esposti A;Guerrini A
2004

Abstract

The circular dichroism (CD) spectra of the powerful antimalarian active principle artemisinin (ART; 1) from Artemisia annua, and of epiartemisinin (EPI, 2), its C(7) epimer, were studied in solution in the presence and absence of ?-cyclodextrin (?-cd). A significant inversion of sign in the region of the second electronic transition was detected. The rotational strengths were successfully calculated within the time-dependent density functional theory (DFT), which enabled us to establish a correlation between the molecular recognition and the biological acitivities of the two isomers.
2004
Istituto per la Sintesi Organica e la Fotoreattivita' - ISOF
DFT
Antimalarial
Circular Dichroism Spectra
Epiartemisinin
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/20.500.14243/37241
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