Heiko Ihmels

Prof. Dr. Heiko Ihmels

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Research Focus & Metrics

Academic Career Length

36Years (1991-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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17 February 2003 in Angewandte Chemie International Edition
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Journal Article
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ZFZhaofu Fei
Zhaofu Fei
NKNikolaus Kocher
Nikolaus Kocher
CMChristian J. Mohrschladt
Christian J. Mohrschladt
HIHeiko Ihmels
Heiko Ihmels
DSDietmar Stalke
Dietmar Stalke

17 January 2007 in Journal of the American Chemical Society
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Journal Article
Closed access
AGAnton Granzhan
Anton Granzhan
HIHeiko Ihmels
Heiko Ihmels
Giampietro ViolaGiampietro Viola
Giampietro Viola

23 April 2009 in Chemical Communications
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Journal Article
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MTMaoqun Tian
Maoqun Tian
HIHeiko Ihmels
Heiko Ihmels
The integration of a selective Hg2+ receptor unit, 1,4-dioxa-7,13-dithia-10-azacyclopentadecane, into the 9-aminoacridizinium fluorophore provides a fluorescent probe which allows a selective ratiometric detection of Hg2+ in water.

23 January 2004 in Chemical Research in Toxicology
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Journal Article
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AMAngela Mally
Angela Mally
HZHerbert Zepnik
Herbert Zepnik
PWPaul Wanek
Paul Wanek
EEErwin Eder
Erwin Eder
KDKaren Dingley
Karen Dingley
WDWolfgang Dekant
Wolfgang Dekant

1 September 2005 in Photochemistry and Photobiology
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Journal Article
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HIHeiko Ihmels
Heiko Ihmels
KFKatja Faulhaber
Katja Faulhaber
DVDaniela Vedaldi
Daniela Vedaldi
FDFrancesco Dall'ACqua
Francesco Dall'ACqua
Giampietro ViolaGiampietro Viola
Giampietro Viola
DNA intercalators represent an important class of compounds with a high potential as DNA‐targeting drugs. In this review it is demonstrated that annelated quinolizinium derivatives such as coralyne and derivatives thereof intercalate into DNA and that this structural motif allows several variations of the substitution pattern without loss of intercalating properties. The commonly applied methods for the evaluation of the DNA association, mainly spectroscopic studies, are pointed out. In addition, studies on the biological activities of annelated quinolizinium derivatives, such as topoisomerase poisoning or cell toxicity, are highlighted.