Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Sandra I. Schweda"'
Autor:
Andreas Masch, Abed Nasereddin, Arne Alder, Megan J. Bird, Sandra I. Schweda, Lutz Preu, Christian Doerig, Ron Dzikowski, Tim W. Gilberger, Conrad Kunick
Publikováno v:
Malaria Journal, Vol 18, Iss 1, Pp 1-10 (2019)
Abstract Background Malaria is one of the most prevalent tropical infectious diseases. Since recently cases of artemisinin resistance were reported, novel anti-malarial drugs are required which differ from artemisinins in structure and biological tar
Externí odkaz:
https://doaj.org/article/86bec5b15da04074875dc25fedb8b09d
Publikováno v:
Molecules, Vol 25, Iss 14, p 3187 (2020)
Malaria causes hundreds of thousands of deaths every year, making it one of the most dangerous infectious diseases worldwide. Because the pathogens have developed resistance against most of the established anti-malarial drugs, new antiplasmodial agen
Externí odkaz:
https://doaj.org/article/db89399e15d342368dca7d1e3ceb4e37
Publikováno v:
Molbank, Vol 2015, Iss 4, p M869 (2015)
The title compound was prepared by a Friedel–Crafts acylation-oxime synthesis-decarboxylation/dehydration sequence starting from commercially available 7-iodoindole with 2-(7-iodo-1H-indol-3-yl)-2-oxoacetic acid as isolated intermediate. The struct
Externí odkaz:
https://doaj.org/article/536b6dc79ad64e9fbcc59ef02c6a0b97
Autor:
Andreas, Masch, Abed, Nasereddin, Arne, Alder, Megan J, Bird, Sandra I, Schweda, Lutz, Preu, Christian, Doerig, Ron, Dzikowski, Tim W, Gilberger, Conrad, Kunick
Publikováno v:
Malaria Journal
Background Malaria is one of the most prevalent tropical infectious diseases. Since recently cases of artemisinin resistance were reported, novel anti-malarial drugs are required which differ from artemisinins in structure and biological target. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::54d0305c9cc8d09b77813ad6550856fd
https://pubmed.ncbi.nlm.nih.gov/30898128
https://pubmed.ncbi.nlm.nih.gov/30898128
Publikováno v:
Molbank, Vol 2015, Iss 4, p M869 (2015)
The title compound was prepared by a Friedel–Crafts acylation-oxime synthesis-decarboxylation/dehydration sequence starting from commercially available 7-iodoindole with 2-(7-iodo-1H-indol-3-yl)-2-oxoacetic acid as isolated intermediate. The struct
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e5cc413f12ea3e91181ca63f57c1d3ff
https://doi.org/10.3390/m869
https://doi.org/10.3390/m869