Synthese von (-) -Pyrenophorol, Bewertung von Heterozyklen gegen Krebs: Benzimidazol-, Benzthiazol- und Sulfonamid-Derivate
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018±0. 0039 μM, A549 = 0.
011±0. 0019 μM, Colo-205 = 0.
12±0. 029 μM und A2780 = 0.
17±0. 023 μM) als Etoposid.
Die Verbindung 117i mit einer elektronenreichen Phenyleinheit zeigte bei allen Zelllinien eine stärkere krebshemmende Wirkung (PC3=0,11±0,068 μM; A549=0,18±0,063 μM; MCF-7= 0,52±0,074 μM und DU-145=0,17±0,082 μM). .
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