Discovery and Structure Optimization of a Series of Isatin Derivatives asMycobacterium tuberculosisChorismate Mutase Inhibitors

C–N bond formation under Cu-catalysis: Synthesis and in vitro evaluation of N-aryl substituted thieno[2,3-d]pyrimidin-4(3H)-ones against chorismate mutase

(2012) Raju Adepu et al.   BIOORGANIC & MEDICINAL CHEMISTRY

AlCl3 induced (hetero)arylation of 2,3-dichloroquinoxaline: A one-pot synthesis of mono/disubstituted quinoxalines as potential antitubercular agents

(2012) K. Shiva Kumar et al.   BIOORGANIC & MEDICINAL CHEMISTRY

When Inhibitors Do Not Inhibit: Critical Evaluation of Rational Drug Design Targeting Chorismate Mutase fromMycobacterium tuberculosis

(2012) Steffi Munack et al.   CHEMISTRY & BIODIVERSITY

Rhodanine carboxylic acids as novel inhibitors of histone acetyltransferases

(2012) Silviya D. Furdas et al.   MedChemComm

A Pd-mediated new strategy to functionalized 2-aminochromenes: Their in vitro evaluation as potential anti tuberculosis agents

(2011) T. Ram Reddy et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Cu-mediated N-arylation of 1,2,3-triazin-4-ones: Synthesis of fused triazinone derivatives as potential inhibitors of chorismate mutase

(2011) K. Shiva Kumar et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Metabolic priming by a secreted fungal effector

(2011) Armin Djamei et al.   NATURE

Evolutionary Cycles for Pericyclic Reactions – Or Why We Keep Mutating Mutases

(2009) Kathrin Roderer et al.   CHIMIA

Structure and function of a complex between chorismate mutase and DAHP synthase: efficiency boost for the junior partner

(2009) Severin Sasso et al.   EMBO JOURNAL