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Bioorg Chem ; 91: 103155, 2019 10.
Article in English | MEDLINE | ID: mdl-31400552

ABSTRACT

The chorismate mutase (CM) is considered as an attractive target for the identification of potential antitubercular agents due to its absence in animals but not in bacteria. A series of 3-indolylmethyl substituted pyrazolotriazinone derivatives were designed and docked into CM in silico as potential inhibitors. These compounds were efficiently synthesized using the Pd/Cu-catalyzed coupling-cyclization in a single pot involving the construction of indole ring. The methodology was later extended to the preparation of corresponding benzo analogs of pyrazolotriazinones i.e. 3-indolylmethyl substituted benzotriazinone derivatives. Several of these novel compounds showed significant inhibition of CM when tested in vitro at 30 µM. The SAR (Structure-Activity-Relationship) studies suggested that benzotriazinone moiety was more favorable over the pyrazolotriazinone ring. The two best active compounds showed IC50 ∼ 0.4-0.9 µM (better than the reference/known compounds used) and no toxicity till 30 µM in vitro.


Subject(s)
Chorismate Mutase/antagonists & inhibitors , Copper/chemistry , Enzyme Inhibitors/chemical synthesis , Enzyme Inhibitors/pharmacology , Indoles/chemistry , Mycobacterium tuberculosis/enzymology , Palladium/chemistry , Triazines/chemical synthesis , Triazines/pharmacology , Animals , Catalysis , Mice , Models, Molecular , Molecular Structure , RAW 264.7 Cells , Structure-Activity Relationship
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