The interaction of human CK2α with a series of tetrabromobenzotriazole (TBBt) and
tetrabromobenzimidazole (TBBz) analogs, in which one of the bromine atoms proximal to …

The interaction of human CK2α (hCK2α) with nine halogenated benzotriazoles, TBBt and its
analogues representing all possible patterns of halogenation on the benzene ring of …

A series of chlorine‐substituted benzotriazole derivatives, representing all possible
substitution patterns of halogen atoms attached to the benzotriazole benzene ring, were …

Binding of a family of brominated benzotriazoles to the catalytic subunit of human protein
kinase CK2 (hCK2α) was used as a model system to assess the contribution of halogen …

To examine the relative role of halogen bonding and hydrophobic interactions in the
inhibition of human CK2α by 4, 5, 6, 7-tetrabromobenzotriazole (TBBt), we have synthesized …

A series of novel benzotriazole derivatives containing iodine atom (s) were synthesized. The
binding of these compounds to the catalytic subunit of human protein kinase CK2 was …

To further clarify the role of the individual bromine atoms of 4, 5, 6, 7-tetrabromotriazole
(TBBt), a relatively selective inhibitor of protein kinase CK2, we have examined the inhibition …

The binding of four bromobenzotriazoles to the catalytic subunit of human protein kinase
CK2 was assessed by two complementary methods: Microscale Thermophoresis (MST) and …

A series of halogenated derivatives of natural flavonoids: baicalein and chrysin were
designed and investigated as possible ligands for the catalytic subunit of tumor‐associated …

Like the previously reported 4, 5, 6, 7-tetrabromobenzotriazole (TBBt), the structurally related
4, 5, 6, 7-tetrabromobenzimidazole (TBBz) is a selective ATP-competitive inhibitor of protein …