# Fat or flat? The impact of dipole moment vectors on non-covalent interactions between aromatic tags and macromolecules

## TL;DR

A 3D aromatic carborane compound was found to be a better inhibitor of a protease drug target in Schistosoma due to its unique dipole interactions.

## Contribution

The study introduces a novel carborane pharmacophore that enhances inhibitor binding through dipole-driven hydrogen bonding.

## Key findings

- Carborane-tagged compounds showed superior inhibitor affinity and bioactivity compared to 2D aromatic phenyl analogs.
- Quantum computations revealed a key hydrogen bond between the carborane's CH vertex and a negatively charged residue in the binding site.
- The carborane pharmacophore conferred specific anti-schistosomal activity, improving protein ligand design.

## Abstract

The closo-1,2-C2B10H12 carborane is a recognized 3D aromatic icosahedral building block, with an electron distribution governed by the outer hydridic BH and acidic CH vertices. We attached the carborane cage to a peptidomimetic scaffold to generate an active-site inhibitor of SmCB1, a protease drug target in the Schistosoma pathogen. The carborane-tagged compound exhibited superior inhibitor affinity and bioactivity compared to its conventional 2D aromatic phenyl analog. Quantum mechanical computations, based on the crystal structure of the protease–inhibitor complex, revealed that the carborane tag contributed to inhibitor binding not only through nonpolar interactions but also via a key hydrogen bond between its CH vertex and a negatively charged residue in the binding site. This interaction, driven by the large dipole moment of the carborane cage, resulted in a more favorable energy contribution than that of the phenyl group in the 2D analog. The carborane pharmacophore boosted affinity for SmCB1 and conferred specific anti-schistosomal activity, highlighting its potential in protein ligand design.

The closo-1,2-C2B10H12 carborane is a recognized 3D aromatic icosahedral building block, with an electron distribution governed by the outer hydridic BH and acidic CH vertices.