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SMART Drugs Engineering Nature’s Solution to the Undruggable Target Challenge

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Two-Pronged Proprietary Discovery Platform<br />

Screening Large Diverse <strong>SMART</strong> Libraries<br />

<strong>SMART</strong> Structure-Based Design<br />

Large-scale library of compounds (10 6 ) all capable<br />

of high affinity binding with FKBP but with highly<br />

diversified variable regions<br />

FKBP<br />

HT screening of library<br />

for <strong>Target</strong> binding<br />

Variable Region<br />

…<br />

Millions of<br />

compounds<br />

<strong>Target</strong><br />

FKBP<br />

<strong>Target</strong><br />

<strong>Target</strong><br />

1. Syn<strong>the</strong>Fc Crystallography<br />

<strong>to</strong> solve Presenter-<strong>Target</strong><br />

Interface<br />

2. Structure-Based Drug<br />

Design <strong>to</strong> build Ligand-<br />

<strong>Target</strong> interface<br />

Novel hits and binding ligands <strong>to</strong> enable<br />

hit-<strong>to</strong>-lead medicinal chemistry<br />

WARP DRIVE BIO, INC. 18

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