Generate Candidates proposes new analogs of your lead across seven medicinal-chemistry strategies, validates each with RDKit, scores them for drug-likeness & synthesizability, and groups them into related series you can explore and export.
R-group / SARBioisostere swapPolarity shiftSteric / shapeLinker editScaffold hopExit-vector
Analyze instead runs a deep single-molecule profile — properties, ADMET, and 3D — without generating new molecules.
