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Samuel H. Foxman

Publications and source records attributed to Samuel H. Foxman.

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onepot CORE -- an enumerated chemical space to streamline drug discovery, enabled by automated small molecule synthesis and AI

The design-make-test-analyze cycle in early-stage drug discovery remains constrained primarily by the "make" step: small-molecule synthesis is slow, costly, and difficult to scale or automate across diverse chemotypes. Enumerated chemical spaces aim to reduce this bottleneck by predefining synthesizable regions of chemical space from available building blocks and reliable reactions, yet existing commercial spaces are still limited by long turnaround times, narrow reaction scope, and substantial manual decision-making in route selection and execution. Here we present the first version of onepot CORE, an enumerated chemical space containing 3.4B molecules and corresponding on-demand synthesis product enabled by an automated synthesis platform and an AI chemist, Phil, that designs, executes, and analyzes experiments. onepot CORE is constructed by (i) selecting a reaction set commonly used in medicinal chemistry, (ii) sourcing and curating building blocks from supplier catalogs, (iii) enumerating candidate products, and (iv) applying ML-based feasibility assessment to prioritize compounds for robust execution. In the current release, the space is supported by seven reactions. We describe an end-to-end workflow - from route selection and automated liquid handling through workup and purification. We further report validation across operational metrics (success rate, timelines, purity, and identity), including NMR confirmation for a representative set of synthesized compounds and assay suitability demonstrated using a series of DPP4 inhibitors. Collectively, onepot CORE illustrates a path toward faster, more reliable access to diverse small molecules, supporting accelerated discovery in pharmaceuticals and beyond.

physics.chem-ph

RapidPIV: Full Flow-Field kHz PIV for Real-Time Display and Control

We present a novel architecture for accelerating PIV calculations. An optical flow hardware accelerator does the brunt of the work, with cross-correlation only providing quick corrections. The result is RapidPIV: a free-to-download software program for real-time particle image velocimetry (PIV) for Linux and Windows computers with an Nvidia Turing-gen (or newer) GPU (RapidPIV download at https://rapidpiv.caltech.edu). Dense vector fields and vorticity can be displayed in real time when connected to compatible camera. Processing pre-existing PIV image files is also supported. We achieve 1,150 frames-per-second on 1 megapixel images. Accuracy, repeatability, and robustness are tested with physical experiments involving an accelerated flat plate and a cylinder wake. RapidPIV's accuracy, precision and ability to handle high displacement, velocity gradients, out-of-plane motion, and low seeding density compare favorably with the trusted multi-grid correlation software. However, RapidPIV is a thousand times faster.

physics.flu-dyn