← Therapeutic programs

MYR-001
Cancer & infectious disease

A small-molecule program targeting protein N-myristoylation, a dependency shared across certain cancers and infectious agents.

Therapeutic area
Oncology & Infectious Disease
Target
Undisclosed (myristoylation pathway)
Modality
Small Molecule
Ownership
Fully Owned
Lead Optimization2 of 7 to approval
Omic Discover screening compounds against a target, with a filtering funnel, binding scores and ADMET properties.
Omic Discover · how this program was run: candidates screened, filtered and scored against the target. Open full size ↗

Why this program

01

A shared cellular dependency

N-myristoylation is a lipid modification that many proteins require to localize correctly and function. A range of tumors and infectious pathogens rely on this pathway more heavily than healthy human cells, which opens a potential therapeutic window.

02

One mechanism, two indications

Because the same enzymatic dependency appears in both oncology and infectious-disease settings, a single small-molecule series has the potential to address multiple indications from a common chemical starting point.

How we got here

01

AI-guided discovery

The program started as a question in Omic. The investigation screened large chemical spaces against the pathway and scored candidates with Omic’s discovery models for selectivity toward diseased over healthy cells. Every result is in the fabric, with its sources.

02

Where it stands

The program is in lead optimization, refining potency, selectivity, and drug-like properties. The specific molecular target remains undisclosed.

Computational program. Laboratory and clinical validation are separate steps, and this program has not reached them. Request the current brief to review what has been run.

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