Calculated reference model · not an experimental or batch-certified structure. All 24 atoms shown.
Model data & sources
- Heavy atoms only; hydrogens are omitted from the reference display.
- Source-defined stereochemistry is checked against the calculated coordinates; no energy-minimum, crystal or solution-structure claim is made.
- Reference molecular species only; batch identity, purity, counterions and excipients are not certified.
- Formula
- C16H11Cl2N3O2S
- Method
- RDKit ETKDGv3 / MMFF94s calculated reference conformer
O-304 (ATX-304)
O-304 (ATX-304) AMPK Activator Research Standard
ATX-304 (also called O-304) is a synthetic research compound studied as a pan-AMPK activator. Its reported identity is CAS 1261289-04-6 with a 1,2,4-thiadiazol-3(2H)-one scaffold, not a benzothiazole. Published work describes protection of AMPK phosphorylation from PP2C-mediated dephosphorylation, with activity dependent on existing upstream kinase tone. This page is for laboratory research use only.
Physical & Handling Properties
| Property | Specification |
|---|---|
| Physical Appearance | White powder |
Mechanism of Action & Research Context
Published work describes ATX-304 as protecting p-T172 AMPK from PP2C-mediated dephosphorylation rather than acting as an AdAM-site allosteric ligand. The reported effect depends on upstream kinase activity, so the experimental model determines whether activation can be observed.
-
Enzyme Interaction: Published work describes O-304 as protecting AMPK phosphorylation from PP2C-mediated dephosphorylation. In in vitro models, the observed effect depends on existing upstream kinase activity.
-
AMPK Activation: By modulating this pathway, the compound allows researchers to study the downstream phosphorylation of metabolic targets and the regulation of lipid and glucose oxidation in isolated cellular environments.
-
Binding Kinetics: The chlorine-substituted 1,2,4-thiadiazol-3(2H)-one scaffold provides structural context for comparing O-304 with other AMPK activators in assay and mechanism studies.
Research Applications
O-304 is utilized as a specialized benchmark for high-fidelity studies in metabolic signaling and enzyme kinetics.
Primary fields of in vitro laboratory investigation include:
-
Enzyme Binding Assays: Measuring the binding strength between O-304 and AMPK in cell-free enzyme preparations, often utilizing competitive displacement techniques.
-
Kinase Assays: Utilizing fluorescence-based probes to observe how O-304 influences the catalytic efficiency of the AMPK complex.
-
Competitive Displacement Studies: Using labeled probes to compete for the same binding pocket, helping to delineate the specificity of the benzothiazole core.
-
Structural Biology: Investigating the interaction patterns of chlorine-substituted heterocycles within kinase catalytic sites.
Storage & Handling Guidelines
Store at controlled room temperature. Keep tightly closed.
Storage guidance is a house recommendation. Analytical documentation is per-lot release testing.
References
-
Sidarala V, et al. (2020) "AMPK Activation by O-304 Improves Metabolic Health and Enhances Insulin Sensitivity." Molecular Metabolism. 31: 1–13.
-
Cokorinos EC, et al. (2017) "Activation of AMPK by O-304 in non-human primates." Cell Chemical Biology. 24(7): 879–889.
-
Kim, J., et al. (2016) "Direct AMPK Activation by Small-Molecule Activators." Cell Metabolism. 23(1): 11–12.
Related Research Compounds
Research Use Disclaimer
Research Use Only Disclaimer: This product is labeled and sold "For Research Use Only — NOT FOR HUMAN CONSUMPTION." It is not a drug, dietary supplement, food, cosmetic, or medical device, and it is not approved by the FDA or any other regulator for human or veterinary use. It is supplied to approved account holders as a research chemical for laboratory use and must be handled in accordance with applicable law.
