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CH 275

This compound is a potent and selective agonist of somatostatin receptor subtype 1 (sst1), with IC50 values demonstrating high selectivity over other sst subtypes. It has been shown to attenuate somatostatin release in the rat nucleus accumbens in vivo, making it a valuable research tool for studying sst1 function in neuroendocrine regulation and related disorders.

Product Specifications

Field of Research

Pharmacology & Drug Discovery

Molecular Weight

1485.8

Storage Conditions

-20°C

Notes

For research use only.

Available Sizes

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