-opioid receptor. Research indicates it has a high affinity for these receptors ( nM) while maintaining a significantly lower affinity for -opioid receptors compared to its parent compound.
-opioid receptor (MOR) agonist. Unlike traditional alkaloids such as morphine, herkinorin is a neoclerodane diterpene and does not contain a basic nitrogen atom, which makes its chemical structure unique among opioid ligands.
: This compound is not approved for human or veterinary use. It has not undergone clinical trials to establish safety, efficacy, or a therapeutic window in humans. herkinorin buy
: In laboratory settings using animal models, herkinorin has demonstrated antinociceptive (pain-relieving) effects. These effects appear to be largely restricted to the site of administration rather than acting centrally. Regulatory and Safety Status
Herkinorin is a semi-synthetic compound derived from Salvinorin A, which is found in the plant Salvia divinorum . It functions as a -opioid receptor
-arrestin-2, a protein associated with many of the side effects of traditional opioids, such as respiratory depression and the development of tolerance. However, more recent research has indicated that these effects may be complex and dependent on the specific biological context or concentration used.
: Herkinorin is classified strictly as a research chemical. It is intended only for use in laboratory settings for biochemical and physiological research. Unlike traditional alkaloids such as morphine, herkinorin is
: Herkinorin acts as a potent and selective agonist at the