Skip to content

Moonhyuk Kwon

3 papers in the library · 91 citations · publishing 2016-2024

Papers

Sort Most recent Most cited

A chromosome level reference genome of Diviner's sage (Salvia divinorum) provides insight into salvinorin A biosynthesis.

BMC plant biology October 1, 2024 Scott A. Ford, Rob W. Ness, Moonhyuk Kwon et al. 9 citations

Diviner's sage (Salvia divinorum; Lamiaceae) is the source of the powerful hallucinogen salvinorin A (SalA). This neoclerodane diterpenoid is an agonist of the human Κ-opioid receptor with potential medical applications in the treatment of chronic pain, addiction, and post-traumatic stress disorder. Only two steps of the approximately twelve step biosynthetic sequence leading to SalA have been...

Identification of clerodane diterpene modifying cytochrome P450 (CYP728D26) in Salvia divinorum - en route to psychotropic salvinorin A biosynthesis.

Physiologia plantarum 2024 Iris Ngo, Rahul Kumar, Liang Li et al. 6 citations

Salvia divinorum is a hallucinogenic plant native to the Oaxaca in Mexico. The active ingredient for psychotropic effects in this plant is salvinorin A, a potent and highly selective κ-opioid receptor agonist. Salvinorin A is distinct from other well-known opioids, such as morphine and codeine, in that it is a non-nitrogenous diterpenoid with no affinity for μ-opioid receptor, the prime...

DOI: 10.1111/ppl.14569 (opens in new tab) Full text (opens in new tab) Salvinorin a Pain management Non-opioid pain relief Alternative analgesics +13

Biosynthesis of the psychotropic plant diterpene salvinorin A: Discovery and characterization of the Salvia divinorum clerodienyl diphosphate synthase

The Plant Journal November 19, 2016 Kyle A. Pelot, Rod Mitchell, Moonhyuk Kwon et al. 76 citations

Salvia divinorum commonly known as diviner's sage, is an ethnomedicinal plant of the mint family (Lamiaceae). Salvia divinorum is rich in clerodane-type diterpenoids, which accumulate predominantly in leaf glandular trichomes. The main bioactive metabolite, salvinorin A, is the first non-nitrogenous natural compound known to function as an opioid-receptor agonist, and is undergoing clinical...

DOI: 10.1111/tpj.13427 (opens in new tab) Diterpene Salvia Atp synthase Traditional medicine +4