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Ingenol: Highly Strained Natural Product as a Core of Powerful Bioactive Compounds
Ingenol is a diterpene isolated from Euphobia family and its structure was determined in 1970.1) Although ingenol has a weak activity against protein kinase C,2) ingenol derivatives show wide range of bioactivity. For instance, ingenol 3-mebutate, an angelate ester at 3-hydroxy group of ingenol, is utilized as a therapeutic medicine for solar keratosis (a precancerous skin condition).3) The mechanism of 1 is considered as an activation of protein kinase C, so it has also been reported to indicate an anticancer4) and anti-HIV5) activities. By the way, ingenol has an “inside-outside structure”, a unique and highly strained structure at a condensed ring moiety of two seven-membered rings, so that it is regarded as a challenging target of total synthesis.6,7)
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References
- 1)Structure determination of the new tetracyclic diterpene ingenol-triacetate with triple product methods
- 2)Specific Binding to Protein Kinase C by Ingenol and Its Induction of Biological Responses
- 3)Ingenol Mebutate Gel 0.015% and 0.05%: In Actinic Keratosis
- 4)The Protein Kinase C Agonist PEP005 (Ingenol 3-Angelate) in the Treatment of Human Cancer: A Balance between Efficacy and Toxicity
- 5)HIV Type 1 Inhibition by Protein Kinase C Modulatory Compounds
- 6)Total Synthesis of Ingenol
- 7)14-Step Synthesis of (+)-Ingenol from (+)-3-Carene