Levopimaric acid
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| Names | |
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| IUPAC name
Abieta-11,13-dien-18-oic acid
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| Systematic IUPAC name
(1R,4aR,4bS,10aR)-1,4a-Dimethyl-7-(propan-2-yl)-1,2,3,4,4a,4b,5,9,10,10a-decahydrophenanthrene-1-carboxylic acid | |
| Other names
13-isopropylpodocarpa-8(14),12-dien-15-oic acid; D6,8(14)-abietadienoic acid; l-pimaric acid; β-pimaric acid; l-sapietic acid
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| Identifiers | |
3D model (JSmol)
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| ChemSpider | |
PubChem CID
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| UNII | |
CompTox Dashboard (EPA)
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| Properties | |
| C20H30O2 | |
| Molar mass | 302.458 g·mol−1 |
| Appearance | Orthorhombic crystals |
| Melting point | 150 °C (302 °F; 423 K) |
| Practically insoluble in water | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Levopimaric acid is an abietane-type of diterpene resin acid.[1] It is a major constituent of pine oleoresin with the chemical formula of C20H30O2. In general, the abietene types of diterpene resin acid have various biological activities, such as antibacterial, cardiovascular and antioxidant. Levopimaric acid accounts for about 18 to 25% of pine oleoresin.[2] The production of oleoresin by conifer species is an important component of the defense response against insect attack and fungal pathogen infection.[3]
Resin acids
[edit]Resin acid is the general name for all kinds of acids that share the same basic skeleton, a three-fused ring and the empirical formula C20H30O2. The resin acids may be classified into two types, abietic and pimaric. The abietic-type group include levopimaric, l-abietic and neoabietic. The structure of these compounds differ only in the position of the conjugated double bond system. This feature influences their chemical reactivity. The pimaric-type acids are dextropimaric and isodextropimaric.[4]
Extraction from pine resin
[edit]Levopimaric acid can be extracted from longleaf pine oleoresin by first dissolving it in a solution of acetone and 2-amino-2-methyl-1-propanol, then acidifying with phosphoric acid.[2]
Biosynthesis
[edit]
The abietane-like skeleton of levopimaric acid is formed by the cyclization of a diterpenoid precursor, geranylgeranyl diphosphate, from which C20 isoprenoids are typically derived.[5] The intermediate which is formed, (+)-copalyl diphosphate, then goes through an oxidation and rearrangement to give levopimaradiene. Then, the levopimaradiene goes through several more steps of oxidation processes via the intermediates levopimaradienol and levepimaradienal to give levopimaric acid.[6]
Role in biology
[edit]Oleoresin in pines is defined as pine gum, which is the nonaqueous secretion of resin acids dissolved in a terpene hydrocarbon oil, which is produced in or exuded from the intercellular resin ducts of a living tree. The viscous oleoresin secretion is composed of a complex mixture of terpenoids, consisting of roughly equal parts of volatile turpentine and rosin (also known as diterpene resin acids). Accumulated resin is released upon tissue injury and/or produced locally at the site of infestation, with the consequence that the beetle and associated fungal pathogens are killed, encased in resin, and expelled from the bore hole point of entry. This process is called pitching out, and it results in not only killing the attackers and flushing the wound site but also moving the oleoresin to the trunk surface where the turpentine evaporates to permit the resin acids to form a formidable physical barrier that seals the wound. Diterpene resin acids (DRA) play important roles in confer defense against insects and microbial pathogens. Levopimaric acid, an abietane-type DRA, is one of the principal resin acids.[3]
References
[edit]- ^ Kersten, P. J.; Kopper, B. J.; Raffa, K. F.; Illman, B. L. (2006). "Rapid Analysis of Abietanes in Conifers". J Chem Ecol. 32 (12): 2679–2685. CiteSeerX 10.1.1.581.2404. doi:10.1007/s10886-006-9191-z. PMID 17082986.
- ^ a b Lloyd, W. D.; Hedrick, G. W. (1965). "Levopimaric acid". Organic Syntheses. 45: 64; Collected Volumes, vol. 5, p. 699.
- ^ a b Trapp, S.; Croteau, R. (2001). "Defensive Biosynthesis of Resin in Conifers". Annual Review of Plant Physiology and Plant Molecular Biology. 52: 689–724. doi:10.1146/annurev.arplant.52.1.689. PMID 11337413.
- ^ Baldwin, D.; Loeblich, V.; Lawrence, R. (1958). "Acidic Composition of Oleoresins and Rosins". Ind. Eng. Chem. Chem. Eng. Data Series. 3 (2): 342–346. doi:10.1021/i460004a036.
- ^ Mohamed Naceur Belgacem; Alessandro Gandini (3 June 2008). Monomers, polymers and composites from renewable resources. Elsevier. ISBN 978-0-08-045316-3. Retrieved 5 December 2011.
- ^ LaFever, R. E.; Vogel, B. S.; Croteau, R. (1994). "Diterpenoid resin acid biosynthesis in conifers: enzymatic cyclization of geranylgeranyl pyrophosphate to abietadiene, the precursor of abietic acid". Arch Biochem Biophys. 313 (1): 139–149. doi:10.1006/abbi.1994.1370. PMID 8053674.