Incensole

Last updated
Incensole
Incensole.svg
Names
IUPAC name
(1R,2R,5E,9Z)-1,5,9-trimethyl-12-propan-2-yl-15-oxabicyclo[10.2.1]pentadeca-5,9-dien-2-ol
Identifiers
3D model (JSmol)
ChemSpider
PubChem CID
  • InChI=1S/C20H34O2/c1-15(2)20-12-11-17(4)8-6-7-16(3)9-10-18(21)19(5,22-20)13-14-20/h7,11,15,18,21H,6,8-10,12-14H2,1-5H3/b16-7+,17-11-/t18-,19-,20?/m1/s1
    Key: SSBZLMMXFQMHDP-AWBFOCMTSA-N
  • CC1=CCCC(=CCC2(CCC(O2)(C(CC1)O)C)C(C)C)C
Properties [1]
C20H34O2
Molar mass 306.490 g·mol−1
Density 1.0±0.1 g/cm3
Boiling point 408.9±45.0 °C at 760 mmHg
Vapor pressure 0.0±2.2 mmHg at 25°C
1.493
Hazards
Flash point 160.7±23.0 °C
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Incensole is a C20 diterpene alcohol and biomarker for some plants of the Boswellia genus. It, along with its acetate ester incensole acetate, is an abundant component of frankincense, the resin collected from Boswellia trees. [2] Incensole is used archaeologically to assist in identifying trade routes and distinguishing the identity of frankincense from other resins which may have been used together in incense and other salves. Incensole has also been deemed to be an active component in medicinal frankincense. [2]  

Contents

History

Incensole was first isolated in 1966 at the University of Rome's Institute of Organic Chemistry by S. Corsano and R. Nicoletti while investigating the neutral components of Boswellia carteri resin. [3] There was some controversy as to whether the sample analyzed by S. Corsano and R. Nicoletti was actually from B. carteri and some believed that the original sample was from a B. papyrifera specimen. Further testing done by H. Obermann in 1977 identified an "Eritrea" type B. carteri sample (so named because it originated from the Eritrea region) which displayed incensole levels consistent with those found by Corsano and Nicoletti, but the sample specimen was likely B. papyrifera misidentified as B. carteri. [4] In 2005, incensole was used as a biomarker for frankincense (also known as olibanum) in order to determine the composition of Ancient Egyptian mummification balms and unguents, [5] speaking to its role in studying the history of religion.

Chemistry

Oily in appearance, incensole has low volatility. It can be synthetically prepared from cembrene, [6] a terpenoid, and cembrenol (serratol), its biologic precursor. [6] Diterpenes and terpenoids are classes of biomarkers which are synthesized in plants and have been found in insects, [7] possibly because of accumulation of terpenoids within their diets. [8] [ page needed ] Terpenoids have gained special interest due to their potential as anti-inflammatories, chemotherapies, and antiparasitics. [7]

Incensole with its proposed biosynthetic precursors Serratol and GGPP GGPP to Incensole via Serratol.jpg
Incensole with its proposed biosynthetic precursors Serratol and GGPP

Biosynthetic pathway

It has been proposed that incensole is produced in Boswellia plants via serratol from geranylgeranyl pyrophosphate (GGPP), [4] a C20 precursor for many metabolic branches such as the chlorophyll, carotenoid, and gibberellin biosynthetic pathways. [9] To begin, GGPP loses its pyrophosphate group enabling it to be 1,14-cyclized to form cembrene after the loss of a proton. Cembrene is then hydrolyzed to form serratol which in turn undergoes epoxidation and intramolecular cyclization to form incensole. [4] Though this has been used to make incensole synthetically, [6] the abundances of incensole, serratol, incensole acetate, and iso-serratol in Boswellia species known to produce incensole are inconsistent with what would be expected if this pathway occurred in situ. [4]

Sources of Incensole

Frankincense resin seeping out of B. sacra trunk Incenso-1.jpg
Frankincense resin seeping out of B. sacra trunk

Incensole is mainly found in the resin of Boswellia trees which grow in a region across Northern Africa from Ethiopia to Nigeria. [10] Boswellia trees prefer to grow in arid, stony regions, [10] and cuts to the body of the trees seep frankincense resin which hardens and darkens when exposed to the air.[ citation needed ] Incensole is a biomarker of frankincense from certain Boswellia species; these species are B. papyrifera , B. occulta, B. carteri, B. sacra , [5] [11] [12] [13] and possibly B. serrata though there are conflicting results as to whether it really produces incensole. [4] B. carteri and B. sacra have been determined to actually be the same species, except that B. carteri is native to Africa while B. sacra is native to South Arabia. [4]

It has also been proposed that incensole and incensole acetate can be derived from other sources such as these: [4]

Gas chromatography and mass spectrometry were used to identify incensole in these specimen, but to conclusively identify these species as producers of incensole/incensole acetate, isolation and structural elucidation from these species would have to occur. [4]

Detection and characterization

Deconvoluted mass spectrum of Incensole from incensole and serratol total ion count peak. RT of 24.02 min. (Baeten et al. 2014) Mass Spectrum of Incensole.png
Deconvoluted mass spectrum of Incensole from incensole and serratol total ion count peak. RT of 24.02 min. (Baeten et al. 2014)

Incensole was originally isolated in 1966 by S. Corsano and R. Nicoletti using several ether extractions and vacuum separations, and then characterized using UV-Vis, IR, and H-NMR spectroscopy. They found incensole to have no UV-Vis absorption above 210 mμ. [3] The distinguishing IR and H-NMR peaks of incensole are reported in the tables below, [3] and the observed mass spectrum of incensole from a study done in 2014 on frankincense in incense pots is pictured to the right. [14]

IR Peaks of Incensole [3]
Wave Number (cm−1)Peak Identity
3620-OH
1670C=C
1375, 1390CH3-C-CH3
1050C-O
NMR Peaks of Incensole in CCl4 at 60 Mc [3]
Chemical Shift (ppm)Protons [15] Group Identity
0.90(d, 6H, J = 6.5 c/s)isopropyl
1.02(s, 3H)CH3-C-O
1.48, 1.61(s, 3H)CH3-C=
3.18(d, 1H, J = 10 c/s)HC-OH
5.06(2H, broad signal)CH3CH=C(CH3)2

Incensole is most often extracted by chromatographic extractions and hydrodistillations, which produce a frankincense essential oil. Incensole is typically characterized by GC/MS although thin layer chromatography and near-infrared spectroscopy [16] . [4]

Unfortunately, within some of the earlier literature, frankincense biomarker compositions have been misattributed to different Boswellia species, as was seen in the mistaken attribution of the first extraction of incensole being from a B. carteri specimen when it likely came from a B. papyrifera specimen. This is likely because the taxonomic certifications for frankincense bought from market as opposed to collected straight from the tree are often faulty or absent. [4]

In archaeology

Frankincense has been used for thousands of years in religious ceremonies and for medicinal purposes. [2] In fact, by tracing incensole's degraded products, historians have been able to use it to understand the historical use of incense in religion. In one such case, the examination of incensole as a biomarker led to the identification of certain porous pots buried in medieval, Belgian, Christian graves as incense burners. Further study indicated that though frankincense was a main component of funerary incense at the time, other, cheaper local resins were mixed into the incense, possibly to reduce cost. [14]

Additionally, frankincense has been used for thousands of years as medicine. It is listed in texts such as the Papyrus Ebers and the Syriac book of medicine and was prescribed by the practitioners Celsus and Culpepper as a remedy for a variety of ailments from stomach ulcers and gastrointestinal hemorrhages to gout and open wounds. [13] Modern analysis on the medicinal efficacy of frankincense has revealed incensole and incensole acetate, along with boswellic acids, to be the bioactive ingredients of frankincense. [2]

Due to its religious and medicinal significance, frankincense and its biomarker components, like incensole, can be found all over the world in Europe, Asia, the Mediterranean, and the Middle East [2] [13] [17] as the result of global trade.

Medicinal properties

Previously, the therapeutic properties of frankincense had been attributed to boswellic acids within the resin, but research from 2019 and 2020 has found incensole and its acetate ester to be major contributors to frankincense's therapeutic efficacy. [2] This research has found incensole to act as an anti-inflammatory and neuroprotective compound after murine head-trauma on top of exhibiting anxiolytic, anti-depressive, and sedative effects in mice. [2]

It is proposed that incensole works as an anti-inflammatory through the inhibition of the NF-κB pathway which is responsible for the increased production of proinflammatory proteins. Insensitivity in the NF-κB pathway is correlated to arthritis, asthma, inflammatory bowel disease, ataxia telangiectasia, cancers, and neurodegenerative diseases. [2] [12] [18]

It has also been found that incensole acetate activates the TRPV3 channel [2] which is responsible for regulating wound healing and the perception of pain and itching, among other things. [19] It is thought that this is another key component of incensole's role as an anti-inflammatory agent.

Incensole has also been cited as a potential antibacterial against Bacillus. [12]

Related Research Articles

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<span class="mw-page-title-main">Myrrh</span> Aromatic resin from the Commiphora myrrha tree

Myrrh is a gum-resin extracted from a number of small, thorny tree species of the genus Commiphora. Myrrh resin has been used throughout history as a perfume, incense and medicine. Myrrh mixed with posca or wine was widely used in many ancient cultures to produce pleasurable feelings and as an analgesic.

<span class="mw-page-title-main">Incense</span> Material that releases fragrant smoke when burnt

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<span class="mw-page-title-main">Frankincense</span> Aromatic resin from Boswellia trees

Frankincense is an aromatic resin used in incense and perfumes, obtained from trees of the genus Boswellia in the family Burseraceae. The word is from Old French franc encens. There are several species of Boswellia that produce true frankincense: Boswellia sacra, B. frereana, B. serrata, and B. papyrifera. Resin from each is available in various grades, which depends on the time of harvesting. The resin is hand-sorted for quality.

<i>Boswellia</i> Genus of flowering plants

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References

  1. ↑ "Incensole | C20H34O2 | ChemSpider".
  2. 1 2 3 4 5 6 7 8 9 Moussaieff A, Mechoulam R (October 2009). "Boswellia resin: from religious ceremonies to medical uses; a review of in-vitro, in-vivo and clinical trials". The Journal of Pharmacy and Pharmacology. 61 (10): 1281–1293. doi:10.1211/jpp.61.10.0003. PMID   19814859. S2CID   98846742.
  3. 1 2 3 4 5 Corsano S, Nicoletti R (January 1967). "The structure of incensole". Tetrahedron. 23 (4): 1977–1984. doi:10.1016/S0040-4020(01)82601-6. ISSN   0040-4020.
  4. 1 2 3 4 5 6 7 8 9 10 Al-Harrasi A, Csuk R, Khan A, Hussain J (May 2019). "Distribution of the anti-inflammatory and anti-depressant compounds: Incensole and incensole acetate in genus Boswellia". Phytochemistry. 161: 28–40. Bibcode:2019PChem.161...28A. doi:10.1016/j.phytochem.2019.01.007. PMID   30802641. S2CID   73501446.
  5. 1 2 Hamm S, Bleton J, Connan J, Tchapla A (June 2005). "A chemical investigation by headspace SPME and GC-MS of volatile and semi-volatile terpenes in various olibanum samples". Phytochemistry. 66 (12): 1499–1514. Bibcode:2005PChem..66.1499H. doi:10.1016/j.phytochem.2005.04.025. PMID   15922374.
  6. 1 2 3 Strappaghetti G, Proietti G, Corsano S, Grgurina I (March 1982). "Synthesis of incensole". Bioorganic Chemistry. 11 (1): 1–3. doi:10.1016/0045-2068(82)90042-6.
  7. 1 2 Majhi S (2020-10-29). "Diterpenoids: Natural Distribution, Semisynthesis at Room Temperature and Pharmacological Aspects‐A Decade Update". ChemistrySelect. 5 (40): 12450–12464. doi:10.1002/slct.202002836. ISSN   2365-6549. S2CID   225109058.
  8. ↑ Peters KE, Walters CC, Moldowan JM. The Biomarker Guide. Cambridge University Press. ISBN   978-1-107-32604-0. OCLC   1030120220.
  9. ↑ Zhou F, Wang CY, Gutensohn M, Jiang L, Zhang P, Zhang D, et al. (June 2017). "A recruiting protein of geranylgeranyl diphosphate synthase controls metabolic flux toward chlorophyll biosynthesis in rice". Proceedings of the National Academy of Sciences of the United States of America. 114 (26): 6866–6871. Bibcode:2017PNAS..114.6866Z. doi: 10.1073/pnas.1705689114 . PMC   5495272 . PMID   28607067.
  10. 1 2 "Boswellia papyrifera (Delile) Hochst". African Plant Database. Retrieved 2023-05-01.
  11. ↑ Mitchell J. "Extraction of Frankincense Resins". Bangor University. Retrieved 2023-05-01.
  12. 1 2 3 Al-Yasiry AR, Kiczorowska B (January 2016). "Frankincense--therapeutic properties". Postepy Higieny I Medycyny Doswiadczalnej. 70: 380–391. doi:10.5604/17322693.1200553. PMID   27117114.
  13. 1 2 3 Michie CA, Cooper E (October 1991). "Frankincense and myrrh as remedies in children". Journal of the Royal Society of Medicine. 84 (10): 602–605. doi:10.1177/014107689108401011. PMC   1295557 . PMID   1744842.
  14. 1 2 Baeten J, Deforce K, Challe S, De Vos D, Degryse P (2014-11-12). "Holy smoke in medieval funerary rites: chemical fingerprints of frankincense in southern Belgian incense burners". PLOS ONE. 9 (11): e113142. Bibcode:2014PLoSO...9k3142B. doi: 10.1371/journal.pone.0113142 . PMC   4229304 . PMID   25391130.
  15. ↑ "NMR Guidelines for ACS Journals" (PDF). American Chemical Society. December 2013. Retrieved 23 May 2023.
  16. ↑ Al-Shidhani S, Rehman NU, Mabood F, Al-Broumi M, Hussain H, Hussain J, et al. (May 2018). "Quantification of Incensole in Three Boswellia Species by NIR Spectroscopy Coupled with PLSR and Cross-Validation by HPLC". Phytochemical Analysis. 29 (3): 300–307. Bibcode:2018PChAn..29..300A. doi:10.1002/pca.2743. PMID   29314317.
  17. ↑ Gebrehiwot K, Muys B, Haile M, Mitloehner R (December 2003). "Introducing Boswellia papyrifera (Del.) Hochst and its non-timber forest product, frankincense". International Forestry Review. 5 (4): 348–353. doi:10.1505/ifor.5.4.348.22661. ISSN   1465-5489.
  18. ↑ Moussaieff A, Shohami E, Kashman Y, Fride E, Schmitz ML, Renner F, et al. (December 2007). "Incensole acetate, a novel anti-inflammatory compound isolated from Boswellia resin, inhibits nuclear factor-kappa B activation". Molecular Pharmacology. 72 (6): 1657–1664. doi:10.1124/mol.107.038810. PMID   17895408. S2CID   539345.
  19. ↑ Yang P, Zhu MX (2014). "TRPV3". In Nilius B, Flockerzi V (eds.). Mammalian Transient Receptor Potential (TRP) Cation Channels: Volume I. Handbook of Experimental Pharmacology. Vol. 222. Berlin, Heidelberg: Springer. pp. 273–291. doi:10.1007/978-3-642-54215-2_11. ISBN   978-3-642-54215-2. PMID   24756710.
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