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Constituent Composition and Biological Activity of Essential Oil from Turczaninowia fastigiata

Suleimen, E. M. ; Iskakova, Zh. B. ; et al.
In: Chemistry of Natural Compounds, Jg. 54 (2018-05-01), S. 597-599
Online unknown

Constituent Composition and Biological Activity of Essential Oil from Turczaninowia fastigiata 

The monotypic genus Turczaninowia DC. (Asteraceae = Compositae) was separated by Augustin De Candolle (DC.) from the genus Aster in 1836. The eastern Asian species Turczaninowia fastigiata (Fisch.) DC. (= Aster fastigiatus Fisch.) grows in eastern Siberia (Dauria), southern Russian Far East (Primorsky Krai, south of Khabarovsk Krai, southeast of Amur Region), Mongolia, northeastern China, Korea, and Japan. It is a biennial plant that inhabits grassy valley meadows and gentle mountain slopes and flowers from July to September [[1] ].

Flavonoids were observed previously in the aerial part of T. fastigiata [[2] ]. To the best of our knowledge, the composition of essential oil from this plant has not been studied.

Raw material for the study was collected during flowering on Aug. 10, 2016, in the vicinity of Turii Rog, Khankaiskii District, Primorsky Krai (Russia), in a grassy dry meadow. Specimens of the plants are preserved in the herbarium of the Chemotaxonomy Laboratory, PIBOCh, FEB, RAS (Vladivostok) under herbarium code T. fastigiata 103606.

Essential oil was obtained from the aerial part of air-dried raw material by steam distillation in a Clevenger apparatus for 2 h using hexane as a trap [[3] ]. GC-MS analysis of essential oils was carried out under conditions analogous to those in the literature [[4] ].

Table 1 shows that the main components of T. fastigiata essential oil were β-pinene (7.3%), trans-nerolidol (4.0%), α-calacorene (3.1%), spathulenol and perhydrofarnesyl acetone (2.2% each), and hexanal and α-humulene epoxide II (2.0% each).

Constituent Composition of Essential Oil from T. fastigiata

ConstituentRI calcd%ConstituentRI calcd%
Hexanal7822.0Citral12030.1
Octane7980.1Carvacrol methyl ether12050.1
2-Hexenal8190.3Perillic aldehyde12270.1
2-Heptanone8640.1Phellandral12300.3
3-(2-Propenyl)cyclohexene8730.15-Isopropenyl-2-methylcyclopent-1-ene carboxaldehyde12390.1
Heptanal8750.2
Nonane9010.2Nonanoic acid12600.2
Tricyclene9130.1Dihydroedulan12630.1
α-Thujene9180.2trans-Sabinyl acetate12651.0
Benzaldehyde9220.1α-Cubebene13360.2
α-Pinene9231.7cis-Geranyl acetate13420.5
Camphene9331.81-(2,6,6-Trimethyl-1,3-cyclohexadien-1-yl)-2-buten-1-one13510.1
Thuja-2,4(10)-diene9370.1
Sabinene9571.1cis-Jasmone13550.2
β-Pinene9597.3Modhephene13581.4
2,3-Dehydro-1,8-cineol9710.4β-Bourbonene13640.2
2-Pentylfuran9740.6β-Elemene13740.6
Octanal9760.2Caryophyllene13950.1
α-Myrcene9791.7β-Copaene14060.4
trans-2-(2-Pentenyl)furan9820.1α-Bergamotene14190.1
α-Phellandrene9890.3Dihydropseudoionone14220.4
α-Terpinene10020.4Humulene14260.8
o-Cymol10050.6Unident. 214310.3
β-Phellandrene10110.6Eudesm-1,4(15),11-triene14360.1
Limonene10141.9trans-β-Farnesene14400.5
trans-β-Ocimene10250.1Unident. 314420.4
Unident. 110280.31,2,9,10-Tetrahydroaristolane14440.4
α-Ocimene10350.3β-Guaiene14470.2
γ-Terpinene10420.6γ-Muurolene14490.4
cis-Linalool oxide10510.2β-Selinene14540.7
1-Methyl-3-(1-methylethenyl)benzene10660.12,6,10-Trimethyltridecane14600.7
Terpinolene10720.2γ-Gurjunene14640.3
6-Methyl-3,5-heptadien-2-one10730.1α-Muurolene14710.6
Nonanal10800.5cis,trans-α-Farnesene14730.4
Linalool10821.8(Z)-α-Bisabolene14780.1
Perillene10830.8β-Bisabolene14840.5
β-Thujene10870.1β-Vatirenene14851.0
α-Campholenal10950.3δ-Cadinene14910.8
trans-Chrysanthenol11060.9α-Calacorene14993.1
trans-Pinocarveol11100.9β-Cadinene15040.2
trans-Sabinol11141.0Elemol15090.2
cis-Verbenol11180.1α-Copaen-11-ol15140.3
Pinocarvone11240.6Germacrene B15170.3
(E)-2-Nonenal11290.1β-Calacorene15190.3
p-Mentha-1,5-dien-8-ol11350.21,5-Epoxysalvial-4(14)-ene15221.1
Cryptone11400.6Palustrol15280.5
Terpinen-4-ol11480.6Spathulenol15332.2
Benichanal11520.8trans-Nerolidol15364.0
1,3,5,8-Unidecatriene11550.1Caryophyllene oxide15420.2
α-Terpineol11590.4trans-Z-α-Bisabolene epoxide15440.2
Myrtenol11650.4Mintketone15480.6
Decanal11780.8Globulol15510.1
β-Cyclocitral11800.1Isoaromadendrene epoxide15540.8
Cuminal11940.6(2E)-2-Methyl-4-(2,6,6-trimethyl-1-cyclohexen-1-yl)-2-butenal15600.3
Carvone11980.2
α-Humulene epoxide II15652.0Calarene epoxide16650.2
2,2,4-Trimethyl-1,3-pentanediol diisobutanoate15700.6Unident. 516840.3
Unident. 415730.4Benzyl benzoate17090.2
γ-Eudesmol15800.2Tetradecanoic acid17550.1
α-Corocalene15840.42-Octylbenzoate17620.2
Patchoulane15880.2n-Octyl benzoate17820.1
Caryophylladienol II15931.2Unident. 618080.3
Cedran-8-ol15990.4Octadecane18110.1
Hexadecane16020.2Unident. 718160.2
τ-Cadinol16070.2Diisobutylphthalate18240.8
β-Eudesmol16090.2Perhydrofarnesyl acetone18362.2
Tetradecanolide16130.8Neophytadiene18440.2
epi-γ-Eudesmol16160.3Farnesyl acetone18920.1
τ-Muurolol16180.4Dibutylphthalate19120.1
α-Santalol16240.3Hydrofol19501.5
Longifolene aldehyde16330.2Tetracosane24010.1
Cadalene16360.9Pentacosane25140.4
Aromadendrene oxide-(2)16410.1Hexacosane26010.1
ent-Germact-4(15),5,10(14)-trien-1β-ol16480.7Heptacosane26960.3
(1R,7S,E)-7-Isopropyl-4,10-dimethylene-cyclodec-5-enol16510.1Squalene28100.2
Hentriacontane30910.2
α-Bisabolol16560.3Total82.8

The cytotoxic activity of T. fastigiata essential oil was determined using the brine shrimp (Artemia salina) lethality test [[5] ]. The experiments established that T. fastigiata essential oil at all tested concentrations (10, 5, and 1 mg/mL) exhibited acute (96%) lethal toxicity, i.e., all larvae died.

The antiradical activity of the essential oils was determined as before [[6] , [7] ]. Essential oil from T. fastigiata had low antiradical activity as compared with butylhydroxyanisole preparation.

Translated from Khimiya Prirodnykh Soedinenii, No. 3, May-June, 2018, pp. 507-508.

References Citations

1 Tamamshyan SG, Genus Turczaninowia DC., Flora of the USSR, 1959, Moscow, Leningrad, Izd. Akad. Nauk SSSR, 136, 138

  • 2 Zdorov′eva EN, Rastit. Resur., 1972, 8, 3, 355
  • 3 State Pharmacopoeia of the USSR, No. 2, General Methods of Analysis. Medicinal Plant Raw Material of the MH USSR [in Russian], 11, th Ed., Moscow, 1990, 400 pp.
  • 4 Suleimen EM, Ibataev ZA, Iskakova ZB, Dudkin RV, Gorovoi PG, Aistova EV, Chem. Nat. Compd., 2017, 53, 169, 10.1007/s10600-017-1940-4
  • 5 Suleimenov EM, Chem. Nat. Compd., 2009, 45, 710, 10.1007/s10600-009-9423-x
  • 6 Sawant O, Kadam VJ, Ghosh R, J. Herb. Med. Toxicol., 2009, 3, 2, 39
  • 7 Sisengalieva GG, Suleimen EM, Ishmuratova IY, Iskakova ZB, Hecke K, Chem. Nat. Compd., 2015, 51, 544, 10.1007/s10600-015-1337-1

By E. M. Suleimen; Zh. B. Iskakova; R. V. Dudkin and P. G. Gorovoi

Titel:
Constituent Composition and Biological Activity of Essential Oil from Turczaninowia fastigiata
Autor/in / Beteiligte Person: Suleimen, E. M. ; Iskakova, Zh. B. ; Gorovoi, P. G. ; Dudkin, R. V.
Link:
Zeitschrift: Chemistry of Natural Compounds, Jg. 54 (2018-05-01), S. 597-599
Veröffentlichung: Springer Science and Business Media LLC, 2018
Medientyp: unknown
ISSN: 1573-8388 (print) ; 0009-3130 (print)
DOI: 10.1007/s10600-018-2421-0
Schlagwort:
  • 010405 organic chemistry
  • Chemistry
  • Biological activity
  • Plant Science
  • General Chemistry
  • 01 natural sciences
  • General Biochemistry, Genetics and Molecular Biology
  • 0104 chemical sciences
  • law.invention
  • 010404 medicinal & biomolecular chemistry
  • law
  • Environmental chemistry
  • Composition (visual arts)
  • Essential oil
Sonstiges:
  • Nachgewiesen in: OpenAIRE
  • Rights: CLOSED

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