Study of chemical composition of Foeniculum vulgare using Fourier transform infrared spectrophotometer and gas chromatography - mass spectrometry

Journal of Pharmacognosy and Phytotherapy

Volumn 8, Issue 3, 2016, Pages 60-89

  Hussein, Hussein J ^a   Hadi, Mohammed Yahya ^b   Hameed, Imad Hadi ^a  

^a UNIVERSITY OF BABYLON   (Iraq)

^b AL QASIM GREEN UNIVERSITY   (Iraq)

Author keywords

Bioactive compounds; Foeniculum vulgare; Fourier transforminfrared spectroscopy (FT IR); Gas chromatography mass spectrometry (GC MS)

Indexed keywords

1 HEPTATRIACOTANOL; 1 PROPYL 3,6 DIAZAHOMOADAMANTAN 9 OL; 2 ETHOXY 4 VINYLPHENOL; 2 HYDROXY 2 (4 METHOXY PHENYL) N METHYL ACETAMIDE; 2 PROPANONE, 1 (4 METHOXYPHENYL); 2 PROPYL TETRAHYDROPYRAN 3 OL; 2,5 OCTADECADIYNOIC ACID; 4 (2,5 DIHYDRO 3 METHOXYPHENYL)BUTYLAMINE; 4 METHOXYBENZOIC ACID , ALLYL ESTER; 6 METHYLENEBICYCLO[3.2.0]HEPT 3 EN 2 ONE; ANETHOLE; APIOLE; ARISALDEHYDE DIMETHYL ACETAL; ASCARIDOLE EPOXIDE; BENZALDEHYDE ,4 METHOXY; BENZENEMETHANOL , 2 (2 AMINOPROPOXY) 3 METHYL; BENZENEMETHANOL,2 (2 AMINOPROPOXY) 3 METHYL; BENZHYDRAZIDE , 4 METHOXY N2 (2 TRIFLUOROACETYLCYCLOHEPTEN 1 YL); CORYMBOLONE; CYCLOPENTA [1,3]CYCLOPROPA[1,2]CYCLOHEPTEN 3(3AH) ONE,1,2,3B,6,7; ESTRAGOLE; FENRETINIDE; FOENICULUM VULGARE EXTRACT; L FENCHONE; MANNOSE; PLANT MEDICINAL PRODUCT; PROPIOLIC ACID , 3 (1 HYDROXY 2 ISOPROPYL 5 METHYLCYCLOHEXYL); PTERIN DERIVATIVE; SPIRO[4.5]DECAN 7 ONE,1,8 DIMETHYL 8,9 EPOXY 4 ISOPROPYL; UNCLASSIFIED DRUG; UNINDEXED DRUG;

ANTIANGIOGENIC ACTIVITY; ANTIARRHYTHMIC ACTIVITY; ANTIBACTERIAL ACTIVITY; ANTIFUNGAL ACTIVITY; ANTIINFLAMMATORY ACTIVITY; ANTIMALARIAL ACTIVITY; ANTINEOPLASTIC ACTIVITY; ANTINOCICEPTION; ANTIOXIDANT ACTIVITY; ANTISPASMOLYTIC ACTIVITY; ARTICLE; BACTERIOSTASIS; BIOLOGICAL ACTIVITY; INFRARED SPECTROSCOPY; MASS FRAGMENTOGRAPHY; NEUROTOXICITY; NONHUMAN; PHYTOCHEMISTRY; PLANT SEED;

EID: 84959519195     PISSN: 21412502     EISSN: None     Source Type: Journal    
DOI: 10.5897/JPP2015.0372     Document Type: Article

References (21)

1. Altameme HJ, Hameed IH, Idan SA, Hadi MY (2015a). Biochemical analysis of Origanum vulgare seeds by Fourier-transform infrared (FT-IR) spectroscopy and gas chromatography-mass spectrometry (GC-MS). J. Pharmacogn. Phytother. 7(9):221-237.
2. Altameme HJ, Hameed IH, Kareem MA (2015b). Analysis of alkaloid phytochemical compounds in the ethanolic extract of Datura stramonium and evaluation of antimicrobial activity Afr. J. Biotechnol. 14(19):1668-1674.
3. El-Awadi ME, Esmat AH (2010). Physiological Responses of Fennel (Foeniculum Vulgare Mill) Plants to Some Growth Substances. J. Am. Sci. 6:985-991.
4. Gross M, Friedman J., Dudia N, Larkov O, Cohen Y, Bare E (2002). Biosynthesis of estragole and t-anethole in bitter fennel (Foeniculum vulgare Mill. var. vulgare) chemotypes. Changes in SAM, phenylpropene o-methyltranferase activities during development. Plant Sci. 163:1047-1053.
5. Hameed IH, Hussein HJ, Kareem MA, Hamad NS (2015a). Identification of five newly described bioactive chemical compounds in methanolic extract of Mentha viridis by using gas chromatography-mass spectrometry (GC-MS). J. Pharmacogn. Phytother. 7(7):107-125.
6. Hameed IH, Ibraheam IA, Kadhim HJ (2015b). Gas chromatography mass spectrum and Fourier-transform infrared spectroscopy analysis of methanolic extract of Rosmarinus oficinalis leaves. J. Pharmacogn. Phytother. 7(6):90-106.
7. Hameed IH, Jasim H, Kareem MA, Hussein AO (2015c). Alkaloid constitution of Nerium oleander using gas chromatography-mass spectroscopy (GC-MS). J. Med. Plants Res. 9 (9):326-334.
8. Hameed IH, Hamza LF, Kamal SA (2015d). Analysis of bioactive chemical compounds of Aspergillus niger by using gas chromatography-mass spectrometry and Fourier-transform infrared spectroscopy. J. Pharmacogn. Phytother. 7(8):132-163.
9. Hamza LF, Kamal SA, Hameed IH (2015). Determination of metabolites products by Penicillium expansum and evaluating antimicobial activity. J. Pharmacogn. Phytother. 7(9):194-220.
10. Hay RK, Waterman PG (1993). Volatile Oil Crops: Their Biology, Biochemistry and Production, Longman Scientific and Technical, Essex, England.
11. Hornok L (1992). The cultivating and Processing of Medicinal Plants. John Wiley, New York. P 338.
12. Hussein AO, Hameed IH, Jasim H, Kareem MA (2015). Determination of alkaloid compounds of Ricinus communis by using gas chromatography-mass spectroscopy (GC-MS). J. Med. Plants Res. 9(10):349-359.
13. Imad H, Mohammed A, Aamera J (2014a). Genetic variation and DNA markers in forensic analysis. Afr. J. Biotechnol. 13(31):3122-3136.
14. Imad H, Mohammed A, Cheah Y, Aamera J (2014b). Genetic variation of twenty autosomal STR loci and evaluate the importance of these loci for forensic genetic purposes. Afr. J. Biotechnol. 13:1-9.
15. Imad H, Muhanned A, Aamera J, Cheah Y (2014c). Analysis of eleven Y-chromosomal STR markers in middle and south of Iraq. Afr. J. Biotechnol. 13(38):3860-3871.
16. Jasim H, Hussein AO, Hameed IH, Kareem MA (2015). Characterization of alkaloid constitution and evaluation of antimicrobial activity of Solanum nigrum using gas chromatography mass spectrometry (GC-MS). J. Pharmacogn. Phytother. 7(4):56-72.
17. Kareem MA, Hussein AO, Hameed IH (2015). Y-chromosome short tandem repeat, typing technology, locus information and allele frequency in different population: A review. Afr. J. Biotechnol. 14(27):2175-2178.
18. Lucinewton S, Raul N, Carvalho J, Mirian B, Lin C, Angela A (2005). Supercritical fluid extraction from fennel (Foeniculum vulgare) global yield, composition and kinetic data. J. Supercrit. Fluids 35:212-219.
19. Marino SD, Gala F, Borbone N, Zollo F, Vitalini S, Visioli F, Iorrizi M (2007). Phenolic glycosides from Foeniculum vulgare fruit and evaluation of antioxidative activity. Phytochem. 68:1805-1812.
20. Mohammed A, Imad H (2013). Autosomal STR: From locus information to next generation sequencing technology. Res. J. Biotechnol. 8(10):92-105.
21. Telci I, Demirtas I, Sahin A (2009). Variation in plant properties and essential oil composition of sweet fennel (Foeniculum vulgare Mill.) fruits during stages of maturity. Ind. Crop Prod. 30:126-130.