1995
DOI: 10.1111/j.1398-9995.1995.tb02515.x
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Cinnamon bark oil, a potent fungitoxicant against fungi causing respiratory tract mycoses

Abstract: Cinnamic aldehyde has been identified as the active fungitoxic constituent of cinnamon (Cinnamomum zeylanicum) bark oil. The fungitoxic properties of the vapours of the oil/active constituent against fungi involved in respiratory tract mycoses, i.e., Aspergillus niger, A. fumigatus, A. nidulans A. flavus, Candida albicans, C. tropicalis, C. pseudotropicalis, and Histoplasma capsulatum, were determined in vitro as minimum inhibitory concentration (MIC), minimum lethal concentration (MLC), inoculum density susta… Show more

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Cited by 75 publications
(36 citation statements)
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“…192 Polygodial-treated yeast cells showed a fragmentation of the cell membrane, formation of many vesicles in the cytoplasma, and changes of mitochondia and nucleus membrane. 193 A database substructure search resulted in the retrieval of a series of anticandidal compounds having a 5-dimethylhex-5-en-2-oyl (2O-DMH) substructure (a-terpineol (70), linalool (66), alphabisabolol (103), nerolidol (95), galanolactone (117), and trans-8b(17)epoxy-12-labdene-15,16-dial (120)), 194 wherein the increase of activity (lowest reported anticandidal MIC: 400, 225, 100, 25, 12,5 mg/mL) is correlated (r ¼ 0.91) to increase of molecular volume (174,179,258,342, 350 cubic angstrom, calculated with 195 ). The 2O-DMH side chain without the oxygen atom is found in zymosterol, a late and fungi specific intermediate in ergosterol biosynthesis.…”
Section: E Vapor Phase Activity Testsmentioning
confidence: 94%
See 1 more Smart Citation
“…192 Polygodial-treated yeast cells showed a fragmentation of the cell membrane, formation of many vesicles in the cytoplasma, and changes of mitochondia and nucleus membrane. 193 A database substructure search resulted in the retrieval of a series of anticandidal compounds having a 5-dimethylhex-5-en-2-oyl (2O-DMH) substructure (a-terpineol (70), linalool (66), alphabisabolol (103), nerolidol (95), galanolactone (117), and trans-8b(17)epoxy-12-labdene-15,16-dial (120)), 194 wherein the increase of activity (lowest reported anticandidal MIC: 400, 225, 100, 25, 12,5 mg/mL) is correlated (r ¼ 0.91) to increase of molecular volume (174,179,258,342, 350 cubic angstrom, calculated with 195 ). The 2O-DMH side chain without the oxygen atom is found in zymosterol, a late and fungi specific intermediate in ergosterol biosynthesis.…”
Section: E Vapor Phase Activity Testsmentioning
confidence: 94%
“…However, several authors have also found the opposite effect, and therefore it was concluded that there is no clear predictability for the degree of hydroxylation and toxicity to microorganism. 121,201 To overview the structural similarities among flavonoids (174)(175)(176)(177)(178)(179)(180)(181)(182)(183)(184)(185)(186)(187)(188)(189)(190)(191)(192)(193), several compounds with a molecular weight higher than 350 Da were respected in Figure 7. The substitution pattern of compounds (186-193) followed rules, which point to a common mode of action, see Figure 8.…”
Section: E Vapor Phase Activity Testsmentioning
confidence: 99%
“…Anticandidal and antidermatophytic activities of the essential oils from various Cinnamomum species have been demonstrated (Mastura et al, 1999). Cinnamaldehyde, isolated from Cinnamomum zeylanicum, has been identified as the major active fungitoxic component of the cinnamon bark oil against various yeasts, especially Candida albicans, which are involved in respiratory tract mycoses (Singh et al, 1995). The essential oil from Cinnamomum also exhibited strong antibacterial properties and its major constituent cinnamaldehyde possessed the strongest antibacterial activity compared with the other components (Chang et al, 2001).…”
Section: Introductionmentioning
confidence: 98%
“…Nevertheless, the excessive addition may be harmful due to allyl sulfide concentrations, which interfere in metabolism, resulting in low growth (LEE; GAO, 2012). The beneficial effects on health of cinnamon are related to the chemical compounds that compose it, such as the active ingredient cinnamaldehyde, which is responsible for the smell, as well as the antioxidant, antimicrobial, and antifungal activities (SINGH et al, 2007). Boudry and Perrier (2008) stated that cinnamaldehyde induced the discharge of HCO 3 -and CL -by intestinal epithelium cells, also having an effect in the adhesion of bacteria to the intestinal microbiota.…”
Section: Resultsmentioning
confidence: 99%