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The genus Cinnamomum

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178 Nguyen Kim Dao<br />

Table 6.11 Composition of the commercial Chinese and Vietnamese cinnamon barks (% dry weight)<br />

Bark grade Coumarin Cinnam- Cinnamic Cinnamyl Cinnamyl Eugenol<br />

aldehyde acid alcohol acetate<br />

Chinese cinnamon<br />

Xijiang cassia barks<br />

Qibian cassia bark 0.15 2.03 0.09 – – –<br />

Peeled cassia bark 0.26 2.54 0.06 – – –<br />

Flat cassia bark 0.01 2.03 0.07 – – –<br />

Oily tube cassia bark<br />

(1) tr 0.92 0.04 tr – –<br />

(2) 0.03 1.68 0.07 tr – –<br />

Non-pressed cassia<br />

Bark-whole (1) 0.05 1.50 0.03 tr – –<br />

(2) tr 2.65 0.06 tr – –<br />

Pressed cassia<br />

Bark-whole (1) 0.04 1.72 0.06 0.001 0.01 –<br />

(2) 0.07 1.17 0.08 tr – –<br />

(3) 0.08 1.66 0.11 0.02 0.05 –<br />

(4) 0.09 2.82 0.15 tr tr –<br />

Cassia branch (1) 0.03 0.69 0.05 – – –<br />

(2) 0.03 0.30 0.07 – – –<br />

Donxing cassia barks<br />

Oily tube cassia bark 0.06 2.19 0.06 0.01 tr –<br />

Non-pressed cassia<br />

Bark-whole 0.02 3.23 0.13 – – –<br />

Pressed cassia<br />

Bark-whole (1) 0.03 1.72 0.16 – – –<br />

(2) 0.49 2.55 0.10 0.01 tr –<br />

Cassia bark-broken 0.04 1.61 0.30 – – –<br />

Vietnamese cassia barks<br />

Yen Bai (YB) cinnamon<br />

YB I 0.58 3.70 0.13 0.03 0.01 tr<br />

YB II 0.47 3.89 0.12 0.16 0.06 –<br />

YB III 0.73 2.73 0.07 0.04 0.09 –<br />

YB IV 0.40 2.70 0.06 0.02 0.01 –<br />

YB V 0.32 2.70 0.08 0.05 0.06 –<br />

YB Guiyisui 0.33 1.93 0.06 0.02 – –<br />

Mien Nam (MN) cinnamon<br />

MN I 0.57 3.57 0.05 0.23 0.34 0.01<br />

MN II 0.53 4.08 0.07 0.08 0.15 0.03<br />

MNK III 0.32 3.02 0.05 0.08 0.15 0.01<br />

MN V 0.51 3.61 0.09 0.12 0.18 0.01<br />

MN Guiyisui 0.51 3.52 0.10 0.09 0.28 0.02<br />

Source: Kondou et al., 1999.<br />

Note<br />

tr: trace.<br />

fractions obtained in the successive fractionation with n-hexane, butanol and acetone, the<br />

butanol insoluble portion was shown to have the activities. In a detailed study on the<br />

effect of Chinese prescriptions and crude drugs on 1,1-diphenyl-2-picrylhyrazyl radical,<br />

cinnamomi cortex ranked third (after Rhus and Rheum) in its inhibitory effect. Cinnamomi<br />

cortex exhibited strong free radical scavenging activity, indicating that it was effective in

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