(10E,12Z,15Z)-9-Hydroxy-10,12,15-octadecatrienoic Acid Methyl Ester as an Anti-inflammatory Compound from Ehretia dicksonii

The methanol extract of Ehretia dicksonii provided (10E,12Z,15Z)-9-hydroxy-10,12,15-octadecatrienoic acid methyl ester (1) which was isolated as an anti-inflammatory compound. Compound 1 suppressed 12-O-tetradecanoyl-phorbol-13-acetate (TPA)-induced inflammation on mouse ears at a dose of 500 μg (the inhibitory effect (IE) was 43%). Linolenic acid methyl ester did not inhibit this inflammation at the same dose. However, the related compounds of 1, (9Z,11E)-13-hydroxy-9,11-octadecadienoic acid (5) and (9Z,11E)- 13-oxo-9,11-octadecadienoic acid (6), showed potent activity (IE500 μg of 63% and 79%, respectively). Compounds 1, 4 ((9Z,12Z,14E)-16-hydroxy-9,12,14-octadecatrienoic acid), 5 and 6 also showed inhibitory activity toward soybean lipoxygenase at a concentration of 10 μg/ml.

[1]  C. Ip,et al.  Conjugated linoleic acid inhibits proliferation and induces apoptosis of normal rat mammary epithelial cells in primary culture. , 1999, Experimental cell research.

[2]  G. Mcneill,et al.  Antiplatelet effects of conjugated linoleic acid isomers. , 1999, Biochimica et biophysica acta.

[3]  S. Tomoda,et al.  Structure and Natural Bond Orbital Analysis of Oxiranes Substituted with a Group 14 Element. A Comment of SN2 Regioselectivity , 1999 .

[4]  A. Cesano,et al.  Conjugated linoleic acid suppresses the growth of human breast adenocarcinoma cells in SCID mice. , 1997, Anticancer research.

[5]  J. Mizutani,et al.  An enzymatic formation of 13-oxo-trideca-9,11-dienoic acid from 13-hydroperoxylinolenic acid by a homolytic hydroperoxide lyase in elicitor-treated soybean cotyledons. , 1995, Biochimica et biophysica acta.

[6]  L. Luedecke,et al.  Inhibitory effect of conjugated dienoic derivatives of linoleic acid and beta-carotene on the in vitro growth of human cancer cells. , 1992, Cancer letters.

[7]  C. Ip,et al.  Mammary cancer prevention by conjugated dienoic derivative of linoleic acid. , 1991, Cancer research.

[8]  Takayuki Okatani,et al.  Studies on inhibitors of skin tumor promotion, VI. Inhibitory effects of quinones on Epstein-Barr virus activation. , 1989, Journal of natural products.

[9]  T. Sugimura,et al.  Diversity in the chemical nature and mechanism of response to tumor promoters. , 1989, Progress in clinical and biological research.

[10]  M. Tabata,et al.  A comparative study on anti-inflammatory activities of the enantiomers, shikonin and alkannin. , 1986, Journal of natural products.

[11]  F. Marks,et al.  The mouse ear edema: a quantitatively evaluable assay for tumor promoting compounds and for inhibitors of tumor promotion. , 1984, Cancer letters.

[12]  N. Harada,et al.  UNSATURATED HYDROXY FATTY ACIDS, THE SELF DEFENSIVE SUBSTANCES IN RICE PLANT AGAINST RICE BLAST DISEASE , 1984 .

[13]  T. Cheesbrough,et al.  [53] Lipoxygenase from soybeans: EC 1.13.11.12 Linoleate:oxygen oxidoreductase , 1981 .

[14]  E. Hecker Structure-activity relationships in diterpene esters irritant and cocarcinogenic to mouse skin , 1978 .

[15]  Y. Isomura,et al.  Antitumor activity of shikonin and its derivatives. , 1977, Chemical & pharmaceutical bulletin.