|
|
1-800-228-0872 |
|
|
|
|
Indole
|
|
The indole nucleus, known to chemists as benzopyrrole, is the parent
member of a broad spectrum of nitrogen heterocyclic biochemicals
commonly found in nature. Indole derivatives occur in flower oils such
as jasmine and orange blossom, and in less pleasant substances such as
coal tar and fecal matter. Indoles also exist as melanin-related
organics and indigoid pigments. One prominent indole configuration, indole-3-carbinol, has achieved
notoriety as a therapeutic phytochemical. This recognition is not only
because of the anticancer activity of indole-3-carbinol, but because the
vegetables in which it occurs belong to the much maligned Brassica
genus of cruciferous vegetables; the ever unpopular broccoli, brussel
sprouts, cabbage, cauliflower, and kale. It would seem that
indole-3-carbinol is partially responsible for the strong flavor that
makes these vegetables so unpopular . . . and so healthy. Indole-3-carbinol is a highly effective anticancer agent, blocking
carcinogenic substances before they reach their cellular targets and
eliminating DNA damage in cell nuclei. It may also turn out to be an
important chemical tool in fighting breast cancer because it inhibits
estrogen-induced growth of cancer cells and converts the more dangerous
forms of estrogen to safer forms. |
|
||||||||||||||||||||||||||||||||||||||
|
|
|||||||||||||||||||||||||||||||||||||||
|
T. J. Clark's Secure Shopping Cart Order Line 1-800-228-0872 Copyright 1998-2005 T. J.
Clark & Company *These statements have
not been evaluated by the Food and Drug Administration. |