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FIELD OF THE INVENTION
The present invention is directed to methods and compositions for treating tumors and other metastatic diseases exhibiting high tyrosinase and saccharide enzyme activity. The invention is further directed to methods and compositions for treating tumors having high tyrosinase
FIELD OF THE INVENTION
The present invention is directed to methods and compositions for treating tumors and other metastatic diseases exhibiting high tyrosinase and .beta.-glucuronidase activity. The invention is further directed to methods and compositions for treating tumors having high
This invention relates to compositions extracted from vegetable matter and more particularly to phytochemicals, including saponogenins and saponins, catechins, lignans, phenolic acids, and isoflavones, and especially those extracted from a family of plants including soy, flax, tea, and cocoa, and
This invention relates to compositions extracted from vegetable matter and more particularly to phytochemicals, including saponogenins and saponins, lignans, phenolic acids, catechins and isoflavones, and especially those extracted from a family of plants including soy, flax, tea, and cocoa and
The present invention relates to polyether-substituted anti-tumor agents, namely the use of polyethers as new synthetic carrier systems serving for infiltrating tremors with low-molecular compounds so as to improve the in vivo tumor diagnosis and tumor therapy using different clinical
RELATED U.S. APPLICATION DATA
Priority is derived herein from U.S. application Ser. No. 11/128,140, filed May 12, 2005, now U.S. Pat. No. 7,098,198, which is a continuation of U.S. application Ser. No. 10/630,578, filed Jul. 30, 2003, now U.S. Pat. No. 6,933,292, and from U.S. Provisional
FIELD OF THE INVENTION
The invention relates to the prevention and/or treatment of cholesterol-associated tumors by means of administering azetidinone-based cholesterol absorption inhibitors. Particularly, hypertrophy of prostate tissues, breast tissues, endometrial tissues, and colon tissues are
RELATED APPLICATIONS/INCORPORATION BY REFERENCE
All documents cited or referenced herein ("herein cited documents"), and all documents cited or referenced in the herein cited documents, together with any manufacturer's instructions, descriptions, product specifications, and product sheets for any
BACKGROUND OF THE INVENTION
The present invention is directed to a method of modulating cellular function and to a pharmaceutical composition containing a phenolic ester of a fatty acid selected to modulate cellular function.
Many drugs interact at the cell membrane surface by combining with cell
BACKGROUND OF THE INVENTION
(1) Field of the Invention
The present invention relates to cytokine inhibitors. More specifically, the present invention identifies and characterizes several inhibitors of macrophage migration inhibitory factor.
(2) Description of the Related Art
Macrophage migration
BACKGROUND OF THE INVENTION
(1) Field of the Invention
The present invention relates to cytokine inhibitors. More specifically, the present invention identifies and characterizes several inhibitors of macrophage migration inhibitory factor.
(2) Description of the Related Art
Macrophage migration
FIELD OF THE INVENTION
This invention relates to a mixture of an extract from a plant belonging to the Zygophyllaceae family containing phenolic compositions and a metal salt. The mixture is useful as a pharmaceutical agent, for example, in the treatment of cancers, non-malignant tumors,
BACKGROUND OF THE INVENTION
The cytoskeletal protein tubulin is among the most attractive therapeutic drug targets for the treatment of solid tumors. A particularly successful class of chemotherapeutics mediates its anti-tumor effect through a direct binding interaction with tubulin. This
BACKGROUND OF THE INVENTION
The cytoskeletal protein tubulin is among the most attractive therapeutic drug targets for the treatment of solid tumors. A particularly successful class of chemotherapeutics mediates its anti-tumor effect through a direct binding interaction with tubulin. This
This invention relates to new phenol derivatives which possess antioestrogenic activity.
Various antioestrogens are now known. Two such compounds, tamoxifen and clomiphene, are commercially available, and others, for example nafoxidine, trioxifene and a number of compounds with code-numbers such as