US2013035305A1PendingUtilityA1
Use of an active ingredient combination that contains hydroxystilbene for preventing and/or treating diseases
Est. expiryFeb 4, 2025(expired)· nominal 20-yr term from priority
A61P 35/00A61P 25/06A61P 25/24A61P 25/22A61P 29/00A61P 13/02A61P 13/08A61K 9/2866A61K 31/085A61K 36/482A61K 9/2846A61K 36/15A23L 33/105A61K 31/7034A61K 36/481A61K 9/2054A61K 36/708
36
PatentIndex Score
0
Cited by
0
References
0
Claims
Abstract
The invention relates to the use of a combination of active ingredients, selected from resveratrol and piceatannol precursors and functional derivatives thereof, in addition to the use of the stereoisomeric forms of said ingredients, in the form of salts or phenol respectively, for producing an agent for the prevention and/or treatment of diseases, whose occurrence and/or progress is associated with an increased IL-6 serum level and/or whose occurrence and/or progress can be treated by a dose of a selective oestrogen receptor .beta. (ER-β) agonist.
Claims
exact text as granted — not AI-modified1 . The use of a hydroxystilbene-containing active ingredient combination comprising at least two compounds selected from precursors of resveratrol and piceatannol, or functional derivatives thereof; and the stereoisomeric forms thereof, in each case in the form of their salts or in the phenol form, for producing a composition for preventing and/or treating disorders whose development and/or progression is associated with an elevated serum IL-6 level and/or whose development and/or progression can be treated by administering a selective estrogen receptor β ERβ agonist.
2 . The use of claim 1 , wherein the disorder is
a) depression and anxiety, b) migraine, c) chronic inflammatory disorders, d) tumorigenesis and/or inhibition of tumor progression for endocrine-dependent and/or—independent tumors, or e) prostate cancer and/or of LUTS.
3 . The use as claimed in claim 1 , wherein the active ingredient combination includes a) a total hydroxystilbene content of more than 90% by weight; and/or b) a total content of glycosidic resveratrol and piceatannol precursors of more than 76% by weight, and/or c) an aglycone content of less than 5% by weight; and/or d) a content of less than 0.5% by weight of anthraquinone and/or anthraquinoids.
4 . The use as claimed in claim 1 , wherein the hydroxystilbene components of the active ingredient combination is chemically synthesized or can be isolated from plants.
5 . The use as claimed in claim 1 , wherein the active ingredient combination substantially comprises rhaponticin and deoxyrhaponticin.
6 . The use as claimed in claim 5 , wherein the active ingredient combination substantially comprises rhaponticin and deoxyrhaponticin in a ratio of about 10:1 to 1:10 by weight.
7 . The use as claimed in claim 1 , wherein the active ingredient combination comprises rhaponticin, deoxyrhaponticin, and rhapontigenin and/or deoxyrhapontigenin.
8 . The use as claimed in claim 1 , wherein the active ingredient combination is substantially free of aglycone derivatives of rhaponticin and deoxyrhaponticin.
9 . The use as claimed in claim 1 , wherein the active ingredient combination substantially consists of approximately
60-70% by weight rhaponticin 30-40% by weight deoxyrhaponticin 0-2% by weight trans-rhapontigenin 0-2% by weight deoxyrhapontigenin.
10 . The use as claimed in claim 1 , wherein the active ingredient or the active ingredient combination can be obtained from plants of the genus Rheum spp, Astragalus spp, Cassia spp or Picea spp.
11 . The use as claimed in claim 1 , wherein where the active ingredient or the active ingredient combination is obtainable from roots and/or other plant parts of Rheum rhaponticum.
12 . The use as claimed in claim 1 , further in combination with at least one further active ingredient which is suitable for the prevention and/or treatment of said disorder and differs from compounds as defined in claim 1 .
13 . The use as claimed in claim 1 , wherein the composition is selected from chemically synthesized, biotechnologically produced, herbal and homeopathic medicaments, other medicinal plant preparations, dietary supplements and dietetic food products.
14 . A dosage form comprising in a pharmaceutically or dietetically acceptable carrier an active ingredient or an active ingredient combination as defined in claim 1 .
15 . The use of an active ingredient combination as claimed in claim 1 for reducing the IL-6 serum level and/or for activating ERβ in vitro or in vivo.
16 . A composition comprising a dosage form as defined in claim 14 .Join the waitlist — get patent alerts
Track US2013035305A1 — get alerts on status changes and closely related new filings.
We store only your email — no account needed. See our privacy policy.