US2007042973A1PendingUtilityA1
Treatment of pain and fever
Est. expiryApr 2, 2016(expired)· nominal 20-yr term from priority
A61P 43/00A23K 20/111A23G 1/32C07D 311/32A61K 31/7048C11B 5/0035C07H 17/06A61P 29/00A61K 31/353A61K 9/2068A61K 9/2018A23G 3/36A23K 50/40A61K 9/4858C07D 311/64C07D 311/62A61K 45/06A61K 36/5777
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Claims
Abstract
This invention relates to a method of treating, decreasing, or preventing pain or fever comprising administering to a subject in need thereof a composition comprising the inventive compounds.
Claims
exact text as granted — not AI-modified1 - 208 . (canceled)
209 . A method of treating pain and/or fever comprising administering to the subject in need thereof a composition comprising an effective amount of a compound having the formula An, a pharmaceutically acceptable salt thereof, or an oxidation product thereof:
wherein
n is an integer from 2 to 18, such that there is at least one terminal monomeric unit A, and one or a plurality of additional monomeric units;
R is 3-(α)—OH, 3-(β)—OH, 3-(α)-O-sugar, or 3-(β)-O-sugar;
bonding between adjacent monomers takes place at positions selected from the group consisting of 4, 6 and 8;
a bond of an additional monomeric unit in position 4 has alpha or beta stereochemistry;
X, Y and Z are selected from the group consisting of monomeric unit A, hydrogen, and a sugar, with the proviso that as to the at least one terminal monomeric unit, bonding of the additional monomeric unit thereto is at position 4 and optionally Y=Z=hydrogen;
the sugar is optionally substituted with a phenolic moiety;
wherein the subject is a human or a veterinary animal.
210 . The method of claim 209 , wherein the compound is a polymeric compound of the formula A n or a pharmaceutically acceptable salt thereof wherein R is 3-(α)—OH or 3-(β)—OH, and X, Y and Z are selected from the group consisting of monomeric unit A or hydrogen.
211 . The method of claim 210 wherein the subject is a human.
212 . The method of claim 211 , wherein n is 2 to 13.
213 . The method of claim 211 , wherein n is 2 to 12.
214 . The method of claim 210 , wherein the adjacent monomers bind at positions (4β→6).
215 . The method of claim 210 , wherein the adjacent monomers bind at positions (4β→6) and/or (4β→8).
216 . The method of claim 210 , wherein the polymeric compound is selected from the group consisting of: dimer EC-(4β→8)-EC, dimer EC-(4β→6)-EC, trimer [EC-(4β→8)] 2 -EC, trimer [EC-(4β→6)] 2 -EC, tetramer [EC-(4β→8)] 3 -EC, pentamer [EC-(4β→8)] 4 -EC, and pentamer [EC-(4β→8)] 3 -EC-(4β→6)-EC, wherein EC is a monomeric unit epicatechin.
217 . The method of claim 216 , wherein the subject is a human.
218 . The method of claim 216 , wherein the subject is a veterinary animal.
219 . The method of claim 210 , wherein the composition is a pharmaceutical composition.
220 . The method of claim 210 , wherein the composition is a dietary supplement.
221 . The method of claim 210 , wherein the composition is a food.
222 . The method of claim 221 , wherein the composition is a pet food.
223 . The method of claim 210 , wherein the composition is a beverage.
224 . The method of claim 209 , wherein the compound is administered orally.
225 . The method of claim 210 , wherein the compound is administered orally.
226 . The method of claim 210 , wherein the composition is a confectionary.
227 . The method of claim 210 , wherein the composition is a chocolate.
228 . The method of claim 225 , wherein the compound is provided as a cocoa extract.
229 . The method of claim 225 , wherein the compound is provided as a cocoa extract fraction.
230 . The method of claim 225 , wherein the compound is provided as a cocoa solid.
231 . The method of claim 230 , wherein the cocoa solid is a cocoa powder.
232 . The method of claim 230 , wherein the cocoa solid is a non-alkalized cocoa solid.
233 . The method of claim 230 , wherein the cocoa solid comprises a conserved level of the compound.
234 . The method of claim 230 , wherein the cocoa solid is a CP-cocoa solid.
235 . The method of claim 211 , wherein the human suffers from pain.
236 . The method of claim 211 , wherein the human suffers from fever.
237 . The method of claim 211 , wherein the human suffers from a headache.
238 . The method of claim 237 , wherein the headache is a migraine headache.
239 . A method of treating pain and/or fever comprising administering to a subject in need thereof a composition comprising an effective amount of a compound selected from the group of catechin, epicatechin, a pharmaceutically acceptable salt thereof, and an oxidation product thereof, wherein the subject is a human or a veterinary animal.
240 . The method of claim 239 , wherein the compound is epicatechin or a pharmaceutically acceptable salt thereof.
241 . The method of claim 239 , wherein the compound is epicatechin.
242 . The method of claim 241 , wherein the subject is a human.
243 . The method of claim 241 , wherein the compound is administered orally.
244 . The method of claim 243 , wherein the compound is provided as a cocoa extract.
245 . The method of claim 243 , wherein the compound is provided as a cocoa extract fraction.
246 . The method of claim 243 , wherein the compound is provided as a cocoa solid.
247 . The method of claim 246 , wherein the cocoa solid is a cocoa powder.
248 . The method of claim 246 , wherein the cocoa solid is a non-alkalized cocoa solid.
249 . The method of claim 246 , wherein the cocoa solid comprises a conserved level of epicatechin.
250 . The method of claim 246 , wherein the cocoa solid is a CP-cocoa solid.
251 . The method of claim 242 , wherein the human suffers from pain.
252 . The method of claim 242 , wherein the human suffers from fever.
253 . The method of claim 242 , wherein the human suffers from a headache.
254 . The method of claim 253 , wherein the headache is a migraine headache.Join the waitlist — get patent alerts
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