Aromatase inhibitors from Broussonetia papyrifera
AssigneeThe Board of Trustees of the University of Illinois
InventorsAlan Douglas Kinghorn, John M. Pezzuto, Dongho Lee, Krishna P.L. Bhat
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Abstract
A composition and method of cancer treatment is disclosed. The composition and method utilized the extract of B. papyrifera, or compounds included therein having aromatase inhibition properties, as active cancer chemopreventative and treating agents in mammals, including humans.
Claims22
A composition comprising (a) a compound selected from the group consisting of 5,7,2′,4′-tetrahydroxy-3-geranylflavone, isogemichalcone C, 3′-(γ-hydroxymethyl-(E)-γ-methylallyl) 2,4,2′,4′-tetrahydroxychalcone 11′-O-coumarate, demethylmoracin 1,2S-2′,4′-dihydroxy-2″-(1-hydroxy -1-methylethyl)-dihydrofuro[2,3-h]flavanone, (2S) -2′,4′-dihydroxy-7-methoxy-8-prenylflavan, isolicoflavonol, (2S)-abyssinone II, (2S)-5,7,2′,4′-tetrahydroxyflavanone, (2S)-euchrenone a7, broussoflavonol F, (2S)-naringenin, broussonin A, 2,4,2′,4′-tetrahydroxy-3′-prenylchalcone, moracin N, albanol A, and mixtures thereof, and (b) an excipient.
A composition consisting essentially of a compound selected from the group consisting of 5,7,2′,4′-tetrahydroxy-3-geranylflavone, isogemichalcone C, 3′-(γ-hydroxymethyl-(E)-γ-methylallyl)2,4,2′,4′-tetrahydroxychalcone 11′-O-coumarate, demethylmoracin 1,2S-2′,4′-dihydroxy-2′-(1-hydroxy-1-methylethyl)-dihydrofuro[2,3-h]flavanone, (2S) -2′,4′-dihydroxy-7-methoxy-8-prenylflavan, isolicoflavonol, (2S)-abyssinone II, (2S)-5,7,2′,4′-tetrahydroxyflavanone, (2S)-euchrenone a7, broussoflavonol F, (2S)-naringenin, broussonin A, 2,4,2′,4′-tetrahydroxy-3′-prenylchalcone, moracin N, albanol A, and mixtures thereof, and (b) an excipient.
A method of treating or preventing a medical condition mediated by aromatase activity comprising administering to an animal in need thereof a therapeutically effective amount of a compound that is present in an extract of Broussonetia papyrifera and that selectively inhibits aromatase activity.
A method of inhibiting the biosynthetic production of estrogen in a mammal comprising administering to the mammal a therapeutically effective amount of a compound that is present in an extract of Broussonetia papyrifera and that selectively inhibits aromatase activity.
A method of treating a hormone-dependent cancer comprising administering a pharmaceutical composition to a mammal in need thereof in a sufficient amount to suppress the initiation, promotion, or progression of the cancer, said composition comprising a compound selected from the group consisting of 5,7,2′,4′-tetrahydroxy-3-geranylflavone, isogemichalcone C, 3′-(γ-hydroxymethyl-(E)γ-methylallyl)2,4,2′,4′-tetrahydroxychalcone 11-O-coumarate, demethylmoracin 1,2S-2′,4′-dihydroxy-2″-(1-hydroxy-1-methylethyl)-dihydrofuro[2,3-h]flavanone, (2S)-2′,4′-dihydroxy-7-methoxy-8-prenylflavan, isolicoflavonol, (2S)-abyssinone II, (2S)-5,7,2′,4′-tetrahydroxyflavanone, (2S)-euchrenone a7, broussoflavonol F, (2S)-naringenin, broussonin A, 2,4,2′,4′-tetrahydroxy-3′-prenylchalcone, moracin N, albanol A, and mixtures thereof, and (b) an excipient.
A compound selected from the group consisting of 5,7,2′,4′-tetrahydroxy-3-geranylflavone, isogemichalcone C, 3′-(γ-hydroxymethyl-(E)γ-methylallyl)-2,4,2′,4′-tetrahydroxychalcone 11′-O-coumarate, demethylmoracin I, and (2S)-2′,4′-dihydroxy-2″-(1-hydroxy-1-methylethyl)-dihydrofuro[2,3-h]flavanone, 5,7,3′,4′-tetrahydroxy-6-geranylflavonol, 5,7,3′,4′-tetrahydroxy-3-methoxy-6-geranylflavone, (2S)-7,4′-dihydroxy-3′-prenylflavan, 1-(2,4-dihydroxyphenyl)-3-(4-hydroxyphenyl)propane, 1-(2,4-dihydroxy-3-prenylphenyl)-3-(4-hydroxyphenyl)propane, and 1-(4-hydroxy-2-methoxyphenyl)-3-(4-hydroxy-3-prenylphenyl)propane.
Dependencies are inferred from the claim text.