摘要:
Aminated isoflavonoid synthesized by aminating the 4-keto group of isoflavanone and isoflavanone ring systems, pharmaceutical compositions containing same and uses thereof as therapeutic agents.
摘要:
Isoflavone compounds are described and recommended as therapeutic agents. Exemplified and preferred compounds are (a). Indications show compounds have good competitive binding to estrogen receptors. This is exemplified.
摘要:
Isoflavone compounds of the formula (I) or (II) Where R can be R7? or OR7? or O and the formula (III) is either a single or double bond extends to Y then Y is an optionally substituted benzyl. W, R1?, Zo? R2? and R7? are as defined in the specification. The compounds are useful for the treatment of certain diseases and disorders, including cancer and inflammation.
摘要翻译:式(I)或(II)的异黄酮化合物其中R可以是R 7? 或OR 7? 或O,式(III)是单键或双键延伸至Y,则Y为任选取代的苄基。 W,R 1 ?, Z o? R 2? 和R 7? 如说明书中所定义。 该化合物可用于治疗某些疾病和病症,包括癌症和炎症。
摘要:
A process for the production of β-(1,3)(1,6) glucan from a glucan containing cellular source is described, together with compositions and uses/methods of treatment involving glucan. The process of the invention comprises the steps of: (a) extracting glucan containing cells with alkali and heat, in order to remove alkali soluble components; (b) acid extracting the cells of step (a) with an acid and heat to form a suspension; (c) extracting the suspension obtained of step (b) or recovered hydrolyzed cells with an organic solvent which is non-miscible with water and which has a density greater than that of water separating the resultant aqueous phase, solvent containing phase and interface so that substantially only the aqueous phase comprising β-(1,3)(1,6) glucan particulate material remains; wherein the extraction with said organic solvent provides separation of glucan subgroups comprising branched β-(1,3)(1,6)-glucan, and essentially unbranched β-(1,3) glucan which is associated with residual non-glucan contaminents; and (d) drying the glucan material from step (c) to give microparticulate glucan.
摘要:
A method and apparatus for eliminating or improving blood flow within incompetent veins to correct venous insufficiency using a barbed bidirectional suture with predetermined breaking point. Said suture may also be utilized for other tissue applications. A two-way barb suture is placed in an insertion device comprised of a tubular body with or without a pointed distal tip. The inserting device and one-way or two-way suture are placed in a position to effectively close off the vein or leave a device within the vein. The insertion device is then withdrawn leaving the suture in place. This barbed suture with predetermined breaking point is used by the method of the present invention to prevent reflux, and as a method to join body tissue, attach dissimilar body tissues, attach devices to body tissues, and alter the position of body tissues by remote percutaneous access with the assistance of ultrasound or fluoroscopy and with the assistance of endoscopic devices.
摘要:
Methods for protecting skin from UV-induced DNA mutagenic damage comprising administration of one or more of equol, dehydroequol, isoflav-3-ene and isoflavan compounds in admixture with a dermally acceptable carrier are described. Also described are methods for preventing skin cancer formation.
摘要:
Therapeutic methods of treatment, compositions and foodstuffs are described which contain isoflavone compounds described by general formula (I), in which Z is H, R1 is H, or RACO where RA is C1-10alkyl or an amino acid, R2 is H, OH, or ORB where RB is an amino acid, or CORA where RA is as previously defined, W is H, A is H or OH, and B is selected from (a), (b), (c), or W is H, and A and B taken together form a six-membered ring selected from (d), or W, A and B taken with the groups with which they are associated comprise (e), or W and A taken together with the groups with which they are associated comprise (f) and B is (g) wherein R3 is H, CORA where RA is as previously defined, CO2RC where RC is C1-10alkyl, or CORB where RB is as previously defined, R4 is H, CORD where RD is H, OH, C1-10alkyl or an amino acid, CO2RC where RC is as previously defined, CORE where RE is H. C1-10alkyl or an amino acid, COOH, CORC where RC is as previously defined, or CONHRE where RE is as previously defined, R5 is H, CORC where RC is as previously defined, or CORCORE where RC and RE are as previously defined, and where the two R5 groups are attached to the same group they are the same or different, R6 is H or hydroxy C1-10alkyl, X is preferably O, but may be N or S, and Y is (h) where R7 is H, or C1-10alkyl.