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    • 3. 发明申请
    • COMPOUNDS EXHIBITING EFFLUX INHIBITOR ACTIVITY AND COMPOSITIONS AND USES THEREOF
    • 表现出EFFLUX抑制剂活性和组成的化合物及其用途
    • WO2007115181A3
    • 2008-06-19
    • PCT/US2007065655
    • 2007-03-30
    • EASTMAN CHEM CO
    • WEMPE MICHAEL FITZPATRICKEDGAR KEVIN JOSEPHZIMA GEORGE CHESTERHYATT JOHN ANTHONY
    • A61K31/353A61K31/355C07D311/30C07D311/38C07D311/72
    • A61K45/06A61K31/00A61K31/352A61K31/355A61K31/56C07J17/00A61K2300/00
    • At least one compound chosen from compounds of Formula 1: a pharmaceutically acceptable salt or ester thereof, a solvate thereof, a chelate thereof, a non-covalent complex thereof, a prodrug thereof, and mixtures of any of the foregoing, wherein: n is a number from 1 to 900, wherein the individual units may be the same or different; W is chosen from alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl; each Of R 2 , R 3 , R 4 and R 5 is independently chosen from -H, alkyl, substituted aikyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl; Z' is chosen from -O-, -N-, -NO-, - NR 4 -, -S-, -SO- and -SO 2 -, wherein R 4 is defined as above; each of X, X', Y and Z is independently chosen from -CR 4 R 5 -, -NH-, -NR 4 -, -NO-. -O-, -NOR 4 -, -S-, -SO-, -SO 2 -, wherein R 4 and R 5 are defined as above; R 1 is chosen from a tocopherol, a steroid and a flavonoid; and R 6 , is chosen from any R 1 , alkyl. substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl.
    • 至少一种选自式1化合物的化合物:其药学上可接受的盐或酯,其溶剂化物,其螯合物,其非共价复合物,其前药以及任何前述物质的混合物,其中:n是 1至900的数字,其中各个单元可以相同或不同; W选自烷基,取代的烷基,环烷基,取代的环烷基,芳基,取代的芳基,芳烷基和取代的芳烷基; R 2,R 3,R 4,R 5和R 5中的每一个独立地选自-H,烷基, 取代的烷基,环烷基,取代的环烷基,芳基,取代的芳基,芳烷基和取代的芳烷基; Z'选自-O - , - N - , - NO - , - NR 4 - , - S - , - SO-和-SO 2 - ,其中 R 4 的定义如上; X,X',Y和Z各自独立地选自-CR 4, - NR 5, , - NO-。 -O - , - NOR 4 - , - S - , - SO - , - SO 2 - ,其中R 4和R 5 的定义如上; R SUB1选自生育酚,类固醇和类黄酮; 和R 6选自任何R 1,烷基。 取代的烷基,环烷基,取代的环烷基,芳基,取代的芳基,芳烷基和取代的芳烷基。
    • 4. 发明申请
    • COMPOUNDS EXHIBITING EFFLUX INHIBITOR ACTIVITY AND COMPOSITIONS AND USES THEREOF
    • 化合物展示抑制剂活性及组合物及其用途
    • WO2007115181A9
    • 2008-04-03
    • PCT/US2007065655
    • 2007-03-30
    • EASTMAN CHEM CO
    • WEMPE MICHAEL FITZPATRICKEDGAR KEVIN JOSEPHZIMA GEORGE CHESTERHYATT JOHN ANTHONY
    • A61B5/05
    • A61K45/06A61K31/00A61K31/352A61K31/355A61K31/56C07J17/00A61K2300/00
    • At least one compound chosen from compounds of Formula 1: a pharmaceutically acceptable salt or ester thereof, a solvate thereof, a chelate thereof, a non-covalent complex thereof, a prodrug thereof, and mixtures of any of the foregoing, wherein: n is a number from 1 to 900, wherein the individual units may be the same or different; W is chosen from alkyl, substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl; each Of R 2 , R 3 , R 4 and R 5 is independently chosen from -H, alkyl, substituted aikyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl; Z' is chosen from -O-, -N-, -NO-, - NR 4 -, -S-, -SO- and -SO 2 -, wherein R 4 is defined as above; each of X, X', Y and Z is independently chosen from -CR 4 R 5 -, -NH-, -NR 4 -, -NO-. -O-, -NOR 4 -, -S-, -SO-, -SO 2 -, wherein R 4 and R 5 are defined as above; R 1 is chosen from a tocopherol, a steroid and a flavonoid; and R 6 , is chosen from any R 1 , alkyl. substituted alkyl, cycloalkyl, substituted cycloalkyl, aryl, substituted aryl, aralkyl and substituted aralkyl.
    • 至少一种选自式1化合物的化合物:其药学上可接受的盐或酯,其溶剂合物,螯合物,其非共价复合物,其前体药物以及上述任何一种的混合物,其中n为 1至900的数字,其中各个单元可以相同或不同; W选自烷基,取代的烷基,环烷基,取代的环烷基,芳基,取代的芳基,芳烷基和取代的芳烷基; R 2,R 3,R 4和R 5各自独立地选自-H,烷基, 取代的芳基,环烷基,取代的环烷基,芳基,取代的芳基,芳烷基和取代的芳烷基; Z'选自-O - , - N-,-NO - , - NR 4 - , - S - , - SO - 和-SO 2 - ,其中 R 4如上定义; X,X',Y和Z中的每一个独立地选自-CR 4 R 5 - , - NH - , - NR 4 - ,-NO-。 -O - , - NOR 4 - , - S - , - SO - , - SO 2 - ,其中R 4和R 2 < > 5 如上所定义; R 1选自生育酚,类固醇和类黄酮; 和R 6,R 6选自任何R 1,C 1-4烷基。 取代的烷基,环烷基,取代的环烷基,芳基,取代的芳基,芳烷基和取代的芳烷基。
    • 7. 发明专利
    • BR9911873A
    • 2001-03-27
    • BR9911873
    • 1999-07-01
    • EASTMAN CHEM CO
    • HYATT JOHN ANTHONY
    • C12P7/04C07B61/00C07C43/166C07C69/145C07D301/19C07D303/16C07D311/72C12P9/00
    • The invention provides processes for producing phytol, isophytol, and certain phytol derivatives by a method of oxidizing or epoxidizing geranylgeraniol or geranylgeraniol derivatives to form epoxygeranylgeraniol derivatives, reducing or hydrogenating the epoxygeranylgeraniol derivatives to produce epoxyphytol derivatives, and then deoxygenating the epoxyphytol derivatives to produce phytol, isophytol, phytene derivatives, isophytene derivatives, or mixtures thereof. The step of deoxygenating is carried out in the presence of deoxygenation catalysts, including rhenium trioxide compounds. The invention also provides methods for the synthesis of certain novel substituted epoxyphytyl compounds and substituted phytene compounds having removable protecting groups. The produce phytol, isophytol, phytene derivatives, isophytene derivatives, substituted epoxyphytyl compounds and substituted phytene compounds are suitable starting materials for condensation with trimethylhydroquinone derivatives in the presence of Lewis acids to give tocopherol derivatives including alpha-tocopherol, vitamin E.