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    • 5. 发明专利
    • 4-AMINO-3-ACYLNAPHTHYRIDINE DERIVATIVES
    • CA2209422C
    • 2001-09-11
    • CA2209422
    • 1996-06-01
    • YUNGJIN PHARMACEUTICAL CO LTD
    • CHUNG KAE JONGCHANG MAN SIKYOO HAN YONGKIM SUNG GYUKANG BOG GOOKIM YOUNG HUNPAEK JANG HOONSOHN SANG KWONKIM YOUNG HEUISEO KWI HYONCHOI WAHN SOOKANG DAE PIL
    • A61K31/435A61K31/4375A61P1/04A61P35/00C07D471/04
    • A novel 4-amino-3-acylnaphthyridine derivatives represented by general formu la (I), wherein R1 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 lower alkoxy group, a C1-C6 lower alkoxyalkyl group, a C3-C6 cycloalkyl group, a C 3- C6 cycloalkyl C1-C6 alkyl group, a substituted or unsubstituted phenyl, or a phenyl C1-C6 alkyl group of which phenyl group may be substituted; R2 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 alkoxy group, a C1-C6 alkylthio group, or a group of a formula: NR6R7 wherein R6 and R7, identical to or different from each other, are independently hydrogen atom or a C1-C6 lower alkyl group, or R6 and R7 may form together 5-membered or 6-membered cycloalkyl group; R3 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 alkoxy group, a C1-C6 alkylthio group, an amino group substituted with one o r two C1-C6 alkyl groups, a halogen atom, a cyano group, a C1-C6 alkanoyl grou p, or trifluoromethyl group; R4 is hydrogen atom or a substituted or unsubstituted C1-C6 alkyl group; R5 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 alkoxy group, an amino group substituted with one or two C1-C 6 alkyl groups, a C1-C6 alkylthio group, a halogen atom, a cyano group, a hydroxycarbamoyl group, a carboxy group, a C1-C6 alkanoyl group, or trifluoromethyl group, or an alkyl group which forms together with R4 a 5- membered or 6-membered cycloalkyl group; m is an integer from 0 to 4, inclusive; and n is an integer from 1 to 3, inclusive; with proviso that all alkyl and alkoxy groups may be linear or branched, and said halogen atom mea ns fluorine, chlorine or bromine atom, or its pharmaceutically acceptable salts are disclosed. These compounds show excellent anti-ulcer activity.
    • 7. 发明专利
    • 4-AMINO-3-ACYLNAPHTHYRIDINE DERIVATIVES
    • CA2209422A1
    • 1997-01-30
    • CA2209422
    • 1996-06-01
    • YUNGJIN PHARMACEUTICAL CO LTD
    • YOO HAN YONGSEO KWI HYONKIM YOUNG HUNCHUNG KAE JONGCHOI WAHN SOOKANG DAE PILKIM YOUNG HEUIKANG BOG GOOCHANG MAN SIKSOHN SANG KWONPAEK JANG HOONKIM SUNG GYU
    • A61K31/435A61K31/4375A61P1/04A61P35/00C07D471/04
    • A novel 4-amino-3-acylnaphthyridine derivatives represented by general formu la (I), wherein R1 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 lower alkoxy group, a C1-C6 lower alkoxyalkyl group, a C3-C6 cycloalkyl group, a C 3- C6 cycloalkyl C1-C6 alkyl group, a substituted or unsubstituted phenyl, or a phenyl C1-C6 alkyl group of which phenyl group may be substituted; R2 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 alkoxy group, a C1-C6 alkylthio group, or a group of a formula: NR6R7 wherein R6 and R7, identical to or different from each other, are independently hydrogen atom or a C1-C6 lower alkyl group, or R6 and R7 may form together 5-membered or 6-membered cycloalkyl group; R3 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 alkoxy group, a C1-C6 alkylthio group, an amino group substituted with one o r two C1-C6 alkyl groups, a halogen atom, a cyano group, a C1-C6 alkanoyl grou p, or trifluoromethyl group; R4 is hydrogen atom or a substituted or unsubstituted C1-C6 alkyl group; R5 is hydrogen atom, a C1-C6 lower alkyl group, a C1-C6 alkoxy group, an amino group substituted with one or two C1-C 6 alkyl groups, a C1-C6 alkylthio group, a halogen atom, a cyano group, a hydroxycarbamoyl group, a carboxy group, a C1-C6 alkanoyl group, or trifluoromethyl group, or an alkyl group which forms together with R4 a 5- membered or 6-membered cycloalkyl group; m is an integer from 0 to 4, inclusive; and n is an integer from 1 to 3, inclusive; with proviso that all alkyl and alkoxy groups may be linear or branched, and said halogen atom mea ns fluorine, chlorine or bromine atom, or its pharmaceutically acceptable salts are disclosed. These compounds show excellent anti-ulcer activity.