Method of depressing fatty acids and triglycerides
    2.
    发明授权
    Method of depressing fatty acids and triglycerides 失效
    消除脂肪酸和苦味酸的方法

    公开(公告)号:US3851056A

    公开(公告)日:1974-11-26

    申请号:US18940971

    申请日:1971-10-14

    IPC分类号: C07H19/16 A61K27/00

    CPC分类号: C07H19/16

    摘要: 1. METHOD OF DEPRESSING FATTY ACIDS AND TRIGLYCERIDES IN MAMMAL IN NEED OF EACH THERAPYL AN EFFECTIVE AMOUNT OF A MAMMALS, WHICH COMPRISES ADMINISTERING TO THE AFFLICTED COMPOUND OF THE GENERA FORMULA

    2-R1,6-(B-X-A-N(-R2)-),9-(3,4-DI(HO-),5-(HO-CH2-)-

    TETRAHYDROFUR-2-YL-)-9H-PURINE

    WHEREIN R1 IS HYDROGEN, CHLORIDE, HYDROXYL OR AMINO; R2 IS HYDROGEN LOWER STRAIGHT-CHAINED OR BRANCHED ALKYL; A IS A VALENCY BOND OR STURATED OR UNSATURATED STRAIGHTCHAINED, LOWER BRANCED OR CYCLIC ALKYLENE, UNSUBSTITUTED OR SUBSTITUTED BY HYDROXYL, CARBOXYL OR LOWER ACYLOXY; X IS A VALENCY BOND OR, IF A IS ALKYLENE, CAN ALSO BE OXYGEN, SULFUR, IMINO, LOWER ALKYLATED IMINO, OR LOWER ACYLATED IMINO; B IS UNSUBSTITUTED OR SUBSTITUTED PHENYL OR NAPHTHYL WHEREIN THE SUBSTITUENTS ARE FROM 1 TO 3 MEMBERS OF THE GROUP CONSISTING OF CHLORO OR FLUORO, LOWER ALKYL, CHLORO- OR FLUORO-ALKYL, ALKOXY, ARYLOXY OF FROM 6 TO 10 CARBON ATOMS, LOWER ACYLOXY, ALKYLTHIO, CARBOXY AND HYDROXYL AND WHEREIN ANY TWO SUBSTITUENTS IN B CAN TOGETHER ALSO REPRESENT A DIOXOMETHYLENE BRIDGE; AND THE PHARMACOLOGICALLY COMPATIBLE SALTS THEREOF.

    N-(6)-aralkyl-adenosine compounds
    3.
    发明授权
    N-(6)-aralkyl-adenosine compounds 失效
    N-(6) - 氨基腺苷化合物

    公开(公告)号:US3817981A

    公开(公告)日:1974-06-18

    申请号:US19972771

    申请日:1971-11-17

    摘要: WHEREIN R1 is hydrogen, halogen or hydroxyl; R2 is hydrogen, halogen, hydroxyl, alkyl or alkoxy; R3 is hydroxyl, amino, alkoxy, alkylamino or dialkylamino; and X is straight or branched-chain alkylene containing up to 3 carbon atoms; and the physiologically compatible salts thereof, ARE OUTSTANDINGLY EFFECTIVE IN PRODUCING A PROLONGED CORONARY VASODILATING EFFECT, AND FURTHERMORE, ARE EFFECTIVE IN DEPRESSING SERUM LIPIDS.

    Novel N(6)-Aralkyl-Adenosine Compounds of the formula

    摘要翻译: 新型N(6) - 烷基 - 腺苷式WHEREIN R1的化合物是氢,卤素或羟基; R2是氢,卤素,羟基,烷基或烷氧基; R3是羟基,氨基,烷氧基,烷基氨基或二烷基氨基; 并且X是含有至多3个碳原子的直链或支链亚烷基; 和其生理上相容的盐,在产生冠状动脉血管扩张作用方面是非常有效的,而且在进一步减少血清脂质中有效。

    Adenosine compounds and therapeutic compositions
    4.
    发明授权
    Adenosine compounds and therapeutic compositions 失效
    腺苷化合物和治疗组合物

    公开(公告)号:US3787391A

    公开(公告)日:1974-01-22

    申请号:US3787391D

    申请日:1971-11-22

    摘要: NEW ADENOSINE COMPOUNDS OF THE FORMULA:

    2-R1,6-((R2,(R3-NH-NH-CO-)PHENYL)-X-A-NH-),9-(3,4-DI(HO-),

    5-(HO-CH2-)-TETRAHYDROFURAN-2-YL)-9H-PURINE

    WHERE R1 IS HYDROGRN OR HALOGEN; R2 IS HYDROGEN, HALOGEN, HYDROXYL, ALKYL OR ALKOXY; R3 IS HYDROGEN OR -CO-R4, WHEREIN R4 IS ARYL WHICH IS OPTIONALLY SUBSTITUTED ONE OR MORE TIMES BY HALOGEN AND/OR LKYL, ALKOXY AND/OR HYDROXYALKYLENEOXY; A IS A STRAIGHTCHAINED OR BRANCHED ALKYLENE RADICAL CONTAINING UP TO 3 CARBON ATOMS AND X IS A VALENCY BOND OR OXYGEN: AND THE PHYSIOLOGICALLY COMPATIBLE SALTS THEREOF, EXHIBIT REMARKABLE EFFECTIVENES IN IMPROVING THE BLOOD CIRCULATION OF MAMMALS AND ALSO BRING ABOUT A DEPRESSION OF SERUM LIPIDS.

    N(6)-disubstituted adenosine compounds
    6.
    发明授权
    N(6)-disubstituted adenosine compounds 失效
    N(6) - 衍生腺苷化合物

    公开(公告)号:US3840521A

    公开(公告)日:1974-10-08

    申请号:US28711572

    申请日:1972-09-07

    IPC分类号: C07H19/16 C07D51/54

    CPC分类号: C07H19/16

    摘要: 1. N(6)-DISUBSTITUTED ADENOSINE COMPOUND OF THE FORMULA

    6-(R1-N(-R2)-),9-(3,4,5-TRI(HO-)-TETRAHYROFUR-2-YL-)-

    9H-PURINE

    WHEREIN R1 IS ALKYL OF FROM 1 TO 6 CARBON ATOMS; AND R2 IS STRAIGHT-CHAINED OR BRANCHED ALKYL OF FROM 4 TO 10 CARBON ATOMS; CYCLOALKYL OR METHYLCYCLOALKYL WHEREIN THE CYCLOALKYL MOIETY CONTAINS FROM 3 TO 10 CARBON ATOMS, CYCLOALKYL-ALKYL WITH FROM 3 TO 10 CARBON ATOMS IN THE CYCLOALKYL GROUP AND FROM 1 TO 4 CARBON ATOMS IN THE ALKYL SIDE-CHAIN OR BICYCLOALKYL OF FROM 5 TO 7 CARBON ATOMS IN EACH RING; AND THE PHARMACOLOGICALLY COMPATIBLE SALTS THEREOF.