Pyrazolo[1,5-a]-1,3,5-triazines
    31.
    发明授权
    Pyrazolo[1,5-a]-1,3,5-triazines 失效
    吡唑并[1,5-a] -1,3,5-三嗪

    公开(公告)号:US4565815A

    公开(公告)日:1986-01-21

    申请号:US614454

    申请日:1984-05-25

    CPC分类号: C07D487/04

    摘要: A compound having anti-ulcer activity and having the formula ##STR1## wherein D is H, SH, NH.sub.2, OH, R.sup.4 S where R.sup.4 is a lower alkyl group; E is OH or NH.sub.2 ; J is H or aryl; X is CH or N; Y is CH, N, or CT, wherein T is a halogen; Z is CH or N; A is ##STR2## and replaces a hydrogen of D, X, or E; R.sup.1 is H or CH.sub.3 ; L is CH.sub.2 S; Q is O or CH.sub.2 S; n is 0 or 1; 2 m 4; each R.sup.2 and R.sup.3, independently, is H, lower alkyl, cycloalkyl, or arylalkyl; or R.sup.2 and R.sup.3, together with the nitrogen atom to which they are attached, form a 4, 5, or 6 membered heterocyclic ring containing 0, 1, or 2 oxygen atoms and 1, 2, or 3 nitrogen atoms and being unsubstituted or lower alkyl substituted; or a pharmaceutically acceptable salt thereof.

    摘要翻译: 具有抗溃疡活性并具有下式的化合物:其中D是H,SH,NH 2,OH,R 4,其中R 4是低级烷基; E是OH或NH 2; J为H或芳基; X是CH或N; Y是CH,N或CT,其中T是卤素; Z是CH或N; A是 + TR ,代替D,X或E的氢; R1是H或CH3; L是CH2S; Q是O或CH2S; n为0或1; 2 m 4; 每个R 2和R 3独立地是H,低级烷基,环烷基或芳基烷基; 或R 2和R 3与它们所连接的氮原子一起形成含有0,1或2个氧原子和1,2或3个氮原子的4,5或6元杂环,并且是未取代的或低级的 烷基取代; 或其药学上可接受的盐。

    Immunomodulators and method of making same
    33.
    发明授权
    Immunomodulators and method of making same 失效
    免疫调节剂及其制备方法

    公开(公告)号:US4871870A

    公开(公告)日:1989-10-03

    申请号:US25850

    申请日:1987-03-16

    申请人: Sun H. Kim

    发明人: Sun H. Kim

    CPC分类号: A61K31/195

    摘要: A compound having the formula ##STR1## or a pharmaceutically acceptable salt thereof, wherein A is an amino acid identifying group; B is a hydrogen atom, an alkyl group having 1-5, inclusive, carbon atoms, or an aralkyl group having 6-12, inclusive, carbon atoms; carbon atom 2 is of the R configuration; and carbon atom 3 is of the R configuration. The compounds of the invention are effective in augmenting immunological responses and are useful therefore in the treatment of diseases such as cancer, viral infections, bacterial infections, and arthritis.

    N-disubstituted glycine and B-amino-propionic acid derivatives having
anti-ulcer activity
    34.
    发明授权
    N-disubstituted glycine and B-amino-propionic acid derivatives having anti-ulcer activity 失效
    N-二取代甘氨酸和具有抗溃疡活性的B-氨基 - 丙酸衍生物

    公开(公告)号:US4785003A

    公开(公告)日:1988-11-15

    申请号:US821071

    申请日:1986-01-21

    申请人: Sun H. Kim

    发明人: Sun H. Kim

    摘要: A compound having the formula ##STR1## or a pharmaceutically acceptable salt thereof, wherein A is N-AC-Sar, pGlu, or homo-pGlu-; B is an aryl group, a heteroaryl group, a cycloalkyl group, an aralkyl group, a heteroalkyl group, a heteroaralkyl group, a benzoyl group, an alkyl group, an acetyl group, or a substituted aryl group wherein the substituent is halogen, hydroxy, alkoxy, nitro, cyano, or hydroxyalkyl; E is H or an alkyl group; B and E being separate substituents or, together with C.sub.1 and the nitrogen atom to which B is attached, forming a 5,6, or 7-membered ring; m is an integer between 0 and 4; either F is ##STR2## wherein R is an alkoxy group or an aralkoxy group; or F is ##STR3## and is capable of forming a 6-membered ring with the nitrogen atom of A, provided that F can only be ##STR4## forming a ring with A when A is pGlu or homo-pGlu.

    摘要翻译: 具有式“IMAGE”的化合物或其药学上可接受的盐,其中A是N-AC-Sar,pGlu或homo-pGlu-; B是芳基,杂芳基,环烷基,芳烷基,杂烷基,杂芳烷基,苯甲酰基,烷基,乙酰基或取代的芳基,其中取代基是卤素,羟基 ,烷氧基,硝基,氰基或羟基烷基; E是H或烷基; B和E是独立的取代基,或者与C1和与B连接的氮原子一起形成5,6或7-元环; m是0和4之间的整数; F是F,其中R是烷氧基或芳烷氧基; 或者F是,并且能够与A的氮原子形成6元环,条件是当A是pGlu或homo-pGlu时,F只能与A形成环。