Azobenzene derivatives as labeling agents and intermediates thereof
    586.
    发明申请
    Azobenzene derivatives as labeling agents and intermediates thereof 审中-公开
    偶氮苯衍生物作为标记试剂及其中间体

    公开(公告)号:US20040067229A1

    公开(公告)日:2004-04-08

    申请号:US10441205

    申请日:2003-05-20

    Abstract: A compound of the formula I 1 wherein R is H or nullNnullN-2-carboxyphenyl; A is (CH2)n or nullCHnullCHnull, wherein n is an integer from 0 to 10, or A may also be nullCH(COOH)null when R is nullNnullN-2-carboxyphenyl; and X is a radical selected from the group consisting of: (i) Cl; (ii) COOR1, wherein R1 is p-nitrophenyl or N-succinimidyl; (iii) CONHnullNHR2, wherein R2 is H, COO(t-butyl) or COObenzyl; (iv) CONHnullnullBnullnullNHR3, wherein R3 is H, COOR1, or CO-nullBnullnull-maleimido, wherein R1 is t-butyl, p-nitrophenyl or N-succinimidyl, and B and Bnull, the same or different, are (CH2)n wherein n is an integer from 2 to 10; (v) CONHnullnullBnullnullCOOR4, wherein R4 is H, C1-C8 alkyl, N-succinimidyl; (vi) CONHnullnullBnullnullOH; (vii) CONHnullnullBnullnullCONHnullNHR2, wherein R2 is H, COO(t-butyl) or COObenzyl; and (viii) NHR2, wherein R2 is H, COO(t-butyl) or COObenzyl, when A is nullCH(COOH)null and R is nullNnullN-2-carboxyphenyl. The 4null-hydroxyazobenzene-2-carboxylic acid (HABA) compounds are novel reagents for labeling, isolation and detection of biological molecules.

    Abstract translation: 式I的化合物,其中R是H或-N = N-2-羧基苯基; A是(CH 2)n或-CH = CH-,其中n是0至10的整数,或当R是-N = N-2-羧基苯基时,A也可以是-CH(COOH) 并且X是选自以下的基团:(i)Cl; (ii)COOR1,其中R1是对硝基苯基或N-琥珀酰亚胺基; (iii)CONH-NHR2,其中R2是H,COO(叔丁基)或COO苄基; (iv)CONH- [B] -NHR 3,其中R 3是H,COOR 1或CO- [B'] - 马来酰亚氨基,其中R 1是叔丁基,对硝基苯基或N-琥珀酰亚胺基,B和B' 相同或不同,为(CH 2)n,其中n为2至10的整数; (v)CONH- [B] -COOR 4,其中R 4是H,C 1 -C 8烷基,N-琥珀酰亚胺基; (vi)CONH- [B] -OH; (vii)CONH- [B] -CONH-NHR2,其中R2是H,COO(叔丁基)或COO苄基; 和(viii)当A为-CH(COOH) - 且R为-N = N-2-羧基苯基时,R 2为H,COO(叔丁基)或COO苄基的NHR 2。 4'-羟基偶氮苯-2-羧酸(HABA)化合物是生物分子标记,分离和检测的新型试剂。

    Preparations and methods for the treatment of T cell mediated diseases
    588.
    发明申请
    Preparations and methods for the treatment of T cell mediated diseases 审中-公开
    用于治疗T细胞介导的疾病的制剂和方法

    公开(公告)号:US20030190323A1

    公开(公告)日:2003-10-09

    申请号:US10307326

    申请日:2002-12-02

    Abstract: The present invention provides pharmaceutical compositions and methods for reducing the incidence or severity of insulin dependent diabetes mellitus, insulitis, null-cell destruction, or latent autoimmune diabetes in adults by administering to a patient a pharmaceutical composition comprising an antigen and a carrier, wherein the antigen is recognized by inflammatory T cells associated with the pathogenesis of the disease and the carrier is a metabolizable lipid emulsion. The composition induces a TH1nullTH2 shift in the cytokines produced by said T cells and it is administered in an amount, which is therapeutically effective to reduce the symptoms of the disease.

    Abstract translation: 本发明提供了通过向患者施用包含抗原和载体的药物组合物来降低成人胰岛素依赖性糖尿病,胰岛炎,β-细胞破坏或潜伏性自身免疫性糖尿病的发病率或严重程度的药物组合物和方法,其中 抗原被与疾病发病相关的炎性T细胞识别,载体是可代谢的脂质乳剂。 所述组合物诱导由所述T细胞产生的细胞因子中的TH1-> TH2位移,并且其用量以治疗方式有效减少疾病症状。

    Methods of kidney transplantation utilizing developing nephric tissue
    589.
    发明申请
    Methods of kidney transplantation utilizing developing nephric tissue 审中-公开
    肾移植方法利用发展中的肾组织

    公开(公告)号:US20030096016A1

    公开(公告)日:2003-05-22

    申请号:US10118933

    申请日:2002-04-10

    CPC classification number: A61K35/22

    Abstract: A method of treating a kidney disease in a subject is disclosed. The method is effected by transplanting into the subject a graft of nephric tissue at a predetermined developmental stage thereby treating the kidney disease in the subject.

    Abstract translation: 公开了治疗受试者的肾脏疾病的方法。 该方法通过在预定的发育阶段向受试者移植肾组织的移植物进行,由此治疗受试者的肾脏疾病。

    Method and pharmaceutical composition for treating inflammation
    590.
    发明申请
    Method and pharmaceutical composition for treating inflammation 失效
    用于治疗炎症的方法和药物组合物

    公开(公告)号:US20030053985A1

    公开(公告)日:2003-03-20

    申请号:US09953206

    申请日:2001-09-17

    CPC classification number: A61K38/217 Y02A50/414

    Abstract: A method of treating an inflammation in a subject in need thereof is disclosed. The method comprises locally or systemically administering to the subject IFN-null in an amount so as to achieve an IFN-null bulk tissue concentration at a site of inflammation of 1-8,000 units per kilogram body weight, thereby ameliorating the inflammation.

    Abstract translation: 公开了治疗需要的受试者的炎症的方法。 该方法包括局部或全身施用本发明的IFN-γ,其用量可达到每千克体重1-8,000单位的炎症部位的IFN-γ体积组织浓度,从而改善炎症。

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