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    Diaminedithiol derivatives and radiorhenium or radiotechnetium complex thereof; a liver cancer-treating composition comprising the radiorhenium complex and lipiodol; and a kit for preparation of the liver cancer-treating composition
    1.
    发明授权
    Diaminedithiol derivatives and radiorhenium or radiotechnetium complex thereof; a liver cancer-treating composition comprising the radiorhenium complex and lipiodol; and a kit for preparation of the liver cancer-treating composition 有权
    二硫代二醇衍生物及其镭或镭鎓络合物; 包含镭配合物和碘油的肝癌治疗组合物; 以及用于制备肝癌治疗组合物的试剂盒

    公开(公告)号：US07067508B2

    公开(公告)日：2006-06-27

    申请号：US10469198

    申请日：2002-03-08

    申请人： Jae Min Jeong ,  Young Ju Kim ,  Yun-Sang Lee ,  Dong Soo Lee ,  June-Key Chung ,  Myung Chul Lee

    发明人： Jae Min Jeong ,  Young Ju Kim ,  Yun-Sang Lee ,  Dong Soo Lee ,  June-Key Chung ,  Myung Chul Lee

    IPC分类号： A01N43/00 ,  A61K31/33

    CPC分类号： C07D285/00 ,  C07C323/41 ,  C07F13/005 ,  Y02P20/55

    摘要： The present invention relates to a novel diaminedithiol derivative or a pharmaceutically acceptable salt thereof; radiorhenium or radiotechneticum complex thereof; a composition for treating liver cancer comprising the radiorhenium complex and lipiodol; and, a preparative kit of the composition for treating liver cancer.In the composition according to the invention, the diaminedithiol derivative is a novel compound in which long chain alkyl groups were introduced to diaminedithiol, capable of forming a radiorhenium or radiotechnetium complex thereof with an ease and leading to stronger van der Waals bonds with lipiodol. As a result, the complex becomes more stable in a medium, lipiodol, whereby the composition of the invention exhibits a high accumulation rate in liver cancer tissue when injected via hepatic artery, thereby capable of achieving an efficient treatment of liver cancer.

    摘要翻译： 本发明涉及一种新的二硫二硫醇衍生物或其药学上可接受的盐; 镭或其无机技术复合物; 用于治疗肝癌的组合物，其包含铑络合物和碘油; 和用于治疗肝癌的组合物的制备试剂盒。 在本发明的组合物中，二硫二硫醇衍生物是一种新的化合物，其中长链烷基被引入到二硫代二醇中，能够容易地形成其镭或镭鎓络合物，并导致与碘碘醇更强的范德华力键。 结果，复合物在培养基，碘油中变得更稳定，由此本发明的组合物通过肝动脉注射时在肝癌组织中表现出高的积累速率，从而能够实现肝癌的有效治疗。

    NANOPARTICLE COATED WITH LIGAND INTRODUCED WITH LONG HYDROPHOBIC CHAIN AND METHOD FOR PREPARING SAME
    2.
    发明申请
    NANOPARTICLE COATED WITH LIGAND INTRODUCED WITH LONG HYDROPHOBIC CHAIN AND METHOD FOR PREPARING SAME 有权
    用长链疏水链引导的纳米复合材料及其制备方法

    公开(公告)号：US20140199235A1

    公开(公告)日：2014-07-17

    申请号：US13982712

    申请日：2012-01-31

    申请人： Jae Min Jeong ,  Young Kyoung Lee ,  Dong Soo Lee ,  June-Key Chung ,  Myung Chul Lee

    发明人： Jae Min Jeong ,  Young Kyoung Lee ,  Dong Soo Lee ,  June-Key Chung ,  Myung Chul Lee

    IPC分类号： A61K51/12 ,  A61K49/00

    CPC分类号： A61K51/1244 ,  A61K49/0067 ,  A61K49/0089 ,  G01N33/54346 ,  G01N33/54353 ,  G01N33/54393

    摘要： The present invention relates to a nanoparticle having a linker connected to a long alkane or alkene chain, and a method for preparing the nanoparticle. The alkyl chain of C10-30 introduced with a ligand of the present invention can be coated on a hydrophobic nanoparticle through a noncovalent bond, enabling easy introduction of various ligands to the nanoparticle, and the nanoparticle having various functional groups prepared using the method can be applied to fluorescent detection, MRI, raman spectroscopy, optical detection, PET, SPECT, or gamma image device, and the ligand of the visualization agents can be modified to be used for new vessels detection, cancer cell detection, immunocyte detection, hepatocyte detection, cell death detection, and gene detection.

    摘要翻译： 本发明涉及具有连接到长链烷烃或链烯链上的连接体的纳米粒子，以及制备纳米粒子的方法。 用本发明的配体引入的C10-30的烷基链可以通过非共价键包被在疏水性纳米颗粒上，使得能够容易地将各种配体引入纳米颗粒，并且具有使用该方法制备的各种官能团的纳米颗粒可以是 应用于荧光检测，MRI，拉曼光谱，光学检测，PET，SPECT或γ图像装置，可视化试剂的配体可用于新血管检测，癌细胞检测，免疫细胞检测，肝细胞检测， 细胞死亡检测和基因检测。

    Benzylideneaniline derivatives and their radioisotope labeled compounds for binding and imaging of beta-amyloid plaques
    6.
    发明申请
    Benzylideneaniline derivatives and their radioisotope labeled compounds for binding and imaging of beta-amyloid plaques 审中-公开
    苯亚甲基苯胺衍生物及其放射性同位素标记化合物，用于结合和成像β-淀粉样蛋白斑

    公开(公告)号：US20070122341A1

    公开(公告)日：2007-05-31

    申请号：US11424741

    申请日：2006-06-16

    申请人： Jae Min Jeong ,  Dong Soo Lee ,  June-Key Chung ,  Myung Chul Lee

    发明人： Jae Min Jeong ,  Dong Soo Lee ,  June-Key Chung ,  Myung Chul Lee

    IPC分类号： A61K51/00 ,  C07D249/02

    CPC分类号： A61K51/04 ,  C07C251/24

    摘要： Benzylideneaniline derivatives of formula 1 wherein R1-R5 are independently selected from hydrogen, C1-C4 alkyl and F (at least one of them is F) and each R6-R10 are independently selected from hydrogen, C1-C4 alkyl, OH, OCH3, NH2, NHCH3 and N(CH3)2 (at least one of them is OH, OCH3, NH2, NHCH3 or N(CH3)2) are disclosed. Benzylideneaniline derivatives according to the present invention have high affinity to β-amyloid plaques. Thus, they can cross the blood-brain-barrier (BBB) and bind to β-amyloid plaques after administration into the body, making them useful for treatment, prevention, or imaging of Alzheimer's disease.

    摘要翻译： 式1的亚苄基苯胺衍生物，其中R 1 -R 5独立地选自氢，C 1 -C 4烷基和F（其中至少一个为F） 取代基，其中R 1，R 2，R 2，R 3，R 4，R 6， 3，NH 2，NHCH 3和N（CH 3）2）（至少一个 它们是OH，OCH 3，NH 2，NHCH 3或N（CH 3 3） 2 ）。 根据本发明的亚苄基苯胺衍生物对β-淀粉样蛋白斑具有高亲和力。 因此，它们可以穿过血脑屏障（BBB）并且在施用于体内后与β-淀粉样蛋白斑结合，使其可用于治疗，预防或成像阿尔茨海默氏病。