테트라메톡시하이드록시플라본을 포함하는 유방암 억제용조성물
    1.
    发明公开
    테트라메톡시하이드록시플라본을 포함하는 유방암 억제용조성물 失效
    含有四羟甲基黄酮的组合物用于抑制乳腺癌

    公开(公告)号:KR1020060121622A

    公开(公告)日:2006-11-29

    申请号:KR1020050043888

    申请日:2005-05-24

    Abstract: A composition for inhibiting breast cancer comprising tetra methoxyhydroxy flavone is provided to inhibit activity, infiltration and mobility of matrix metalloproteinase(MMP) without toxicity to breast cells, so that progress and metastasis of breast cancer are inhibited. The composition for inhibiting breast cancer comprises tetra methoxyhydroxy flavone(5,6,3',5'-tetramethoxy 7,4'-hydroxyflavone) represented by the formula(1) as an effective ingredient, and pharmaceutically acceptable carriers or excipients, wherein the effective concentration of tetra methoxyhydroxy flavone is 10-50 muM; and the composition is formulated as tablet, pill, powder, sachet, elixir, suspension, emulsion, solution, syrup, aerosol, soft or hard gelatin capsule, sterilized injection solution or sterilized powder.

    Abstract translation: 提供了包含四甲氧基羟基黄酮的用于抑制乳腺癌的组合物,以抑制对乳腺细胞没有毒性的基质金属蛋白酶(MMP)的活性,浸润和迁移性,从而抑制乳腺癌的进展和转移。 用于抑制乳腺癌的组合物包含作为有效成分的由式(1)表示的四甲氧基羟基黄酮(5,6,3',5'-四甲氧基-7,4'-羟基黄酮)和药学上可接受的载体或赋形剂,其中 四甲氧基羟基黄酮的有效浓度为10-50μM; 组合物配制成片剂,药丸,粉剂,香囊,酏剂,悬浮液,乳液,溶液,糖浆,气雾剂,软或硬明胶胶囊,灭菌注射液或灭菌粉末。

    엔테로코쿠스 파에시움 CBG-5 KACC 91002균체의 초음파 파쇄물을 유효성분으로 함유하는 염증감소용조성물
    2.
    发明公开
    엔테로코쿠스 파에시움 CBG-5 KACC 91002균체의 초음파 파쇄물을 유효성분으로 함유하는 염증감소용조성물 无效
    含有肠易激综合征CBG-C5 KACC 91002的消炎减少组合物作为有效成分

    公开(公告)号:KR1020060114481A

    公开(公告)日:2006-11-07

    申请号:KR1020050036424

    申请日:2005-04-29

    CPC classification number: A61K35/74

    Abstract: A composition for reducing inflammation comprising Enterococcus faecium CBG-C5(KACC 91002) as an effective ingredient is provided to reduce inflammation cheaply and simply by removing isolation and purification of conjugated linoleic acid accumulated in Enterococcus faecium CBG-C5(KACC 91002). The composition for reducing inflammation comprises destroyed Enterococcus faecium CBG-C5(KACC 91002) as an effective ingredient, wherein the concentration of the destroyed Enterococcus faecium CBG-C5(KACC 91002) in the composition is 1.25 mug/ml; and the destroyed Enterococcus faecium CBG-C5(KACC 91002) is prepared by dissolving cultured Enterococcus faecium CBG-C5(KACC 91002) in phosphate buffered saline(PBS), destroying the cultured Enterococcus faecium CBG-C5(KACC 91002) with ultrasonic wave and freeze-drying it, and suspending the freeze-dried product in PBS and sterilizing it with heating.

    Abstract translation: 提供一种用于减少包含屎肠球菌CBG-C5(KACC91002)作为有效成分的炎症的组合物,通过去除在屎肠球菌CBG-C5(KACC 91002)中积累的共轭亚油酸的分离和纯化,便宜且简单地减少炎症。 用于减少炎症的组合物包括破坏的屎肠球菌CBG-C5(KACC 91002)作为有效成分,其中组合物中破坏的屎肠球菌CBG-C5(KACC 91002)的浓度为1.25mug / ml; 通过将培养的屎肠球菌CBG-C5(KACC91002)溶解在磷酸盐缓冲盐水(PBS)中,用超声波破坏培养的屎肠球菌CBG-C5(KACC91002),制备被破坏的屎肠球菌CBG-C5(KACC91002) 冷冻干燥,将冻干物悬浮于PBS中,加热灭菌。

    에피갈로카테킨 갈레트 및 공액 리놀레인산을 유효성분으로함유하는 것을 특징으로 하는 항암 조성물
    4.
    发明公开

    公开(公告)号:KR1020070097610A

    公开(公告)日:2007-10-05

    申请号:KR1020060027710

    申请日:2006-03-28

    Abstract: An anticancer agent containing epigallocatechin gallate(EGCG) and conjugated linoleic acid is provided to inhibit side effects of epigallocatechin gallate including inhibition of intercellular signal transfer through the gap junction channel and increase inhibition of matrix metalloproteinase(MMP) activity. An anticancer composition contains 0.1-50 wt.% of effective ingredients including epigallocatechin gallate(EGCG) and conjugated linoleic acid in a weight ratio of 10:1 to 1:10 and is formulated as medicine, food, food additive and beverage, wherein the cancer is large intestine cancer, breast cancer, stomach cancer or liver cancer.

    Abstract translation: 提供含有表没食子儿茶素没食子酸酯(EGCG)和共轭亚油酸的抗癌剂,以抑制表没食子儿茶素没食子酸酯的副作用,包括通过间隙连接通道抑制细胞间信号转移并增加基质金属蛋白酶(MMP)活性的抑制。 抗癌组合物含有0.1-50重量%的有效成分,包括表没食子儿茶素没食子酸酯(EGCG)和共轭亚油酸,重量比为10:1至1:10,并配制成药物,食品,食品添加剂和饮料,其中 癌症是大肠癌,乳腺癌,胃癌或肝癌。

    테트라메톡시하이드록시플라본을 포함하는 유방암 억제용조성물
    5.
    发明授权
    테트라메톡시하이드록시플라본을 포함하는 유방암 억제용조성물 失效
    含有四甲氧基羟基黄酮的组合物,用于抑制乳腺癌

    公开(公告)号:KR100700358B1

    公开(公告)日:2007-03-27

    申请号:KR1020050043888

    申请日:2005-05-24

    Abstract: 본 발명은 테트라메톡시하이드록시플라본(5,6,3',5'-tetramethoxy 7,4'-hydroxyflavone)을 포함하는 유방암 억제용 조성물에 관한 것으로, 본 발명에 따른 조성물은 매트릭스 메탈로프로티나아제(Matrix metalloproteinase : MMP)의 활성과 침윤성, 이동성을 저해함으로써 유방암의 진행과 전이를 억제하는데 유용하게 사용될 수 있으며, 이러한 목적을 갖는 약제, 가공 식품, 기능성 식품, 음료 및 주류의 제조에도 이용될 수 있다.
    테트라메톡시하이드록시플라본, 메트릭스 메탈로프로티나아제, 유방암, 약제, 식품

    9Z, 11E 공액 리놀레인산을 유효성분으로 함유함을특징으로 하는 세포 간 갭 결합 장애 매개 질환의 예방용조성물
    6.
    发明公开
    9Z, 11E 공액 리놀레인산을 유효성분으로 함유함을특징으로 하는 세포 간 갭 결합 장애 매개 질환의 예방용조성물 有权
    含有9Z,11E结合的亚麻酸作为有效成分的组合物,用于预防与GAP JUNCTION损伤相关的疾病

    公开(公告)号:KR1020060114460A

    公开(公告)日:2006-11-07

    申请号:KR1020050036398

    申请日:2005-04-29

    Abstract: A composition for prevention of disease mediated with gap junction damage comprising 9Z, 11E conjugated linoleic acid as an effective ingredient is provided to recover the intercellular communication through the damaged gap junction, and maintain homeostasis. The composition for prevention of disease mediated with gap junction damage comprises 9Z, 11E conjugated linoleic acid as an effective ingredient, wherein the 9Z, 11E conjugated linoleic acid is produced from Enterococcus faecium CBG-C5(KACC 91002), and inhibits phosphorylation of extracellular signal-regulated kinase that is produced when the gap junctional intercellular communication is inhibited by hydrogen peroxide.

    Abstract translation: 提供用于预防由间隙连接损伤介导的疾病的组合物,其包含9Z,11E共轭亚油酸作为有效成分,以通过损伤的间隙连接处恢复细胞间连通,并维持体内平衡。 用间隙连接损伤介导的疾病预防组合物包含9Z,11E共轭亚油酸作为有效成分,其中9Z,11E共轭亚油酸由屎肠球菌CBG-C5(KACC 91002)产生,并抑制细胞外信号的磷酸化 当间隙连接的细胞间通讯被过氧化氢抑制时产生的 - 调节的激酶。

    자시오시딘을 포함하는 유방암 전이 억제용 식품 조성물
    8.
    发明公开
    자시오시딘을 포함하는 유방암 전이 억제용 식품 조성물 无效
    含有JACEOSIDIN用于抑制乳腺癌的食物组合物

    公开(公告)号:KR1020070038480A

    公开(公告)日:2007-04-10

    申请号:KR1020070023923

    申请日:2007-03-12

    Abstract: 본 발명은 자시오시딘(Jaceosidin; 5,7,4'-tetramethoxy 6,3'-dimethoxyflavone)을 포함하는 유방암 전이 억제용 식품 조성물에 관한 것으로, 본 발명에 따른 조성물은 매트릭스 메탈로프로티나아제 (Matrix metalloproteinase : MMP)의 활성과 침윤성, 이동성을 저해함으로써 유방암의 진행과 전이를 억제하는데 유용하게 사용될 수 있으며, 이러한 목적을 갖는 가공 식품, 기능성 식품, 음료 및 주류의 제조에도 이용될 수 있다.
    자시오시딘, 매트릭스 메탈로프로티나아제, 유방암, 식품

    비타민 K3 및 공액 리놀레인산을 유효성분으로 함유하는것을 특징으로 하는 항암 조성물
    10.
    发明授权
    비타민 K3 및 공액 리놀레인산을 유효성분으로 함유하는것을 특징으로 하는 항암 조성물 失效
    비타민K3및공액리놀레인산을유효성분으로함유하는것을특징으로하는항암조성물

    公开(公告)号:KR100749115B1

    公开(公告)日:2007-08-13

    申请号:KR1020060027711

    申请日:2006-03-28

    Abstract: An anticancer composition containing vitamin K3 and conjugated linoleic acid is provided to improve side effect caused by vitamin K3 such as inhibition of intercellular signal transfer through gap junction channel, and increase MMP(matrix metalloproteinase)-inhibiting effects compared to use of single vitamin K3 by using vitamin K3 and conjugated linoleic acid. The anticancer composition contains 0.1-50 wt.% of effective ingredients including vitamin K3 and conjugated linoleic acid in a weight ratio of 10:1 to 1:10, and pharmaceutically acceptable carriers, diluents or excipients, wherein the cancer is large intestine cancer, breast cancer or liver cancer; the daily dosage of effective ingredients is 0.1-100 mg/kg; and the composition is formulated as plaster, granule, lotion, liniment, lemonade, aromatic water, powder, syrup, ophthalmic ointment, liquid and solution, aerosol, extract, elixir, ointment, fluid extract, emulsion, suspension, decoction, infusion, ophthalmic solution, tablet, suppository, injection, spirit, cataplasma, capsule, cream, troche, tincture, paste, pill or soft or hard gelatin capsule.

    Abstract translation: 提供含有维生素K3和共轭亚油酸的抗癌组合物以改善由维生素K3引起的副作用,例如通过间隙连接通道抑制细胞间信号转移,并增加MMP(基质金属蛋白酶)抑制作用,与​​使用单一维生素K3相比, 使用维生素K3和共轭亚油酸。 该抗癌组合物含有重量比为10:1至1:10的包括维生素K3和共轭亚油酸在内的有效成分0.1-50重量%,以及药学上可接受的载体,稀释剂或赋形剂,其中癌症为大肠癌, 乳腺癌或肝癌; 有效成分的日剂量为0.1-100mg / kg; 该组合物配制成膏药,颗粒,洗剂,擦剂,柠檬水,芳香水,粉剂,糖浆,眼膏,液体和溶液,气雾剂,提取物,酏剂,软膏,液体提取物,乳剂,混悬剂,煎剂,输液剂,眼科 溶液剂,片剂,栓剂,注射剂,精神剂,泥敷剂,胶囊剂,霜剂,锭剂,酊剂,糊剂,丸剂或软或硬明胶胶囊。

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