공역화 리놀렌산을 생산하는 신규한 균주, 이를 함유하는 캡슐제 및 이를 이용한 기능성 식품
    11.
    发明公开
    공역화 리놀렌산을 생산하는 신규한 균주, 이를 함유하는 캡슐제 및 이를 이용한 기능성 식품 有权
    可生产含有联氨酸的新型微生物,包含其的封装组合物及其制备方法

    公开(公告)号:KR1020030081180A

    公开(公告)日:2003-10-17

    申请号:KR1020030023164

    申请日:2003-04-12

    Applicant: (주)케비젠

    Abstract: PURPOSE: A novel microorganism capable of producing conjugated linoleic acid, a capsulated composition comprising the same, and a preparation method thereof are provided. The microorganism has high conjugated linoleic acid production yield and gastric juice and bile acid tolerance. CONSTITUTION: A microorganism capable of producing conjugated linoleic acid is provided, wherein the microorganism is Bifidobacterium breve CBG-C2 KACC 91001 and KCTC 10462BP, Bifidobacterium pseudocartenulatum CBG-C4 KACC 91003, and Enterococcus faecium CBG-C5 KACC 91002 and KCTC 10208BP. The capsulated composition for prevention and treatment of diseases capable of being inhibited by the conjugated linoleic acid, such as cancer, sclerosis of the arteries, diabetes and corpulence comprises the microorganism capable of producing conjugated linoleic acid.

    Abstract translation: 目的:提供一种能够生产共轭亚油酸的新型微生物,包含其的包封组合物及其制备方法。 该微生物具有高共轭亚油酸产量和胃液和胆汁酸耐受性。 构成:提供能够产生共轭亚油酸的微生物,其中微生物是双歧双歧杆菌CBG-C2KACC91001和KCTC10462BP,假双歧杆菌CBG-C4KACC 91003和屎肠球菌CBG-C5 KACC 91002和KCTC 10208BP。 用于预防和治疗能够被共轭亚油酸抑制的疾病的包封组合物,例如癌症,动脉硬化,糖尿病和败血症包括能够产生共轭亚油酸的微生物。

    효소 활성이 증가된 인간 베타, 베타 - 카로틴 15, 15' -디옥시게나제의 유전자 변이체
    12.
    发明公开
    효소 활성이 증가된 인간 베타, 베타 - 카로틴 15, 15' -디옥시게나제의 유전자 변이체 无效
    人类BETA,具有改善酶活性的十五碳十二烷酸的突变体基因

    公开(公告)号:KR1020030062126A

    公开(公告)日:2003-07-23

    申请号:KR1020020002561

    申请日:2002-01-16

    Applicant: (주)케비젠

    CPC classification number: C12N9/0069 C12P7/02 C12Y113/11063

    Abstract: PURPOSE: Mutant genes of human beta, beta-carotene 15, 15'-dioxygenase having improved enzyme activity are provided, so that enzyme proteins expressed from the mutant genes can be used in various fields related to the vitamin A production. CONSTITUTION: Mutant genes of human beta, beta-carotene 15, 15'-dioxygenase are produced by error-prone PCR using a human beta, beta-carotene 15, 15'-dioxygenase gene as templates, and have the enzyme activity of the expressed protein of 1100 pmol/h. A method for producing vitamin A comprises digesting beta-carotene using the expressed human beta, beta-carotene 15, 15'-dioxygenase. A method for producing vitamin A comprises transforming a host cell using the mutant genes of human beta, beta-carotene 15, 15'-dioxygenase, and culturing the transformed host cell in a medium, wherein the host cell is a plant cell, a prokaryotic cell, a yeast cell, an insect cell, a mammal cell or a poultry cell.

    Abstract translation: 目的:提供具有改善的酶活性的人β,β-胡萝卜素15,15'-双加氧酶的突变基因,使得从突变基因表达的酶蛋白可用于与维生素A生产相关的各种领域。 构成:使用人β,β-胡萝卜素15,15'-双加氧酶基因作为模板,通过易错PCR产生人β,β-胡萝卜素15,15'-双加氧酶的突变基因,并具有表达的酶活性 蛋白质为1100 pmol / h。 生产维生素A的方法包括使用表达的人β,β-胡萝卜素15,15'-双加氧酶消化β-胡萝卜素。 生产维生素A的方法包括使用人β,β-胡萝卜素15,15'-双加氧酶的突变基因转化宿主细胞,并在培养基中培养转化的宿主细胞,其中宿主细胞是植物细胞,原核 细胞,酵母细胞,昆虫细胞,哺乳动物细胞或家禽细胞。

    시스 형태의 레티노이드 유도체 및 이의 제조방법
    13.
    发明授权
    시스 형태의 레티노이드 유도체 및 이의 제조방법 有权
    类视黄醇衍生物和生产所述化合物的方法

    公开(公告)号:KR100822757B1

    公开(公告)日:2008-04-17

    申请号:KR1020020052026

    申请日:2002-08-30

    Applicant: (주)케비젠

    Abstract: 본 발명은 화학식(I)로 표시되는 신규한 시스 형태의 레티노이드 유도체 화합물 또는 이의 약제학적으로 허용되는 염에 관한 것이다:

    (I)

    상기식에서, X, R
    1 , R
    2 및 R
    3 은 본원에 정의한 바와 같다. 또한, 본 발명은 상기 레티노이드 유도체 화합물의 제조 방법 및 그러한 화합물을 함유하는 항암제 조성물에 관한 것이다. 본 발명에 따른 화학식(I)의 화합물은 고도의 항암 활성을 나타내면서 유해한 부작용을 유발하지 않는다.
    항암제, 레티노이드 유도체, 아폽토시스

    유산균 다중 마이크로캡슐의 제조방법, 이 방법에 의해제조된 마이크로캡슐 및 이를 포함하는 제품
    14.
    发明公开
    유산균 다중 마이크로캡슐의 제조방법, 이 방법에 의해제조된 마이크로캡슐 및 이를 포함하는 제품 有权
    制备多糖微生物细菌的方法,方法制备的微生物和包含微生物的文章

    公开(公告)号:KR1020070104140A

    公开(公告)日:2007-10-25

    申请号:KR1020060036360

    申请日:2006-04-21

    Applicant: (주)케비젠

    CPC classification number: A23C9/123 A23C2210/40 A61K9/50 B01J13/02

    Abstract: A multi-microcapsule of lactic acid bacteria, a method for preparing the same, and a product comprising the same are provided to improve the dispersibility and the stability of the multi-microcapsule, and maintain a large quantity of lactic acid bacterial even during a long storage period. A first coating material is prepared by sterilizing and gelatinizing low-fat skimmed milk, glycerin, and a media solution, and homogenizing a mixture of lactic acid bacteria and the resultant material. A second coating material is prepared by mixing refined process oil, polyglycerol fatty acid ester, and glycerin succinylated fatty acid into the first coating material, and homogenizing the mixture. A third coating material is prepared by mixing, gelatinizing, and homogenizing carbohydrate, protein, germ type binder, and emulsifier, and homogenizing a mixture of the second coating material and the resultant material. The third coating material is sprayed in sterilized cool water.

    Abstract translation: 提供乳酸菌的多微胶囊,其制备方法及其制备方法,以提高多微胶囊的分散性和稳定性,并且即使在长时间内也能维持大量的乳酸菌 储存期 通过对低脂脱脂乳,甘油和培养基溶液进行消毒和凝胶化,并将乳酸菌和所得物质的混合物均质化来制备第一涂层材料。 通过将精制工艺油,聚甘油脂肪酸酯和甘油琥珀酰化脂肪酸混合到第一涂料中并将混合物均化来制备第二涂料。 通过混合,凝胶化和均化碳水化合物,蛋白质,胚芽型粘合剂和乳化剂,并均化第二涂料和所得材料的混合物来制备第三涂层材料。 第三种涂料在无菌冷水中喷雾。

    퓨에라리아 속 식물 뿌리의 알콜 추출물을 함유하는 조성물
    15.
    发明授权
    퓨에라리아 속 식물 뿌리의 알콜 추출물을 함유하는 조성물 有权
    含有葛属植物根的酒精提取物的组合物

    公开(公告)号:KR100548058B1

    公开(公告)日:2006-01-31

    申请号:KR1020020066071

    申请日:2002-10-29

    Applicant: (주)케비젠

    Abstract: 본 발명은 퓨에라리아 속 식물 뿌리의 알콜 추출물을 함유하는 항암용 조성물에 관한 것으로, 항암 효과가 뛰어나며 부작용이 적어 각종 암의 예방과 치료에 유용하게 사용될 수 있다.
    또한, 본 발명의 퓨에라리아 속 식물 뿌리의 알콜 추출물은 피부에 안정할 뿐 아니라, 보습효과, 피부 탄력 효과, 잔주름, 기미, 잡티 등의 예방에 효과적이므로, 화장료 조성물로 유용하게 사용될 수 있다.

    Abstract translation: 本发明涉及含有pyuerariah的在植物根部的醇提取物的抗癌组合物,以及优良的抗肿瘤活性具有副作用少,可以是各种癌症的预防和治疗是有用的。

    공역화 리놀렌산을 생산하는 신규한 균주, 이를 함유하는 캡슐제 및 이를 이용한 기능성 식품
    18.
    发明公开
    공역화 리놀렌산을 생산하는 신규한 균주, 이를 함유하는 캡슐제 및 이를 이용한 기능성 식품 有权
    生产微生物的共轭亚油酸(CLA),其将CLA分解成生物质中的中和和累积物,包含其的包封组合物和使用其的功能性食品

    公开(公告)号:KR1020050023364A

    公开(公告)日:2005-03-09

    申请号:KR1020050004128

    申请日:2005-01-17

    Applicant: (주)케비젠

    Abstract: PURPOSE: Provided are a conjugated linoleic acid(CLA) producing microorganism, a capsulated composition comprising the same microorganism, and the functional food using the same composition, which microorganism has improved conjugated linoleic acid(CLA) producing activity, secretes CLA into the medium and accumulates CLA within the biomass, and has tolerance against acids such as acid in the stomach and bile juice and antibiotics. CONSTITUTION: The CLA producing microorganism which converts linoleic acid(LA) into conjugated linoleic acid(CLA) is provided, wherein the CLA producing microorganism is Enterococcus faecium CBG-C5(KACC 91002). The capsulated composition for prevention and treatment of cancer, arteriosclerosis, diabetes and obeseness comprises the CLA producing microorganism Enterococcus faecium CBG-C5(KACC 91002), wherein the coating material is water-soluble polysaccharides. The functional food containing the capsulated composition is provided, wherein the food is yoghurt, cheese, kimchi and jang(fermented soybean).

    Abstract translation: 目的:提供共轭亚油酸(CLA)生产微生物,包含相同微生物的包封组合物和使用相同组成的功能性食品,该微生物具有改善的共轭亚油酸(CLA)产生活性,将CLA分泌到培养基中, 在生物质内积累CLA,并且具有对胃酸,胆汁和抗生素等酸的耐受性。 构成:提供将亚油酸(LA)转化为共轭亚油酸(CLA)的CLA产生微生物,其中CLA产生微生物是屎肠球菌CBG-C5(KACC91002)。 用于预防和治疗癌症,动脉硬化,糖尿病和软绵绵的包封组合物包括CLA产生微生物屎肠球菌CBG-C5(KACC91002),其中涂层材料是水溶性多糖。 提供含有封装组合物的功能性食品,其中食品是酸奶,奶酪,泡菜和姜(发酵大豆)。

    신규한 레티노이드 유도체 및 이의 제조방법 및 그화합물을 함유한 항암제 조성물
    19.
    发明公开
    신규한 레티노이드 유도체 및 이의 제조방법 및 그화합물을 함유한 항암제 조성물 有权
    含有衍生物的新型复方衍生物,制剂方法和抗癌药物组合物

    公开(公告)号:KR1020020090850A

    公开(公告)日:2002-12-05

    申请号:KR1020020015016

    申请日:2002-03-20

    Applicant: (주)케비젠

    Abstract: PURPOSE: A novel retinoid derivative, its preparation method, a compound used for preparing the derivative, and an anticancer medicine composition containing the derivative are provided, which retinoid derivative shows the excellent anticancer activity and no toxic side effect. CONSTITUTION: The retinoid derivative is represented by the formula I, wherein R¬1 and R¬2 are independent each other and are OH, SH, NH2, COOH, -R(CH2)mCH3, -RCOCO(CH2)mCH3, -RCO(CH2)mCHCH3CH3, or -RCOCH(NCOCH3)CH2CH2CONH2, and R¬3 is H; R¬1 and R¬3 are independent each other and are OH, SH, NH2, COOH, -R(CH2)mCH3, -RCOCO(CH2)mCH3, or -RCOCH(NCOCH3)CH2CH2CONH2, and R¬2 is H; R¬1 is OH, SH, NH2, COOH, -R(CH2)mCH3, R¬2 is H, and R¬3 is H, OH or Cl; R¬3 is OH, SH, NH2, COOH, -R(CH2)mCH3, or -RCOCH(NCOCH3)CH2CH2CONH2, R¬2 is H, and R¬1 is H, OH or Cl; or R¬1, R¬2 and R¬3 are independent each another and are OH, SH, NH2, COOH, -R(CH2)mCH3, or -RCOCH(NCOCH3)CH2CH2CONH2; and R is CH2, O, NH or S, R¬4 is H or an alkyl group of C1-C6, and m is an integer of 0-5.

    Abstract translation: 目的:提供一种新型类视黄醇衍生物及其制备方法,用于制备衍生物的化合物和含有该衍生物的抗癌药物组合物,其视黄酸衍生物显示出优异的抗癌活性,无毒副作用。 构型:类视黄醇衍生物由式I表示,其中R 1和R 2彼此独立,为OH,SH,NH 2,COOH,-R(CH 2)m CH 3,-RCOCO(CH 2)m CH 3,-RCO (CH 2)m CHCH 3 CH 3或-RCOCH(NCOCH 3)CH 2 CH 2 CONH 2,R 3 3是H; R 1和R 3彼此独立地是OH,SH,NH 2,COOH,-R(CH 2)mCH 3,-OCOO(CH 2)mCH 3或-RCOCH(NCOCH 3)CH 2 CH 2 CONH 2,R 12是H; R 1是OH,SH,NH 2,COOH,-R(CH 2)mCH 3,R 2是H,R 3是H,OH或Cl; R 3是OH,SH,NH 2,COOH,-R(CH 2)m CH 3或-RCOCH(NCOCH 3)CH 2 CH 2 CONH 2,R 2是H,R 1是H,OH或Cl; 或R 1,R 2和R 3彼此独立,并且是OH,SH,NH 2,COOH,-R(CH 2)mCH 3或-RCOCH(NCOCH 3)CH 2 CH 2 CONH 2; 且R为CH 2,O,NH或S,R 4为H或C 1 -C 6烷基,m为0-5的整数。

    알파-엘-아스파틸-엘-페닐알라닌 메틸 에스테르 염산염의새로운 제조방법
    20.
    发明公开
    알파-엘-아스파틸-엘-페닐알라닌 메틸 에스테르 염산염의새로운 제조방법 失效
    ALPHA-L-ASPARTYL-L-苯丙氨酸甲酯盐酸盐的新型制备方法

    公开(公告)号:KR1020020085491A

    公开(公告)日:2002-11-16

    申请号:KR1020010025012

    申请日:2001-05-08

    Abstract: PURPOSE: A novel method for preparing α-L-aspartyl-L-phenylalanine methyl ester·HCl salt is provided, to reduce the amount of by-products, to allow the by-products to be reused after hydrolysis and to increase the production yield by 20% or more. CONSTITUTION: The method comprises the steps of reacting L-aspartic acid with trimethyl silyl chloride in the presence of an alcohol solvent to esterify the β-COOH selectively to obtain α-L-aspartyl-L-phenylalanine methyl ester·HCl. Preferably the alcohol solvent is selected from the group consisting of methyl alcohol, ethyl alcohol, allyl alcohol and benzyl alcohol. Preferably the method comprises further the steps of protecting an amine group with -CHO, Boc, benzyloxycarbonyl group, or -C(O)OR¬2 (R2 is methyl. ethyl or isobutyl group) by using acetic anhydride and formic acid.

    Abstract translation: 目的:提供一种制备α-L-天冬氨酰-L-苯丙氨酸甲酯·HCl盐的新方法,以减少副产物的含量,使副产物在水解后再次使用,并提高产量 减少20%以上。 方法:该方法包括在醇溶剂存在下使L-天冬氨酸与三甲基甲硅烷基氯反应,选择性地酯化β-COOH,得到α-L-天冬氨酰-L-苯丙氨酸甲酯·HCl。 醇溶剂优选选自甲醇,乙醇,烯丙醇和苄醇。 优选地,所述方法还包括通过使用乙酸酐和甲酸保护具有-CHO,Boc,苄氧基羰基或-C(O)OR 2(R2为甲基,乙基或异丁基)的胺基的步骤。

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