밤껍질 추출물을 포함하는 화장료 조성물
    41.
    发明公开
    밤껍질 추출물을 포함하는 화장료 조성물 有权
    化妆品组合包括CHESTNUT壳提取物

    公开(公告)号:KR1020120027436A

    公开(公告)日:2012-03-21

    申请号:KR1020117031696

    申请日:2010-06-18

    CPC classification number: A61Q19/005 A61K8/97 A61K36/49

    Abstract: PURPOSE: A cosmetic composition containing nutshell extract is provided to suppress proteinase-activated receptor-2(PAR-2) and to relieve itching. CONSTITUTION: A cosmetic composition for relieving or suppressing itching contains nutshell extract as an active ingredient. The composition prevents or relieves itching caused by inflammatory dermatitis, atopic dermatitis, miliaria, frostbite, contact dermatitis, seborrheic dermatitis, or pruritus. A cosmetic composition improving skin barrier function contains the nutshell extract as an active ingredient. The extract is prepared using water, low alcohol of C1-4, 1,3-butylene glycol, or mixture thereof.

    Abstract translation: 目的:提供含有坚果壳提取物的化妆品组合物,以抑制蛋白酶激活的受体-2(PAR-2)并缓解瘙痒。 构成:用于缓解或抑制瘙痒的化妆品组合物含有坚果壳提取物作为活性成分。 该组合物预防或缓解由炎症性皮炎,特应性皮炎,睫毛膏,冻伤,接触性皮炎,脂溢性皮炎或瘙痒引起的瘙痒。 改善皮肤屏障功能的化妆品组合物含有坚果壳提取物作为活性成分。 提取物是使用C 1-4,1,3-丁二醇或其混合物的水,低级醇制备的。

    콩 추출물을 함유하는 혈액 순환 개선 및 혈관 건강 증진용 조성물
    42.
    发明公开
    콩 추출물을 함유하는 혈액 순환 개선 및 혈관 건강 증진용 조성물 审中-实审
    包含用于改善血液循环和血管健康的豆提取物的组合物

    公开(公告)号:KR1020100127728A

    公开(公告)日:2010-12-06

    申请号:KR1020100049181

    申请日:2010-05-26

    Abstract: PURPOSE: A composition containing soybean extract isolated with low alcohol is provided to improve blood circulation and to treat obesity, diabetes, and hyperlipidemia. CONSTITUTION: A composition for improving blood circulation contains soybean extract isolating with 1-7% of C1-5 alcohol or fraction. The C1-5 alcohol is methanol, ethanol, isopropylalcohol, n-propylalcohol, n-butanol or isobutanol. The soybean extract or fraction contains adenosine. The fraction is an ethylacetate or butanol fraction. The composition suppresses thrombosis or cholesterol generation.

    Abstract translation: 目的:提供含有用低分子量分离的大豆提取物的组合物,以改善血液循环和治疗肥胖症,糖尿病和高脂血症。 构成:用于改善血液循环的组合物含有用1-7%的C1-5醇或级分分离的大豆提取物。 C 1-5醇是甲醇,乙醇,异丙醇,正丙醇,正丁醇或异丁醇。 大豆提取物或级分含有腺苷。 馏分是乙酸乙酯或丁醇馏分。 该组合物抑制血栓形成或胆固醇的产生。

    바닐로이드 수용체 길항물질로서의 신규 화합물, 이의이성체 또는 이의 약학적으로 허용가능한 염, 및 이를함유하는 약학 조성물
    44.
    发明公开
    바닐로이드 수용체 길항물질로서의 신규 화합물, 이의이성체 또는 이의 약학적으로 허용가능한 염, 및 이를함유하는 약학 조성물 有权
    新化合物,其异构体,或其药学上可接受的盐作为VANILLOID受体拮抗剂; 和含有它们的药物组合物

    公开(公告)号:KR1020080007329A

    公开(公告)日:2008-01-18

    申请号:KR1020077024002

    申请日:2006-03-15

    Abstract: A compound as a vanilloid receptor antagonist is provided to obtain a pharmaceutical composition effective for preventing or treating pain, migraine, arthralgia, nerve injury, skin diseases, overactive bladder, irritable bowel syndrome, or the like. A compound as a vanilloid receptor antagonist, an isomer or a pharmaceutically acceptable salt thereof is represented by the following formula I. In formula I, X is NHCH2, CR11=CR12, NH, CHR11CHR12 or C=C, wherein each of R11 and R12 represents H, halogen, C1-C5 alkyl, C1-C5 alkoxy, halo(C1-C5)alkyl or phenyl; R1 is a C2-C5 alkenyl or C2-C5 alkynyl; R2 is H, halogen, nitro, cyano, C1-C5 alkyl, C1-C5 alkoxy, halo(C1-C5)alkyl, C2-C5 alkenyl, or C2-C5 alkynyl; R2 is H, halogen, nitro, cyano, C1-C5 alkyl, C1-C5 alkoxy, halo(C1-C5)alkyl, C2-C5 alkenyl, C2-C5 alkynyl, carboxyl, C1-C5 alkoxycarbonyl, C1-C5 alkylthio, phenyl or phenyl(C1-C3)alkyl, wherein is each phenyl group is non-substituted or substituted with at least one substituent; R3 is H, C1-C5 alkyl, C1-C5 alkoxy or halo(C1-C5)alkyl; each of R4, R5 R6, R7 and R8 independently represents H, carboxyl, C1-C5 alkyl, nitro, C2-C5 alkenyl, C1-C5 alkoxy, C2-C5 alkynyl, halo(C1-C5)alkyl, C1-C5 alkylthio, C1-C5 alkylsulfonyl, C1-C5 alkylcarbonyl, C1-C5 alkoxycarbonyl, hydroxy, C2-C5 alkenyloxy, C1-C5 alkoxy(C1-C5)alkoxy, C1-C5 alkoxy(C1-C5)alkoxy(C1-C5)alkyl, C1-C3 alkylpiperazinyl, piperazinyl(C1-C5)alkoxy, piperidinyl(C1-C5)alkoxy, C1-C5 alkoxy (C1-C5)alkylamino, C1-C7 alkylamino, morpholinyl, morpholinyl(C1-C5)alkyloxy, tetrahydropyranyloxy, phenyl or halogen, wherein each phenyl group is non-substituted or substituted with at least one substituent; each of R9 and R10 independently represents H, -SO2R13, -SOR13, C1-C5 alkyl, C1-C5 alkoxy, halo (C1-C5)alkyl, C2-C5 alkenyl, C1-C5 alkoxycarbonyl, C1-C5 alkylthio, phenyl or phenyl (C1-C3)alkyl, wherein each phenyl group is non-substituted or substituted with at least one substituent, and R13 is H, amino, C1-C5 alkyl, C2-C5 alkenyl, C1-C5 alkoxy, halo(C1-C5)alkyl, trifluoromethyl, phenyl or phenyl(C1-C3)alkyl.

    Abstract translation: 提供作为香草素受体拮抗剂的化合物以获得有效预防或治疗疼痛,偏头痛,关节痛,神经损伤,皮肤疾病,膀胱过度活动症,肠易激综合征等的药物组合物。 作为香草酸受体拮抗剂的化合物,其异构体或其药学上可接受的盐由下式I表示。在式I中,X为NHCH 2,CR 11 = CR 12,NH,CHR 11 CHR 12或C = C,其中R 11和R 12 表示H,卤素,C 1 -C 5烷基,C 1 -C 5烷氧基,卤代(C 1 -C 5)烷基或苯基; R1是C2-C5烯基或C2-C5炔基; R2是H,卤素,硝基,氰基,C1-C5烷基,C1-C5烷氧基,卤代(C1-C5)烷基,C2-C5烯基或C2-C5炔基; R2是H,卤素,硝基,氰基,C1-C5烷基,C1-C5烷氧基,卤代(C1-C5)烷基,C2-C5烯基,C2-C5炔基,羧基,C1-C5烷氧羰基,C1-C5烷硫基, 苯基或苯基(C1-C3)烷基,其中每个苯基是未取代的或被至少一个取代基取代; R3是H,C1-C5烷基,C1-C5烷氧基或卤代(C1-C5)烷基; R 4,R 5,R 6,R 7和R 8各自独立地表示H,羧基,C 1 -C 5烷基,硝基,C 2 -C 5烯基,C 1 -C 5烷氧基,C 2 -C 5炔基,卤代(C 1 -C 5)烷基,C 1 -C 5烷硫基 ,C1-C5烷基磺酰基,C1-C5烷基羰基,C1-C5烷氧基羰基,羟基,C2-C5链烯氧基,C1-C5烷氧基(C1-C5)烷氧基,C1-C5烷氧基(C1-C5)烷氧基(C1-C5)烷基 (C1-C5)烷氧基,C1-C5烷氧基(C1-C5)烷基氨基,C1-C7烷基氨基,吗啉基,吗啉基(C1-C5)烷氧基,四氢吡喃基氧基, 苯基或卤素,其中每个苯基未被取代或被至少一个取代基取代; R 9和R 10各自独立地表示H,-SO 2 R 13,-SOR 13,C 1 -C 5烷基,C 1 -C 5烷氧基,卤代(C 1 -C 5)烷基,C 2 -C 5烯基,C 1 -C 5烷氧基羰基,C 1 -C 5烷硫基,苯基或 苯基(C1-C3)烷基,其中每个苯基未被取代或被至少一个取代基取代,R 13是H,氨基,C 1 -C 5烷基,C 2 -C 5烯基,C 1 -C 5烷氧基,卤代(C1- C5)烷基,三氟甲基,苯基或苯基(C1-C3)烷基。

    바닐로이드 수용체 길항물질로서의 신규 화합물, 이의이성체 또는 이의 약학적으로 허용가능한 염, 및 이를함유하는 약학 조성물
    45.
    发明公开
    바닐로이드 수용체 길항물질로서의 신규 화합물, 이의이성체 또는 이의 약학적으로 허용가능한 염, 및 이를함유하는 약학 조성물 有权
    新化合物,其异构体,或其药学上可接受的盐作为VANILLOID受体拮抗剂; 和含有它们的药物组合物

    公开(公告)号:KR1020070114821A

    公开(公告)日:2007-12-04

    申请号:KR1020077024004

    申请日:2006-03-17

    Abstract: A compound as a vanilloid receptor antagonist is provided to obtain a high activity in preventing or treating pain, migraine, arthralgia, neuralgia, neural diseases, neural injury, skin diseases, irritable bowel syndrome, inflammatory diseases, cardiac diseases, etc. A compound as a vanilloid receptor antagonist is a compound represented by the following formula Ia or an isomer and/or pharmaceutically acceptable salt thereof. In formula Ia, X is CR11=CR12 or C=C, wherein each of R11 and R12 independently represents H, a halogen atom, C1-C5 alkyl or phenyl; each of R1 and R2 independently represents H, carboxyl, C1-C5 alkyl, halogen, nitro, C1-C5 alkoxy, halo(C1-C5)alkyl, C1-C5 alkylcarbonyl, C1-C5 alkylcarbonylamino, C1-C5 alkylsulfonylamino, phenylsulfonylamino, C1-C5 alkylthio, C1-C5 alkylsulfonyl or C1-C5 alkoxycarbonyl; R3 is H, C1-C5 alkyl, C1-C5 alkoxy or halo(C1-C5)alkyl; each of R4, R5, R6, R7 and R8 independently represents H, carboxyl, C1-C5 alkyl, nitro, C2-C5 alkenyl, C1-C5 alkoxy, C2-C5 alkynyl, halo(C1-C5)alkyl, C1-C5 alkylthio, C1-C5 alkylsulfonyl, C1-C5 alkylcarbonyl, C1-C5 alkoxycarbonyl, phenyl or halogen, wherein the phenyl is non-substituted or substituted with at least one substituent selected from carboxyl, C1-C5 alkyl, halogen, nitro, C2-C5 alkenyl, C1-C5 alkoxy, halo(C1-C5)alkyl, C1-C5 alkylcarbonyl, C1-C5 alkylthio, C1-C5 alkylsulfonyl and C1-C5 alkoxycarbonyl; R9 is C1-C5 alkylsulfonyl or C2-C5 alkenylsulfonyl; and R10 is H, with the proviso that when R3 is not H, R11 and R13 cannot represent H at the same time.

    Abstract translation: 提供了一种作为香草素受体拮抗剂的化合物,用于预防或治疗疼痛,偏头痛,关节痛,神经痛,神经疾病,神经损伤,皮肤病,肠易激综合征,炎性疾病,心脏病等中的高活性。 香草酸受体拮抗剂是由下式Ia表示的化合物或其异构体和/或其药学上可接受的盐。 在式Ia中,X是CR 11 = CR 12或C = C,其中R 11和R 12各自独立地表示H,卤素原子,C 1 -C 5烷基或苯基; R1和R2各自独立地表示H,羧基,C1-C5烷基,卤素,硝基,C1-C5烷氧基,卤代(C1-C5)烷基,C1-C5烷基羰基,C1-C5烷基羰基氨基,C1-C5烷基磺酰基氨基,苯基磺酰基氨基, C1-C5烷硫基,C1-C5烷基磺酰基或C1-C5烷氧基羰基; R3是H,C1-C5烷基,C1-C5烷氧基或卤代(C1-C5)烷基; R4,R5,R6,R7和R8各自独立地表示H,羧基,C1-C5烷基,硝基,C2-C5烯基,C1-C5烷氧基,C2-C5炔基,卤代(C1-C5)烷基,C1-C5 烷基硫代,C 1 -C 5烷基磺酰基,C 1 -C 5烷基羰基,C 1 -C 5烷氧基羰基,苯基或卤素,其中苯基是未取代的或被至少一个选自羧基,C 1 -C 5烷基,卤素,硝基, C5链烯基,C1-C5烷氧基,卤代(C1-C5)烷基,C1-C5烷基羰基,C1-C5烷硫基,C1-C5烷基磺酰基和C1-C5烷氧基羰基; R9为C1-C5烷基磺酰基或C2-C5链烯基磺酰基; R 10为H,条件是当R3不为H时,R11和R13不能同时表示H。

    피부 미백용 조성물
    49.
    发明授权

    公开(公告)号:KR101902242B1

    公开(公告)日:2018-10-01

    申请号:KR1020110108051

    申请日:2011-10-21

    Abstract: 본발명은효소처리오가피를유효성분으로함유하는피부미백용조성물을제공한다. 본발명의효소처리오가피추출물을함유하는피부미백용조성물은효소를처리한오가피추출물을함유함으로써멜라닌생성의주효소인티로시나제를억제효과를나타내고, 멜라닌생성억제효과를나타내어기미또는주근깨개선, 색소침착억제및 피부미백효과가우수하므로, 피부외용제, 화장료조성물및 약학조성물등에사용될수 있다.

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