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    페닐아세트아미드 유도체 및 그의 제조방법
    25.
    发明授权
    페닐아세트아미드 유도체 및 그의 제조방법 失效
    苯乙酸衍生物及其制备方法

    公开(公告)号：KR1019920009574B1

    公开(公告)日：1992-10-19

    申请号：KR1019900001274

    申请日：1990-02-02

    Applicant: 한국화학연구원

    Inventor： 박노상 ,  하덕찬 ,  최중권 ,  김현숙 ,  임희종 ,  이광숙

    IPC: C07C233/08 ,  C07C235/18

    Abstract: Phenylacetamide derivs. of formula (I) and their acid addn. salts are new. In (I), R=C1-8 alkyl or cyclid alkyl; X= halogen, nitro, R1, OR1, SR1, or NR1R2; R1 and R2 each =H, C1-8 alkyl, cyclic alkyl or substd. phenyl; l = 0-5; m = 0-5; n = 1-6. Also claimed is the prepn. of (I) which comprises condensing a cpd. of formula (II) with phenylacetic acid of formula (III). The cpds. (I) may be used as an anti-inflammatory analgesic.

    Abstract translation: 苯乙酰胺衍生物。 的式（I）和它们的酸加成。 盐是新的。 在（I）中，R = C 1-8烷基或环烷基; X =卤素，硝基，R 1，OR 1，SR 1或NR 1 R 2; R1和R2各自为H，C1-8烷基，环烷基或取代基。 苯基; l = 0-5; m = 0-5; n = 1-6。 还声称是prepn。 （I），其包括冷凝cpd。 式（II）与式（III）的苯乙酸反应。 cpds。 （I）可以用作消炎止痛剂。

    벤조산유도체의 제조방법
    27.
    发明授权
    벤조산유도체의 제조방법 失效
    制备苯甲酸衍生物的方法

    公开(公告)号：KR1019900007369B1

    公开(公告)日：1990-10-08

    申请号：KR1019870012931

    申请日：1987-11-17

    Applicant: 한국화학연구원 ,  씨제이 주식회사

    Inventor： 최중권 ,  홍성엽 ,  장영길 ,  김대황

    IPC: C07C61/15 ,  C07C51/235

    Abstract: Benzoic acid deriv. of formula (I) is prepd. by oxidizing benzaldehyde of formula (II) with H2O2 in the presence of arylselenium deriv. of formula (III) as a catalyst at 0-100 deg.C. In the formulas, A, B, C, R1 and R2 are each H, C1-3 alkyl, C1-3 alkoxy, halogen or nitro; Z is H, Cl or hydroxy; n is 0 or 1. The arylselenium deriv. is diaryldiselenide, arylselenic acid etc.

    Abstract translation: 苯甲酸衍生物 式（I）的化合物是制备的。 通过在芳基硒衍生物存在下用H 2 O 2氧化式（II）的苯甲醛。 的式（III）作为催化剂在0-100℃下反应。 在式中，A，B，C，R 1和R 2各自为H，C 1-3烷基，C 1-3烷氧基，卤素或硝基; Z是H，Cl或羟基; n为0或1.芳基硒衍生物。 是二芳基二硒，芳基硒酸等

    퀴놀린올 화합물을 유효성분으로 포함하는 항진균 조성물
    29.
    发明公开
    퀴놀린올 화합물을 유효성분으로 포함하는 항진균 조성물 有权
    包含喹啉醇化合物作为活性成分的抗真菌组合物

    公开(公告)号：KR1020120081690A

    公开(公告)日：2012-07-20

    申请号：KR1020110002945

    申请日：2011-01-12

    Applicant: 순천대학교 산학협력단 ,  한국화학연구원

    Inventor： 최상기 ,  최중권 ,  고아라

    IPC: A61K31/437 ,  A61P31/10 ,  A61P31/00

    CPC classification number: A61K31/4745

    Abstract: PURPOSE: An anti-fungal composition containing quinoline compounds is provided to enhance anti-fungal activity against pathogenic fungi and to be applied to pharmaceutical compositions, food preservative, and antifungal agrochemical. CONSTITUTION: An anti-fungal composition contains 0.001-99.9 wt% of quinoline compounds of chemical formula 1 as an active ingredient. An antifungal composition has an antifungal function to Candida albicans, Cryptococcus neoformans, Candida glabrata, Candida lusitaniae, Candida tropicalis, Candida glabrata, Candida lusitaniae, Candida tropicalis, Aspergillus niger, Aspergillus fumigates, and Fusarium oxysporum.

    Abstract translation: 目的：提供含有喹啉化合物的抗真菌组合物，以增强对致病真菌的抗真菌活性，并用于药物组合物，食品防腐剂和抗真菌农药。 构成：抗真菌组合物含有0.001-99.9重量％的化学式1的喹啉化合物作为活性成分。 抗真菌组合物对白色念珠菌，新型隐球酵母，光滑假丝酵母，念珠菌，念珠菌，玻璃假丝酵母，益热假丝酵母，热带假丝酵母，黑曲霉，烟曲霉和尖孢镰刀具有抗真菌功能。

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