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1. 发明申请

WO2004014898A1 BENZOPYRAN DERIVATIVES SUBSTITUTED WITH SECONDARY AMINES INCLUDING IMIDAZOLE, THEIR PREPARATION AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM 审中-公开
标题翻译：二氯苯胺衍生物，其中包括咪达唑，其制剂和含有它们的药物组合物
公开(公告)号：WO2004014898A1
公开(公告)日：2004-02-19
申请号：PCT/KR2003/001534
申请日：2003-07-30
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , YI, Kyu Yang , LEE, Sun Kyung , YOO, Sung-Eun , SUH, Jee Hee , KIM, Nak Jeong , HWANG, Sun Kyung , LEE, Byung-Ho , SEO, Ho Won , LEE, Chong Ock , CHOI, Sang-Un
发明人： YI, Kyu Yang , LEE, Sun Kyung , YOO, Sung-Eun , SUH, Jee Hee , KIM, Nak Jeong , HWANG, Sun Kyung , LEE, Byung-Ho , SEO, Ho Won , LEE, Chong Ock , CHOI, Sang-Un
IPC分类号： C07D405/12
CPC分类号： C07D405/12
摘要： The present invention relates to benzopyran derivatives substituted with secondary amines including imidazole, their preparation, and pharmaceutical compositions containing them. The present invention is pharmacologically useful for the treatment of cancer, rheumatoid arthritis, and diabetic retinopathies through anti-angiogenic properties, and also pharmacologically useful in the protection of heart and neuronal cells against ischemia-reperfusion injury or preserving organs.
摘要翻译：本发明涉及被仲胺包括咪唑取代的苯并吡喃衍生物，其制备方法和含有它们的药物组合物。本发明在药理学上可用于通过抗血管生成特性治疗癌症，类风湿性关节炎和糖尿病性视网膜病变，并且还可用于保护心脏和神经细胞免受缺血再灌注损伤或保存器官的药理作用。

2. 发明申请

WO2009051417A3 PHENANTHRENE LACTAM DERIVATIVES HAVING ANTICANCER ACTIVITY AND METHOD FOR THE PREPARATION THEREOF 审中-公开
标题翻译：具有抗癌活性的苯丙氨酸衍生物及其制备方法
公开(公告)号：WO2009051417A3
公开(公告)日：2009-06-04
申请号：PCT/KR2008006110
申请日：2008-10-16
申请人： KOREA RES INST CHEM TECH , HEO JUNG NYOUNG , KIM BUM TAE , MIN YONG KI , CHOI SANG UN , LEE HYUK , CHANG SUNG YOUN , PARK NO KYUN , KIM JOA KYUM , KIM YOUNG HA , PARK MI KYUNG
发明人： HEO JUNG NYOUNG , KIM BUM TAE , MIN YONG KI , CHOI SANG UN , LEE HYUK , CHANG SUNG YOUN , PARK NO KYUN , KIM JOA KYUM , KIM YOUNG HA , PARK MI KYUNG
IPC分类号： C07D209/90
CPC分类号： C07D491/04
摘要： The present invention relates to a phenanthrene lactam derivative having anticanter activity, a method for the preparation thereof, and a pharmaceutical composition comprising same.
摘要翻译：本发明涉及具有抗癌活性的菲内酰胺衍生物，其制备方法和包含其的药物组合物。

3. 发明申请

WO2009051417A2 PHENANTHRENE LACTAM DERIVATIVES HAVING ANTICANCER ACTIVITY AND METHOD FOR THE PREPARATION THEREOF 审中-公开
标题翻译：具有抗癌活性的吩L内酰胺衍生物及其制备方法
公开(公告)号：WO2009051417A2
公开(公告)日：2009-04-23
申请号：PCT/KR2008/006110
申请日：2008-10-16
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , HEO, Jung Nyoung , KIM, Bum Tae , MIN, Yong Ki , CHOI, Sang Un , LEE, Hyuk , CHANG, Sung Youn , PARK, No Kyun , KIM, Joa Kyum , KIM, Young Ha , PARK, Mi Kyung
发明人： HEO, Jung Nyoung , KIM, Bum Tae , MIN, Yong Ki , CHOI, Sang Un , LEE, Hyuk , CHANG, Sung Youn , PARK, No Kyun , KIM, Joa Kyum , KIM, Young Ha , PARK, Mi Kyung
IPC分类号： C07D209/90
CPC分类号： C07D491/04
摘要： The present invention relates to a phenanthrene lactam derivative having anticanter activity, a method for the preparation thereof, and a pharmaceutical composition comprising same.
摘要翻译：本发明涉及具有抗心律不齐活性的菲内酰胺衍生物，其制备方法以及包含它的药物组合物。

4. 发明申请

WO1995025096A1 BENZOYLUREA DERIVATIVES AND ANTINEOPLASTIC COMPOSITIONS CONTAINING THEM 审中-公开
标题翻译：苯甲酰衍生物和含有它们的抗生素组合物
公开(公告)号：WO1995025096A1
公开(公告)日：1995-09-21
申请号：PCT/KR1995000021
申请日：1995-03-15
申请人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY , HWANG, Ki-Jun , PARK, Kyung-Ho , LEE, Chong, Ock , CHOI, Sang, Un
发明人： KOREA RESEARCH INSTITUTE OF CHEMICAL TECHNOLOGY
IPC分类号： C07D239/34
CPC分类号： C07D231/26 , C07D231/22
摘要： The present invention concerns benzoylurea derivatives represented by formula (I), wherein R and R are the same or different, and each represents hydrogen; one or more halogen atoms selected from the group consisting of fluorine, chlorine and bromine; straight or branch chained alkoxy group having 1 to 6 carbon atoms; haloalkyl group or nitro group; R represents hydrogen; straight or branch chained alkyl group having 1 to 6 carbon atoms; W, X and Y are the same or different, and each represents hydrogen; one or more halogen atoms selected from the group consisting of fluorine, chlorine and bromine; straight or branch chained alkyl group having 1 to 6 carbon atoms; straight or branch chained haloalkyl group having 1 to 6 carbon atoms; or phenyl group, optionally substituted with halogen, alkyl group having 1 to 6 carbon atoms or haloalkyl group; and Z represents oxygen or sulfur atom, and pharmaceutically acceptable salts thereof.
摘要翻译：本发明涉及由式（I）表示的苯甲酰基脲衍生物，其中R和R 2相同或不同，各自表示氢; 一个或多个选自氟，氯和溴的卤素原子; 具有1至6个碳原子的直链或支链烷氧基; 卤代烷基或硝基; R 1表示氢; 具有1-6个碳原子的直链或支链烷基; W，X和Y相同或不同，各自表示氢; 一个或多个选自氟，氯和溴的卤素原子; 具有1-6个碳原子的直链或支链烷基; 具有1至6个碳原子的直链或支链的卤代烷基; 或苯基，任选被卤素取代，具有1至6个碳原子的烷基或卤代烷基; Z表示氧或硫原子，及其药学上可接受的盐。

5. 发明授权

KR790000026B1 PREPARATION OF STABILIZED (TYPE) COPPER PHTHALOCYANINE BLU 失效
公开(公告)号：KR790000026B1
公开(公告)日：1979-02-26
申请号：KR770002481
申请日：1977-10-27
申请人： CHOI SANG UN , CHOI IN SIK
发明人： CHOI SANG UN , CHOI IN SIK
摘要： β-type copper phthalocyanine blue (I) was obtained by reaction of polyhydric alcohol, copper phthalocyanine blue compds., common salt and derivatives of phthalocyanine. The reaction mixts. were kneaded at 120-140≦̸C for 6-8hr, and refined by water and 98% H2SO4 at 90≦̸C for 1hr. The thermal stability, dispersive power and fluidity of I were excellent. The viscosity of I was increased.

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