Abstract: A 1,2,4-triazole derivative of formula 1 or a non-toxic salt thereof, a preparation method thereof, and a pharmaceutical composition containing the derivative or the salt as an active ingredient are provided: wherein, Ar represents naphthyl; 3,4-methylenedioxyphenyl: phenyl; or phenyl substituted with the group selected from C1-C6 alkyl, C1-C6 alkoxy, or halogen.
Type:
Grant
Filed:
July 31, 2003
Date of Patent:
February 1, 2005
Assignee:
CJ Corp.
Inventors:
Il Hwan Cho, Dong Hyun Ko, Myeong Yun Chae, Taerho Kim, Kyoung Rae Kang, Jong Hoon Kim, Sung Hak Jung, Sang Wook Park, Hyung Ok Chun, Hyung Chul Ryu, Ji Young Noh, Hyun Jung Park, Jie Eun Park, Young Mee Chung
Abstract: Disclosed are a novel organic acid salt of amlodipine, its preparation method, and a pharmaceutical composition containing the same as a therapeutically active ingredient.
Type:
Grant
Filed:
August 19, 2003
Date of Patent:
January 25, 2005
Assignee:
CJ Corp
Inventors:
Yong Sik Youn, Seong Hwan Cho, Choong Sil Park, Yun Cheul Kim, Dong Kwon Lim, Sung Hak Jung, Sung Hak Lee, Hyun Suk Kang, Kyung Mi Park, Yun Taek Jung, Young Hoon Kim, Kyu Jeong Yeon, Myeong Yun Chae, Hae Tak Jin, Hea Ran Suh, Kwang Hyeg Lee, Hyuk Koo Lee
Abstract: A thiazolidine-4-one derivative of formula 1 or a non-toxic salt thereof, a preparation method thereof, and a pharmaceutical composition containing the derivative or the salt as an active ingredient are provided:
wherein:
R1 and R2 each independently represent hydrogen, C1-C3 alkyl, halogen, methyl substituted with halogen, C1-C3 alkoxy substituted with halogen, cyano, or nitro.
Type:
Grant
Filed:
May 16, 2003
Date of Patent:
August 17, 2004
Assignee:
CJ Corp.
Inventors:
Il Hwan Cho, Jee Woong Lim, Sang Wook Park, Ji Young Noh, Hyung Chul Ryu, Jong Hoon Kim, Myeong Yun Chae, Hyun Jung Park, Sung Hak Jung, Kyu Jeong Yeon, Hae Tak Jin
Abstract: Disclosed are a novel organic acid salt of amlodipine with superb physicochemical properties, its preparation method, and a pharmaceutical composition containing the same as a therapeutically active ingredient.
Type:
Grant
Filed:
July 29, 2003
Date of Patent:
June 29, 2004
Assignee:
CJ Corp.
Inventors:
Seong Hwan Cho, Yong Sik Youn, Yun Taek Jung, Choong Sil Park, Hyuk Koo Lee, Kwang Hyeg Lee, Eun Ju Jeong, Young Hoon Kim, Hae Tak Jin, Jun Hee Cheon, Sung Hak Lee, Sung Hak Jung, Dong Kwon Lim, Kyu Jeong Yeon, Yun Cheul Kim, Kyung Mi Park, Hyun Suk Kang
Abstract: Disclosed is a toothbrush having soft and hard bristles together. The toothbrush having soft and hard bristles with 6-10 mm in tapered length and 0.01-0.08mm in diameter of end portions comprises: longer bristles(1) located at both edges; and shorter bristles(2) located at the central portion, wherein the bristles are generally in a semicircular form at their top portions when seen from a side, and a difference in length between the longer bristles(1) and the shorter bristles(2) is about 2-4mm. The toothbrush can increase brushing efficiency and effectively remove foreign matters between teeth and inside periodontal pockets.
Abstract: A 2-thioxothiazole derivative of formula 1 or a non-toxic salt thereof, a preparation method thereof, and a pharmaceutical composition containing the derivative or the salt as an active ingredient are provided:
wherein:
R represents hydrogen or methyl;
X represents hydrogen, methyl, halogen, nitro, or methanesulfonyl.
Type:
Grant
Filed:
June 13, 2003
Date of Patent:
April 27, 2004
Assignee:
CJ Corp.
Inventors:
Il Hwan Cho, Jee Woong Lim, Sang Wook Park, Hyung Chul Ryu, Ji Young Noh, Jong Hoon Kim, Myeong Yun Chae, Sung Hak Jung, Hyun Jung Park, Kyu Jeong Yeon, Kyoung Rae Kang
Abstract: The present invention relates to an isothiazole derivative of the following formula 1 or nontoxic salt thereof: 1
Type:
Application
Filed:
October 9, 2003
Publication date:
April 15, 2004
Applicant:
CJ Corp.
Inventors:
II Hwan Cho, Dong Hyun Ko, Myeong Yun Chae, In Ki Min, Young Hoon Kim, Young Mee Chung, Hyun Jung Park, Ji Young Noh, II Hwan Kim, Hyung Chul Ryu, Sang Wook Park, Sung Hak Jung, Jong Hoon Kim
Abstract: Disclosed are a novel organic acid salt of amlodipine, its preparation method, and a pharmaceutical composition containing as a therapeutically active ingredient the same.
Type:
Application
Filed:
July 29, 2003
Publication date:
February 12, 2004
Applicant:
CJ Corp
Inventors:
Seong Hwan Cho, Yong Sik Youn, Yun Taek Jung, Choong Sil Park, Hyuk Koo Lee, Kwang Hyeg Lee, Eun Ju Jeong, Young Hoon Kim, Hae Tak Jin, Jun Hee Cheon, Sung Hak Lee, Sung Hak Jung, Dong Kwon Lim, Kyu Jeong Yeon, Yun Cheul Kim, Kyung Mi Park, Hyun Suk Kang
Abstract: Disclosed are a novel organic acid salt of amlodipine, its preparation method, and a pharmaceutical composition containing the same as a therapeutically active ingredient.
Type:
Application
Filed:
July 29, 2003
Publication date:
February 12, 2004
Applicant:
CJ Corp
Inventors:
Seong Hwan Cho, Yong Sik Youn, Yun Taek Jung, Choong Sil Park, Hyuk Koo Lee, Kwang Hyeg Lee, Eun Ju Jeong, Young Hoon Kim, Hae Tak Jin, Jun Hee Cheon, Sung Hak Lee, Sung Hak Jung, Dong Kwon Lim, Kyu Jeong Yeon, Yun Cheul Kim, Kyung Mi Park, Hyun Suk Kang
Abstract: A pyrazole-3-one derivative of formula 1 or a non-toxic salt thereof, a preparation method thereof, and a pharmaceutical composition containing the derivative or the salt as an active ingredient are provided:
wherein:
R1 and R2 each independently represent C1-C3 alkyl, aryl, or substituted aryl;
R3 represents amino or methyl;
R4 and R5 each independently represent hydrogen, C1-C3 alkyl, halogen, methyl substituted with halogen, C1-C3 alkoxy, cyano, or nitro;
or a non-toxic salt thereof.
Type:
Grant
Filed:
June 13, 2003
Date of Patent:
February 10, 2004
Assignee:
CJ Corp.
Inventors:
Il Hwan Cho, Ji Young Noh, Sang Wook Park, Hyung Chul Ryu, Jee Woong Lim, Jong Hoon Kim, Myeong Yun Chae, Dal Hyun Kim, Sung Hak Jung, Hyun Jung Park, Young Hoon Kim, In Ki Min
Abstract: The present invention relates to a processing method for preparing lovastatin and simvastatin which comprises the steps of (1) performing lactonization of mevinic acid and its homologous compounds in the presence of a mixed organic solvent without an acid catalyst through nitrogen sweep; and (2) making crystals. In the process of the present invention, lovastatin and simvastatin highly purified can be produced in a high yield and especially, heterodimers formed as a by-product can be reduced remarkably. Therefore, the processing method of the present invention can be convenient and economical.
Type:
Application
Filed:
November 14, 2002
Publication date:
June 12, 2003
Applicant:
CJ CORP.
Inventors:
Kwang-hyeg Lee, Jin-wan Kim, Kwang-do Choi, Sang-ho Lee, Hong-suk Cho