Cj Corporation

Cj Cheiljedang Corporation

Myeong Yun Chae

Sung Hak Jung

Jong Hoon Kim

Sang Wook Park

Il Hwan Cho

Ji Young Noh

Hyung Chul Ryu

Hyun Jung Park

Young Hoon Kim

Kyu Jeong Yeon

Young Mee Chung

Dong Hyun Ko

Jee Woong Lim

Hae Tak Jin

Kyoung Rae Kang

Jie Eun Park

In Ki Min

Sung Hak Lee

Kyung Mi Park

Yong Sik Youn

Dong Kwon Lim

Kwang Hyeg Lee

Hyun Suk Kang

Seong Hwan Cho

Choong Sil Park

Hyung Ok Chun

Yun Taek Jung

Hea Ran Suh

Yun Cheul Kim

Hyuk Koo Lee

Dal Hyun Kim

Il Hwan Kim

Chun Seon Lyu

Taerho Kim

Jun Hee Cheon

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.

Thione derivative, method for the preparation thereof, and pharmaceutical composition containing the same

1,2,4-triazole derivatives, processes for the preparation thereof, and pharmaceutical compositions containing the same

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: Rrepresents naphthyl, indolyl, benzofuranyl, benzothienyl, benzimidazolyl, benzothiazolyl, benzotriazolyl, benzooxazolyl, quinolinyl, or isoquinolinyl; wherein, Ris optionally substituted at a substitutable position with one or more radicals independently selected from halogen, hydroxy, nitro, C-Calkyl, C-Chaloalkyl, C-Calkoxy, C-Chaloalkoxy, cyano, amino, monoalkylamino, and dialkylamino; Rrepresents methyl or amino; and A, B, E, and D each independently represent carbon or nitrogen.

1,2,4-triazole derivative, method for preparing the same, and pharmaceutical composition containing the same

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.

1,2,4-Triazole derivative, method for preparing the same, and pharmaceutical composition containing the same

A novel crystalline organic acid salt of amlodipine having improved physiochemical properties, a preparation method thereof and a pharmaceutical composition comprising the same are provided.

Crystalline organic acid salt of amlodipine

The present invention relates to an isothiazole derivative of the following formula 1 or nontoxic salt thereof: According to the present invention, isothiazole derivative or nontoxic salt thereof having antipyretic, analgesic and antiphlogistic activity and an improved side effect; process for the preparation thereof; and pharmaceutical composition including the same can be provided.

Isothiazole derivatives, process for the preparation thereof, and pharmaceutical composition including the same

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:

Disclosed are a novel organic acid salt of amlodipine, its preparation method, and a pharmaceutical composition containing the same as a therapeutically active ingredient.

Organic acid salt of amlodipine

Thiazolidine-4-one derivative, method for preparing the same, and pharmaceutical composition containing the same

2-thioxothiazole derivative, method for preparing the same, and pharmaceutical composition containing the same

Pyrazole-3-one derivative, method for preparing the same, and pharmaceutical composition containing the same

Growing community of inventors

Seongnam, South Korea

Myeong Yun Chae