CAS No.: | 128-13-2 |
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Formula: | C24h40o4 |
EINECS: | 204-879-3 |
Environmental Protection: | Yes |
Certification: | ISO |
Color: | White |
Customization: |
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Ursodeoxycholic acid (UDCA), also known as ursodiol, is a naturally-occurring bile acid that constitutes a minor fraction of the human bile acid pool. UDCA has been used to treat liver disease for decades: its first use in traditional medicine dates back more than a hundred years.1,6 UDCA was first characterized in the bile of the Chinese black bear and is formed by 7b-epimerization of chenodeoxycholic acid, which is a primary bile acid. Due to its hydrophilicity, UDCA is less toxic than cholic acid or chenodeoxycholic acid.
UDCA was first approved by the FDA in 1987 for dissolution of gallstones and for primary biliary cirrhosis in 1996. UDCA works by replacing the hydrophobic or more toxic bile acids from the bile acid pool.
Huadi Group is a national high-tech enterprise. It is invested and established by a group of professionals who are specialized in the R&D of the biopharmaceutical field and have rich experience in production management and operation. It is a group company that invests in the production of diversified industries such as pharmaceuticals, medical devices, food, health products, cosmetics, and biological agriculture products.
Huadi Group has a total of 8 subsidiaries: Zhejiang Huadi Pharmaceutical Group Co., Ltd., Hangzhou Huajin Pharmaceutical Co., Ltd., Zhejiang Huajun Pharmaceutical Co., Ltd., Zhejiang Huadi Pharmaceutical Group Pharmaceutical Development Co., Ltd., Hangzhou Huadi Health Technology Co., Ltd., Leizhou Huadi Biotechnology Co., Ltd., Hainan Huadi Pharmaceutical Co., Ltd., Hunan Huadi Biotechnology Co., Ltd.
Huadi Group is the vice president unit of the China Biochemical Pharmaceutical Industry Association and the vice president unit of the Zhejiang Health Industry Research Association. Its controlling subsidiary, Zhejiang Huadi Pharmaceutical Group, is the drafting unit of the GMP appendix for biochemical drugs of the National Good Manufacturing Practice for Drugs. The group has two provincial-level R&D centers, the Chief Scientist is a senior scientist and overseas returnee PhD from a fortune 500 company in the United States. The company has long hired domestic and foreign experts and scholars as technical consultants, with strong technological innovation capabilities. With nearly 30 years of R&D and industrial transformation experience in biochemical extraction products, multi-component biochemical drugs, and synthetic peptide products, the technical level is leading domestically; In 2019, the group jointly launched internationally leading biopharmaceutical cutting-edge projects with senior research teams from the United States and Zhejiang University: The preparation of medicinal proteins using plant instantaneous expression systems, and the personalized treatment of tumors - neoantigen peptide project. All of these projects have made breakthrough progress and their technical level is internationally leading.
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