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MUC (Sal de magnésio do tri-hidrato do ácido ursodeoxicólico e do ácido quenodeoxicólico)

ICE

At ICE Pharma, we are a leading global manufacturer and supplier of Ursodeoxycholic Acid and Chenodeoxycholic Acid Trihydrate Magnesium salt, a combination bile acid salt renowned for its efficacy in dissolving cholesterol gallstones and providing hepatoprotective effects. Using our existing bovine derived bile acid API’s, ICE Pharma manufactures this trihydrated salt of CDCA and UDCA in a crystalline form. Our product is synthesized under stringent Good Manufacturing Practice (GMP) conditions, ensuring exceptional purity and consistency for pharmaceutical applications.

Descrição do produto

Ursodeoxycholic Acid and Chenodeoxycholic Acid Trihydrate Magnesium salt is a synthetic bile acid salt combining the therapeutic properties of ursodeoxycholic acid (UDCA) and chenodeoxycholic acid (CDCA) in a magnesium trihydrate form. This enhances the solubility and bioavailability of bile acids, facilitating effective dissolution of cholesterol-rich gallstones and offering protective benefits to liver tissues.

Aplicações

This API is utilised in the formulation of pharmaceutical products aimed at treating various hepatobiliary disorders, including:

  • Cholesterol Gallstones: Effective in dissolving radiolucent cholesterol gallstones in patients with functioning gallbladders, providing a non-surgical treatment option.
  • Hepatoprotective Agent: Offers protective effects against liver fibrosis and oxidative stress-induced liver damage.

Utilizações finais

MUC (Ursodeoxycholic Acid and Chenodeoxycholic Acid Trihydrate Magnesium Salt) is used as an active pharmaceutical ingredient in certain formulations for the treatment of biliary indigestion and gallstone dissolution. Its combined bile acid profile enhances therapeutic efficacy in managing hepatobiliary conditions where improved bile flow and cholesterol solubilization are critical.

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Visão geral do produto

  • Fórmula molecular

    C48H86MgO11

  • Peso molecular

    839,14

  • Formulário

    Pó cristalino branco

Unidades de produção

Locais
Nota
Embalagem
Standard Specification
Em conformidade com as BPF
DMF disponível
CEP Químico
BSETSE CEP

Reggio Emilia, Itália

N/A

25 kg

N/A

Sim

Não

Não

Sim

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