Dehydrocholic Acid

Dehydrocholic Acid

製品名 Dehydrocholic Acid
CAS番号 81-23-2
別名 3,7,12-Trioxo-5β-cholan-24-oic acid; Dehydrocholate; DHCA
分子式 C24H34O5
分子量 402.52 g/mol
外観 白色からオフホワイトの結晶性粉末
分析(HPLC) ≥98.0%
融点 233-237°C (decomposes)
溶解度 Soluble in ethanol, acetone; slightly soluble in water
乾燥減量 ≤0.5%
焼失残渣 ≤0.11 TP3T
重金属 10 ppm以下
パッケージ 25 kg fiber drum with inner polyethylene bag

Dehydrocholic Acid Structure

同義語: 3,7,12-Trioxo-5β-cholan-24-oic acid; Dehydrocholate; DHCA; 5β-Cholan-24-oic acid, 3,7,12-trioxo-; Triketocholanic acid

Dehydrocholic acid is a synthetic bile acid derivative characterized by three ketone groups at positions 3, 7, and 12 on the steroid nucleus. This oxidation pattern distinguishes it from natural bile acids like cholic acid, which carry hydroxyl groups at these positions. The resulting flat, rigid structure enhances its interaction with hepatic transporters and enzymes, making it a valuable tool in pharmaceutical research and a key intermediate in the synthesis of other bile acid analogs.

Commercially, dehydrocholic acid is produced through the oxidation of cholic acid, typically using chromic acid or other oxidizing agents. It is available in high purity grades, often exceeding 98% as determined by HPLC. The compound is a white to off-white crystalline powder, sparingly soluble in water but freely soluble in organic solvents such as ethanol and acetone. Its stability under normal storage conditions makes it suitable for various applications.

In the pharmaceutical industry, dehydrocholic acid serves as a choleretic agent, stimulating bile production and flow. It is also used as an intermediate in the manufacture of ursodeoxycholic acid and other therapeutic bile acids. Research applications include studies on bile acid metabolism, liver function, and drug delivery systems. Its unique chemical properties continue to drive interest in both medicinal chemistry and process development.

化学構造と性質

Dehydrocholic acid belongs to the family of C24 bile acids, featuring a steroid nucleus with a carboxyl side chain. The three ketone groups at C3, C7, and C12 create a more planar and hydrophobic molecule compared to its hydroxylated counterparts. This structural feature influences its physicochemical behavior, including its solubility profile and chromatographic retention. The compound exhibits strong UV absorption due to the conjugated ketone system, which facilitates its detection and quantification.

作用機序

  • Choleretic effect: Dehydrocholic acid stimulates bile secretion by hepatocytes, increasing bile flow and volume. This effect is mediated through activation of nuclear receptors such as FXR and PXR, which regulate bile acid synthesis and transport.
  • Enzyme inhibition: It inhibits 7α-hydroxylase (CYP7A1), the rate-limiting enzyme in bile acid biosynthesis, thereby modulating cholesterol metabolism.
  • Transport modulation: The compound interacts with bile salt export pump (BSEP) and multidrug resistance-associated protein 2 (MRP2), affecting biliary excretion of endogenous and exogenous substances.
  • Metabolic regulation: Through activation of farnesoid X receptor (FXR), it influences lipid and glucose homeostasis, making it a subject of research in metabolic disorders.

品質仕様

パラメータ 仕様
外観 白色からオフホワイトの結晶性粉末
分析(HPLC) ≥98.0%
融点 233-237°C (decomposes)
乾燥減量 ≤0.5%
焼失残渣 ≤0.11 TP3T
重金属 10 ppm以下
溶解度 Soluble in ethanol, acetone; slightly soluble in water

供給および書類

  • 容量: 10 metric tons per year
  • リードタイム: 3~5営業日(在庫品)
  • ドキュメント: COA, MSDS, TDS available upon request
  • パッケージ: 25 kg fiber drum with inner polyethylene bag

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