700122P

campestanol

Avanti Research^™ - A Croda Brand 700122P, powder

• 別名: 5α-campestan-3β-ol
• 実験式（ヒル表記法）: C₂₈H₅₀O
• CAS番号: 474-60-2
• 分子量: 402.70
• MDL番号: MFCD00201592
• UNSPSCコード: 12352211
• NACRES: NA.25

特性

• アッセイ: >99% (TLC)
• フォーム: powder
• 包装: pkg of 1 × 1 mg (700122P-1mg)
• メーカー／製品名: Avanti Research^™ - A Croda Brand 700122P
• 輸送温度: dry ice
• 保管温度: −20°C
• SMILES記法: O[C@@H]1C[C@H]2[C@@]([C@@H]3[C@H]([C@H]4[C@@]([C@H](CC4)[C@@H](CC[C@H](C(C)C)C)C)(CC3)C)CC2)(CC1)C
• InChI: 1S/C28H50O/c1-18(2)19(3)7-8-20(4)24-11-12-25-23-10-9-21-17-22(29)13-15-27(21,5)26(23)14-16-28(24,25)6/h18-26,29H,7-17H2,1-6H3/t19-,20-,21+,22+,23+,24-,25+,26+,27+,28-/m1/s1
• InChI Key: ARYTXMNEANMLMU-ATEDBJNTSA-N

詳細

詳細

Campestanol has a methyl group at the C-24. It comprises the 10-30% of stanol content in vegetable oil. It is naturally occurring and has similar structure as cholesterol. Campestanol is synthesized by the hydrogenation of campesterol.

Campestanol is a saturated plant stanol.

生物化学的／生理学的作用

Campestanol absorption in intestine is similar to that of cholesterol absorption pathway. However, in sitosterolemic homozygotes, it is hyperabsorbed from the intestine.

Intestinal absorption of campestanol is lesser compared to cholesterol due to the presence of side chain. Due to the structural similarity with cholesterol, campestanol reduces cholesterol absorption in the intestine and the plasma level of LDL cholesterol.

包装

5 mL Amber Glass Screw Cap Vial (700122P-1mg)

法的情報

Avanti Research is a trademark of Avanti Polar Lipids, LLC

安全性情報

• 保管分類コード: 11 - Combustible Solids