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.[1] It is naturally occurring and has similar structure as cholesterol.[2] Campestanol is synthesized by the hydrogenation of campesterol.[3]

Campestanol is a saturated[4] 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.[2] However, in sitosterolemic homozygotes, it is hyperabsorbed from the intestine.[1]

Intestinal absorption of campestanol is lesser compared to cholesterol due to the presence of side chain.[5] Due to the structural similarity with cholesterol, campestanol reduces cholesterol absorption in the intestine and the plasma level of LDL cholesterol.[4]

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