52444

ビオラキサンチン

≥90.0% (HPLC), solid

• 別名: (3S,3′S,5R,5′R,6S,6′S)-5,6:5′,6′-ジエポキシ-5,5′,6,6′-テトラヒドロ-β,β-カロテン-3,3′-ジオール
• 実験式（ヒル表記法）: C₄₀H₅₆O₄
• CAS番号: 126-29-4
• 分子量: 600.87
• Beilstein: 101269
• MDL番号: MFCD00075896
• UNSPSCコード: 12352202
• PubChem Substance ID: 329757838
• NACRES: NA.32

特性

• 製品名: ビオラキサンチン, ≥90.0% (HPLC)
• アッセイ: ≥90.0% (HPLC)
• フォーム: solid
• λ: in ethanol
• UV吸収: λ: 438-442 nm A_max
• 保管温度: −20°C
• SMILES記法: CC(/C=C/[C@@]12[C@](C)(O2)C[C@@H](O)CC1(C)C)=C\C=C\C(C)=C\C=C\C=C(C)\C=C\C=C(\C=C\[C@]34C(C)(C)C[C@H](O)C[C@]3(O4)C)C
• InChI: 1S/C40H56O4/c1-29(17-13-19-31(3)21-23-39-35(5,6)25-33(41)27-37(39,9)43-39)15-11-12-16-30(2)18-14-20-32(4)22-24-40-36(7,8)26-34(42)28-38(40,10)44-40/h11-24,33-34,41-42H,25-28H2,1-10H3/b12-11+,17-13+,18-14+,23-21+,24-22+,29-15+,30-16+,31-19+,32-20+/t33-,34-,37+,38+,39-,40-/m0/s1
• InChI Key: SZCBXWMUOPQSOX-WVJDLNGLSA-N

詳細

詳細

Violaxanthin is an epoxidized carotenoid obtained from plants.[1] It is an orange-colored natural xanthophyll pigment.[2]

アプリケーション

Violaxanthin has been used as a standard/control in high-pressure liquid chromatography (HPLC) analysis of pigment extracts to confirm the high-level astaxanthin accumulation suspected from the visual phenotype of Nt-AXT plants.[3]

生物化学的／生理学的作用

Violaxanthin is a carotene epoxide that is a precursor to capsanthin. It is one of three xanthophylls involved in the evolution of plastids of green plants (oxygen evolution) and participating in photo-induced interconversions known as the violaxanthin cycle. The cleavage of 9-cis-epoxycarotenoids (violaxanthin) to xanthoxin is the key regulatory step of abscisic acid biosynthesis.[4][5]

Violaxanthin is a powerful antioxidant and a vital precursor to important compounds like fucoxanthin and β-damascenone.[1] It is a non-photochemical fluorescence quenching structural component of the xanthophyll cycle that shields the photosynthetic system from excessive light. The 2,2′-azinobis-3-ethylbenzothiazoline-6-sulfonic acid (ABTS⁺) radical scavenging action of violaxanthin extracted from water spinach/water morning glory is strong, and it also inhibits lipid peroxidation and red blood cell hemolysis. Hence, it has the potential to be used in a wide range of medicinal and health products.[2]

安全性情報

• 保管分類コード: 11 - Combustible Solids
• WGK: WGK 3
• 引火点(°F): Not applicable
• 引火点(℃): Not applicable