基本情報
- 標準SMILES
COc1cc(CCC(=O)CC(=O)CCc2ccc(O)c(OC)c2)ccc1O- InChIKey
LBTVHXHERHESKG-UHFFFAOYSA-N- 分子式
- C21H24O6
- 平均分子量
- 372.4 g/mol
- 単同位体質量
- 372.15728849
概要
Tetrahydrocurcumin is a beta-diketone that is curcumin in which both of the double bonds have been reduced to single bonds. It has a role as a metabolite. It is a polyphenol, a beta-diketone and a diarylheptanoid. It is functionally related to a curcumin.
名称と識別子
- 優先名称
- Tetrahydrocurcumin
- IUPAC
- 1,7-bis(4-hydroxy-3-methoxyphenyl)heptane-3,5-dione
- 現地名
- テトラヒドロジフェルロイルメタン
- 英語名
- Tetrahydrocurcumin
- 分子式
- C21H24O6
- 分子量
- 372.41
名称と別名
名称をさらに表示
データベース識別子
- CAS
36062-04-1- PubChem CID
- 124072
- DTXSID
DTXSID30865801- ChEMBL
CHEMBL318743- ChEBI
CHEBI:67263- UNII
- 00U0645U03
- EC Number
- 609-201-3
- Nikkaji
- J478.221F
物性
構造計算による物性
- XLogP
- 2.8
- 極性表面積
- 93.1 Ų
- 水素結合供与体数
- 2
- 水素結合受容体数
- 6
- 回転可能結合数
- 10
- 重原子数
- 27
- 形式電荷
- 0
- 複雑度
- 437
実験および物理化学的性質
物理化学的性質
- 融点
- 95 · 95-97 ºC
- 沸点
- 564.1 · 564.1±45.0 °C(Predicted)
- 比重(密度)
- 1.222 · 1.222
- 闪点
- 196 ℃ · 196℃
- 貯蔵温度
- Inert atmosphere,Room Temperature
- 溶解性
- DMSO(微量)、メタノール(微量、加温)
- 酸解離定数(Pka)
- 9.12 · 9.12±0.10(Predicted)
- 外見
- 粉
- 色
- 薄黄色~黄色
- BRN
- 3485469 · 3485469
- 安定性
- 光に敏感
- 主な用途
- 食品および飲料
- 化粧品成分の機能
- 抗酸化物質
- InChI
- InChI=1S/C21H24O6/c1-26-20-11-14(5-9-18(20)24)3-7-16(22)13-17(23)8-4-15-6-10-19(25)21(12-15)27-2/h5-6,9-12,24-25H,3-4,7-8,13H2,1-2H3
- InChIKey
- LBTVHXHERHESKG-UHFFFAOYSA-N
- SMILES
- C(C1=CC=C(O)C(OC)=C1)CC(=O)CC(=O)CCC1=CC=C(O)C(OC)=C1
- LogP
- 2.728 · 2.728 (est)
化学的性質
化学的特性Off-white crystalline powder or Yellow Solid, soluble in methanol, ethanol, DMSO and other organic solvents, derived from turmeric bulbs.
安全と法規制
GHS分類
GHS Classification
This chemical does not meet GHS hazard criteria for 100% (2 of 2) of all reports.
Not Classified
Aggregated GHS information provided per 2 reports by companies from 1 notifications to the ECHA C&L Inventory.
危険有害性情報
Regulatory Information
Chemical: 3,5-Heptanedione, 1,7-bis(4-hydroxy-3-methoxyphenyl)-
Status: Active Update: 18-06-2014 https://echa.europa.eu/registration-dossier/-/registered-dossier/7283
3,5-Heptanedione, 1,7-bis(4-hydroxy-3-methoxyphenyl)-: Does not have an individual approval but may be used as a component in a product covered by a group standard. It is not approved for use as a chemical in its own right.
安全データ
- wgk
- 3
- ストレージクラス
- 11 - Combustible Solids
化学と産業
薬理情報
用途と製造
応用分野
説明Tetrahydrocurcumin (THC), the active metabolite of curcumin, is gaining popularity amongst scientist due to its wide spectrum of pharmacological activities, better stability and colourless nature. Tetrahydrocurcumin has a similar structure to that of curcumin. THC lacks the α, β-unsaturated carbonyl moiety in its chemical structure. It is naturally sourced from the roots of Curcuma zedoaria, Zingiber mioga, and Zingiber officinale and has potent antioxidant activity and depigmentation of the skin. THC is being studied for the treatment of cancer and dementia. THC is also known to epigenetically ameliorate mitochondrial dysfunction in brain vasculature during Ischemic Stroke. Tetrahydrocurcumin (THC) has been used as a neuroprotective agent to study its therapeutic potential in improving mitochondrial dysfunction in the ischemic stroke mice model.
使用Tetrahydrocurcumin is an antioxidant and skin-whitening ingredient. It is a major curcuminoid metabolite of curcumin that has been shown to have protective effects against diabetes and vascular dysfunction via alleviation of oxidative stress.The interest in tetrahydrocurcumin research is increasing because it is superior to curcumin in its solubility in water, chemical stability, bioavailability, and anti-oxidative activity. Curcumin metabolizes into tetrahydrocurcumin by bacterial enzyme NADPH-dependent curcumin reductase in the intestine.
調製方法
製造方法Tetrahydrocurcumin can also be chemically synthesized from curcumin by catalytic hydrogenation using PtO2 or palladium as a catalyst.One gram (1.0 g) of curcumin was dissolved in 20 ml of acetone and placed in a 100-ml glass reactor for reduction, to which was then added 500 mg of activated Raney-nickel catalyst. Subsequently, the atmosphere of the reactor was replaced for hydrogen gas by the routine method. A rubber-made balloon filled with hydrogen gas was arranged on the upper portion of the reactor in order to keep hydrogen gas pressure constant in the reactor by supplying hydrogen gas to make up for the consumed amount of hydrogen gas. The reactor was stirred while maintained at a given temperature in a constant-temperature water bath kept at 30° C. for 2-hour reduction.After completion of the reaction, the Raney-nickel catalyst was removed from the solution by filtering, which was then evaporated and dried by concentration under reduced pressure and was dissolved again in a small amount of acetone.Subsequently, the eluate was concentrated and dried under reduced pressure to obtain 674 mg of tetrahydrocurcumin.Method for making tetrahydrocurcumin and a substance containing the antioxidative substance tetrahydrocurcumin
上流・下流製品情報
上流原料
サプライヤー50 社
補足説明
定義本品は、次の化学式で表される芳香族化合物である。
定義ChEBI: Tetrahydrocurcumin is a beta-diketone that is curcumin in which both of the double bonds have been reduced to single bonds. It has a role as a metabolite. It is a beta-diketone, a polyphenol and a diarylheptanoid. It derives from a curcumin.
関連反応
関連ノート
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