原花青素C1
原花青素C1(Procyanidin C1,簡稱PCC1)是一種B型前花青素(B type proanthocyanidin),是一種可在釀酒葡萄中找到的表兒茶素三聚體。[1]
原花青素C1 | |
---|---|
![]() | |
IUPAC名 (12R,13R,14R,22R,23R,24S,32R,33R)-12,22,32-Tris(3,4-dihydroxyphenyl)-12H,22H,32H-[14,28:24,38-ter-1-benzopyran]-13,15,17,23,25,27,33,35,37-nonol | |
别名 | Procyanidin C1 Procyanidol C1 Epicatechin-(4.beta.-->8)epicatechin-(4.beta.-->8)epicatechin Epicatechin-(4β→8)-epicatechin--(4β→8)-epicatechin |
识别 | |
CAS号 | 37064-30-5 ![]() |
PubChem | 169853 |
ChemSpider | 148540 |
SMILES |
|
InChI |
|
InChIKey | MOJZMWJRUKIQGL-XILRTYJMBW |
ChEBI | 75643 |
KEGG | C17624 |
性质 | |
化学式 | C45H38O18 |
866.77 g/mol g·mol⁻¹ | |
若非注明,所有数据均出自标准状态(25 ℃,100 kPa)下。 |
自然中的分布與功用
原花青素C1可從釀酒葡萄的種子萃取物中分離出來。[2]
化學合成
有七種芐酯前花青素三聚體(其中包括原花青素C1、原花青素C2及其他幾種「表兒茶素-(4β-8)-兒茶素-(4α-8)-表兒茶素」三聚體),可透過以三氟甲磺酸三甲基硅酯進行催化的凝結反應進行高產量的不对称合成;而苄酯化的原花青素C2的結構可藉由比較以兩種不同路徑合成的受保護的原花青素C2的1H NMR光譜進行確認;此外,對「(+)-兒茶素」以及「(-)-表兒茶素」三聚體衍生物的去保護作用,可以相當良好的產量製成四種自然的原花青素三聚體。[3]
外部連結
- Carissa Wong: Grape seed chemical allows mice to live longer by killing aged cells (页面存档备份,存于). NewScientist, 6 December 2021
參考資料
- Proanthocyanidin composition of red Vitis vinifera varieties from the Douro valley during ripening : Influence of cultivation altitude. Mateus Nuno, Marques Sara, Goncalves Ana C., Machado José M. and De Freitas Victor, American journal of enology and viticulture, 2001, vol. 52, no2, pp. 115-121, INIST:1129642
- Carissa Wong. . New Scientist. Dec 6, 2021 [2022-02-07]. (原始内容存档于2021-12-21).
- Efficient Stereoselective Synthesis of Proanthocyanidin Trimers with TMSOTf-Catalyzed Intermolecular Condensation. Akiko Saito, Akira Tanaka, Makoto Ubukata and Noriyuki Nakajima, Synlett, 2004, volume 6, pages 1069-1073, doi:10.1055/s-2004-822905
- Xu, Qixia; et al. . Nature Metabolism. Dec 6, 2021 [2022-02-07]. doi:10.1038/s42255-021-00491-8. (原始内容存档于2022-02-18).
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.