跳轉至內容
Merck
全部照片(3)

重要文件

C1251

Sigma-Aldrich

(+)-儿茶素 水合物

≥98% (HPLC), powder

同義詞:

(+)-儿茶精-3, (2R,3S)-2-(3,4-二羟基苯基)-3,4-二氢-1(2H)-苯并吡喃-3,5,7-三醇

登入查看組織和合約定價


About This Item

經驗公式(希爾表示法):
C15H14O6 · xH2O
CAS號碼:
分子量::
290.27 (anhydrous basis)
Beilstein:
3595244
EC號碼:
MDL號碼:
分類程式碼代碼:
12352200
PubChem物質ID:
NACRES:
NA.77
暫時無法取得訂價和供貨情況

化驗

≥98% (HPLC)

形狀

powder

顏色

yellow to yellow with tan cast

mp

175-177 °C (anhydrous) (lit.)

溶解度

ethanol: 50 mg/mL

儲存溫度

2-8°C

SMILES 字串

[H]O[H].O[C@H]1Cc2c(O)cc(O)cc2O[C@@H]1c3ccc(O)c(O)c3

InChI

1S/C15H14O6.H2O/c16-8-4-11(18)9-6-13(20)15(21-14(9)5-8)7-1-2-10(17)12(19)3-7;/h1-5,13,15-20H,6H2;1H2/t13-,15+;/m0./s1

InChI 密鑰

OFUMQWOJBVNKLR-NQQJLSKUSA-N

尋找類似的產品? 前往 產品比較指南

一般說明

儿茶素是植物化学物质,在黑葡萄、桃子、草莓和蚕豆中含量丰富。儿茶素有各种形式,如儿茶素、表儿茶素、表儿茶素没食子酸酯、表焙儿茶素和表没食子儿茶素没食子酸酯。[1]

應用

(+)-水合儿茶素已用于以下情形:
  • 作为多酚标准品,测定红葡萄酒副产物中的多酚总量[2]
  • 作为添加剂,通过三重进料批量方法研究对体外甲烷生产和底物降解的效果[3]
  • 作为底物,测定L. plantarum CECT 748T 14重组鞣酸酶对儿茶素的活性[4]

生化/生理作用

一种植物来源的抗氧化性黄酮类化合物;自由基清除剂,可在各种生物系统中防止自由基介导的损伤。例如,在生理pH条件下,儿茶素可抑制羟基自由基介导的DNA链断裂。它还可以防止人体血浆氧化。它延迟了内源性脂溶性抗氧化剂的消耗并抑制脂质氧化。儿茶素还可以作为脂肪酸合酶的抑制剂。

象形圖

Exclamation mark

訊號詞

Warning

危險聲明

危險分類

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

標靶器官

Respiratory system

儲存類別代碼

11 - Combustible Solids

水污染物質分類(WGK)

WGK 3

閃點(°F)

Not applicable

閃點(°C)

Not applicable

個人防護裝備

dust mask type N95 (US), Eyeshields, Gloves


從最近期的版本中選擇一個:

分析證明 (COA)

Lot/Batch Number

未看到正確版本?

如果您需要一個特定的版本,您可以透過批號來尋找特定憑證。

已經擁有該產品?

您可以在文件庫中找到最近購買的產品相關文件。

存取文件庫

Hadeer M Ezzat et al.
International journal of pharmaceutics, 565, 488-498 (2019-05-18)
Catechin hydrate is a phytopharmaceutical with promising anticancer effects but poor bioavailability. This study aimed to elaborate catechin loaded chitosan-tethered liposomes (chitosomes) to enhance catechin oral bioavailability. Nanocarriers were optimized via ethanol injection method followed by physicochemical, ex vivo and
Christine Ziegler et al.
Molecular microbiology, 78(1), 13-34 (2010-10-07)
Increases in the environmental osmolarity are key determinants for the growth of microorganisms. To ensure a physiologically acceptable level of cellular hydration and turgor at high osmolarity, many bacteria accumulate compatible solutes. Osmotically controlled uptake systems allow the scavenging of
S B Lotito et al.
Free radical biology & medicine, 24(3), 435-441 (1998-01-23)
Based on the recognized capacity of (+)-catechin (CTCH) to prevent free radical-mediated damage in different biological systems, its role in the protection of human plasma from oxidation was investigated. Samples of human blood plasma were incubated with 50 mM AAPH
Nutrition and Health Info Sheet: Catechins (2008)
J Ueda et al.
Archives of biochemistry and biophysics, 333(2), 377-384 (1996-09-15)
The reactivities of various antioxidative compounds including catechol derivatives and endogenous radical scavengers toward hydroxyl radical (.OH) were investigated by an electron spin resonance-spin trapping method, thiobarbituric acid method, and DNA strand scission assay. Hydroxyl radical was generated by both

文章

Fatty acid synthesis supports cancer cell proliferation, essential for membrane generation, protein modification, and bioenergetics.

脂肪酸合成有助於癌細胞增殖,對於膜生成、蛋白質修飾和生物能來說是不可或缺的。

DISCOVER Bioactive Small Molecules for Nitric Oxide & Cell Stress Research

Antioxidants protect biological systems from oxidative damage produced by oxygen-containing free radicals and from redoxactive transition metal ions such as iron, copper, and cadmium.

查看全部

條款

Protocol for HPLC Analysis of Flavonoids on Ascentis® RP-Amide

在 Ascentis® RP-Amide 上進行類黃酮 HPLC 分析的規程

Questions

  1. Is the origin of "Catechin hydrate C1251" natural or synthetic?

    1 answer
    1. Currently, this product is of synthetic origin.

      Helpful?

Reviews

No rating value

Active Filters

我們的科學家團隊在所有研究領域都有豐富的經驗,包括生命科學、材料科學、化學合成、色譜、分析等.

聯絡技術服務