102067-92-5 Usage
General Description
Epitheaflagallin 3-O-gallate is a powerful antioxidant compound belonging to the family of catechins. It is found in various plant sources, especially in tea leaves. This chemical has been studied extensively for its potential health benefits, including its ability to protect cells from oxidative damage, reduce inflammation, and potentially lower the risk of various chronic diseases. Epitheaflagallin 3-O-gallate has also been investigated for its potential anti-cancer properties and its ability to support cardiovascular health. Overall, this chemical shows promise as a natural bioactive compound with numerous potential health benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 102067-92-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,0,6 and 7 respectively; the second part has 2 digits, 9 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 102067-92:
(8*1)+(7*0)+(6*2)+(5*0)+(4*6)+(3*7)+(2*9)+(1*2)=85
85 % 10 = 5
So 102067-92-5 is a valid CAS Registry Number.
102067-92-5Relevant articles and documents
Tannins and related compounds. XXXVI. Isolation and structures of theaflagallins, new red pigments from black tea
Nonaka,Hashimoto,Nishioka
, p. 61 - 65 (1986)
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Enzymatic synthesis of tea theaflavin derivatives and their anti-inflammatory and cytotoxic activities
Sang, Shengmin,Lambert, Joshua D.,Tian, Shiying,Hong, Jungil,Hou, Zhe,Ryu, Jae-He,Stark, Ruth E.,Rosen, Robert T.,Huang, Mou-Tuan,Yang, Chung S.,Ho, Chi-Tang
, p. 459 - 467 (2007/10/03)
Derivatives based on a benzotropolone skeleton (9-26) have been prepared by the enzymatic coupling (horseradish peroxidase/H2O2) of selected pairs of compounds (1-8), one with a vic-trihydroxyphenyl moiety, and the other with an ortho-dihydroxyphenyl structure. Some of these compounds have been found to inhibit TPA-induced mice ear edema, nitric oxide (NO) synthesis, and arachidonic acid release by LPS-stimulated RAW 264.7 cells. Their cytotoxic activites against KYSE 150 and 510 human esophageal squamous cell carcinoma and HT 29 human colon cancer cells were also evaluated.
