Detail of > 4233-96-9
- CAS Number:
- 4233-96-9
- Name:
Benzoic acid,3,4,5-trihydroxy-,(2S,3R)-3,4-dihydro-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-3-ylester
- Superlist Name:
- (-)-Gallocatechin gallate
- Formula:
- C22H18O11
- Molecular Structure:

- Synonyms:
- Benzoicacid, 3,4,5-trihydroxy-, 3,4-dihydro-5,7-dihydroxy-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-3-ylester, (2S-trans)-;Gallocatechol, 3-gallate, (-)- (8CI);Gallic acid, esterwith gallocatechol, (-) (8CI);(-)-Gallocatechin 3-O-gallate;(-)-Gallocatechin3-gallate;(-)-Gallocatechol gallate;
- Molecular Weight:
- 458.37
- Density:
- 1.9 g/cm3
- Boiling Point:
- 909.1 °C at 760 mmHg
- Flash Point:
- 320 °C
- Hazard Symbols:
Xi- Risk Codes:
- 36/37/38
- Safety:
- 26-36Details
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Reference
- Theaflavin derivatives in black tea and catechin derivatives in green tea inhibit HIV-1 entry by targeting gp41
- All Rights Reserved. Theaflavin derivatives in black tea and catechin derivatives in green tea inhibit HIV-1 entry by targeting gp41. [Erratum to document cited in CA]. Liu, Shuwen; Lu, Hong; Zhao, Qian; He, Yuxian; Niu, Jinkui; Debnath, Asim K.; Wu, Shuguang; Jiang, Shibo (The New York Blood Center, Lindsley F. Kimball Research Institute, New York, NY 10021, USA). Biochimica et Biophysica Acta, General Subjects, 1770(2), 312 (English) 2007 Elsevier Ltd. CODEN: BBGSB3. ISSN: 0304-4165. DOCUMENT TYPE: Journal CA Section: 1 (Pharmacology) On page 279, Figure 7 is incorrect. The cor. Figure 7 and its legend is given.Except for chemicals metioned above, 989-51-5 and 4233-96-9 are also used. .
- Influence of tea catechins on lipid metabolism
- All Rights Reserved. Influence of tea catechins on lipid metabolism. Ikeda, Ikuo (Laboratory of Food and Biomolecular Science, Graduate School of Agricultural Science, Tohoku University, Sendai 981-8555, Japan). Tohoku Journal of Agricultural Research, 57(1-2), 11-17 (English) 2006 Tohoku University, Graduate School of Agricultural Science. CODEN: TJARAJ. ISSN: 0040-8719. DOCUMENT TYPE: Journal; General Review CA Section: 1 (Pharmacology) A review. Tea catechins reduce serum cholesterol concn. and suppress postprandial hypertriacylglycerolemia in exptl. animals and humans. These effects are mainly ascribed to gallate esters of catechins, (-)-epicatechin gallate (ECG) and (-)-epigallocatechin gallate (EGCG). During heat treatment for pasteurization, tea catechins are epimerized to so-called heat-treated tea catechins such as (-)-catechin gallate (CG) and (-)-gallocatechin gallate (GCG). We showed that both tea catechins and heat-treated tea catechins with galloyl moiety lower intestinal absorption of cholesterol by inhibiting micellar soly. 989-51-5 and 4233-96-9 which are cas registry numbers are also used here. of cholesterol. Since they inhibited pancreatic lipase in vitro and slowed down lymphatic absorption of triacylglycerol, we think that delayed intestinal absorption of triacylglycerol in the feeding of the catechin prepns. causes suppression of postprandial hypertriacylglycerolemia. It has been reported that tea catechins and heat-treated tea catechins with galloyl moiety suppress deposition of visceral fat in exptl. animals and humans. Some studies suggested that stimulation of hepatic b-oxidn. might be a cause of reduced deposition of visceral fat. However, our study did not show any acceleration of b-oxidn. in rat liver. Although there are some controversial observations, results obtained suggest a possibility that tea catechins and heat-treated tea catechins with galloyl moiety improve lipid metab. and contribute to prevention of life-style related diseases. .
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