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Benzoic acid, 3,4,5-trihydroxy-, 1,2-ethanediyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

53653-60-4

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53653-60-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 53653-60-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,6,5 and 3 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 53653-60:
(7*5)+(6*3)+(5*6)+(4*5)+(3*3)+(2*6)+(1*0)=124
124 % 10 = 4
So 53653-60-4 is a valid CAS Registry Number.

53653-60-4SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-(3,4,5-trihydroxybenzoyloxy)ethyl 3,4,5-trihydroxybenzoate

1.2 Other means of identification

Product number -
Other names 1,2-bis[(3,4,5-trihydroxybenzoyl)oxy]ethane

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:53653-60-4 SDS

53653-60-4Downstream Products

53653-60-4Relevant academic research and scientific papers

Promotion of mitochondrial biogenesis by synthetic 1,2- or 1,3-digallates through activation of an energy sensing network

Lee, Taegum,Kim, Mi Kyoung,Chong, Youhoon

, p. 407 - 411 (2022/01/08)

Based on the observations suggesting that a digallate functionality might serve as a novel scaffold for inducers of mitochondrial biogenesis, we prepared a series of digallates and evaluated their activity in an in vitro model widely used in PD research (

Double-gallic acid ester derivative in the preparation of the use in the medicament for treating hyperuricemia

-

, (2017/08/25)

The invention discloses application of a digallate derivative which has a formula (I) and a pharmaceutically acceptable salt thereof to preparation of a medicine for treating hyperuricemia. The digallate derivative has a strong effect of inhibiting xanthi

Plasminogen activator inhibitor-1 inhibitors and methods of use thereof to modulate lipid metabolism

-

, (2015/09/22)

The invention relates to plasminogen activator-1 (PAI-1) inhibitor compounds and uses thereof in the treatment of any disease or condition associated with elevated PAI-1. The invention includes, but is not limited to, the use of such compounds to modulate lipid metabolism and treat conditions associated with elevated PAI-1, cholesterol, or lipid levels.

New synthetic inhibitors of fatty acid synthase with anticancer activity

Turrado, Carlos,Puig, Teresa,García-Cárceles, Javier,Artola, Marta,Benhamú, Bellinda,Ortega-Gutiérrez, Silvia,Relat, Joana,Oliveras, Gloria,Blancafort, Adriana,Haro, Diego,Marrero, Pedro F.,Colomer, Ramón,López-Rodríguez, María L.

experimental part, p. 5013 - 5023 (2012/07/30)

Fatty acid synthase (FASN) is a lipogenic enzyme that is highly expressed in different human cancers. Here we report the development of a new series of polyphenolic compounds 5-30 that have been evaluated for their cytotoxic capacity in SK-Br3 cells, a hu

Plasminogen Activator Inhibitor-1 Inhibitors And Methods Of Use Thereof To Modulate Lipid Metabolism

-

, (2009/01/23)

The invention relates to plasminogen activator-1 (PAI-1) inhibitor compounds and uses thereof in the treatment of any disease or condition associated with elevated PAI-1. The invention includes, but is not limited to, the use of such compounds to modulate lipid metabolism and treat conditions associated with elevated PAI-1, cholesterol, or lipid levels.

Structure-activity relationship of bis-galloyl derivatives related to (-)-epigallocatechin gallate

Dodo, Kosuke,Minato, Taro,Hashimoto, Yuichi

experimental part, p. 190 - 194 (2009/11/30)

Green tea and (-)-epigallocatechin gallate (EGCG: one of main components of green tea) are well known to have preventive activities against human cancers. Previously, using a galloyl group as a core structure derived from EGCG, we developed alkyl gallate and gallamide derivatives, which showed strong antiproliferative activity towards human leukemia HL-60 cells by inducing apoptosis. Here, as a further structural development study, we planned to introduce an additional galloyl group into alkyl gallates and gallamides. According to this strategy, various bisgallate and bisgallamide derivatives were synthesized and tested for antiproliferative activity towards HL-60 cells. In gallamide derivatives having a short alkyl chain, the additional galloyl group enhanced the antiproliferative activity. In contrast, in the gallate derivatives, the additional galloyl group had no effect on the antiproliferative activity.

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