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Prodelphinidin B4 is a polymeric tannin that is composed of Gallocatechin and can be synthesized from (-)-Epigallocatechin Gallate, a tumor-inhibiting constituent found in green tea.

68964-95-4

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68964-95-4 Usage

Uses

Used in Pharmaceutical Industry:
Prodelphinidin B4 is used as a pharmaceutical agent for its tumor-inhibiting properties. It is derived from green tea, which is known for its health benefits and cancer-fighting potential.
Used in Anticancer Applications:
Prodelphinidin B4 is used as an anticancer agent, leveraging its ability to inhibit tumor growth and potentially contribute to cancer treatment and prevention strategies.
Used in Nutraceutical Industry:
Prodelphinidin B4 can be used as a nutraceutical ingredient, given its presence in green tea and its potential health benefits, including its role in cancer prevention and treatment.
Used in Cosmetic Industry:
Prodelphinidin B4 may be used in cosmetic products for its potential skin health benefits, such as providing antioxidant protection and potentially reducing the risk of skin cancer.
Used in Food and Beverage Industry:
Prodelphinidin B4 can be incorporated into food and beverage products as a functional ingredient, capitalizing on the health-promoting properties of green tea and its constituents.

Check Digit Verification of cas no

The CAS Registry Mumber 68964-95-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,8,9,6 and 4 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 68964-95:
(7*6)+(6*8)+(5*9)+(4*6)+(3*4)+(2*9)+(1*5)=194
194 % 10 = 4
So 68964-95-4 is a valid CAS Registry Number.

68964-95-4SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name (2R,3R)-2-(3,4,5-trihydroxyphenyl)-8-[(2R,3S,4S)-3,5,7-trihydroxy-2-(3,4,5-trihydroxyphenyl)-3,4-dihydro-2H-chromen-4-yl]-3,4-dihydro-2H-chromene-3,5,7-triol

1.2 Other means of identification

Product number -
Other names Gallocatechin-(4alpha->8)-epigallocatechin

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:68964-95-4 SDS

68964-95-4Downstream Products

68964-95-4Relevant academic research and scientific papers

Syntheses of prodelphinidin B1, B2, and B4 and their antitumor activities against human PC-3 prostate cancer cell lines

Fujii, Wataru,Toda, Kazuya,Matsumoto, Kiriko,Kawaguchi, Koichiro,Kawahara, Sei-Ichi,Hattori, Yasunao,Fujii, Hiroshi,Makabe, Hidefumi

supporting information, p. 7188 - 7192 (2013/12/04)

Total synthesis of prodelphinidin B1, B2, and B4 has been accomplished. The key step is Lewis acid-mediated equimolar condensations between an epigallocatechin and/or a gallocatechin nucleophile and an epigallocatechin and/or a gallocatechin electrophile. The antitumor effects of synthetic prodelphinidin B1-B4 against human PC-3 prostate cancer cell lines have been investigated. These compounds showed significant antitumor effects. Their activity seemed to be little bit stronger than EGCG and prodelphinidin B3, known antitumor agent.

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