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1-Propanone, 3-phenyl-1-(2,3,4,6-tetrahydroxyphenyl)- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

126380-10-7

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126380-10-7 Usage

Source

Fruits of the embelia ribes plant

Traditional medicine uses

Anti-inflammatory, anti-microbial, and anti-cancer properties

Potential medicinal uses

Cancer, diabetes, and inflammatory conditions

Mechanism of action

Inhibits the activity of NF-kappaB, a protein complex involved in the regulation of immunity, inflammation, and cell survival

Safety and efficacy

Further research needed to determine safety and efficacy for medicinal use

Check Digit Verification of cas no

The CAS Registry Mumber 126380-10-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,3,8 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 126380-10:
(8*1)+(7*2)+(6*6)+(5*3)+(4*8)+(3*0)+(2*1)+(1*0)=107
107 % 10 = 7
So 126380-10-7 is a valid CAS Registry Number.

126380-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-phenyl-1-(2,3,4,6-tetrahydroxyphenyl)propan-1-one

1.2 Other means of identification

Product number -
Other names 2',3',4',6'-tetrahydroxydihydrochalcone

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:126380-10-7 SDS

126380-10-7Downstream Products

126380-10-7Relevant academic research and scientific papers

α-Glucosidase inhibition of 6-hydroxyflavones. Part 3: Synthesis and evaluation of 2,3,4-trihydroxybenzoyl-containing flavonoid analogs and 6-aminoflavones as α-glucosidase inhibitors

Gao, Hong,Kawabata, Jun

, p. 1661 - 1671 (2007/10/03)

The SAR studies suggested that the C-ring of baicalein (1) was not necessary for the activity, and validated the importance of 2,3,4- trihydroxybenzoyl structure of 1. Thus, a series of 2,3,4-trihydroxybenzoyl- containing flavonoid analogs were investigat

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