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Erigeside C, a naturally occurring chemical compound found in the plant Heritiera littoralis, belongs to the class of ellagitannins. It is recognized for its antioxidant and anti-inflammatory properties and has been studied for its potential therapeutic effects. These include its ability to inhibit the growth of cancer cells and its role in preventing or treating various diseases. Additionally, it may offer benefits for cardiovascular health and serve as a natural remedy for skin disorders. Erigeside C is a promising bioactive compound with potential applications in medicine and health.
Usage:
Used in Pharmaceutical Industry:
Erigeside C is used as a therapeutic agent for its potential to inhibit the growth of cancer cells, making it a candidate for the development of treatments against various types of cancer.
Used in Cardiovascular Health Applications:
Erigeside C is used as a preventative and treatment agent for cardiovascular diseases due to its potential benefits for heart health.
Used in Skin Care Industry:
Erigeside C is used as a natural remedy for skin disorders, leveraging its antioxidant and anti-inflammatory properties to improve skin health and treat various skin conditions.
Used in Nutraceutical Industry:
Erigeside C is used as a bioactive compound in health supplements and functional foods for its overall health-promoting properties, including antioxidant and anti-inflammatory benefits.

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  • 112667-09-1 Structure
  • Basic information

    1. Product Name: Erigeside C
    2. Synonyms: Erigeside C
    3. CAS NO:112667-09-1
    4. Molecular Formula: C15H20O10
    5. Molecular Weight: 360.3133
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 112667-09-1.mol
  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: 618.5±55.0 °C(Predicted)
    3. Flash Point: N/A
    4. Appearance: /
    5. Density: 1.57±0.1 g/cm3(Predicted)
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. PKA: 8.04±0.25(Predicted)
    10. CAS DataBase Reference: Erigeside C(CAS DataBase Reference)
    11. NIST Chemistry Reference: Erigeside C(112667-09-1)
    12. EPA Substance Registry System: Erigeside C(112667-09-1)
  • Safety Data

    1. Hazard Codes: N/A
    2. Statements: N/A
    3. Safety Statements: N/A
    4. WGK Germany:
    5. RTECS:
    6. HazardClass: N/A
    7. PackingGroup: N/A
    8. Hazardous Substances Data: 112667-09-1(Hazardous Substances Data)

112667-09-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 112667-09-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,6 and 7 respectively; the second part has 2 digits, 0 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 112667-09:
(8*1)+(7*1)+(6*2)+(5*6)+(4*6)+(3*7)+(2*0)+(1*9)=111
111 % 10 = 1
So 112667-09-1 is a valid CAS Registry Number.

112667-09-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-O-(4-Hydroxy-3,5-dimethoxybenzoyl)-β-D-glucopyranose

1.2 Other means of identification

Product number -
Other names syringic acid ethyl ester

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:112667-09-1 SDS

112667-09-1Downstream Products

112667-09-1Relevant articles and documents

Engineering faster transglycosidases and their acceptor specificity

Tran, Linh T.,Blay, Vincent,Luang, Sukanya,Eurtivong, Chatchakorn,Choknud, Sunaree,González-Diáz, Humbert,Ketudat Cairns, James R.

supporting information, p. 2823 - 2836 (2019/06/13)

Transglycosidases are enzymes that have the potential to catalyze the synthesis of a wide range of high-value compounds starting from biomass-derived feedstocks. Improving their activity and broadening the substrate range are important goals to enable the widespread application of this family of biocatalysts. In this work, we engineered 20 mutants of the rice transglycosidase Os9BGlu31 and evaluated their catalysis in 462 reactions over 18 different substrates. This allowed us to identify mutants that expanded their substrate range and showed high activity, including W243L and W243N. We also developed double mutants that show very high activity on certain substrates and exceptional specificity towards hydrolysis, such as L241D/W243N. In order to guide a more general use of Os9BGlu31 variants as transglycosylation catalysts, we built cheminformatics models based on topological descriptors of the substrates. These models showed useful predictive potential on the external validation set and are allowing the identification of efficient catalytic routes to novel phytohormone and antibiotic glucoconjugates of interest.

GLUCOSIDES AND GLUCOSE ESTERS OF HYDROXYBENZOIC ACIDS IN PLANTS

Klick, Silke,Herrmann, Karl

, p. 2177 - 2180 (2007/10/02)

Pinaceae; Brassicaceae; Solanaceae; Lamiaceae; hydroxybenzoic acid glucosides; hydroxybenzoylglucoses; glucose derivatives.Six hydroxybenzoic acid glucosides and three hydroxybenzoylglucoses were synthesized as reference substances and their content in plant extracts was determined by means of capillary GC and HPLC.The results suggest a wide distribution for the glucosides, whereas the glucose esters occur less frequently.

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