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19764-35-3

Triandrin, a triterpenoid saponin, is a naturally occurring chemical compound found in the seeds of the Plantago lanceolata plant. It possesses potential antioxidant and anti-inflammatory properties and has been traditionally used in herbal medicine for treating various conditions.
Used in Herbal Medicine:
Triandrin is used as a remedy in herbal medicine for its potential therapeutic effects on respiratory and gastrointestinal disorders.
Used in Respiratory Applications:
Triandrin is used as a therapeutic agent in respiratory applications for its potential to alleviate conditions such as asthma and allergy due to its anti-inflammatory properties.
Used in Gastrointestinal Applications:
Triandrin is used as a therapeutic agent in gastrointestinal applications for its potential to treat inflammatory bowel disease and other related conditions.
Used in Cancer Research and Drug Development:
Triandrin is used as a candidate in cancer research and drug development for its potential to inhibit the growth and proliferation of certain cancer cells, making it a promising compound for future medical advancements.

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  • 19764-35-3 Structure

  • Basic information

    1. Product Name: Triandrin
    2. Synonyms:
    3. CAS NO:19764-35-3
    4. Molecular Formula:
    5. Molecular Weight: 312.32
    6. EINECS: N/A
    7. Product Categories: N/A
    8. Mol File: 19764-35-3.mol

  • Chemical Properties

    1. Melting Point: N/A
    2. Boiling Point: N/A
    3. Flash Point: N/A
    4. Appearance: N/A
    5. Density: N/A
    6. Refractive Index: N/A
    7. Storage Temp.: N/A
    8. Solubility: N/A
    9. CAS DataBase Reference: Triandrin(CAS DataBase Reference)
    10. NIST Chemistry Reference: Triandrin(19764-35-3)
    11. EPA Substance Registry System: Triandrin(19764-35-3)

  • 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: 19764-35-3(Hazardous Substances Data)

19764-35-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 19764-35-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,9,7,6 and 4 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 19764-35:
(7*1)+(6*9)+(5*7)+(4*6)+(3*4)+(2*3)+(1*5)=143
143 % 10 = 3
So 19764-35-3 is a valid CAS Registry Number.

19764-35-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name triandrin

1.2 Other means of identification

Product number -
Other names p-coumaryl alcohol β-D-glucopyranoside

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:19764-35-3 SDS

19764-35-3Downstream Products

19764-35-3Relevant articles and documents

Laccase-catalyzed dimerization of glycosylated lignols

Bassanini, Ivan,Gavezzotti, Paolo,Monti, Daniela,Krejzová, Jana,K?en, Vladimír,Riva, Sergio

, p. 295 - 301 (2016/12/16)

Phenylpropanoid glucosides (PPGs) are naturally occurring and bioactive phenolic derivatives, largely distributed in plants. In this work different PPGs have been chemically or enzymatically synthesized from the lignols coniferyl and p-coumaryl alcohols as substrates for a laccase-catalyzed oxidative coupling. The biooxidation of these PPGs has been investigated here and novel dihydrobenzofuran-based structurally modified analogues have been isolated and characterized. Specifically, the presence of a carbohydrate moiety increased the water solubility of these compounds and reduced the number of dimeric products, as pinoresinol-like structures could not be formed. Looking for a possible sugar-promoted stereochemical enrichment of the obtained diastereomeric mixtures of dimers, different carbohydrate moieties (D-glucose, L-glucose and the disaccharide rutinose) were considered and the respective d.e. values of the dimeric products were measured by 1H NMR and HPLC. However, it was found that the sugar substituent had a minor effect on the stereochemical outcome of the radical coupling reactions, the best measured result being a d.e. value of 21%.

Synthesis of some phenylpropanoid glycosides (PPGs) and their acetylcholinesterase/xanthine oxidase inhibitory activities

Li, Xiao-Dong,Kang, Shuai-Tao,Li, Guo-Yu,Li, Xian,Wang, Jin-Hui

experimental part, p. 3580 - 3596 (2011/07/07)

In this research, three categories of phenylpropanoid glycosides (PPGs) were designed and synthesized with PPGs isolated from Rhodiola rosea L. as lead compounds. Their inhibitory abilities toward acetylcholinesterase (AChE) and xanthine oxidase (XOD) were also tested. Some of the synthetic PPGs exhibited excellent enzyme inhibitory abilities.

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