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Salirepin, a natural chemical compound derived from the Salvia homiletics plant, also known as the sage plant, is a member of the diterpenoid class. These compounds are recognized for their wide range of biological activities. Salirepin has garnered attention for its potential pharmacological properties, particularly its anti-inflammatory and analgesic effects, and is being studied for its possible role in treating inflammatory-related diseases. Moreover, its antioxidant characteristics suggest it could be instrumental in the development of new drugs or nutraceuticals. Further research is essential to fully explore the therapeutic potential and safety of salirepin for human applications.

26652-12-0

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26652-12-0 Usage

Uses

Used in Pharmaceutical Industry:
Salirepin is used as a potential therapeutic agent for its anti-inflammatory and analgesic effects, targeting the treatment of inflammatory-related diseases.
Used in Nutraceutical Development:
Given its antioxidant properties, salirepin is used as a component in the development of new nutraceuticals aimed at promoting health and wellness.
Used in Drug Discovery:
Salirepin's diverse biological activities position it as a candidate for drug discovery, potentially leading to the creation of novel medications for various health conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 26652-12-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,6,6,5 and 2 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 26652-12:
(7*2)+(6*6)+(5*6)+(4*5)+(3*2)+(2*1)+(1*2)=110
110 % 10 = 0
So 26652-12-0 is a valid CAS Registry Number.

26652-12-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-Hydroxy-2-(hydroxymethyl)phenyl β-D-glucopyranoside

1.2 Other means of identification

Product number -
Other names 1-Methyl-4-hydroxy-4-piperidyl-phenylketon

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:26652-12-0 SDS

26652-12-0Downstream Products

26652-12-0Relevant articles and documents

Phenyl glycosides from the leaves of Flacourtia indica (Burm. f.) Merr (Salicaceae)

Lavaud, Catherine,Massiot, Georges,Nguyen, Phuc-Dam,Sayagh, Charlotte

, (2021)

Thirteen phenolic glycosides, together with fourteen various known compounds, were isolated from the methanolic extract of leaves of Flacourtia indica. Twelve of these were composed of gentisyl or salicyl alcohols, glycosylated on the phenol and acylated on the primary alcohol with various more or less oxidized forms of pyrocatechuic acid. A number of positions on the glucose or on the acid were further acylated by benzoic or cinnamic acid. In addition to these, a glucoside of a phenyl propanoid was also isolated. The gross structures were elucidated by spectroscopic means including 1D and 2D NMR experiments and HR-ESI-MS analyses. Several of these structures, for example, xylosmin, were previously described but it proved extremely difficult to conclude on their exact identity with the absence of clear data on absolute configuration in the literature.

Poliothrysoside and its derivatives as novel insulin sensitizers potentially driving AMPK activation and inhibiting adipogenesis

Sashidhara, Koneni V.,Singh, Suriya P.,Varshney, Salil,Beg, Muheeb,Gaikwad, Anil N.

, p. 570 - 577 (2014)

In our efforts to develop safe and active chemical entities from nature, we first identified poliothrysoside (1), a phytoconstituent isolated from Flacourtia indica, possessing antidiabetic potential. Subsequently, fifteen derivatives (2-16) were synthesi

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