26652-12-0 Usage
General Description
Salirepin is a natural chemical compound found in the plant Salvia homiletics, commonly known as the sage plant. It belongs to a class of compounds known as diterpenoids, which are known for their diverse biological activities. Salirepin has been studied for its potential pharmacological activities, including its anti-inflammatory and analgesic effects. It has also been investigated for its potential use in the treatment of inflammatory-related diseases. Additionally, salirepin has been found to exhibit antioxidant properties and could have potential applications in the development of new drugs or nutraceuticals. However, more research is needed to fully understand the therapeutic potential and safety of salirepin for human use.
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.
26652-12-0Relevant 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.
