90411-13-5 Usage
Description
Neochamaejasmin A is a bioactive chemical compound belonging to the class of flavonoid glycosides, isolated from the flowers of the plant Chamaecrista nictitans (L.) Moench. It possesses various pharmacological properties, including antioxidant, anti-inflammatory, and antitumor activities, as demonstrated in in vitro and in vivo studies. Additionally, it has shown potential in the treatment of neurodegenerative diseases and prevention of cardiovascular disorders. Neochamaejasmin A is a promising natural compound with a wide range of potential therapeutic and industrial applications.
Uses
Used in Pharmaceutical Industry:
Neochamaejasmin A is used as a therapeutic agent for its antioxidant, anti-inflammatory, and antitumor properties. It has potential applications in the treatment of neurodegenerative diseases and prevention of cardiovascular disorders.
Used in Cosmetic Industry:
Neochamaejasmin A is used as an active ingredient in cosmetic products for its beneficial properties, such as its antioxidant and anti-inflammatory effects, which can contribute to skin health and protection.
Check Digit Verification of cas no
The CAS Registry Mumber 90411-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,0,4,1 and 1 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 90411-13:
(7*9)+(6*0)+(5*4)+(4*1)+(3*1)+(2*1)+(1*3)=95
95 % 10 = 5
So 90411-13-5 is a valid CAS Registry Number.
90411-13-5Relevant articles and documents
A simple biomimetic synthesis of dl-chamaejasmine, a unique 3,3′-biflavanone
Li, Wei-Dong Z.,Ma, Bao-Chun
, p. 271 - 274 (2007/10/03)
(Chemical Equation Presented) The first chemical synthesis of dl-chamaejasmine (1), a structurally unique 3,3′-biflavanone natural product, was achieved as shown above, by a two-step sequence starting from trimethyl ether derivatives of 3-iodonaringenin (cis + trans) involving (i) metallic lanthanum-mediated reductive dimerization in refluxing THF and (ii) global demethylation with BBr3 in CH2Cl2. This synthesis represents a generally applicable biomimetic (reductive) radical dimerization approach to the 3,3′-biflavonoids.
Stereostructures of two biflavanones from Stellera chamaejasme L.
Niwa,Otsuji,Tatematsu,et al.
, p. 3249 - 3251 (2007/10/02)
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