2798-25-6 Usage
Description
Bellidifolin, also known as 1,5,8-Trihydroxy-3-methoxy-9H-xanthen-9-one, is a member of the xanthone family and is a natural product predominantly found in Swertia chirata and Gentianella campestris. It is an important chemotaxonomic marker of the Swertia genus and has been recognized for its various biological activities.
Uses
Used in Pharmaceutical Applications:
Bellidifolin is used as a hepatoprotective agent for its notable protective effects against carbon tetrachloride (CCl4)-induced HepG2 cell damage. It helps in alleviating the levels of aspartate transaminase (AST), lactate dehydrogenase (LDH), superoxide dismutase (SOD), and malonic dialdehyde, thereby supporting liver health and functioning.
Used in Traditional Medicine:
Bellidifolin is also utilized in traditional medicine, particularly in the Swertia genus, for its various therapeutic properties. As a chemotaxonomic marker, it aids in the identification and classification of plant species within the Swertia genus, which are known for their medicinal values.
Check Digit Verification of cas no
The CAS Registry Mumber 2798-25-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,9 and 8 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2798-25:
(6*2)+(5*7)+(4*9)+(3*8)+(2*2)+(1*5)=116
116 % 10 = 6
So 2798-25-6 is a valid CAS Registry Number.
InChI:InChI=1/C14H10O6/c1-19-6-4-9(17)11-10(5-6)20-14-8(16)3-2-7(15)12(14)13(11)18/h2-5,15-17H,1H3
2798-25-6Relevant articles and documents
-
Ghosal et al.
, p. 1286,1287 (1974)
-
-
Asahina et al.
, p. 104,105 (1942)
-
XANTHONE AND FLAVONOL CONSTITUENTS OF SWERTIA HOOKERI
Ghosal, Shibnath,Biswas, Kanika,Jaiswal, Dinesh K.
, p. 123 - 126 (2007/10/02)
The whole plant of Swertia hookeri, collected at flowering has been shown to contain two tri- and nine tetraoxygenated free, glucosyloxy, and stearyl ester xanthones and one flavonol stearyl ester.Among these, three are previously unreported in nature and one was known previously only as a synthetic compound.The xanthones are based on 1,3,5-, 1,3,5,8- and 1,3,7,8-oxygenated systems with the middle oxygenation pattern predominating.The two ester compounds appeared only at the flowering stage.Plants collected at the pre-flowering stage gave the corresponding free compounds.The biochemical and biological significance of these findings are appraised.Key Word Index - Swertia hookeri; Gentianaceae; 1-O-stearyl-3,5-dimethoxyxanthone; 3-O-stearyl-3',4',5,7-tetra-O-methylquercetin; 1-hydroxy-3,5-dimethoxyxanthone; tetraoxygenated xanthones; 8-O-β-D-glucosyl-1,3-dihydroxy-5-methoxyxanthones; 8-O-β-D-glucosyl-1,5-dihydroxy-3-methoxyxanthone.
