25406-56-8 Usage
Uses
Used in Pharmaceutical Applications:
[(3β)-17-Carboxy-28-norolean-12-en-3-yl]3-O-β-D-glucopyranosyl-β-D-glucopyranosiduronic acid is used as a potential therapeutic agent for various medical conditions due to its anti-inflammatory and antioxidant properties. These properties make it a promising candidate for the development of new drugs to treat inflammation-related diseases and oxidative stress-related disorders.
Used in Nutraceutical Applications:
In the nutraceutical industry, [(3β)-17-Carboxy-28-norolean-12-en-3-yl]3-O-β-D-glucopyranosyl-β-D-glucopyranosiduronic acid is used as an ingredient in dietary supplements and functional foods. Its potential health benefits, such as anti-inflammatory and antioxidant effects, contribute to the overall wellness and prevention of various diseases.
Further research is necessary to fully understand the pharmacological properties and potential uses of [(3β)-17-Carboxy-28-norolean-12-en-3-yl]3-O-β-D-glucopyranosyl-β-D-glucopyranosiduronic acid in different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 25406-56-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,4,0 and 6 respectively; the second part has 2 digits, 5 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 25406-56:
(7*2)+(6*5)+(5*4)+(4*0)+(3*6)+(2*5)+(1*6)=98
98 % 10 = 8
So 25406-56-8 is a valid CAS Registry Number.
InChI:InChI=1/C42H66O14/c1-37(2)14-16-42(36(51)52)17-15-40(6)20(21(42)18-37)8-9-24-39(5)12-11-25(38(3,4)23(39)10-13-41(24,40)7)54-35-30(48)31(29(47)32(56-35)33(49)50)55-34-28(46)27(45)26(44)22(19-43)53-34/h8,21-32,34-35,43-48H,9-19H2,1-7H3,(H,49,50)(H,51,52)/t21-,22+,23-,24+,25-,26+,27-,28+,29-,30+,31-,32-,34-,35+,39-,40+,41+,42-/m0/s1
25406-56-8Relevant academic research and scientific papers
SAPONINS FROM ROOTS OF KALOPANAX SEPTEMLOBUS (THUNB.) KOIDZ., CIQIU: STRUCTURES OF KALOPANAX-SAPONINS C, D, E AND F
Shao, Chun-Jie,Kasai, Ryoji,Xu, Jing-Da,Tanaka, Osamu
, p. 311 - 314 (2007/10/02)
Four new triterpenoid saponins named kalopanax-saponins C (4), D (5), E (6) and F (7) were isolated from the roots of Kalopanax septemlobus (THUNB.) KOIDZ. together with three known saponins, kalopanax-saponins A (1) and B (2), and chikusetsusaponin IV (3).On the basis of chemical and spectral data, the structures of these new saponins were elucidated to be as follows: (4), 3-O-α-rhamnopyranosyl-(1->2)-3)>-α-arabinopyranosyl hederagenin 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (5), 3-O-α-rhamnopyranosyl-(1->2)-3)>-α-arabinopyranosyl oleanolic acid 28-O-α-rhamnopyranosyl-(1->4)-β-glucopyranosyl-(1->6)-β-glucopyranosyl ester; (6), 3-O-β-glucopyranosyl-(1->3)-β-glucuronopyranosyl oleanolic acid; (7), 3-O-α-arabinopyranosyl-(1->2)-3)>-β-glucuronopyranosyl oleanolic acid 28-O-β-glucopyranosyl ester.Keywords - Kalopanax septemlobus; Araliaceae; saponin; kalopanax-saponin; oleanolic acid glycoside; hederagenin glycoside; Chinese folk medicine; ciqiu
