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Ecliptasaponin D, a triterpenoid saponin compound, is derived from the plant Eclipta prostrata, commonly known as false daisy. It exhibits a range of biological activities, such as anti-inflammatory, hepatoprotective, and anti-cancer properties. ecliptasaponin D's diverse therapeutic potential makes it a subject of interest for various medical applications.

206756-04-9

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206756-04-9 Usage

Uses

Used in Pharmaceutical Industry:
Ecliptasaponin D is used as a hepatoprotective agent for its ability to treat liver damage. It also serves as an anti-inflammatory agent, making it a promising candidate for treating a variety of conditions characterized by inflammation.
Used in Cancer Treatment:
Ecliptasaponin D is used as an anti-cancer agent due to its capacity to inhibit cancer cell growth. Its potential role in cancer treatment is currently under investigation, with further research needed to understand its mechanisms of action and therapeutic potential fully.
Used in Antimicrobial Applications:
Ecliptasaponin D is used as an antimicrobial agent for its potential in treating microbial infections. Its effectiveness against various pathogens could contribute to the development of new treatments for infectious diseases.

Check Digit Verification of cas no

The CAS Registry Mumber 206756-04-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,0,6,7,5 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 206756-04:
(8*2)+(7*0)+(6*6)+(5*7)+(4*5)+(3*6)+(2*0)+(1*4)=129
129 % 10 = 9
So 206756-04-9 is a valid CAS Registry Number.

206756-04-9Downstream Products

206756-04-9Relevant academic research and scientific papers

Oleanane glycosides from Eclipta alba

Yahara,Ding,Nohara

, p. 1336 - 1338 (2007/10/02)

From the whole parts of Eclipta alba HASSK., six new oleanane triterpene glycosides, named eclalbasaponins I-VI (1-6), were isolated. The structures of 1-6 were characterized as echinocystic acid glycosides, and of those, 5 and 6 were revealed to be sulfated saponins on the basis of chemical and spectral data.

THE STRUCTURE OF PROSAPOGENIN OBTAINED FROM THE SAPONIN OF GLEDITSIA JAPONICA

Konoshima, Takao,Fukushima, Hiroyuki,Inui,Hideo,Sato, Keiko,Sawada, Tokunosuke

, p. 139 - 142 (2007/10/02)

Key Word Index - Gleditsia japonica; Leguminosae; saponins; bisdesmoside; echinocystic acid derivatives; Gleditsia saponin C. Prosapogenin was obtained by alkaline hydrolysis of Gleditsia saponin GS-C (echinocystic acid 3,28-O-bisdesmoside), a new triterpenoid saponin isolated from Gleditsia japonica.Prosapogenin was shown on the basis of chemical and physicochemical data to be echinocystic acid 3-O-β-D-xylopyranosyl-(1-2)-α-L-arabinopyranosyl-(1-6)-β-D-glucopyranoside.

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