Madecassoside

Madecassoside
Names
Other names
Redermic, Asiaticoside A
Identifiers
3D model (JSmol)
ChEBI
ChEMBL
ChemSpider
DrugBank
ECHA InfoCard 100.047.327 Edit this at Wikidata
EC Number
  • 252-076-1
UNII
  • InChI=1S/C48H78O20/c1-19-10-11-48(13-12-46(6)22(28(48)20(19)2)8-9-27-44(4)14-24(52)39(61)45(5,18-50)38(44)23(51)15-47(27,46)7)43(62)68-42-35(59)32(56)30(54)26(66-42)17-63-40-36(60)33(57)37(25(16-49)65-40)67-41-34(58)31(55)29(53)21(3)64-41/h8,19-21,23-42,49-61H,9-18H2,1-7H3
    Key: BNMGUJRJUUDLHW-HCZMHFOYSA-N
  • CC1CCC2(CCC3(C)C(=CCC4C5(C)CC(O)C(O)C(C)(CO)C5C(O)CC34C)C2C1C)C(=O)OC1OC(COC2OC(CO)C(OC3OC(C)C(O)C(O)C3O)C(O)C2O)C(O)C(O)C1O
Properties
C48H78O20
Molar mass 975.132 g·mol−1
Appearance white crystals
Density 1.47 g/cm3
Melting point 220–223 °C (428–433 °F; 493–496 K)
Boiling point 1,043.55 °C (1,910.39 °F; 1,316.70 K)
soluble
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

Madecassoside is a pentacyclic triterpenoid extracted from the plant Centella asiatica.[1]

Uses

Scientific studies have confirmed the anti-inflammatory activity of this substance, already known in traditional medicine through the use of the plant from which it is extracted.[2][3]

See also

References

  1. ^ James, Jacinda T.; Dubery, Ian A. (9 October 2009). "Pentacyclic Triterpenoids from the Medicinal Herb, Centella asiatica (L.) Urban". Molecules. 14 (10): 3922–3941. doi:10.3390/molecules14103922. PMC 6255425. PMID 19924039.
  2. ^ Pullaiah, T. (15 December 2021). An Introduction to Nephroprotective Plants. Bentham Science Publishers. p. 346. ISBN 978-981-5036-61-9. Retrieved 21 July 2025.
  3. ^ Barkat, Md Abul (29 December 2021). Nanotechnology Driven Herbal Medicine for Burns: From Concept to Application. Bentham Science Publishers. p. 30. ISBN 978-981-5039-60-3. Retrieved 21 July 2025.

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