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Madecassoside - 98%, high purity , CAS No.34540-22-2

COA

Grade & Purity:

Moligand™

≥98%

Cas Number: 34540-22-2
Molecular Weight: 975.12
PubChem CID: 45356919
PubChem SID: 488201164

In stock

Item Number

M107331

Grouped product items
SKU	Size	Availability	Price
M107331-25mg	25mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$75.90
M107331-100mg	100mg	1	$312.90
M107331-500mg	500mg	Available within 8-12 weeks(?) Production requires sourcing of materials. We appreciate your patience and understanding.	$499.90

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Basic Description

Synonyms	CCG-270599 \| MFCD03411893 \| AC-6056 \| AS-15335 \| Madecassoside \| Q-100419 \| AKOS008901372 \| ASIATICOSIDE A \| s3843 \| BNMGUJRJUUDLHW-CIZDPPTDSA-N
Specifications & Purity	Moligand™, ≥98%
Biochemical and Physiological Mechanisms	Centella asiatica glycoside is a triterpenoid compound found in Centella asiatica (Gotu Kola) and is a medicinal herb used in traditional Chinese medicine (TCM), Ayurvedic medicine, and traditional African medicine. According to reports, centella asiatica
Storage Temp	Store at 2-8°C,Protected from light,Argon charged
Shipped In	Wet ice This product requires cold chain shipping. Ground and other economy services are not available.
Grade	Moligand™
Product Description	Madecassoside is one of the major pentacyclic triterpenoid saponin compounds extracted from Centella asiatica. Application: Madecassoside has been used to study its cytotoxic effects on mouse macrophage cell lines (J774A.1).It has also been used as a potential inhibitor of serine racemase (SR) for in vitro and ex vivo studies.

Taxonomic Classification

Taxonomy Tree

Kingdom Organic compounds
- Superclass Lipids and lipid-like molecules
  - Class Prenol lipids
    - Subclass Terpene glycosides
      - Level5 Triterpene glycosides
        Level6 Triterpene saponins

Kingdom	Organic compounds
Superclass	Lipids and lipid-like molecules
Class	Prenol lipids
Subclass	Terpene glycosides
Intermediate Tree Nodes	Triterpene glycosides
Direct Parent	Triterpene saponins
Alternative Parents	Triterpenoids Oligosaccharides 7-alpha-hydroxysteroids 12-beta-hydroxysteroids O-glycosyl compounds Oxanes Secondary alcohols Cyclic alcohols and derivatives Carboxylic acid esters Polyols Oxacyclic compounds Monocarboxylic acids and derivatives Acetals Primary alcohols Organic oxides Hydrocarbon derivatives Carbonyl compounds
Molecular Framework	Aliphatic heteropolycyclic compounds
Substituents	Triterpene saponin - Triterpenoid - Oligosaccharide - 12-beta-hydroxysteroid - 7-hydroxysteroid - 7-alpha-hydroxysteroid - Hydroxysteroid - 12-hydroxysteroid - Steroid - O-glycosyl compound - Glycosyl compound - Oxane - Cyclic alcohol - Secondary alcohol - Carboxylic acid ester - Oxacycle - Organoheterocyclic compound - Polyol - Monocarboxylic acid or derivatives - Carboxylic acid derivative - Acetal - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Primary alcohol - Organooxygen compound - Carbonyl group - Alcohol - Aliphatic heteropolycyclic compound
Description	This compound belongs to the class of organic compounds known as triterpene saponins. These are glycosylated derivatives of triterpene sapogenins. The sapogenin moiety backbone is usually based on the oleanane, ursane, taraxastane, bauerane, lanostane, lupeol, lupane, dammarane, cycloartane, friedelane, hopane, 9b,19-cyclo-lanostane, cycloartane, or cycloartanol skeleton.
External Descriptors	Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61. DOI: 10.1186/s13321-016-0174-y

Names and Identifiers

Pubchem Sid	488201164
Pubchem Sid Url	https://pubchem.ncbi.nlm.nih.gov/substance/488201164
IUPAC Name	[(2S,3R,4S,5S,6R)-6-[[(2R,3R,4R,5S,6R)-3,4-dihydroxy-6-(hydroxymethyl)-5-[(2S,3R,4R,5R,6S)-3,4,5-trihydroxy-6-methyloxan-2-yl]oxyoxan-2-yl]oxymethyl]-3,4,5-trihydroxyoxan-2-yl] (1S,2R,4aS,6aR,6aR,6bR,8R,8aR,9R,10R,11R,12aR,14bS)-8,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydro-1H-picene-4a-carboxylate
INCHI	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/t19-,20+,21+,23-,24-,25-,26-,27-,28+,29+,30-,31-,32+,33-,34-,35-,36-,37-,38-,39+,40-,41+,42+,44-,45+,46+,47-,48+/m1/s1
InChIKey	BNMGUJRJUUDLHW-CIZDPPTDSA-N
Smiles	CC1CCC2(CCC3(C(=CCC4C3(CC(C5C4(CC(C(C5(C)CO)O)O)C)O)C)C2C1C)C)C(=O)OC6C(C(C(C(O6)COC7C(C(C(C(O7)CO)OC8C(C(C(C(O8)C)O)O)O)O)O)O)O)O
Isomeric SMILES	C[C@@H]1CC[C@@]2(CC[C@]3(C(=CC[C@H]4[C@]3(C[C@H]([C@@H]5[C@@]4(C[C@H]([C@@H]([C@@]5(C)CO)O)O)C)O)C)[C@@H]2[C@H]1C)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO[C@H]7[C@@H]([C@H]([C@@H]([C@H](O7)CO)O[C@H]8[C@@H]([C@@H]([C@H]([C@@H](O8)C)O)O)O)O)O)O)O)O
Molecular Weight	975.12
Reaxy-Rn	24283150
Reaxys-RN_link_address	https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=24283150&ln=

Certificates（CoA,COO,BSE/TSE and Analysis Chart)

C of A & Other Certificates(BSE/TSE, COO):

Analytical Chart:

Find and download the COA for your product by matching the lot number on the packaging.

13 results found

Lot Number	Certificate Type	Date	Item
B2526342	Certificate of Analysis	Mar 01, 2025	M107331
B2526343	Certificate of Analysis	Mar 01, 2025	M107331
B2526290	Certificate of Analysis	Mar 01, 2025	M107331
B2526291	Certificate of Analysis	Mar 01, 2025	M107331
B2526292	Certificate of Analysis	Mar 01, 2025	M107331
B2526293	Certificate of Analysis	Mar 01, 2025	M107331
B2526294	Certificate of Analysis	Mar 01, 2025	M107331
B2526295	Certificate of Analysis	Mar 01, 2025	M107331
J2326572	Certificate of Analysis	Oct 31, 2023	M107331
D1606081	Certificate of Analysis	Aug 03, 2023	M107331
C2331524	Certificate of Analysis	Apr 12, 2023	M107331
C2331560	Certificate of Analysis	Apr 12, 2023	M107331
D2219083	Certificate of Analysis	Apr 29, 2022	M107331

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Chemical and Physical Properties

Sensitivity	Light sensitive
Molecular Weight	975.100 g/mol
XLogP3	-1.200
Hydrogen Bond Donor Count	13
Hydrogen Bond Acceptor Count	20
Rotatable Bond Count	10
Exact Mass	974.509 Da
Monoisotopic Mass	974.509 Da
Topological Polar Surface Area	335.000 Å²
Heavy Atom Count	68
Formal Charge	0
Complexity	1860.000
Isotope Atom Count	0
Defined Atom Stereocenter Count	28
Undefined Atom Stereocenter Count	0
Defined Bond Stereocenter Count	0
Undefined Bond Stereocenter Count	0
The total count of all stereochemical bonds	0
Covalently-Bonded Unit Count	1

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