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Asiaticoside - analytical standard,≥98%, high purity , CAS No.16830-15-2

In stock
Item Number
A111276
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Price Qty
A111276-10mg
10mg
3
$29.90
A111276-20mg
20mg
2
$49.90
A111276-50mg
50mg
2
$99.90
A111276-250mg
250mg
2
$299.90
A111276-1g
1g
Available within 8-12 weeks(?)
Production requires sourcing of materials. We appreciate your patience and understanding.
$699.90

Triterpene glycoside. Stimulates collagen biosynthesis and glycosaminoglycan synthesis.

Basic Description

Synonyms (-)-SENECIONINE | NSC-36002 | (2alpha,3beta,4alpha)-2,3,23-TRIHYDROXYURS-12-EN-28-OIC ACID O-6-DEOXY-alpha-L-MANNOPYRANOSYL-(1->4)-O-beta-D-GLUCOPYRANOSYL-(1->6)-O-beta-D-GLUCOPYRANOSYL ESTER | Madecassol | Prost-13-en-1-oic acid, 11,15-dihydroxy-6,9-diox
Specifications & Purity analytical standard, Moligand™, ≥98%
Biochemical and Physiological Mechanisms Triterpene glycoside. Stimulates collagen biosynthesis and glycosaminoglycan synthesis. Displays wound-healing activity. Antiaging and anti-infective agent. Active in vivo and in vitro .
Storage Temp Store at 2-8°C,Argon charged
Shipped In
Wet ice
This product requires cold chain shipping. Ground and other economy services are not available.
Grade analytical standard, Moligand™
Note Wherever possible, you should prepare and use solutions on the same day. However, if you need to make up stock solutions in advance, we recommend that you store the solution as aliquots in tightly sealed vials at -20°C. Generally, these will be useable for up to one month. Before use, and prior to opening the vial we recommend that you allow your product to equilibrate to room temperature for at least 1 hour. Need more advice on solubility, usage and handling? Please visit our frequently asked questions (FAQ) page for more details.
Product Description

Asiaticoside (Madecassol) is the active chemical component of the plant Centella asiatica. Asiaticoside is used to study potential treatments for wounds and burns.
Is used to study potential treatments for wounds and burns

Taxonomic Classification

Taxonomy Tree

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  12-beta-hydroxysteroids  O-glycosyl compounds  Oxanes  Secondary alcohols  Carboxylic acid esters  Cyclic alcohols and derivatives  Monocarboxylic acids and derivatives  Acetals  Polyols  Oxacyclic compounds  Primary alcohols  Hydrocarbon derivatives  Carbonyl compounds  Organic oxides  
Molecular Framework Aliphatic heteropolycyclic compounds
Substituents Triterpene saponin - Triterpenoid - Oligosaccharide - 12-hydroxysteroid - Hydroxysteroid - 12-beta-hydroxysteroid - Steroid - Glycosyl compound - O-glycosyl compound - Oxane - Cyclic alcohol - Secondary alcohol - Carboxylic acid ester - Polyol - Organoheterocyclic compound - Oxacycle - Monocarboxylic acid or derivatives - Acetal - Carboxylic acid derivative - Organooxygen compound - Hydrocarbon derivative - Organic oxide - Organic oxygen compound - Carbonyl group - Alcohol - Primary 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 triterpenoid saponin

Associated Targets(Human)

AMY2A Tclin Pancreatic alpha-amylase (74 Activities)
Activity Type Relation Activity value Units Action Type Journal PubMed Id doi Assay Aladdin ID

Mechanisms of Action

Mechanism of Action Action Type target ID Target Name Target Type Target Organism Binding Site Name References

Names and Identifiers

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,6aS,6bR,8aR,9R,10R,11R,12aR,14bS)-10,11-dihydroxy-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/C48H78O19/c1-20-10-13-48(15-14-46(6)23(29(48)21(20)2)8-9-28-44(4)16-24(51)39(60)45(5,19-50)27(44)11-12-47(28,46)7)43(61)67-42-36(58)33(55)31(53)26(65-42)18-62-40-37(59)34(56)38(25(17-49)64-40)66-41-35(57)32(54)30(52)22(3)63-41/h8,20-22,24-42,49-60H,9-19H2,1-7H3/t20-,21+,22+,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 WYQVAPGDARQUBT-FGWHUCSPSA-N
Smiles CC1CCC2(CCC3(C(=CCC4C3(CCC5C4(CC(C(C5(C)CO)O)O)C)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(CC[C@@H]5[C@@]4(C[C@H]([C@@H]([C@@]5(C)CO)O)O)C)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
WGK Germany 3
Molecular Weight 959.12
Reaxy-Rn 25443182
Reaxys-RN_link_address https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=25443182&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.

22 results found

Lot Number Certificate Type Date Item
K1414085 Certificate of Analysis Jun 16, 2025 A111276
D2522378 Certificate of Analysis Apr 10, 2025 A111276
D2522379 Certificate of Analysis Apr 10, 2025 A111276
D2522380 Certificate of Analysis Apr 10, 2025 A111276
D2522381 Certificate of Analysis Apr 10, 2025 A111276
H2429450 Certificate of Analysis Aug 03, 2024 A111276
H2429451 Certificate of Analysis Aug 03, 2024 A111276
H2429456 Certificate of Analysis Aug 03, 2024 A111276
J2219048 Certificate of Analysis Jul 19, 2024 A111276
D2429116 Certificate of Analysis Apr 10, 2024 A111276
D2429133 Certificate of Analysis Apr 10, 2024 A111276
D2429134 Certificate of Analysis Apr 10, 2024 A111276
D2429099 Certificate of Analysis Apr 10, 2024 A111276
D2429136 Certificate of Analysis Apr 10, 2024 A111276
D2429129 Certificate of Analysis Apr 10, 2024 A111276
D2429132 Certificate of Analysis Apr 10, 2024 A111276
D2429135 Certificate of Analysis Apr 10, 2024 A111276
H2312088 Certificate of Analysis Jul 31, 2023 A111276
H2312096 Certificate of Analysis Jul 31, 2023 A111276
I2110054 Certificate of Analysis Jun 09, 2023 A111276
J2219049 Certificate of Analysis Aug 08, 2022 A111276
K1827220 Certificate of Analysis Jul 11, 2022 A111276

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Chemical and Physical Properties

Sensitivity Moisture sensitive;Heat sensitive
Melt Point(°C) 230-233°C
Molecular Weight 959.100 g/mol
XLogP3 0.100
Hydrogen Bond Donor Count 12
Hydrogen Bond Acceptor Count 19
Rotatable Bond Count 10
Exact Mass 958.514 Da
Monoisotopic Mass 958.514 Da
Topological Polar Surface Area 315.000 Ų
Heavy Atom Count 67
Formal Charge 0
Complexity 1820.000
Isotope Atom Count 0
Defined Atom Stereocenter Count 27
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

Citations of This Product

1. Wang Pei, Wang Yun, Yi Yang, Gong Yan, Ji Haoran, Gan Yuci, Xie Fei, Fan Jinchen, Wang Xiansong.  (2022)  MXenes-integrated microneedle combined with asiaticoside to penetrate the cuticle for treatment of diabetic foot ulcer.  JOURNAL OF NANOBIOTECHNOLOGY,  20  (1): (1-14). 
2. Keyan Wu, Guanghuai Yao, Xiaolei Shi, Huan Zhang, Qingtian Zhu, Xinnong Liu, Guotao Lu, Lianghao Hu, Weijuan Gong, Qi Yang, Yanbing Ding.  (2021)  Asiaticoside ameliorates acinar cell necrosis in acute pancreatitis via toll-like receptor 4 pathway.  MOLECULAR IMMUNOLOGY,  130  (122). 

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