Home Immunology & Inflammation ROS inhibitor Asiaticoside For research use only.

Asiaticoside

Synonyms: Ba 2742, BRN0078195, CCRIS8995, NSC166062, Emdecassol,Madecassol

Asiaticoside (Ba 2742, BRN0078195, CCRIS8995, NSC166062, Emdecassol,Madecassol), the major active principle of Centella asiatica, prevents ultraviolet A-dependent photoaging by suppressing ultraviolet A-induced reactive oxygen species production. It also decreases DNA binding by MITF.

Asiaticoside Chemical Structure

Asiaticoside Chemical Structure

CAS: 16830-15-2

Selleck's Asiaticoside has been cited by 1 publication

Purity & Quality Control

Batch: Purity: 99.99%
99.99

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Biological Activity

Description Asiaticoside (Ba 2742, BRN0078195, CCRIS8995, NSC166062, Emdecassol,Madecassol), the major active principle of Centella asiatica, prevents ultraviolet A-dependent photoaging by suppressing ultraviolet A-induced reactive oxygen species production. It also decreases DNA binding by MITF.
In vitro
In vitro In the central nervous system, Asiaticoside has been shown to attenuate in vitro neuronal damage caused by exposure to β-amyloid. In cultured mouse cortical neurons exposed to glutamate-induced excitotoxicity invoked by N-methyl-D-aspartate, pretreatment with Asiaticoside decreases neuronal cell loss in a con­centration-dependent manner and restored changes in expression of apoptotic-related proteins Bcl-2 and Bax. Asiaticoside pretreatment also attenuates the upregulation of NR2B expression, a subunit of N-methyl-D-aspartate receptors, but does not affect expression of NR2A subunits. It also significantly inhibits Ca 2+ influx induced by N-methyl-D-aspartate[1]. Presence of asiaticoside along with the DNA during irradiation prevents the relaxation of the supercoiled form to the open circular form[2].
Cell Research Cell lines Cortical neurons
Concentrations 0.1, 1, 10, 100 μM
Incubation Time 24 h
Method Cortical neurons cultured for 7 days in vitro are divided into three groups: control, NMDA treatment (200 μmol/L NMDA and 10 μmol/L glycine, NMDA receptor co-activa­tor) and Asiaticoside pretreatment (Asiaticoside (less than 1%) pretreatment for 24 hours, then NMDA (200 μmol/L) and glycine (10 μmol/L) treatment for another 30 minutes). The NR2B receptor specific antagonist, RO-25-6981, is used as a positive control. The cells are then returned to the original culture medium for further 24 hours.
In Vivo
In vivo In vivo studies demonstrate that Asiaticoside could attenu­ate neurobehavioral, neurochemical and histological changes in transient focal middle cerebral artery occlusion animals. In addition, Asiaticoside shows anxiolytic effects in acute and chronic stress animals. It has been shown to have wound healing effects, anti-infammatory effects, and promotes liver protective activity[1]. Administration of asiaticoside prior to whole-body radiation exposure of the mice prevents this increase in radiation-induced increase in comet parameters, which could be the result of protection to DNA under in vivo conditions of radiation exposure[2].
NCT Number Recruitment Conditions Sponsor/Collaborators Start Date Phases
NCT03814850 Withdrawn Unruptured Cerebral Aneurysm Sebastian Koch|University of Miami December 1 2024 Not Applicable
NCT06108232 Not yet recruiting Follicular Lymphoma|Tumor M.D. Anderson Cancer Center|Bristol-Myers Squibb March 31 2024 Phase 2
NCT06154005 Not yet recruiting Degenerative Disc Disease|Degenerative Spondylolisthesis|Spinal Stenosis|Spine Disease|Lumbar Radiculopathy|Lumbar Spinal Stenosis|Lumbar Disc Herniation|Lumbar Disc Disease|Lumbar Spine Degeneration|Lumbar Spondylolisthesis Theradaptive Inc March 2024 Phase 1|Phase 2
NCT05906758 Not yet recruiting Acute Kidney Injury Tulane University March 2024 Phase 3

Chemical lnformation & Solubility

Molecular Weight 959.12 Formula

C48H78O19
CAS No. 16830-15-2 SDF Download Asiaticoside SDF
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
Storage (From the date of receipt)

In vitro
Batch:

DMSO : 100 mg/mL ( (104.26 mM)； Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Water : Insoluble

Ethanol : Insoluble


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In vivo
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