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Ginsenoside Rg1 Beta Amyloid inhibitor

Cat.No.S3923

Ginsenoside Rg1 (Ginsenoside A2, Panaxoside A, Panaxoside Rg1, Sanchinoside C1, Sanchinoside Rg1), one of the major active components of ginseng, is identified as a protopanaxatriol-type and has pharmacological actions such as neuroprotective and anti-tumor effects on various cancer types. This compound reduces cerebral Aβ levels and NF-κB nuclear translocation.
Ginsenoside Rg1 Beta Amyloid inhibitor Chemical Structure

Chemical Structure

Molecular Weight: 801.01

Quality Control

Chemical Information, Storage & Stability

Molecular Weight 801.01 Formula

C42H72O14

Storage (From the date of receipt)
CAS No. 22427-39-0 -- Storage of Stock Solutions

Synonyms Ginsenoside A2, Panaxoside A, Panaxoside Rg1, Sanchinoside C1, Sanchinoside Rg1 Smiles CC(=CCCC(C)(C1CCC2(C1C(CC3C2(CC(C4C3(CCC(C4(C)C)O)C)OC5C(C(C(C(O5)CO)O)O)O)C)O)C)OC6C(C(C(C(O6)CO)O)O)O)C

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Mechanism of Action

Targets/IC50/Ki
[5]
NF-κB [6]
In vitro

Ginsenoside Rg1 (Rg1) activates promyogenic kinases, p38MAPK (mitogen-activated protein kinase) and Akt signaling, that in turn promotes the heterodimerization with MyoD and E proteins, resulting in enhancing myogenic differentiation. Through the activation of Akt/mammalian target of rapamycin pathway, this compound induces myotube growth and prevents dexamethasone-induced myotube atrophy. Furthermore, it increases MyoD-dependent myogenic conversion of fibroblast. This chemical enhances glucose uptake in insulin-resistant myoblasts[1]. It possesses the capacity for anti-aging activity in HSCs both in vitro and vivo[2]. This compound promotes endothelial progenitor cells (EPCs) adhesion, proliferation, migration and in vitro vasculogenesis in a dose- and time-dependent manner[3]. It could prevent cellular apoptosis via initiating an autophagic survival response, during which time this chemical could promote the expression of Beclin1 and Bcl-2 and weaken the interaction between Beclin1 and Bcl-2[4].

In vivo

Rg1 can protect BMSCs against senescence and affect cell cycle phase distribution of bone marrow stromal cells (BMSCs) in aged rats. It affects inflammatory cytokine and stem cell factor (SCF) levels of BMSCs. This compound affects inflammatory cytokine and SCF levels of BMSCs. It improves the anti-aging ability of hematopoietic microenvironment through enhancing the anti-oxidant and anti-inflammatory capacities of BMSCs[2]. This chemical has neuroprotective properties in neurodegenerative diseases such as AD. It could ameliorate cognitive impairment in the mouse model of AD, improve the learning and memory abilities, decrease the levels of cerebral Aβ, maintain hippocampal neuron activity, and prevent cellular apoptosis induced by Aβ accumulation. On the other hand, this compound also could protect against brain aging by enhancing the scavenging of free radicals in the brain[5].

References
  • [4] https://pubmed.ncbi.nlm.nih.gov/27228978/
  • [5] https://www.hindawi.com/journals/omcl/2017/6473506/#B16
  • [6] https://pubmed.ncbi.nlm.nih.gov/28903427/

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