Salidroside

Name: Salidroside
Brand: Selleck Chemicals
SKU: S2396
Rating: 5 (2 reviews)

For research use only.

Catalog No.S2396 Synonyms: Rhodioloside

2 publications

CAS No. 10338-51-9

Salidroside (Rhodioloside), a phenylpropanoid glycoside isolated from Rhodiola rosea, has been reported to have a broad spectrum of pharmacological properties. Salidroside is a prolyl endopeptidase inhibitor. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy.

Selleck's Salidroside has been cited by 2 publications

Curr Med Sci, 2021, 10.1007/s11596-021-2374-6

PubMed: 34181207 ( click the link to review the publication )

J Med Virol, 2019, 91(8):1440-1447

PubMed: 30900754 ( click the link to review the publication )

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Biological Activity

Description	Salidroside (Rhodioloside), a phenylpropanoid glycoside isolated from Rhodiola rosea, has been reported to have a broad spectrum of pharmacological properties. Salidroside is a prolyl endopeptidase inhibitor. Salidroside alleviates cachexia symptoms in mouse models of cancer cachexia via activating mTOR signalling. Salidroside protects dopaminergic neurons by enhancing PINK1/Parkin-mediated mitophagy.
In vitro	Salidroside inhibits the growth of various human cancer cell lines in concentration- and time-dependent manners, and the sensitivity to salidroside is different in those cancer cell lines. Salidroside could cause G1-phase or G2-phase arrest in different cancer cell lines, meanwhile, salidroside resultes in a decrease of CDK4, cyclin D1, cyclin B1 and Cdc2, and upregulates the levels of p27(Kip1) and p21(Cip1). ^[1] Salidroside also alleviates cell viability loss and apoptotic cell death induced by H(2)O(2) stimulation in cultured NGF-differentiated PC12 cells by activating ERK1/2 pathway and inhibiting caspase-3 activation. ^[2] Salidroside activates the PI3K/Akt pathway resulting in protective effects against MPP(+)-induced apoptosis in PC12 cells, which may be used in the treatment of Parkinson's disease (PD). ^[3]
In vivo	Salidroside (20, 50 and 100 mg/kg) protects liver tissue from the oxidative stress elicited by D-galactosamine and lipopolysaccharide. ^[4]

Protocol

References

[4] Wu YL, et al. J Pharm Pharmacol, 2009, 61(10), 1375-1382.

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Solubility (25°C)

In vitro	DMSO	60 mg/mL (199.8 mM)
	Water	60 mg/mL (199.8 mM)
	Ethanol	4 mg/mL (13.32 mM)

* Please note that Selleck tests the solubility of all compounds in-house, and the actual solubility may differ slightly from published values. This is normal and is due to slight batch-to-batch variations.

Chemical Information Download Salidroside SDF

Molecular Weight	300.3
Formula	C₁₄H₂₀O₇
CAS No.	10338-51-9
Storage	3 years-20°C powder 2 years-80°C in solvent
Synonyms	Rhodioloside
Smiles	C1=CC(=CC=C1CCOC2C(C(C(C(O2)CO)O)O)O)O

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Salidroside