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Saikosaponin D

Cat. No. M3936

All AbMole products are for research use only, cannot be used for human consumption.

Saikosaponin D Structure
Synonym:

Ssd

Size Price Availability Quantity
1mg USD 25  USD25 In stock
5mg USD 55  USD55 In stock
10mg USD 80  USD80 In stock
20mg USD 140  USD140 In stock
50mg USD 260  USD260 In stock
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Quality Control & Documentation
Biological Activity

Saikosaponin D inhibits cell growth of human cancer cells by inducing apoptosis and blocking cell cycle progression in the G1 phase.Saikosaponin D was found to stimulate corticotropin-releasing factor (CRF) gene expression and CRF release.Ssd was shown to increase cytosolic calcium level via direct inhibition of sarcoplasmic/endoplasmic reticulum Ca(2+) ATPase pump,leading to autophagy induction through the activation of the Ca(2+)/calmodulin-dependent kinase kinase-AMP-activated protein kinase-mammalian target of rapamycin pathway.Ssd treatment causes the disruption of calcium homeostasis, which induces endoplasmic reticulum stress as well as the unfolded protein responses pathway.Ssd also proved to be a potent cytotoxic agent in apoptosis-defective or apoptosis-resistant mouse embryonic fibroblast cells, which either lack caspases 3, 7 or 8 or had the Bax-Bak double knockout.SSd markedly suppressed phosphorylation of nuclear factor kappa B (NF-κB) and signal transducer and activator of transcription 3 (STAT3) and reversed the APAP-induced increases in the target genes of NF-κB, such as pro-inflammatory cytokine Il6 and Ccl2, and those of STAT3, such as Socs3, Fga, Fgb and Fgg. SSd also enhanced the expression of the anti-inflammatory cytokine Il10 mRNA.

Product Citations
Customer Product Validations & Biological Datas
Source Front Pharmacol (2021). Figure 5. Saikosaponin D (Abmole Bioscience, Houston, TX, USA)
Method Administration
Cell Lines chronic mild stress (CMS) mice
Concentrations -
Incubation Time -
Results Consistent with the abovementioned observation, the expression of the neuronal marker MAP2 was decreased in CMS mice (Figure 5C), whereas MAP2 expression was significantly increased in the MePD of CMS+SSD mice.
Source Front Pharmacol (2021). Figure 2. Saikosaponin D (Abmole Bioscience, Houston, TX, USA)
Method Administration
Cell Lines chronic mild stress (CMS) mice
Concentrations -
Incubation Time -
Results SSD treatment remarkably alleviated the adverse effects of CMS, with a statistically significant increase in the time spent exploring an estrous female mouse than a sexually active male mouse.
Chemical Information
Molecular Weight 780.98
Formula C42H68O13
CAS Number 20874-52-6
Solubility (25°C) DMSO
Storage Powder          -20°C   3 years ;  4°C   2 years
In solvent       -80°C   6 months ;  -20°C   1 month
References

[1] Liu RY, et al. Eur Rev Med Pharmacol Sci. Saikosaponin-d inhibits proliferation of human undifferentiated thyroid carcinoma cells through induction of apoptosis and cell cycle arrest.

[2] Liu A, et al. Chem Biol Interact. Saikosaponin d protects against acetaminophen-induced hepatotoxicity by inhibiting NF-κB and STAT3 signaling.

[3] Ying ZL, et al. Exp Ther Med. Saikosaponin-d affects the differentiation, maturation and function of monocyte-derived dendritic cells.

[4] Yao M, et al. Mol Med Rep. Saikosaponin‑d inhibits proliferation of DU145 human prostate cancer cells by inducing apoptosis and arresting the cell cycle at G0/G1 phase.

[5] Wong VK, et al. Cell Death Dis. Saikosaponin-d, a novel SERCA inhibitor, induces autophagic cell death in apoptosis-defective cells.

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Keywords: Saikosaponin D, Ssd supplier, COX, inhibitors, activators

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