Dextran sulfate sodium salt (MW 5000) [9011-18-1]

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Cat# NB-64-05231-25g

Size : 25g

Brand : Neo Biotech

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Dextran sulfate sodium salt (MW 5000) (Synonyms: DSS, Dextran sulfate sodium salt (MW 5000))

Catalog No. T13647 Copy Product Info
Dextran sulfate sodium salt (MW 4500-5500) is a polymer of dehydrated glucose and an inhibitor of complement and coagulation pathways. Dextran sulfate sodium salt (MW 4500-5500) can be used as an anticoagulant, antiviral agent and antilipidemic agent. Dextran sulfate sodium salt (MW 4500-5500) can prevent the HIV-1 virus from adsorbing onto host cells. Dextran sulfate sodium salt (MW 4500-5500) can inhibit NK cell-mediated cytotoxicity. Dextran sulfate sodium salt (MW 4500-5500) can inhibit the immediate blood-mediated inflammatory response (IBMIR).

Dextran sulfate sodium salt (MW 5000)

Copy Product Info
Synonyms DSS, Dextran sulfate sodium salt (MW 5000)

Dextran sulfate sodium salt (MW 4500-5500) is a polymer of dehydrated glucose and an inhibitor of complement and coagulation pathways. Dextran sulfate sodium salt (MW 4500-5500) can be used as an anticoagulant, antiviral agent and antilipidemic agent. Dextran sulfate sodium salt (MW 4500-5500) can prevent the HIV-1 virus from adsorbing onto host cells. Dextran sulfate sodium salt (MW 4500-5500) can inhibit NK cell-mediated cytotoxicity. Dextran sulfate sodium salt (MW 4500-5500) can inhibit the immediate blood-mediated inflammatory response (IBMIR).

Dextran sulfate sodium salt (MW 5000)
Cas No. 9011-18-1
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Appearance:Solid
Color:White
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Product Introduction

Bioactivity
Description
Dextran sulfate sodium salt (MW 4500-5500) is a polymer of dehydrated glucose and an inhibitor of complement and coagulation pathways. Dextran sulfate sodium salt (MW 4500-5500) can be used as an anticoagulant, antiviral agent and antilipidemic agent. Dextran sulfate sodium salt (MW 4500-5500) can prevent the HIV-1 virus from adsorbing onto host cells. Dextran sulfate sodium salt (MW 4500-5500) can inhibit NK cell-mediated cytotoxicity. Dextran sulfate sodium salt (MW 4500-5500) can inhibit the immediate blood-mediated inflammatory response (IBMIR).
Targets&IC50
HIV-1:9.1 µg/mL
In vitro
METHODS: MT-4 cells were treated with Dextran sulfate sodium salt (MW 4500-5500) (25 μg/mL) for 24 hours. The inhibitory effect on HIV-1 replication was observed, and the effects of the drug on cytotoxicity and reverse transcriptase activity were evaluated.
RESULTS: Dextran sulfate sodium salt (MW 4500-5500) has a significant selective inhibitory effect on HIV-1, with an IC50 value of 2.3-8.8 µg/ml, and does not show toxicity to host cells at high concentrations. [1]
In vivo
METHODS: To investigate the effect of Dextran sulfate sodium salt (MW 4500-5500) on endothelial injury after ischemia and reperfusion in a rat model of inferior renal aortic clamp, Dextran sulfate sodium salt (MW 4500-5500)(5 mg/mL, 200 μL) was immediately locally infused into the ischemic aortic segment of rats before reperfusion.
RESULTS: Dextran sulfate sodium salt (MW 4500-5500) inhibits complement activation and reduces endothelial injury after ischemia and reperfusion in the rat model of inferior renal aortic clamp. [2]
Disease Modeling Protocol
Ulcerative colitis model
  • Modeling Mechanism:

    Dextran sulfate sodium salt (MW 5000) (DSS) disrupts the tight junctions of the intestinal epithelium and damages the integrity of the mucosal barrier, causing intestinal flora imbalance, activating innate and adaptive immune responses, inducing neutrophil infiltration and the release of pro-inflammatory factors such as TNF-α and IL-6, ultimately leading to colonic mucosal congestion, edema, erosion and ulcer formation.

  • Related Products:

    Dextran sulfate sodium salt (MW 5000) (T13647)

  • Modeling Method:

    Experimental Subject:

    Mouse, C57BL/6J, Male, 6 weeks old

    Dosage and Administration Route:

    2.5% DSS aqueous solution (prepared with sterile water), sole drinking water source, ad libitum consumption

    Dosing Frequency and Duration Model:

    Initial 14-day adaptation period (gavage with corresponding reagent), followed by continuous drinking of 2.5% DSS for 7 days (total experimental period: 21 days)

  • Validation:

    The colonic tissue showed mucosal erosion, inflammatory cell infiltration, and ulceration, and the colon length was shortened; the DAI score (weight loss, abnormal stool characteristics, and hematochezia) was significantly elevated; serum LPS and FITC-glucan levels were elevated, and intestinal permeability was increased; the expression of ZO-1, Occludin, and Claudin-1 in the colonic tissue was decreased; the levels of IL-1β, TNF-α, IL-6, and iNOS mRNA and protein in serum and colonic tissue were elevated, while the expression of IL-10 was decreased; the intestinal flora was disordered (the firmicutes/bacteroidota ratio was decreased, harmful bacteria such as Escherichia-Shigella and Helicobacter increased, and beneficial bacteria such as Akkermansia decreased); the expression of antioxidant-related genes and proteins such as Nrf2, HO-1, SOD, GPX4, and CAT was decreased.

*Precautions: All mice were anesthetized and sacrificed on day 22 after modeling (day 15 after the end of DSS administration), and serum, colon tissue, and fecal samples were collected simultaneously.

*References:Li Y, et,al. Mare milk and fermented mare milk alleviate dextran sulfate sodium salt-induced ulcerative colitis in mice by reducing inflammation and modulating intestinal flora. J Dairy Sci. 2025 Mar;108(3):2182-2198.

SynonymsDSS, Dextran sulfate sodium salt (MW 5000)
Chemical Properties
Molecular Weight9000-20000
Formula(C6H7Na3O14S3)n
Cas No.9011-18-1
Relative Density.no data available
Storage & Solubility Information
StoragePowder: -20°C for 3 years | In solvent: -80°C for 1 year
Solubility Information
H2O: 100 mg/mL, Sonication is recommended.
DMSO: Insoluble

Citations

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