O-6-Deoxy-α-L-mannopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl (3β)-3-[(4-O-β-D-glucopyranosyl-α-L- arabinopyranosyl)oxy]olean-12-en-28-oate

≥95%(HPLC)

Reagent Code: #221952
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CAS Number 1175042-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 1220 g/mol
Formula C₅₉H₉₆O₂₆
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This compound is a triterpenoid saponin derivative with complex glycosylation, making it highly polar and bioactive. It is primarily investigated for its immunomodulatory and adjuvant properties in vaccine formulations. The molecule enhances antigen presentation by promoting dendritic cell maturation and stimulating both humoral and cellular immune responses. Due to its natural origin and low toxicity profile, it is used in experimental vaccines to boost efficacy without excessive inflammation. Additionally, it shows potential in anticancer therapies by inducing apoptosis in tumor cells and inhibiting angiogenesis. Its sugar moieties contribute to solubility and target specificity, enabling improved pharmacokinetics in drug delivery systems. Research also explores its use in topical formulations for anti-inflammatory and skin-barrier enhancing effects.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days $1,293.04
O-6-Deoxy-α-L-mannopyranosyl-(1→4)-O-β-D-glucopyranosyl-(1→6)-β-D-glucopyranosyl (3β)-3-[(4-O-β-D-glucopyranosyl-α-L- arabinopyranosyl)oxy]olean-12-en-28-oate
This compound is a triterpenoid saponin derivative with complex glycosylation, making it highly polar and bioactive. It is primarily investigated for its immunomodulatory and adjuvant properties in vaccine formulations. The molecule enhances antigen presentation by promoting dendritic cell maturation and stimulating both humoral and cellular immune responses. Due to its natural origin and low toxicity profile, it is used in experimental vaccines to boost efficacy without excessive inflammation. Additionally, it shows potential in anticancer therapies by inducing apoptosis in tumor cells and inhibiting angiogenesis. Its sugar moieties contribute to solubility and target specificity, enabling improved pharmacokinetics in drug delivery systems. Research also explores its use in topical formulations for anti-inflammatory and skin-barrier enhancing effects.
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