Rathbunioside R1

≥90%

Reagent Code: #230789
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CAS Number 350689-78-0

science Other reagents with same CAS 350689-78-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 568.78 g/mol
Formula C₃₂H₅₆O₈
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Rathbunioside R1 is primarily investigated for its potential anti-inflammatory and immunomodulatory properties. It has shown activity in suppressing pro-inflammatory cytokines, making it a candidate for research in autoimmune and chronic inflammatory conditions. Preliminary studies suggest it may influence cellular signaling pathways involved in immune response, particularly NF-κB and MAPK pathways. Due to its natural origin and structural complexity, it is also studied in the context of drug development for metabolic and degenerative diseases. However, its application remains largely experimental, with most data derived from in vitro and animal models. Further research is needed to evaluate bioavailability, toxicity, and therapeutic efficacy in humans.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿43,230.00

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Rathbunioside R1
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Rathbunioside R1 is primarily investigated for its potential anti-inflammatory and immunomodulatory properties. It has shown activity in suppressing pro-inflammatory cytokines, making it a candidate for research in autoimmune and chronic inflammatory conditions. Preliminary studies suggest it may influence cellular signaling pathways involved in immune response, particularly NF-κB and MAPK pathways. Due to its natural origin and structural complexity, it is also studied in the context of drug development

Rathbunioside R1 is primarily investigated for its potential anti-inflammatory and immunomodulatory properties. It has shown activity in suppressing pro-inflammatory cytokines, making it a candidate for research in autoimmune and chronic inflammatory conditions. Preliminary studies suggest it may influence cellular signaling pathways involved in immune response, particularly NF-κB and MAPK pathways. Due to its natural origin and structural complexity, it is also studied in the context of drug development for metabolic and degenerative diseases. However, its application remains largely experimental, with most data derived from in vitro and animal models. Further research is needed to evaluate bioavailability, toxicity, and therapeutic efficacy in humans.

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