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Tribenoside
CAS No. 10310-32-4
Tribenoside( Ba 2140 | BG-356 | Glivenol | Glyvenal | Glyvenol | TBGF )
Catalog No. M27173 CAS No. 10310-32-4
Tribenoside is a vasoprotectant with mild anti-inflammatory, analgesic, and wound healing properties.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 37 | In Stock |
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| 10MG | 33 | In Stock |
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| 25MG | 53 | In Stock |
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| 50MG | 86 | In Stock |
|
| 100MG | Get Quote | In Stock |
|
| 200MG | Get Quote | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
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Product NameTribenoside
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NoteResearch use only, not for human use.
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Brief DescriptionTribenoside is a vasoprotectant with mild anti-inflammatory, analgesic, and wound healing properties.
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DescriptionTribenoside is a vasoprotectant with mild anti-inflammatory, analgesic, and wound healing properties.(In Vitro):Administration of 1 nM-100 μM Tribenoside exhibits cytotoxic effect(EC50 = 13.74 μM) in HeLa cells.(In Vivo):Oral administration in doses of 500 and 1,200 mg/kg Tribenoside weekly significantly decreases in the development of osteoporosis in male mice.
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In VitroTribenoside (1 nM-100 μM) exhibits cytotoxic effect against HeLa cells with the EC50 of 13.74 μM. Cell Viability Assay Cell Line:HeLa cells Concentration:1 nM, 10 nM, 100 nM, 1 μM, 10 μM, 100 μM Incubation Time:72 hours Result:Reduced HeLa cells viability in a dose-responsive manner.
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In VivoTribenoside (oral administration in doses of 500 and 1,200 mg/kg weekly) significantly decreases in the development of osteoporosis. Animal Model:male C57 black mice Dosage:500 and 1,200 mg/kg weekly Administration:Oral administration Result:Led to a significant reduction in the overall arthrotic involvement.
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SynonymsBa 2140 | BG-356 | Glivenol | Glyvenal | Glyvenol | TBGF
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PathwayOthers
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TargetOther Targets
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RecptorEP3
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Research Area——
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Indication——
Chemical Information
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CAS Number10310-32-4
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Formula Weight478.585
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Molecular FormulaC29H34O6
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Purity>98% (HPLC)
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Solubility——
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SMILESCCOC1O[C@H]([C@@H](COCc2ccccc2)OCc2ccccc2)[C@H](OCc2ccccc2)[C@H]1O
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Chemical Name——
Shipping & Storage Information
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Storage(-20℃)
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ShippingWith Ice Pack
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Stability≥ 2 years
Reference
1.Singh J, et al. Antagonists of the EP3 receptor for prostaglandin E2 are novel antiplatelet agents that do not prolong bleeding. ACS Chem Biol. 2009 Feb 20;4(2):115-26.
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