Etiprednol dicloacetate
CAS No. 199331-40-3
Etiprednol dicloacetate( —— )
Catalog No. M34592 CAS No. 199331-40-3
Etiprednol dicloacetate (BNP-166) is a corticosteroid with anti-inflammatory activity.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 5MG | 247 | In Stock |
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| 10MG | 371 | In Stock |
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| 25MG | 620 | In Stock |
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| 50MG | 863 | In Stock |
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| 100MG | 1172 | In Stock |
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| 200MG | Get Quote | In Stock |
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| 500MG | Get Quote | In Stock |
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| 1G | Get Quote | In Stock |
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Biological Information
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Product NameEtiprednol dicloacetate
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NoteResearch use only, not for human use.
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Brief DescriptionEtiprednol dicloacetate (BNP-166) is a corticosteroid with anti-inflammatory activity.
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DescriptionEtiprednol dicloacetate (BNP 166) is an anti-inflammatory agent. Etiprednol dicloacetate inhibits eosinophil accumulation. Etiprednol dicloacetate can be used in the research of inflammatory airway diseases, such as asthma.
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In VitroEtiprednol dicloacetate (1 nM-1 μM) inhibits LPS-induced TNF-α production by human blood.
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In VivoEtiprednol dicloacetate (0-100 μg/kg, intranasal inhalation) attenuates peribronchial eosinophilia in the lung of the allergen sensitized and challenged rats.Etiprednol dicloacetate (0.1 μg/kg, intranasal inhalation) inhibits eosinophil accumulation in rats (antigen-induced airway eosinophil infiltration).Etiprednol dicloacetate (0-20 mg/kg, p.o., 28 days) is well tolerated in rats and dogs.Animal Model: Allergen sensitized and challenged Brown Norway rats Dosage:0.1, 1, 10, and 100 μg/kg Administration: Intranasal inhalation Result:Decreased the number of eosinophils at the perivascular area of the lung tissue.Decreased the number of mucus secreting cells and antigen-induced formation of perivascular edema.
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Synonyms——
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PathwayOthers
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TargetOther Targets
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RecptorOthers
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Research Area——
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Indication——
Chemical Information
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CAS Number199331-40-3
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Formula Weight485.4
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Molecular FormulaC24H30Cl2O6
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Purity>98% (HPLC)
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Solubility——
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SMILESO(C(C(Cl)Cl)=O)[C@@]1(C(OCC)=O)[C@]2(C)[C@@](CC1)([C@]3([C@]([C@@H](O)C2)([C@]4(C)C(CC3)=CC(=O)C=C4)[H])[H])[H]
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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
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S26131
S26131 behaves as an antagonist on MT1 and MT2 receptors with Ki of 0.5 and 112 nM respectively.
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