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Bucladesine sodium

Bucladesine sodium
Bucladesine sodium (DC2797) is a cAMP analog with cell-permeable properties. Bucladesine sodium is also a cAMP-dependent protein kinase (PKA) activator and a phosphodiester (PDE) inhibitor. Bucladesine sodium has anti-inflammatory activity.
Catalog No. T1418Cas No. 16980-89-5
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Purity:99.58%
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Bucladesine sodium

Purity: 99.58%
Catalog No. T1418Alias Sodium dibutyryl cAMP, Dibutyryl-cAMP sodium salt, Dibutyryl-cAMP, DC2797, dbcAMP, Bucladesine sodium salt, BucladesineCas No. 16980-89-5

Bucladesine sodium (DC2797) is a cAMP analog with cell-permeable properties. Bucladesine sodium is also a cAMP-dependent protein kinase (PKA) activator and a phosphodiester (PDE) inhibitor. Bucladesine sodium has anti-inflammatory activity.
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Pack SizePriceAvailabilityQuantity
25 mg$31In Stock
50 mg$42In Stock
100 mg$79In Stock
200 mg$117In Stock
500 mg$193In Stock
2 g$419In Stock
1 mL x 10 mM (in DMSO)$46In Stock
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Product Introduction

Bioactivity
Description
Bucladesine sodium (DC2797) is a cAMP analog with cell-permeable properties. Bucladesine sodium is also a cAMP-dependent protein kinase (PKA) activator and a phosphodiester (PDE) inhibitor. Bucladesine sodium has anti-inflammatory activity.
In vitro
METHODS: Human eosinophil EoL-1 cells were treated with Bucladesine sodium (10-100 µM) for 8 days and activity was measured using PKA assay.
RESULTS: Proliferation of EoL-1 cells treated with Bucladesine sodium increased in a time-dependent manner. [1]
METHODS: PC12 cells were treated with Bucladesine sodium (1 mM) for 72 h. TNF-α levels were measured by ELISA assay.
RESULTS: Bucladesine sodium increased the activity of PKA. [2]
In vivo
METHODS: To study the anti-inflammatory activity in vivo, Bucladesine sodium (0.24-0.7 µg/kg) was administered intraperitoneally to a mouse model of copper pine demyelination once daily for seven days.
RESULTS: Bucladesine had a protective effect on myelin formation. Enhanced intracellular cAMP prevented demyelination and exerted anti-inflammatory and anti-apoptotic properties in a mouse model of copper pine demyelination. [3]
METHODS: To investigate the effects on liver injury, Bucladesine sodium (0.5-500 mg/kg) was intraperitoneally injected into C57BL/6J jcl mice, and liver injury was induced by the intravenous injection of rTNF-α (1.0 µg/kg) and intraperitoneal injection of D-gal (500 mg/kg) after 1 h. The RESULTS showed that Bucladesine protected against hepatic injury in C57BL/6J jcl mice.
RESULTS: Bucladesine protected mice from TNF-α/D-gal-induced liver injury.Bucladesine significantly enhanced the expression of Hsp70 in hepatocytes of D-gal/TNFα-injected mice, which was closely related to the inhibition of liver injury. [4]
Animal Research
Animal: Mice. Formulation: water/DMSO (9:1). Dosages: 600 nM. Administration: i.p.
AliasSodium dibutyryl cAMP, Dibutyryl-cAMP sodium salt, Dibutyryl-cAMP, DC2797, dbcAMP, Bucladesine sodium salt, Bucladesine
Chemical Properties
Molecular Weight491.37
FormulaC18H23N5NaO8P
Cas No.16980-89-5
Storage & Solubility Information
Storagestore at low temperature | Powder: -20°C for 3 years | In solvent: -80°C for 1 year | Shipping with blue ice.
Solubility Information
H2O: 49.1 mg/mL (100 mM)
DMSO: 55 mg/mL (111.93 mM)
Solution Preparation Table
H2O/DMSO
1mg5mg10mg50mg
1 mM2.0351 mL10.1756 mL20.3513 mL101.7563 mL
5 mM0.4070 mL2.0351 mL4.0703 mL20.3513 mL
10 mM0.2035 mL1.0176 mL2.0351 mL10.1756 mL
20 mM0.1018 mL0.5088 mL1.0176 mL5.0878 mL
50 mM0.0407 mL0.2035 mL0.4070 mL2.0351 mL
100 mM0.0204 mL0.1018 mL0.2035 mL1.0176 mL

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