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Chemical Structure| 16980-89-5 Chemical Structure| 16980-89-5

Structure of Bucladesine sodium
CAS No.: 16980-89-5

Chemical Structure| 16980-89-5

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Dibutyryl-cAMP inhibits neuronal glucose uptake via PKA activation.

Synonyms: Dibutyryl cAMP sodium salt; DBcAMP sodium salt; DC 2797

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Product Details of Bucladesine sodium

CAS No. :16980-89-5
Formula : C18H23N5NaO8P
M.W : 491.37
SMILES Code : O=C(CCC)O[C@H]1[C@H](N2C(N=CN=C3NC(CCC)=O)=C3N=C2)O[C@@](CO4)([H])[C@@]1([H])OP4([O-])=O.[Na+]
Synonyms :
Dibutyryl cAMP sodium salt; DBcAMP sodium salt; DC 2797

Safety of Bucladesine sodium

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Related Pathways of Bucladesine sodium

Hedgehog

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Hepatocyte couplets 10 µM 30 min To study the protective effect of DBcAMP against TLC-induced cholestasis, results showed DBcAMP significantly improved cVA of CLF Gut. 2002 Jul;51(1):113-9.
oligodendrocyte progenitor cells (OPCs) 3.21 mM 48 h dbcAMP promotes OPC differentiation in the presence of myelin-associated inhibitors, increasing O4 and Mbp expression EMBO Mol Med. 2013 Dec;5(12):1918-34
L6 cells 1mM 2.5h To test the effect of DBcAMP on glucose uptake (GU). Results showed that DBcAMP significantly increased GU. Br J Pharmacol. 2006 Feb;147(4):446-54

In Vivo:

Species
Animal Model
Administration Dosage Frequency Description References
Rats Acute cardiac allograft rejection model Intraperitoneal injection 15 mg/kg/day Once daily for the entire experimental period Db-cAMP inhibits inflammatory gene expression, NO-mediated cytotoxicity, and caspase-3-dependent apoptotic events, prolonging cardiac allograft survival Exp Mol Med. 2010 Jan 31;42(1):69-79
Lewis rats Spinal cord contusion model Intravenous injection 50 mg/kg Single injection, lasting 24 hours Systemic administration of Cyclic AMP and IL-4 after spinal cord injury significantly promotes M1 to M2a phenotypic conversion and reduces inflammatory responses. J Neuroinflammation. 2016 Jan 13;13:9

Protocol

Bio Calculators
Preparing Stock Solutions 1mg 5mg 10mg

1 mM

5 mM

10 mM

2.04mL

0.41mL

0.20mL

10.18mL

2.04mL

1.02mL

20.35mL

4.07mL

2.04mL

Dissolving Methods
Please choose the appropriate dissolution scheme according to your animal administration guide.For the following dissolution schemes, clear stock solution should be prepared according to in vitro experiments, and then cosolvent should be added in turn:

in order to ensure the reliability of the experimental results, the clarified stock solution can be properly preserved according to the storage conditions; The working fluid for in vivo experiment is recommended to be prepared now and used on the same day;

The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1
Protocol 2
The prepared working fluid is recommended to be prepared now and used up as soon as possible in a short period of time. The percentage shown in front of the following solvent refers to the volume ratio of the solvent in the final solution; If precipitation or precipitation occurs in the preparation process, it can be assisted by heating and/or ultrasound.
Protocol 1

References

 

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