research use only

8-Bromo-cAMP Sodium Salt PKA activator

Cat.No.S7857

8-Bromo-cAMP sodium salt is a cell permeable analog of cAMP that activates cyclic-AMP-dependent protein kinase with a Ka value of 0.05 μM; and a PKA activator.
8-Bromo-cAMP Sodium Salt PKA activator Chemical Structure

Chemical Structure

Molecular Weight: 430.08

Quality Control

Cell Culture, Treatment & Working Concentration

Cell Lines Assay Type Concentration Incubation Time Formulation Activity Description PMID
RAW 264.7 Function assay 50 μM 20 min the ADP-enhanced ERK signaling was significantly decreased. 27867196
HUVECs Function assay enhances capillary network formation 24493289
MC3T3-E1 Function assay 1 day significant increases in ALP activities 24493289
CHO  Function assay 0, 10, and 100 μmol/L 8-Br-cAMP increased [Ca2+]i in NCX1 transfectants at reverse mode 23564083
N2a cells Function assay 1-1,000 μM 24 h Aβ40, Aβ42 and sAPPα were significantly increased 23297063
Click to View More Cell Line Experimental Data

Chemical Information, Storage & Stability

Molecular Weight 430.08 Formula

C10H10BrN5NaO6P

Storage (From the date of receipt)
CAS No. 76939-46-3 Download SDF Storage of Stock Solutions

Synonyms 8-Br-Camp sodium salt Smiles C1C2C(C(C(O2)N3C4=NC=NC(=C4N=C3Br)N)O)OP(=O)(O1)[O-].[Na+]

Solubility

In vitro
Batch:

DMSO : 86 mg/mL (199.96 mM)
(Moisture-contaminated DMSO may reduce solubility. Use fresh, anhydrous DMSO.)

Water : 86 mg/mL

Ethanol : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

Step 1: Enter information below (Recommended: An additional animal making an allowance for loss during the experiment)

mg/kg g μL

Step 2: Enter the in vivo formulation (This is only the calculator, not formulation. Please contact us first if there is no in vivo formulation at the solubility Section.)

% DMSO % % Tween 80 % ddH2O
%DMSO %

Calculation results:

Working concentration: mg/ml;

Method for preparing DMSO master liquid: mg drug pre-dissolved in μL DMSO ( Master liquid concentration mg/mL, Please contact us first if the concentration exceeds the DMSO solubility of the batch of drug. )

Method for preparing in vivo formulation: Take μL DMSO master liquid, next addμL PEG300, mix and clarify, next addμL Tween 80, mix and clarify, next add μL ddH2O, mix and clarify.

Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

Note: 1. Please make sure the liquid is clear before adding the next solvent.
2. Be sure to add the solvent(s) in order. You must ensure that the solution obtained, in the previous addition, is a clear solution before proceeding to add the next solvent. Physical methods such
as vortex, ultrasound or hot water bath can be used to aid dissolving.

Mechanism of Action

Targets/IC50/Ki
PKA [1]
0.05 μM(Ka)
In vitro

8-Bromo-cAMP improves the reprogramming efficiency of human neonatal foreskin fibroblast (HFF1) cells. [1]

In bronchial epithelial cells, 8-Bromo-cAMP decreases HDE-stimulated tumor necrosis factor (TNF)-α-converting enzyme (TACE; ADAM-17) activity and subsequent TNF-α release. [2]

References

Tech Support

Handling Instructions

Tel: +1-832-582-8158 Ext:3

If you have any other enquiries, please leave a message.

Please enter your name.
Please enter your email. Please enter a valid email address.
Please write something to us.