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Chemical Structure| 76939-46-3 Chemical Structure| 76939-46-3

Structure of 76939-46-3

Chemical Structure| 76939-46-3

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8-Bromo-cAMP 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.

Synonyms: 8-Bromo-cAMP sodium salt; 8-Br-Camp sodium salt; 8 Br cAMP Na

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Product Details of 8-Bromoadenosine 3',5'-cyclic monophosphate sodium salt

CAS No. :76939-46-3
Formula : C10H10BrN5NaO6P
M.W : 430.08
SMILES Code : NC1=C(N=C(Br)N2[C@@H]3O[C@@](COP(O4)([O-])=O)([H])[C@]4([H])[C@H]3O)C2=NC=N1.[Na+]
Synonyms :
8-Bromo-cAMP sodium salt; 8-Br-Camp sodium salt; 8 Br cAMP Na
MDL No. :MFCD00005844
InChI Key :DMRMZQATXPQOTP-GWTDSMLYSA-M
Pubchem ID :23702958

Safety of 8-Bromoadenosine 3',5'-cyclic monophosphate sodium salt

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

Related Pathways of 8-Bromoadenosine 3',5'-cyclic monophosphate sodium salt

Hedgehog

Isoform Comparison

Biological Activity

In Vitro:

Cell Line
Concentration Treated Time Description References
Nonpregnant uterine artery endothelial cells (NP-UAECs) 1 µM and 1 mM 0 to 60 minutes or 12 hours 8-Br-cAMP did not significantly increase Cx43 S365 signal in NP-UAECs. Hypertension. 2017 Aug;70(2):401-411.
Pregnant uterine artery endothelial cells (P-UAECs) 1 µM and 1 mM 0 to 60 minutes or 12 hours 8-Br-cAMP significantly increased nonphosphorylated Cx43 S365 signal and total Cx43 phosphorylation, but not S368 phosphorylation. Hypertension. 2017 Aug;70(2):401-411.
Human umbilical vein endothelial cells (HUVECs) 200 µM 1 hour Mimicked the effect of caffeine in inducing AMPK phosphorylation and enhanced endothelial cell migration Acta Pharmacol Sin. 2021 Dec;42(12):2033-2045.
Wharton's jelly-derived mesenchymal stem cells (WJ-MSCs) 0.5 mM 21 days 8-Br-cAMP upregulated vimentin and CD13 and downregulated CK and CD9, promoting the differentiation of WJ-MSCs into ESC-like cells. Stem Cell Res Ther. 2017 Nov 2;8(1):246.
Human endometrial stromal (hES) cells 0.5 mM 2-4 days Investigate the differential regulation of mTORC1 and mTORC2 during 8-Br-cAMP-induced decidualization. Results showed increased mTORC1 activity and decreased mTORC2 activity, leading to reduced Akt phosphorylation and activation of FOXO1, promoting the expression of decidualization markers PRL and IGFBP1. Exp Mol Med. 2018 Oct 30;50(10):1-11.
Human esophageal cancer cell line Eca-109 20 µM 24 hours To investigate the effects of 8-Br-cAMP on differentiation and apoptosis of Eca-109 cells. Results showed that the signals of wt p53 and iNOS were markedly stronger, while the signals of c-myc and EGFR were obviously weaker in E1 group (24-hour treatment). World J Gastroenterol. 2005 Nov 7;11(41):6538-42.
JEG-3 cells 250 µM 36 hours Induced trophoblastic differentiation and upregulated LGALS16 and CGB3/5 gene expression Biomolecules. 2021 Dec 20;11(12):1909.
Human esophageal cancer cell line Eca-109 20 µM 48 hours To investigate the effects of 8-Br-cAMP on differentiation and apoptosis of Eca-109 cells. Results showed that the signals of wt p53, iNOS, p38 kinase, and caspase-3 were significantly stronger, whereas the signals of bcl-2, c-myc, and Fas/FasL were markedly weaker in E2 group (48-hour treatment). World J Gastroenterol. 2005 Nov 7;11(41):6538-42.
BeWo cells 250 µM 48 hours Induced trophoblastic differentiation and upregulated LGALS16 and CGB3/5 gene expression Biomolecules. 2021 Dec 20;11(12):1909.
Rat heart cells 10 µM 5 minutes To evaluate the protective effects of 8-Br on the heart, results showed that 8-Br significantly reduced ventricular arrhythmias, improved hemodynamic function, and reduced infarct size Cells. 2021 May 17;10(5):1223.
Differentiated HL-60 neutrophil-like cells (dHL-60) 10 µM 7 hours Inhibited NETosis induced by PMA or rabbit anti-B19V-VP1u IgG Int J Mol Sci. 2024 Sep 13;25(18):9917.
Canine ventricular myocytes 250 µM To investigate the effect of 8-Br-cAMP on IKr and IKs, results showed that 8-Br-cAMP significantly increased the current amplitudes of IKr and IKs Br J Pharmacol. 2011 Feb;162(4):890-6.

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