8-Bromo-cAMP, sodium salt

8-Bromo-cAMP, sodium salt

Catalog Number:
FC01366395APE
Mfr. No.:
APE-B9000
Price:
$177
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          Background

          8-Bromo-cAMP is a cAMP-analogues. [1]
          cAMP can have an effect on the proliferative response of a cell. Either the effect is a positive or a negative regulator depending on the cell types. There is also variable effect of cAMP in hematopoietic cell lines. CAMP-analogues can significantly inhibit the erythropoietin-stimulated proliferation.[1]
          8-Bromo-cAMP increased the cellular content of mRNA encoding the hCG a- and β-subunits and prevented the increase in fibronectin mRNA. This is determined by blot hybridization analysis using specific cDNA probes. 8-Bromo-cAMP also induced phosphorylation of Erk1,2 in AML193 cells. 8-Bromo-cAMP is an agent in AML193 cells and activates Erk1,2 , this condition happens does not accompanied by the involvement of Shc phosphorylation.[1,2]
          8-bromo-cAMP increases catecholamine biosynthesis and produces an increase both in the activity and phosphorylation of tyrosine hydroxylase. 8-bromo-cAMP also promotes alterations in the synthesis and secretion of specific proteins, including fibronectin and the subunits of hCG by regulating mRNA expression.[2,3]

          [1]Ulloa-Aguirre A,?August AM,?etal. , 8-Bromo-adenosine?3',5'-monophosphate?regulates?expression?of?chorionic?gonadotropin?and fibronectin in human cytotrophoblasts. J Clin Endocrinol Metab.?1987 May;64(5):1002-9.
          [2] Rene e M. Y. Barge, J.H. Frederik Falkenburg, etal., 8-Bromo-cAMP induces a proliferative response in an IL-3 dependent leukemic cell line and activates Erk1,2 via a Shc-independent pathway. Biochimica et Biophysica Acta 1355 (1997) 141–146.
          [3] Haycock JW, Bennett WF, etal. , Multiple site phosphorylation of tyrosine hydroxylase. Differential regulation in situ by a 8-bromo-cAMP and acetylcholine. J Biol Chem. 1982 Nov 25;257(22):13699-703.

      • Properties
        • Categories
          Cell-permeable cAMP analog that activates PKA
          Alternative Name
          sodium (4aR,6R,7R,7aS)-6-(6-amino-8-bromo-9H-purin-9-yl)-7-hydroxytetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinin-2-olate 2-oxide
          CAS Number
          76939-46-3
          Molecular Formula
          C10H10BrN5NaO6P
          Molecular Weight
          430.09
          Appearance
          A solid
          Purity
          98.00%
          Solubility
          ≥43 mg/mL in H2O; insoluble in EtOH; ≥22.43 mg/mL in DMSO with gentle warming and ultrasonic
          Storage
          Store at -20°C
          SMILES
          NC1=C(N=C(Br)N2[[email protected]@H]3O[[email protected]](COP(O4)([O-])=O)[[email protected]@H]4[[email protected]]3O)C2=NC=N1.[Na+]

          * For Research Use Only

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