CAS 23583-48-4
:8-Bromo-cAMP
Description:
8-Bromo-cAMP, with the CAS number 23583-48-4, is a synthetic derivative of cyclic adenosine monophosphate (cAMP), a crucial second messenger in various biological processes. This compound is characterized by the presence of a bromine atom at the 8-position of the adenine ring, which enhances its stability and alters its biological activity compared to natural cAMP. 8-Bromo-cAMP is often used in biochemical research to study signal transduction pathways, particularly those involving protein kinase A (PKA), as it can mimic the effects of cAMP while being resistant to degradation by phosphodiesterases. The compound is typically soluble in water and organic solvents, making it versatile for laboratory applications. Its ability to activate PKA and influence cellular responses makes it a valuable tool in pharmacology and cell biology. However, like many chemical substances, it should be handled with care, following appropriate safety protocols due to its potential biological effects.
Formula:C10H11BrN5O6P
InChI:InChI=1/C10H11BrN5O6P/c11-10-15-4-7(12)13-2-14-8(4)16(10)9-5(17)6-3(21-9)1-20-23(18,19)22-6/h2-3,5-6,9,17H,1H2,(H,18,19)(H2,12,13,14)/t3-,5-,6-,9-/m1/s1
InChI key:InChIKey=DVKQVRZMKBDMDH-UUOKFMHZSA-N
SMILES:BrC=1N(C=2C(N1)=C(N)N=CN2)[C@H]3[C@H](O)[C@]4([C@](O3)(COP(=O)(O)O4)[H])[H]
Synonyms:- (4aR,6R,7R,7aS)-6-(6-amino-8-bromo-9H-purin-9-yl)tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinine-2,7-diol 2-oxide
- 23583-48-4
- 3',5'-(Hidrogenofosfato) Ciclico De 8-Bromoadenosina
- 3',5'-(Hydrogenophosphate) Cyclique De 8-Bromoadenosine
- 4H-Furo[3,2-d]-1,3,2-dioxaphosphorin, adenosine deriv.
- 6-(6-amino-8-bromo-9H-purin-9-yl)tetrahydro-4H-furo[3,2-d][1,3,2]dioxaphosphinine-2,7-diol 2-oxide
- 8-Bromadenosin-cyclisch-3',5'-(hydrogenphosphat)
- 8-Bromo-cAMP
- 8-Bromo-cyclic 3',5'-AMP
- 8-Bromo-cyclic 3′,5′-AMP
- 8-Bromoadenosine Cyclic 3',5'-(Hydrogen Phosphate)
- 8-Bromoadenosine cyclic 3',5'-monophosphate
- 8-Bromoadenosine cyclic 3',5'-phosphate
- 8-Bromoadenosine cyclic 3′,5′-monophosphate
- 8-Bromoadenosine cyclic 3′,5′-phosphate
- 8-Bromoadenosine-cAMP
- Adenosine, 8-bromo-, cyclic 3',5'-(hydrogen phosphate)
- Adenosine, 8-bromo-, cyclic 3′,5′-(hydrogen phosphate)
- Cyclic 8-bromoadenosine 3',5'-monophosphate
- Cyclic 8-bromoadenosine 3′,5′-monophosphate
- Nsc 171719
- 8-Bromo Cyclic Adenosine Monophosphate
- 8-BROMOADENOSINE-3-5-CYCLICMONOPHOSPHATE FREE ACID
- 8-Bromoadenosine 3',5'-monophosphate
- 8-Br-A-3:5-MP
- 8-BROMOADENOSINE 3':5'-CYCLIC MONOPHOSPHATE USP/EP/BP
- -CyclicMonophosphate
- 8-BR-CAMP
- 8-BROMOADENOSINE 3' 5'-CYCLIC
- 8-bromo-3',5'-cyclic AMP
- 8-BR-CAMP,98+%
- B-cAMP
- 8-BROMOADENOSINE 3':5'-CYCLIC MONOPHOSPHATE
- 8-Bromoadenosine 3',5'-phosphoric acid
- 8-Bromoadenosine-3'',-5''-cyclic monophosphoric acid
- 8-BROMOADENOSINE-3',5'-CYCLOPHOSPHATE
- 8-Bromocyclic AMP
- 8-BROMOADENOSINE-3',5'-CYCLIC MONOPHOSPHATE
- Cyclic amp, 8-bromo
- 8-BROMOADENOSINE-3',5'-CYCLOPHOSPHORIC ACID
- See more synonyms
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Found 7 products.
8-Bromoadenosine-3',5'-cyclic monophosphate
CAS:<p>This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C10H11BrN5O6PMolecular weight:408.118-Bromoadenosine cyclic 3',5'-monophosphate
CAS:Formula:C10H11BrN5O6PPurity:98%Color and Shape:SolidMolecular weight:408.10208-Bromo-cAMP
CAS:<p>8-Bromo-cAMP is a cell-permeable cAMP analogue and activator of CAMP-dependent protein kinase A that induces cell death and reduces proliferation.</p>Formula:C10H11BrN5O6PPurity:97.30%Color and Shape:SolidMolecular weight:408.18-Bromoadenosine 3',5'-cyclic monophosphate
CAS:<p>8-Bromoadenosine 3',5'-cyclic monophosphate (8-Br-cAMP) is a cyclic nucleotide that is involved in the regulation of energy metabolism. It is a pharmacological agent that regulates the intracellular levels of cAMP and plays an important role in regulating cell proliferation, differentiation, and survival. 8-Br-cAMP binds to specific protein kinases and alters their activity. It also inhibits the enzymatic activity of DNA polymerase II. 8-Br-cAMP has been shown to inhibit tumor growth in mice with bone cancer. The mechanism by which this drug exerts its antitumor effect appears to be related to increased expression of basic proteins and decreased expression of phosphatase 2A, leading to increased activation of protein kinase A. 8-Br-cAMP also causes cellular accumulation of Ca2+ ions by stimulating an increase in the activity of phospholipase C, which hydrolyzes phosphat</p>Formula:C10H11BrN5O6PPurity:Min. 98 Area-%Color and Shape:Beige PowderMolecular weight:408.11 g/mol







