Cart
sales@molnova.com
8-Bromo-cAMP(sodium salt)
CAS No. 76939-46-3
8-Bromo-cAMP(sodium salt)( 8-Br-cAMP sodium | 8 Br cAMP Na )
Catalog No. M19095 CAS No. 76939-46-3
8-Bromo-cAMP is a long-acting derivative of cyclic AMP. It is an activator of cyclic AMP-dependent protein kinase, but resistant to degradation by cyclic AMP phosphodiesterase.
Purity : >98% (HPLC)
COA
Datasheet
HNMR
HPLC
MSDS
Handing Instructions
| Size | Price / USD | Stock | Quantity |
| 1 mL x 10 mM in DMSO | 44 | In Stock |
|
| 5MG | 39 | In Stock |
|
| 10MG | 55 | In Stock |
|
| 25MG | 74 | In Stock |
|
| 50MG | 123 | In Stock |
|
| 100MG | 211 | In Stock |
|
| 200MG | 322 | In Stock |
|
| 500MG | Get Quote | In Stock |
|
| 1G | Get Quote | In Stock |
|
Biological Information
-
Product Name8-Bromo-cAMP(sodium salt)
-
NoteResearch use only, not for human use.
-
Brief Description8-Bromo-cAMP is a long-acting derivative of cyclic AMP. It is an activator of cyclic AMP-dependent protein kinase, but resistant to degradation by cyclic AMP phosphodiesterase.
-
Description8-Br-cAMP sodium is a cell-permeable activator of protein kinase A.
-
In Vitro——
-
In Vivo——
-
Synonyms8-Br-cAMP sodium | 8 Br cAMP Na
-
PathwayAngiogenesis
-
TargetALK
-
RecptorPKA
-
Research AreaOthers-Field
-
Indication——
Chemical Information
-
CAS Number76939-46-3
-
Formula Weight430.08
-
Molecular FormulaC10H10BrN5NaO6P
-
Purity>98% (HPLC)
-
SolubilityDMSO : 125 mg/mL 290.64 mM; H2O : ≥ 33.33 mg/mL 77.50 mM
-
SMILES[Na+].Nc1ncnc2c1nc(Br)n2[C@@H]1O[C@@H]2COP(=O)([O-])O[C@H]2[C@H]1O
-
Chemical Namesodium (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
Shipping & Storage Information
-
Storage(-20℃)
-
ShippingWith Ice Pack
-
Stability≥ 2 years
Reference
1.Wang Y,etal.A cyclic AMP analog, 8-Br-cAMP, enhances the induction of pluripotency in human fibroblast cells.Stem Cell Rev. 2011 Jun;7(2):331-41.
molnova catalog
related products
-
LDN193189
LDN193189 is a potent, selective BMP type I receptor that inhibits BMP4-induced phosphorylation of SMAD1/5/8 with IC50 of 5 nM.
-
SM 16
SM 16 is a ALK5/ALK4 kinase inhibitor (Ki: 10/1.5 nM).
-
LDK378 dihydrochlori...
Ceritinib dihydrochloride is a selective, orally bioavailable and ATP-competitive inhibitor of ALK tyrosine kinase(IC50 of 200 pM), and also inhibits IGF-1R, InsR, and STK22D (IC50 values of 8, 7, and 23 nM, respectively).
