8-Br-cADPR sodium salt
8-Br-cADPR sodium salt (8-Bromo-Cyclic ADP-Ribose sodium salt) is a membrane-permeable competitive antagonist of Cyclic ADP-ribose (cADPR) (HY-N7395) and an antagonist of TRPM2 ion channels. 8-Br-cADPR sodium salt blocks cADPR-dependent RyR, SR calcium mobilization, and cADPR-mediated signaling; reduces Paclitaxel (HY-B0015)-induced axonal calcium flux, and protects against Paclitaxel-induced axonal degeneration/peripheral neuropathy. 8-Br-cADPR sodium salt blocks isoproterenol-induced pulmonary artery dilation, angiotensin II-induced arterial calcium signaling/contraction, and hypoxic pulmonary vasoconstriction. 8-Br-cADPR sodium salt can be used in research related to neurological diseases and cancer.
For research use only. We do not sell to patients.
- Formula: C15H18BrN5Na2O13P2
- Molecular Weight:664.16
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Storage:
-80°C
All Calcium Channel Isoforms
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Biological Activity
Description
In Vitro
8-Br-cADPR sodium salt partially reduces Paclitaxel (HY-B0015)-induced intra-axonal calcium flux in DRG sensory axons/sensory neuron axons, partially inhibits sTIR dimerization-induced axonal calcium elevation, and reduces Paclitaxel-induced axonal degeneration in a concentration-dependent manner[3].
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
In Vivo
MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.
Chemical Information
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Appearance Solid
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Molecular Weight 664.16
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Formula C15H18BrN5Na2O13P2
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Color White to off-white
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SMILES
O[C@H]1[C@@H](O)[C@H](N2C(Br)=NC3=C2N=CN([C@H]4[C@H](O)[C@H](O)[C@@H](COP(O5)(O[Na])=O)O4)C3=N)O[C@@H]1COP5(O[Na])=O
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Synonyms
8-Bromo-Cyclic ADP-Ribose sodium salt
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Shipping
Shipping with dry ice.
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Storage
-80°C
Purity & Documentation
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Data Sheet (293 KB)
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SDS (252 KB)
- English - EN (252 KB)
- Français - FR (252 KB)
- Deutsch - DE (252 KB)
- Norwegian - NO (252 KB)
- Español - ES (252 KB)
- Swedish - SV (252 KB)
- Italian - IT (252 KB)
- Korean - KR (252 KB)
- Portuguese - PT (252 KB)
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Handling Instructions (2659 KB)
References
[1]. Zhong J, et al. Cyclic ADP-Ribose and Heat Regulate Oxytocin Release via CD38 and TRPM2 in the Hypothalamus during Social or Psychological Stress in Mice. Frontiers in neuroscience. 2016;10:304. [Content Brief]
[3]. Li Y, et al. Sarm1 activation produces cADPR to increase intra-axonal Ca++ and promote axon degeneration in PIPN. The Journal of cell biology. 2022 Feb 07;221(2):e202106080. [Content Brief]
Calculators
Concentration (start) × Volume (start) = Concentration (final) × Volume (final)