Product Data Sheet

8-Br-7-CH-cADPR

Catalog No. A66376

main product photo
8-Br-7-CH-cADPR (7-Deaza-8-bromo-cADPR) functions as a potent cADPR antagonist. It exhibits partial inhibition of calcium elevation induced by sTIR dimerization, making it valuable in studies related to calcium signaling pathways. Furthermore, 8-Br-7-CH-cADPR has been shown to significantly reduce axon degeneration caused by Paclitaxel treatment, providing insights into neuroprotective mechanisms and potential therapeutic applications in neurodegenerative research.
Chemical Information
Catalog NumA66376
M. Wt619.21
FormulaC16H21BrN4O13P2
Purity>98%
Storageat -20 °C 3 years (powder form); at -20 °C 6 months (Solution base)
CAS No.189876-06-0
Synonyms7-Deaza-8-bromo-cADPR; 7-Deaza-8-bromo-cyclic ADP ribose
SMILESN=C1C(C=C(Br)N2[C@H]3[C@H](O)[C@H](O)[C@@H](COP4(O)=O)O3)=C2N=CN1[C@H]5[C@H](O)[C@H](O)[C@@H](COP(O)(O4)=O)O5
Biological Activity
Description8-Br-7-CH-cADPR (7-Deaza-8-bromo-cADPR) functions as a potent cADPR antagonist. It exhibits partial inhibition of calcium elevation induced by sTIR dimerization, making it valuable in studies related to calcium signaling pathways. Furthermore, 8-Br-7-CH-cADPR has been shown to significantly reduce axon degeneration caused by Paclitaxel treatment, providing insights into neuroprotective mechanisms and potential therapeutic applications in neurodegenerative research.
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SHIPPING AND STORAGE
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