Rp-8-bromo-Cyclic GMPS sodium salt (Rp-8-bromo-cGMPS)

98%

Reagent Code: #109480
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CAS Number 208445-06-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 462.1 g/mol
Formula C₁₀H₁₀BrN₅NaO₆PS
inventory_2 Storage & Handling
Storage -20°C, airtight, dry

description Product Description

Rp-8-bromo-cGMPS is widely used in biochemical and pharmacological research as a potent and selective inhibitor of cyclic GMP-dependent protein kinase (PKG). It is particularly valuable in studies aimed at understanding the role of PKG in various cellular processes, including smooth muscle relaxation, platelet aggregation, and neuronal signaling. Researchers utilize this compound to dissect the signaling pathways mediated by cGMP, helping to elucidate the mechanisms underlying cardiovascular, neurological, and other physiological functions. Additionally, Rp-8-bromo-cGMPS is employed in experiments to investigate the therapeutic potential of targeting PKG in diseases such as hypertension, heart failure, and erectile dysfunction. Its ability to block PKG activation makes it a critical tool for studying the downstream effects of cGMP in cellular and tissue models.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿61,371.00
Rp-8-bromo-Cyclic GMPS sodium salt (Rp-8-bromo-cGMPS)
Rp-8-bromo-cGMPS is widely used in biochemical and pharmacological research as a potent and selective inhibitor of cyclic GMP-dependent protein kinase (PKG). It is particularly valuable in studies aimed at understanding the role of PKG in various cellular processes, including smooth muscle relaxation, platelet aggregation, and neuronal signaling. Researchers utilize this compound to dissect the signaling pathways mediated by cGMP, helping to elucidate the mechanisms underlying cardiovascular, neurological, and other physiological functions. Additionally, Rp-8-bromo-cGMPS is employed in experiments to investigate the therapeutic potential of targeting PKG in diseases such as hypertension, heart failure, and erectile dysfunction. Its ability to block PKG activation makes it a critical tool for studying the downstream effects of cGMP in cellular and tissue models.
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