8-Chloroadenosine 3',5'-cyclic-monophosphate (C1081) - High-Quality cAMP Analog

REF #: 3199521
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Short description

8-Chloroadenosine 3′,5′-cyclic-monophosphate

  • Chemical Name: 8-Chloroadenosine 3′,5′-cyclic-monophosphate
  • Purity: >= 85%
  • Description: Membrane-permeable cAMP analog
  • Stability: Resistant to hydrolysis by phosphodiesterases

Catalog Numbers: C1081, 8-Chloroadenosine 3′, 5′-cyclic-monophosphate, u226585%, 8-Chloro-cAMP, 8-Chloroadenosine 3′, 5′-monophosphate, 8-Cl-cAMP, 41941-56-4

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Description

8-Chloroadenosine 3',5'-cyclic-monophosphate (C1081) - High-Quality cAMP Analog for Cellular Signaling Research

  • Chemical Name: 8-Chloroadenosine 3',5'-cyclic-monophosphate
  • Purity: ≥85%
  • Description: Membrane-permeable cAMP analog
  • Stability: Resistant to hydrolysis by phosphodiesterases

The 8-Chloroadenosine 3',5'-cyclic-monophosphate, also known as C1081, is a high-quality, membrane-permeable cAMP analog widely used in various research applications. With its purity level of at least 85%, this compound is an essential tool for scientists studying cellular signaling pathways, second messenger systems, and other vital biological processes.

Features:

  • Purity: The 8-Chloroadenosine 3',5'-cyclic-monophosphate has a purity level of ≥85%, guaranteeing a high-quality and reliable product for research purposes.
  • Membrane-permeable: This cAMP analog is capable of crossing cell membranes, allowing for easy and efficient delivery to target cells.
  • Stability: Resistant to hydrolysis by phosphodiesterases, ensuring the compound remains intact and active throughout experiments.
  • Research tool: Widely used in scientific research to investigate cellular signaling pathways, second messenger systems, and other important biological processes.

Applications:

8-Chloroadenosine 3',5'-cyclic-monophosphate has a wide range of applications in cellular and molecular biology research. Some of its common uses include:

  • Studying cAMP-mediated signaling pathways: By mimicking the function of natural cAMP, this compound helps researchers investigate the various cellular processes regulated by cAMP, including gene expression, protein phosphorylation, and ion channel activity.
  • Second messenger systems: cAMP is a well-known second messenger that plays a crucial role in transmitting signals from cell surface receptors to intracellular effectors. The use of 8-Chloroadenosine 3',5'-cyclic-monophosphate allows scientists to study the downstream effects of cAMP activation and its impact on cellular processes.
  • Phosphodiesterase research: 8-Chloroadenosine 3',5'-cyclic-monophosphate's resistance to hydrolysis by phosphodiesterases makes it an excellent tool for studying the role of these enzymes in cAMP regulation and degradation.
  • Drug discovery: Understanding the complex signaling pathways involving cAMP is vital for the development of therapeutic agents targeting various diseases. 8-Chloroadenosine 3',5'-cyclic-monophosphate is frequently used in drug discovery research to assay the effects of novel compounds on cAMP-mediated pathways and identify potential drug candidates.

Product Details:

8-Chloroadenosine 3',5'-cyclic-monophosphate, also known as 8-Chloro-cAMP or 8-Cl-cAMP, has the catalog numbers C1081 and 41941-56-4. It is supplied in a high-quality form with a purity level of at least 85%. The compound is carefully formulated to ensure stability and reliability, making it an excellent choice for researchers conducting rigorous scientific studies.

It is important to note that while 8-Chloroadenosine 3',5'-cyclic-monophosphate is a potent research tool, caution should be exercised during handling and storage. Proper safety precautions, including the use of appropriate personal protective equipment, should be followed to minimize potential risks associated with this compound.

In summary, 8-Chloroadenosine 3',5'-cyclic-monophosphate is a highly valuable research tool for scientists in the field of cellular and molecular biology. With its membrane-permeable properties, stability, and resistance to hydrolysis, this cAMP analog serves as a reliable and efficient means for investigating cellular signaling pathways, second messenger systems, and other important biological processes.

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