CasNo.118-00-3,Guanosine manufacture,(118-00-3) Suppliers

10 Gram	Negotiable

Min.Order :10 Gram
Purity: 98.0%
Payment Terms : L/C,T/T,

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Guanosine suppiler Guanosine high quality Guanosine

Quick Details

Appearance:A white or almost white crystalline powder
Application:Guanosine is thought to have neuroprotective properties. It can reduce neuroinflammation, oxidative stress, and excitotoxicity, as well as exerting trophic effects in neuronal and glial cells
PackAge:10kg/drum
ProductionCapacity:30|Metric Ton|Month
Storage:keep sealed and keep from direct light
Transportation:According to client's requirements

Superiority:

Product name: Guanosine

Synonyms:Guanosine hydrate;Guanine-9-β-D-ribofuranoside;2-Amino-9-((2R,3R,4S,5R)-3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-1H-purin-6(9H)-one

CAS No.: 118-00-3

Molecular formula: C10H13N5O5

Molecular weight: 283.24

Appearance:A white or almost white crystalline powder

Loss on drying:≤5.0%

Residue on ignition:≤0.2%

Heavy metals:≤10ppm

Purity（HPLC）:≥98.0%

Assay(UV):97.0%-103.0%

Guanosine is a purine nucleoside, in which the guanine attached to the C1 carbon of a ribose (ribofuranose) ring via a β-N9-glycosidic bond. Its phosphorylated derivatives include GMP (guanosine monophosphate), cGMP (cyclic guanosine monophosphate), GDP (guanosine diphosphate), and GTP (guanosine triphosphate). These guanosine derivatives are very important in various biochemical processes, such as synthesis of nucleic acids and proteins, photosynthesis, muscle contraction, and intracellular signal transduction.
Guanosine is thought to have neuroprotective properties. It can reduce neuroinflammation, oxidative stress, and excitotoxicity, as well as exerting trophic effects in neuronal and glial cells. It is shown to be protective in central nervous system diseases including ischemic stroke, Alzheimer’s disease, Parkinson’s disease, spinal cord injury, nociception, and depression. Guanosine is found to be associated with purine nucleoside phosphorylase (PNP) deficiency, which is an inborn error of metabolism.

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