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MilliporeSigma

85030

Sigma-Aldrich

Serotonin creatinine sulfate salt monohydrate

purum, ≥98.0% (T)

Sinónimos:

5-Hydroxytryptamine creatinine sulfate salt

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About This Item

Fórmula empírica (notación de Hill):
C10H12N2O · C4H9N3O5S · H2O
Número de CAS:
Peso molecular:
405.43
Beilstein:
3886526
Número CE:
Número MDL:
Código UNSPSC:
12352100
ID de la sustancia en PubChem:

grado

purum

Ensayo

≥98.0% (T)

mp

~220 °C (dec.)

temp. de almacenamiento

2-8°C

cadena SMILES

O.OS(O)(=O)=O.CN1CC(=O)NC1=N.NCCc2c[nH]c3ccc(O)cc23

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Linda Booij et al.
PloS one, 10(3), e0119061-e0119061 (2015-03-18)
Serotonin plays an important role in the etiology of depression. Serotonin is also crucial for brain development. For instance, animal studies have demonstrated that early disruptions in the serotonin system affect brain development and emotion regulation in later life. A
Mathieu Desclaux et al.
Journal of neuroscience research, 93(1), 43-55 (2014-08-19)
In spinal cord injury (SCI), absence of functional recovery and lack of spontaneous axonal regeneration are attributed, among other factors, to the formation of a glial scar that forms both physical and chemical barriers. The glial scar is composed mainly
Di Wang et al.
Journal of neurophysiology, 112(1), 30-38 (2014-04-18)
The lamprey central nervous system has been used extensively as a model system for investigating the networks underlying vertebrate motor behavior. The locomotor networks can be activated by application of glutamate agonists, such as N-methyl-D-aspartic acid (NMDA), to the isolated
Toko Maehara et al.
British journal of pharmacology, 172(4), 1136-1147 (2014-11-08)
Post-operative ileus (POI) is induced by intestinal inflammation. Here, we aimed to clarify the effects of 5-HT3 receptor antagonists against POI. We administered three 5-HT3 receptor antagonists, ondansetron, tropisetron and palonosetron, to a mouse model of POI induced by surgical
Kirsty Bannister et al.
Neuropharmacology, 85, 375-383 (2014-06-18)
Dynorphin A is an endogenous opioid peptide derived from the precursor prodynorphin. The proteolytic fragment dynorphin A (1-17) exhibits inhibitory effects via opioid receptors. Paradoxically, the activity of the dynorphin system increases with chronic pain and neuropathy is associated with

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