ChemicalBook--->CAS DataBase List--->18525-25-2

18525-25-2

18525-25-2 Structure

18525-25-2 Structure
IdentificationBack Directory
[Name]

5-HYDROXYTRYPTAMINE MALEATE SALT
[CAS]

18525-25-2
[Synonyms]

5-HT
serotoninmaleate
SEROTONIN BIMALEATE
SEROTONIN HYDROGEN MALEATE
5-HYDROXYTRYPTAMINE MALEATE
5-HYDROXYTRYPTAMINE BIMALEATE
5-HYDROXYTRYPTAMINE MALEATE SALT
3-(2-aminoethyl)-indol-5-omaleate
Serotonin hydrogen maleate powder
3-(2-aminoethyl)indole-5-ol,maleate
5-HYDROXYTRYPTAMINE HYDROGEN MALEATE
3-(2-AMINOETHYL)-5-HYDROXYINDOLE MALEATE
3-(2-AMINOETHYL)-5-HYDROXYINDOLE MALEATE SALT
3-(2-ammonioethyl)-5-hydroxy-1H-indolium maleate
3-(2-AMINOETHYL)-5-HYDROXYINDOLE HYDROGEN MALEATE
3-(2-Aminoethyl)-5-hydroxyindole hydrogen maleate, 5-HT, 5-Hydroxytryptamine hydrogen maleate
Serotonin hydrogen maleate,3-(2-Aminoethyl)-5-hydroxyindole hydrogen maleate, 5-HT, 5-Hydroxytryptamine hydrogen maleate
[EINECS(EC#)]

242-399-6
[Molecular Formula]

C14H16N2O5
[MDL Number]

MFCD00043256
[MOL File]

18525-25-2.mol
[Molecular Weight]

292.29
Chemical PropertiesBack Directory
[Melting point ]

154-158 °C (dec.)
[storage temp. ]

2-8°C
[form ]

powder
[color ]

off-white to yellow
[BRN ]

8173182
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H302
[Precautionary statements ]

P264-P270-P301+P312-P330-P501
[Hazard Codes ]

Xn
[Risk Statements ]

22
[WGK Germany ]

3
[RTECS ]

NM2560000
[F ]

3-8-10
Hazard InformationBack Directory
[Uses]

Serotonin hydrogen maleate is a monoamine neurotransmitter in the CNS and an endogenous 5-HT receptor agonist. Serotonin hydrogen maleate is also a catechol O-methyltransferase (COMT) inhibitor with a Ki of 44 μM [1] [2].
[References]

[1] Tsao D, et al. Serotonin-induced hypersensitivity via inhibition of catechol O-methyltransferase activity. Mol Pain. 2012 Apr 13;8:25. DOI:10.1186/1744-8069-8-25
[2] Shajib MS, et al. Interleukin 13 and serotonin: linking the immune and endocrine systems in murine models of intestinal inflammation. PLoS One. 2013 Aug 28;8(8):e72774. DOI:10.1371/journal.pone.0072774
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