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Merck

M109

2-Methylserotonin maleate salt

≥98% (HPLC)

Sinonimo/i:

2-Methyl-5-hydroxytryptamine maleate salt, 3-(2-Aminoethyl)-2-methyl-1H-indol-5-ol maleate salt

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Informazioni su questo articolo

Formula empirica (notazione di Hill):
C11H14N2O · C4H4O4
Numero CAS:
Peso molecolare:
306.31
UNSPSC Code:
12352200
PubChem Substance ID:
MDL number:
Servizio Tecnico
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assay

≥98% (HPLC)

form

solid

color

tan

solubility

H2O: 4.5 mg/mL

storage temp.

−20°C

SMILES string

OC(=O)\C=C/C(O)=O.Cc1[nH]c2ccc(O)cc2c1CCN

Gene Information

Biochem/physiol Actions

5-HT3 serotonin receptor agonist.


Classe di stoccaggio

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)



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D M Gillies et al.
European journal of pharmacology, 303(1-2), 1-12 (1996-05-06)
5-Hydroxytryptamine (5-HT) is involved in the modulation of dopaminergic activity in the mesolimbic system, but its sites of action and the receptors involved are not well understood. Locomotor activity responses in rats were monitored in Animex automated activity boxes following
T Endo et al.
Research communications in molecular pathology and pharmacology, 104(2), 145-155 (2000-01-14)
The object of this study was to evaluate the involvement of 5-HT3 receptors in the regulation of 5-HT release from the small intestine using ferrets, an animal model of emesis. 2-Methyl-5-HT, a 5-HT3 receptor agonist, produced a concentration-dependent increase of
A M Ismaiel et al.
Journal of medicinal chemistry, 33(2), 755-758 (1990-02-01)
alpha-Methyl-5-hydroxytryptamine (alpha-Me-5-HT; 2) and 2-methyl-5-hydroxytryptamine (2-Me-5-HT; 3) are considered to be 5-HT2-selective and 5-HT3-selective agents, respectively. These agents were synthesized and examined at serotonin (5-HT) binding sites because there is relatively little documentation as to their selectivity and because they