M1514
Nω-Methyl-5-hydroxytryptamine oxalate salt
≥90% (HPLC)
Synonym(s):
Nω-Methylserotonin oxalate salt
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About This Item
Empirical Formula (Hill Notation):
C11H14N2O · C2H2O4
CAS Number:
Molecular Weight:
280.28
MDL number:
UNSPSC Code:
12352116
PubChem Substance ID:
NACRES:
NA.77
Quality Level
Assay
≥90% (HPLC)
storage temp.
2-8°C
SMILES string
OC(=O)C(O)=O.CNCCc1c[nH]c2ccc(O)cc12
InChI
1S/C11H14N2O.C2H2O4/c1-12-5-4-8-7-13-11-3-2-9(14)6-10(8)11;3-1(4)2(5)6/h2-3,6-7,12-14H,4-5H2,1H3;(H,3,4)(H,5,6)
InChI key
DYOZWAJOUTVNAF-UHFFFAOYSA-N
Gene Information
Biochem/physiol Actions
Serotonin receptor ligand.
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Niels Hadrup et al.
Drug and chemical toxicology, 42(1), 76-83 (2018-07-24)
Selenium (Se) nanoparticles have been proposed as food supplements. However, the particle formulation may exert unexpected toxicity. The aim was therefore to compare toxicity of low doses of Se nanoparticles and the dissolved, ionized Se species selenite. Female rats were
A R Johnston et al.
Experimental brain research, 93(2), 293-298 (1993-01-01)
The effects of 5-hydroxytryptamine (5-HT) and related compounds on the discharge rate of tonically active medial vestibular nucleus (MVN) neurones were studied in an in vitro slice preparation of the dorsal brainstem of the rat. The majority (87 of 107
D Alberghina et al.
Research in veterinary science, 90(3), 392-395 (2010-07-17)
To evaluate the changes in plasma and platelet serotonin (5-HT) as markers of the serotoninergic system in equines, 5-HT content was measured by high performance liquid chromatography (HPLC) in deproteinized plasma obtained from peripheral blood samples of 12 clinically healthy
G L Laekeman et al.
Agents and actions, 16(5), 443-445 (1985-07-01)
Pharmacological effects of 5-hydroxykynuramine (5-HK) were investigated in chicken whole blood. It was shown that 5-HK had a time-depending inhibiting activity on platelet aggregation induced by 5-hydroxytryptamine (5-HT). Experiments were carried out in order to determine whether the inhibitory effect
N Takeda et al.
Neuroreport, 6(17), 2378-2380 (1995-11-27)
We have analyzed products of the serotonin-degradative pathway, in which both N-methylserotonin and bufotenine are formed in urine specimens of products with psychiatric disorders by three-dimensional HPLC with electrochemical detection. Bufotenine was detected in urine from all autistic patients with
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