α-Me-5-HT

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Names

[ CAS No. ]:
97469-12-0

[ Name ]:
α-Me-5-HT

[Synonym ]:
|A-Methylserotonin maleate salt
2-methyl-5-HT
HMS3262F07

Chemical & Physical Properties

[ Melting Point ]:
191 - 193 °C

[ Molecular Formula ]:
C15H18N2O5

[ Molecular Weight ]:
306.31400

[ Exact Mass ]:
306.12200

[ PSA ]:
136.64000

[ LogP ]:
2.17530

[ Storage condition ]:
20°C

MSDS

Safety Information

[ Personal Protective Equipment ]:
Eyeshields;Gloves;type N95 (US);type P1 (EN143) respirator filter

[ RIDADR ]:
NONH for all modes of transport

[ HS Code ]:
2933990090

Customs

[ HS Code ]: 2933990090

[ Summary ]:
2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

Articles

5-HT1 and 5-HT2 binding profiles of the serotonergic agents alpha-methylserotonin and 2-methylserotonin.

J. Med. Chem. 33 , 755-758, (1990)

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 syn...

Serotonin via 5-HT1B and 5-HT2B receptors stimulates anion secretion in the rat epididymal epithelium.

J. Physiol. 519 , 519, (1999)

1. The short-circuit current (Isc) technique was used to study the role of 5-hydroxytryptamine (5-HT) in the regulation of anion secretion in cultured rat cauda epididymal epithelia. 2. 5-HT, the 5-HT...

Effects of serotonin-1 and serotonin-2 receptor agonists on neuronal activity in the nucleus tractus solitarius.

J. Auton. Nerv. Syst. 56 , 119-124, (1995)

Spontaneous neuronal activity in the solitary tract nucleus was recorded extracellularly in a brain slice preparation during bath-application of 5-HT1 and 5-HT2 receptor-selective agonists and antagon...


More Articles


Related Compounds

  • 2-Methyl-5-HT
  • α-Me-D-Phe(3-NO2)-OH·H2O
  • α-Me-D-Phe(2-Br)-OH·H2O
  • α-Me-D-Phe(4-CF3)-OEt·HCl·H2O
  • α-Me-Phe(2-NO2)-OH·H2O
  • α-Me-Phe(4-Ph)-OH·H2O
  • 4-((Cyclohexylamino)methyl)benzoic acid hydrochloride
  • 1-[(2,4-Dichlorophenyl)methyl]-N-(1,1-dimethylethyl)-2-methyl-1H-indole-3-methanamine
  • 2-Methoxy-6-(pyrazol-1-yl)-benzonitrile
  • 2-[(3-ethyl-4-oxo-3,4-dihydro[1]benzofuro[3,2-d]pyrimidin-2-yl)sulfanyl]-N-(4-methylbenzyl)acetamide
  • 1H-3-Benzazepin-7-ol, 8-chloro-2,3,4,5-tetrahydro-5-(3-iodophenyl)-3-methyl-, (S)-
  • (4-Methyl-tetrahydro-furan-2-yl)-methanol
  • 2-(5-(4-fluorophenyl)isoxazol-3-yl)-N-(2-(methylthio)phenyl)acetamide
  • N-(1-cyanocyclopentyl)-2-[4-(4-fluorobenzenesulfonyl)-1,4-diazepan-1-yl]acetamide
  • 4,5,6,7-Tetrahydrobenzo[d]isoxazole-3-carbaldehyde
  • 4-(Cyclopropylformamido)butanoic acid