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
  • N1-(2-(benzofuran-2-yl)-2-hydroxypropyl)-N2-(2-methoxybenzyl)oxalamide
  • (-)-Avarone
  • 4-(2-Chloro-pyridin-3-yloxy)-phenylamine
  • 2-Acetamido-4-(4-fluorophenyl)thiophene-3-carboxylic acid
  • (2Z)-3-(7-Methoxy-1,3-benzodioxol-5-yl)-2-propenoic acid
  • 3-cyano-6-cyclopropyl-N-(5-methyl-1,3-thiazol-2-yl)-2-(methylsulfanyl)pyridine-4-carboxamide
  • 1,1-Dioxo-1lambda6-thiolan-3-yl 3-[4,6-dimethyl-2-(methylsulfanyl)pyrimidin-5-yl]propanoate
  • 6-Nitro-1,1-dioxo-2,3-dihydro-1-benzothiophene-3-sulfonyl chloride
  • 2-(5-Ethyl-1,3,4-oxadiazol-2-yl)morpholine
  • 2-[5-(Propan-2-yl)-1,3,4-oxadiazol-2-yl]morpholine
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