Basic information Safety Supplier Related

3-(2-AMINO-ETHYL)-1H-INDOLE-5-CARBOXYLIC ACID AMIDE

Basic information Safety Supplier Related

3-(2-AMINO-ETHYL)-1H-INDOLE-5-CARBOXYLIC ACID AMIDE Basic information

Product Name:
3-(2-AMINO-ETHYL)-1H-INDOLE-5-CARBOXYLIC ACID AMIDE
Synonyms:
  • 3-(2-AMINO-ETHYL)-1H-INDOLE-5-CARBOXYLIC ACID AMIDE
  • 5-CARBOXAMINODOTRYPTAMINE
  • 5-CT
  • 5-CARBOXAMIDOTRYPTAMINE HEMIETHANOLATE MALEATE SALT
  • 5-carboxamidotryptamine
  • 2-Carboxyamidotryptamine
  • 3-(2-Aminoethyl)-1H-indole-5-carboxamide
  • 5-Carboxyamidotryptamine
CAS:
74885-09-9
MF:
C11H13N3O
MW:
203.24
Product Categories:
  • pharmacetical
  • Serotonin receptor
Mol File:
74885-09-9.mol
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3-(2-AMINO-ETHYL)-1H-INDOLE-5-CARBOXYLIC ACID AMIDE Chemical Properties

Boiling point:
513.6±35.0 °C(Predicted)
Density 
1.293±0.06 g/cm3(Predicted)
storage temp. 
−20°C
solubility 
H2O: 10 mg/mL
form 
solid
pka
16.32±0.30(Predicted)
color 
white or off-white
Stability:
Hygroscopic
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Safety Information

Hazard Codes 
Xi
Risk Statements 
36/37/38
Safety Statements 
26-36
WGK Germany 
3
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3-(2-AMINO-ETHYL)-1H-INDOLE-5-CARBOXYLIC ACID AMIDE Usage And Synthesis

Uses

5-Carboxamidotryptamine maleate is an agonist of the 5-HT1 receptors.

Definition

ChEBI: 5-carboxamidotryptamine is a member of tryptamines.

in vivo

5-Carboxamidotryptamine (0.03-3 mg/kg i.p. and 0.125-5 μg i.c.v.) causes a dose-dependent reduction in rectal temperature of mice[3].
5-Carboxamidotryptamine (0.1-1 mg/kg; i.p.) reduces rectal temperature in wild type mice but not 5-HT7 receptor knockout mice[3].
5-Carboxamidotryptamine (0.0 1-1 μg/kg; i.v.) causes consistent, dose-related decreases in diastolic blood pressure and carotid arterial vascular resistance and increases in heart rate of cats. In contrast, 5-HT (1-100 μg/kg; i.v.) causes tachycardia but variable and complex effects on diastolic blood pressure and carotid arterial vascular resistance[5].
5-Carboxamidotryptamine does not cause bronchoconstriction in cats. In contrast, 5-HT causes dose-related bronchoconstriction[5].

Animal Model:Male Swiss Webster mice (20-25 g)[3]
Dosage:0.03-3 mg/kg (i.p.) and 0.125-5 μg (i.c.v.)
Administration:i.p. and i.c.v.
Result:Caused dose-dependent reduction in rectal temperature.
Animal Model:5-HT7 receptor knockout mice (background=50% 129SvEv/50% C57Bl/6J)[3]
Dosage:0.1-1 mg/kg
Administration:i.p. and i.c.v.
Result:Reduced rectal temperature in wild type but not 5-HT7 receptor knockout mice.

IC 50

5-HT1A Receptor; 5-HT1B Receptor; 5-HT1D Receptor; 5-HT5A Receptor; 5-HT7 Receptor

3-(2-AMINO-ETHYL)-1H-INDOLE-5-CARBOXYLIC ACID AMIDESupplier

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