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Tryptamine TAAR agonist

Cat.No.S3627

Tryptamine is a monoamine alkaloid and may play a role as a neuromodulator or neurotransmitter. It is an agonist of hTAAR1. This compound acts as a non-selective serotonin receptor agonist and serotonin-norepinephrine-dopamine releasing agent (SNDRA).
Tryptamine TAAR agonist Chemical Structure

Chemical Structure

Molecular Weight: 160.22

Quality Control

Batch: S362701 DMSO]32 mg/mL]false]Ethanol]32 mg/mL]false]Water]Insoluble]false Purity: 99.55%
99.55

Chemical Information, Storage & Stability

Molecular Weight 160.22 Formula

C10H12N2

Storage (From the date of receipt)
CAS No. 61-54-1 Download SDF Storage of Stock Solutions

Synonyms N/A Smiles C1=CC=C2C(=C1)C(=CN2)CCN

Solubility

In vitro
Batch:

DMSO : 32 mg/mL ( (199.72 mM) Moisture-absorbing DMSO reduces solubility. Please use fresh DMSO.)

Ethanol : 32 mg/mL

Water : Insoluble

Molarity Calculator

Mass Concentration Volume Molecular Weight

In vivo
Batch:

In vivo Formulation Calculator (Clear solution)

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Method for preparing in vivo formulation: Take μL DMSO master liquid, next add μL Corn oil, mix and clarify.

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Mechanism of Action

Targets/IC50/Ki
hTAAR1 [2]
(COS-7 cells)
1.08 μM(Ki)
In vitro
High concentrations of tryptamine (0.1-1 mM) induce autophagy in HT22 and SK-N-SH nerve cell lines and in primary cultures of astrocytes, glial cells being less sensitive than neurons[2].
In vivo
Tryptamine at a dose of 50 mg/kg i.p. induces an inhibition of locomotor activity and, at doses ranging from 150 to 300 mg/kg, induces peculiar behaviors such as head twitch, head weaving, forepaw treading, hindlimb abduction and Straub tail. This compound induces both the depression and excitation in the behavior of mice depending on the dosage and its excitatory behaviors may be attributed to both its direct stimulation of 5-HT receptors and facilitation of 5-HT release[3].
References

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