1. Neuronal Signaling GPCR/G Protein
  2. Monoamine Oxidase 5-HT Receptor
  3. 5,7-Dihydroxytryptamine

5,7-Dihydroxytryptamine (5,7-DHP) is an autofluorescent (λex≈365 nm), selective neurotoxin and a transport substrate for MAO-A and 5-HT. 5,7-Dihydroxytryptamine can specifically target and damage central and peripheral 5-HTergic neurons, while affecting 5-HT-related pathways and neurotransmitter balance. 5,7-Dihydroxytryptamine can be used to establish 5-HTergic neuron injury models for studies on neural development, neurodegenerative diseases, as well as mechanisms related to platelet function and retinal neurons.

For research use only. We do not sell to patients.

5,7-Dihydroxytryptamine

5,7-Dihydroxytryptamine Chemical Structure

CAS No. : 31363-74-3

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Description

5,7-Dihydroxytryptamine (5,7-DHP) is an autofluorescent (λex≈365 nm), selective neurotoxin and a transport substrate for MAO-A and 5-HT. 5,7-Dihydroxytryptamine can specifically target and damage central and peripheral 5-HTergic neurons, while affecting 5-HT-related pathways and neurotransmitter balance. 5,7-Dihydroxytryptamine can be used to establish 5-HTergic neuron injury models for studies on neural development, neurodegenerative diseases, as well as mechanisms related to platelet function and retinal neurons[1][2][3].

IC50 & Target

MAO-A

 

In Vitro

5,7-dihydroxytryptamine (25 μM; 60 min at 37°C) specifically labels serotonergic cells (but not dopaminergic cells) in 10-day-old primary mesencephalic cultures from 14-day-old Wistar rat foetuses[2].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

In Vivo

5,7-Dihydroxytryptamine (12.5-50.0 μg; intracerebroventricular administration; single dose) depletes norepinephrine and 5-HT in the hippocampus of mice. The depletion of norepinephrine is blocked by non-selective MAO inhibition but not by selective MAO-B inhibition[1].
5,7-Dihydroxytryptamine (10 μg base; intracerebroventricular injection; single administration; 10 days prior to seizure induction) depletes 5-HT levels in the spinal cord of rats, but does not affect electrically induced spinal cord seizures in rats[3].

MedChemExpress (MCE) has not independently confirmed the accuracy of these methods. They are for reference only.

Animal Model: C57BL/6 male mice (2 months old, 20-30 g)[1]
Dosage: 12.5, 25, 50.0 μg
Administration: intracerebroventricularly; single dose
Result: Depleted hippocampal norepinephrine by 68% and serotonin by 71% in mice not pretreated with MAO inhibitors.
Animal Model: Sprague-Dawley (female, 180-220 g)[3]
Dosage: 10 µg of the base
Administration: i.c.v.; single dose; 10 days before seizure induction
Result: Reduced spinal cord 5-hydroxytryptamine levels to 0.21 µg/g ± 0.04; produced no changes in spinal cord norepinephrine content or electrically-induced spinal cord seizure parameters (duration of tonic flexion, tonic extension, or total seizure duration)
Molecular Weight

192.21

Formula

C10H12N2O2

CAS No.
SMILES

NCCC1=CNC2=C(O)C=C(O)C=C12

Structure Classification
Initial Source

rat

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Storage

Please store the product under the recommended conditions in the Certificate of Analysis.

Purity & Documentation
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  • Do most proteins show cross-species activity?

    Species cross-reactivity must be investigated individually for each product. Many human cytokines will produce a nice response in mouse cell lines, and many mouse proteins will show activity on human cells. Other proteins may have a lower specific activity when used in the opposite species.

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Product Name:
5,7-Dihydroxytryptamine
Cat. No.:
HY-N18471
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