1. GPCR/G Protein Neuronal Signaling
  2. Dopamine Receptor
  3. Cyclo(glycyl-L-leucyl)

Cyclo(glycyl-L-leucyl)  (Synonyms: Cyclo(leu-gly))

Cat. No.: HY-W152604
Handling Instructions

Cyclo(glycyl-L-leucyl) (Cyclo(leu-gly)), a neuropeptide, down-regulates dopamine (DA) receptors and attenuates dopaminergic supersensitivity. Cyclo(glycyl-L-leucyl) inhibits the development of Morphine induced pain relief as well as dopamine receptor supersensitivity in rats. Cyclo(glycyl-L-leucyl) has the potential for the prevention of tardive and/or L-DOPA.html" class="link-product" target="_blank">L-DOPA (HY-N0304)-induced dyskinesias.

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

Cyclo(glycyl-L-leucyl) Chemical Structure

Cyclo(glycyl-L-leucyl) Chemical Structure

CAS No. : 5845-67-0

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Description

Cyclo(glycyl-L-leucyl) (Cyclo(leu-gly)), a neuropeptide, down-regulates dopamine (DA) receptors and attenuates dopaminergic supersensitivity. Cyclo(glycyl-L-leucyl) inhibits the development of Morphine induced pain relief as well as dopamine receptor supersensitivity in rats. Cyclo(glycyl-L-leucyl) has the potential for the prevention of tardive and/or L-DOPA.html" class="link-product" target="_blank">L-DOPA (HY-N0304)-induced dyskinesias[1][2].

IC50 & Target[1]

Dopamine Receptor

 

In Vivo

Cyclo(glycyl-L-leucyl) (8 mg/kg; s.c.) given 24h after apomorphine (APO) attenuates the DA receptor supersensitivity caused by acute high dose APO (5 mg/kg; s.c.)[1].

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

Animal Model: Male Swiss-Webster mice, 20-25g[1]
Dosage: 8 mg/kg
Administration: SC; single dose given 24h after apomorphine (APO)
Result: Attenuated the DA receptor supersensitivity caused by acute high dose APO (5 mg/kg; s.c.).
Molecular Weight

170.21

Formula

C8H14N2O2

CAS No.
SMILES

CC(C[C@H]1C(NCC(N1)=O)=O)C

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

Purity & Documentation
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Cyclo(glycyl-L-leucyl)
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