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DAMGO

Catalog No. T4351   CAS 78123-71-4
Synonyms: Dagol, DAGO, RX-783006

DAMGO (DAGO) is an opioid receptor agonist with the ability to affect the locomotive activity in rodents. Possible analgesic agent due to μ-opiod receptor interaction.

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DAMGO Chemical Structure
DAMGO, CAS 78123-71-4
Pack Size Availability Price/USD Quantity
1 mg In stock $ 43.00
2 mg In stock $ 55.00
5 mg In stock $ 79.00
10 mg In stock $ 143.00
25 mg In stock $ 297.00
50 mg In stock $ 445.00
100 mg In stock $ 656.00
1 mL * 10 mM (in DMSO) In stock $ 90.00
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Purity: 99.92%
Purity: 98.83%
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Biological Description
Chemical Properties
Storage & Solubility Information
Description DAMGO (DAGO) is an opioid receptor agonist with the ability to affect the locomotive activity in rodents. Possible analgesic agent due to μ-opiod receptor interaction.
Targets&IC50 μ opioid receptor (Native):3.46±0.84 nM (Kd)
In vivo (1) DAMGO inhibits GABAergic inputs in VTA-DA neurons at presynaptic sites; (2) effect of DAMGO on GABAergic inputs in VTA-DA neurons is inhibited by potassium channel blocker 4-aminopyridine (4-AP) and Gi protein inhibitor N-ethyl maleimide (NEM); (3) phospholipase A2 (PLA2) does not mediate the effect of DAMGO on GABAergic inputs in VTA-DA neurons, but mediates it in the periaqueductal gray (PAG); (4) multiple downstream signaling molecules of l receptors do not mediate the effect of DAMGO on GABAergic inputs in VTA-DA neurons. These results suggest that DAMGO depresses inhibitory synaptic transmission via l receptor-Gi protein-Kv channel pathway in VTA-DA neurons, but via l receptor-PLA2 pathway in PAG
Synonyms Dagol, DAGO, RX-783006
Molecular Weight 513.59
Formula C26H35N5O6
CAS No. 78123-71-4

Storage

store at low temperature,keep away from moisture

Powder: -20°C for 3 years | In solvent: -80°C for 1 year

Solubility Information

DMSO: 33.33 mg/mL (64.90 mM), Sonication is recommended.

TargetMolReferences and Literature

1. Zhang W, etal. DAMGO depresses inhibitory synaptic transmission via different downstream pathways of μ opioid receptors in ventral tegmental area and periaqueductal gray[J]. Neuroscience, 2015, 301: 144-154. 2. Yan J, etal. Activation of μ-opioid receptors in the central nucleus of the amygdala induces hypertonic sodium intake[J]. Neuroscience, 2013, 233(39):28-43.

TargetMolCitations

1. Xu C, Zhou Y, Liu Y, et al.Specific pharmacological and Gi/o protein responses of some native GPCRs in neurons.Nature Communications.2024, 15(1): 1990.

Related compound libraries

This product is contained In the following compound libraries:
Anti-Neurodegenerative Disease Compound Library Membrane Protein-targeted Compound Library GPCR Compound Library Peptide Compound Library Bioactive Compounds Library Max Neuronal Signaling Compound Library Endocrinology-Hormone Compound Library NO PAINS Compound Library Bioactive Compound Library Neurotransmitter Receptor Compound Library

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Keywords

DAMGO 78123-71-4 Endocrinology/Hormones GPCR/G Protein Neuroscience Opioid Receptor Dagol RX783006 μ-opioid receptor DAGO RX 783006 RX-783006 inhibit μ-OPR Inhibitor analgesic effect inhibitor

 

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