DAMGO

€54.00

Excl. VAT

Item no.	HY-P0210-1mg
Manufacturer	MedChem Express
CASRN	78123-71-4
Amount	1 mg
Category	Peptides & Proteins Peptides
Type	Peptides
Specific against	other
Purity	99.90
Formula	C26H35N5O6
Citations	[1]FEBS Lett. 1995 Jan 2;357(1):93-7. Onogi T, et al. DAMGO, a mu-opioid receptor selective agonist, distinguishes between mu- and delta-opioid receptors around their first extracellular loops. [2]Patel JP, et al. Modulation of neuronal CXCR4 by the micro-opioid agonist DAMGO. J Neurovirol. 2006 Dec;12(6):492-500. [3]Gold MS, et al. DAMGO inhibits prostaglandin E2-induced potentiation of a TTX-resistant Na+ current in rat sensory neurons in vitro. Neurosci Lett. 1996 Jul 12;212(2):83-6. [4]Desmeules JA, et al. Selective opioid receptor agonists modulate mechanical allodynia in an animal model of neuropathic pain. Pain. 1993 Jun;53(3):277-285.
Smiles	OC1=CC=C(C[C@H](N)C(N[C@H](C)C(NCC(N(C)[C@H](C(NCCO)=O)CC2=CC=CC=C2)=O)=O)=O)C=C1
ECLASS 10.1	32160409
ECLASS 11.0	32160409
UNSPSC	12352202
Alias	78123-71-4
Available
Product Description	DAMGO is a μ-opioid receptor (μ-OPR ) selective agonist with a Kd of 3.46 nM for native μ-OPR[1].
StorageTemperature	-80°C, 2 years; -20°C, 1 year (Powder, sealed storage, away from moisture and light)
Shipping	Blue Ice
Manufacturers Applications	Cancer-programmed cell death
Molecular Weight	513.59
Clinical Information	No Development Reported
Solubility	DMSO : 33.33 mg/mL (ultrasonic)\|H2O : ≥ 100 mg/mL
Isoform	μ Opioid Receptor/MOR
Pathway	GPCR/G Protein; Neuronal Signaling
Manufacturers Product type	Peptides

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HY-P0210-1mg-safety-datasheet.pdf