Basic information Safety Supplier Related

GALANIN (2-11) PORCINE, RAT

Basic information Safety Supplier Related

GALANIN (2-11) PORCINE, RAT Basic information

Product Name:
GALANIN (2-11) PORCINE, RAT
Synonyms:
  • H-TRP-THR-LEU-ASN-SER-ALA-GLY-TYR-LEU-LEU-NH2
  • GALANIN (2-11) PORCINE, RAT
  • AR-M 1896
  • GALANIN (2-11)
  • TRP-THR-LEU-ASN-SER-ALA-GLY-TYR-LEU-LEU-NH2
  • Galanin (2-11) (AR-M 1896)
  • L-Leucinamide, L-tryptophyl-L-threonyl-L-leucyl-L-asparaginyl-L-seryl-L-alanylglycyl-L-tyrosyl-L-leucyl-
CAS:
367518-31-8
MF:
C54H81N13O14
MW:
1136.3
Product Categories:
  • Galanin receptor
  • Galanins
  • Neuropeptides
  • Peptides for Cell Biology
Mol File:
367518-31-8.mol
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GALANIN (2-11) PORCINE, RAT Chemical Properties

Boiling point:
1595.4±65.0 °C(Predicted)
Density 
1.291±0.06 g/cm3(Predicted)
storage temp. 
−20°C
solubility 
Soluble to 1 mg/ml in 20% formic acid
pka
9.82±0.15(Predicted)
form 
lyophilized powder
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Safety Information

WGK Germany 
3

MSDS

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GALANIN (2-11) PORCINE, RAT Usage And Synthesis

Biological Activity

binding ic50: 1.76 nm for rgalr2; 879 nm for hgalr1galanin is a 29-aa neuropeptide with a complex role in pain processing. galanin receptor subtypes are present in dorsal root ganglia and spinal cord with a differential distribution. three galanin receptors, galr1, galr2 and galr3, have been identified and cloned. ar-m1896 is a specific galanin r2 (galr2) agonist.

in vitro

additional removal of the glycine residue in position 1 resulted in ar-m1896 with almost unchanged galr2 affinity and functional activity, and 500-fold selectivity for galr2-rs over galr1-rs. this compound represents a truly galr2-selective galanin analog and, thus, could be used as a pharmacological tool to differentiate between these two receptors [1].

in vivo

in normal rats mechanical and cold allodynia of the hindpaw are induced by intrathecal infusion of low-dose galanin. the same effect is seen with equimolar doses of ar-m1896 or ar-m961 (an agonist both at galr1 and galr2 receptors). in allodynic bennett model rats, the mechanical threshold dose-dependently increased after intrathecal injection of a high ar-m961dose, whereas no effect was observed in the control or ar-m1896 group. no effect of either compounds was observed in nonallodynic bennett model rats [1].

References

[1] liu hx, brumovsky p, schmidt r, brown w, payza k, hodzic l, pou c, godbout c, hökfelt t. receptor subtype-specific pronociceptive and analgesic actions of galanin in the spinal cord: selective actions via galr1 and galr2 receptors. proc natl acad sci u s a. 2001 aug 14;98(17):9960-4.

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