Basic information Safety Supplier Related

FMRF AMIDE

Basic information Safety Supplier Related

FMRF AMIDE Basic information

Product Name:
FMRF AMIDE
Synonyms:
  • PHE-MET-ARG-PHE AMIDE
  • PHE-MET-ARG-PHE-NH2
  • PHE-MET-ARG-PHE-NH2 1/2ACOH 2H2O
  • MOLLUSCAN CARDIOEXCITATORY PEPTIDE
  • MOLLUSCAN CARDIOEXCITATORY NEUROPEPTIDE
  • MOLLUSCAN CARDIOEXCITATORY NEUROPEPTIDE 1 1/2 ACOH 2H2O
  • MOLLUSCAN CARDIOEXCITATORY NEUROPEPTIDE ACETATE SALT
  • H-PHE-MET-ARG-PHE-NH2
CAS:
152165-14-5
MF:
C29H42N8O4S
MW:
598.76
Product Categories:
  • Peptide
Mol File:
152165-14-5.mol
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FMRF AMIDE Chemical Properties

storage temp. 
−20°C
Sequence
Phe-Met-Arg-Phe-NH2
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Safety Information

WGK Germany 
3

MSDS

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FMRF AMIDE Usage And Synthesis

Uses

Phe-Met-Arg-Phe, amide acetate dose dependently (ED50=23 nM) activates a K+ current in the peptidergic caudodorsal neurons[1].

in vivo

Phe-Met-Arg-Phe, amide (FMRFamide) acetate stimulates growth hormone secretion in conscious OVX rats. The presence of Phe-Met-Arg-Phe, amide-like immunoreactivity in neuronal elements in the hypothalamus suggested a role for this in the hypothalamic control of the anterior pituitary function. The injection of 200 ng (313.8 pM) of FMRFamide (in 2 uL) produces a significantly increased plasma GH 15 min after injection. The GH-increasing effect of 400-800 ng (627-1255 pM) of FMRFamide is already developed after 5 min and lasted up to 30 min[3].

References

[1] Kits KS, et al. Phe-Met-Arg-Phe-amide activates a novel voltage-dependent K+ current through a lipoxygenasepathway in molluscan neurones. J Gen Physiol. 1997 Nov;110(5):611-28. DOI:10.1085/jgp.110.5.611
[2] Sorenson RL, et al. Phe-met-arg-phe-amide (FMRF-NH2) inhibits insulin and somatostatin secretion and anti-FMRF-NH2 sera detects pancreatic polypeptide cells in the rat islet. Peptides. 1984 Jul-Aug;5(4):777-82. DOI:10.1016/0196-9781(84)90021-4
[3] Ottlecz A, et al. Phe-Met-Arg-Phe-amide (FMRFamide) stimulated growth hormone secretion in conscious OVX rats. Neuropeptides. 1987 Feb-Mar;9(2):161-7. DOI:10.1016/0143-4179(87)90054-0

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