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NEUROPEPTIDE FF

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NEUROPEPTIDE FF Basic information

Product Name:
NEUROPEPTIDE FF
Synonyms:
  • PHE-LEU-PHE-GLN-PRO-GLN-ARG-PHE AMIDE
  • PHE-LEU-PHE-GLN-PRO-GLN-ARG-PHE-NH2
  • NPFF
  • NEUROPEPTIDE FF
  • H-PHE-LEU-PHE-GLN-PRO-GLN-ARG-PHE-NH2
  • F-8-F-NH2
  • ninamide
  • phenylalanyl-leucyl-phenylalanyl-glutaminyl-prolyl-glutaminyl-arginyl-phenylala
CAS:
99566-27-5
MF:
C54H76N14O10
MW:
1081.27
Product Categories:
  • Peptide
Mol File:
99566-27-5.mol
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NEUROPEPTIDE FF Chemical Properties

storage temp. 
−20°C
solubility 
Water: 1 mg/ml
form 
Solid
color 
White to off-white
Water Solubility 
Soluble to 0.50 mg/ml in water.
Sequence
Phe-Leu-Phe-Gln-Pro-Gln-Arg-Phe-NH2
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Safety Information

WGK Germany 
3

MSDS

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NEUROPEPTIDE FF Usage And Synthesis

Description

Neuropeptide FF (NPFF) is a peptide expressed in the brain and spinal cord that shares a precursor protein with neuropeptide AF. NPFF is expressed primarily in the posterior pituitary, hypothalamus, and medulla. It is an agonist at NPFF1 and NPFF2 receptors (Kis = 2.82 and 0.21 nM, respectively, for human recombinant receptors) that inhibits forskolin-induced cAMP production in CHO cells (EC50s = 236 and 2.3 nM, respectively). NPFF activates parvocellular neurons in the paraventricular nucleus (PVN) of the hypothalamus to stimulate oxytocin release from their projections in the brain stem, thereby regulating baroreflex control of heart rate. However, it inhibits magnocellular PVN neurons by enhancing GABAergic input. It is also found in plasma and exogenous administration briefly increases mean arterial pressure (MAP) by 40 mm Hg in rats, an effect that is only partially blocked by the norepinephrine competitor guanethidine and the α1-adrenergic receptor antagonist prazosin . NPFF has anti-opioid effects in rodent models, inhibiting morphine-induced analgesia and inducing abstinence in morphine-tolerant rats. It also inhibits acquisition of conditioned place preference to cocaine in rats when administered at doses of 10 and 20 nmol.

Uses

Endogenous antiopioid peptide and agonist at NPFF1 and NPFF2 receptors (Ki values are 2.82 and 0.21 nM respectively). Exhibits anorexigenic effects.

storage

Store at -20°C

References

[1] PERTTI PANULA  Krzysztof W ?  Antti A Aarnisalo. Neuropeptide FF, a mammalian neuropeptide with multiple functions[J]. Progress in Neurobiology, 1996, 48 4: Pages 461-479, 481-487. DOI: 10.1016/0301-0082(96)00001-9
[2] CATHERINE MOLLEREAU . Pharmacological characterization of human NPFF1 and NPFF2 receptors expressed in CHO cells by using NPY Y1 receptor antagonists[J]. European journal of pharmacology, 2002, 451 3: Pages 245-256. DOI: 10.1016/s0014-2999(02)02224-0
[3] JACK H JHAMANDAS V G. Role of neuropeptide FF in central cardiovascular and neuroendocrine regulation.[J]. ACS Applied Electronic Materials, 2013: 8. DOI: 10.3389/fendo.2013.00008
[4] BRYAN L. ROTH . Elevation of arterial pressure in rats by two new vertebrate peptides FLF QPQRF-NH2 and AGE GLSSPFWSLAAPQRF-NH2 which are immunoreactive to FMRF-NH2 antiserum[J]. Neuropeptides, 1987, 10 1: Pages 37-42. DOI: 10.1016/0143-4179(87)90087-4
[5] QINGYUN LIU. Identification and Characterization of Novel Mammalian Neuropeptide FF-like Peptides That Attenuate Morphine-induced Antinociception*[J]. The Journal of Biological Chemistry, 2001, 25 1: 36961-36969. DOI: 10.1074/jbc.m105308200
[6] JOLANTA KOTLINSKA  Jerzy S  Agnieszka Pachuta. Neuropeptide FF (NPFF) reduces the expression of cocaine-induced conditioned place preference and cocaine-induced sensitization in animals[J]. Peptides, 2008, 29 6: Pages 933-939. DOI: 10.1016/j.peptides.2008.01.008

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