Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  Biochemical Engineering >  Polypeptide >  NEUROPEPTIDE FF

NEUROPEPTIDE FF

Basic information Safety Supplier Related

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
More
Less

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.
More
Less

Safety Information

WGK Germany 
3

MSDS

More
Less

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

NEUROPEPTIDE FFSupplier

GL Biochem (Shanghai) Ltd
Tel
21-61263452 13641803416
Email
ymbetter@glbiochem.com
Shanghai Hanhong Scientific Co.,Ltd.
Tel
021-54306202 13764082696
Email
info@hanhongsci.com
Chemsky(shanghai)International Co.,Ltd.
Tel
021-50135380
Email
shchemsky@sina.com
Cellmano Biotech Limited
Tel
0551-65326643 18156095617
Email
info@cellmano.com
Nanjing Sunlida Biological Technology Co., Ltd.
Tel
025-57798810
Email
sales@sunlidabio.com