NEUROPEPTIDE FF manufacturers
- NEUROPEPTIDE FF
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- $1.00
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2020-03-06
- CAS:99566-27-5
- Min. Order: 1g
- Purity: ≥98%
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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 | | EINECS: | | | Product Categories: | Peptide | | Mol File: | 99566-27-5.mol |  |
| | 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 |
| | 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 |
| | NEUROPEPTIDE FF Preparation Products And Raw materials |
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