About 13 results found for searched term "Neuropeptide FF" (0.127 seconds)
| Cat.No. | Name | Target |
|---|---|---|
| M53030 | Neuropeptide FF (5-8) | Neuropeptide Receptor |
| Neuropeptide FF (5-8) is a Neuropeptide FF-related peptide. | ||
| M54443 | Neuropeptide FF | Neuropeptide Receptor |
| Neuropeptide FF (NPFF), an octapeptide belonging to the RF-amide family of peptides, interacts with two distinct G-protein-coupled receptors, NPFF(1) and NPFF(2). | ||
| M6303 | JNJ-31020028 | Neuropeptide Receptor |
| JNJ-31020028 is a selective brain penetrant antagonist of neuropeptide Y2 receptor with high affinity(pIC50=8.07, human; pIC50=8.22 rat); >100-fold selective versus human Y1/Y4/Y5 receptors. | ||
| M7629 | BIBP3226 TFA | Neuropeptide Receptor |
| BIBP3226 TFA is a novel, selective non-peptide neuropeptide Y Y1 receptor antagonist, with Ki values of 1.1, 79, and 108 nM for rNPY Y1, hNPFF2, and rNPFF, respectively. | ||
| M11364 | α-MSH TFA | Melanocortin Receptor |
| alpha-MSH Trifluoroacetate; α-Melanocyte-stimulating hormone TFA, | ||
| As an endogenous neuropeptide, alpha-melanocyte-stimulating hormone (TFA) is an endogenous melanocortin receptor 4 (MC4R) agonist with anti-inflammatory and antipyretic effects. α-MSH TFA is a posttranslational derivative of preopelanocorticoid (POMC). | ||
| M25543 | GR231118 | Neuropeptide Receptor |
| 1229U91; GW1229 | ||
| GR231118, an analogue of the C-terminus of neuropeptide Y, is a potent, competitive and relative seletive antagonist at human neuropeptide Y Y receptor with a pKi of 10.4. GR231118 a potent agonist at the human neuropeptide Y Y4 receptor (pEC50=8.6; pKi=9.6) and a weak agonist at the human and rat neuropeptide YY2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide Y Y6 receptor (pKi= 8.8). | ||
| M25544 | GR231118 TFA | Neuropeptide Receptor |
| 1229U91 TFA; GW1229 TFA | ||
| GR231118 TFA, an analogue of the C-terminus of neuropeptide Y, is a potent, competitive and relative seletive antagonist at human neuropeptide YY receptor with a pKi of 10.4. GR231118 a potent agonist at the human neuropeptide YY4 receptor (pEC50=8.6; pKi=9.6) and a weak agonist at the human and rat neuropeptide Y Y2 and Y5 receptors. GR231118 also has high affinity for the mouse neuropeptide YY6 receptor (pKi= 8.8). | ||
| M28638 | BIBP3226 | Neuropeptide Receptor |
| BIBP3226 is a potent and selective neuropeptide Y Y1 (NPY Y1) and neuropeptide FF (NPFF) receptor antagonist, with Kis of 1.1, 79, and 108 nM for rNPY Y1, hNPFF2, and rNPFF, respectively. BIBP3226 displays anxiogenic-like effect. | ||
| M29873 | Lu AA33810 | Neuropeptide Receptor |
| Lu AA33810 is a potent and selective antagonist of neuropeptide Y5 receptor with a Ki of 1.5 nM for the human receptor. Lu AA33810 exhibts antianxiolytic-like and antidepressant-like effects. | ||
| M53012 | Neuropeptide SF(mouse, rat) | Neuropeptide Receptor |
| Neuropeptide SF (mouse,rat) is a potent neuropeptide FF receptor agonist with Ki values are 48.4 nM and 12.1 nM for NPFF1 and NPFF2, respectively. | ||
| M53022 | Galanin (1-13)-Neuropeptide Y (25-36) amide | Neuropeptide Receptor |
| Galanin (1-13)-Neuropeptide Y (25-36) amide is a high-affinity ligand for galanin receptors, and galanin itself. | ||
| M53099 | Neuropeptide EI, rat | GPR/FFAR |
| Neuropeptide EI, rat displays functional melanin concentrating hormone (MCH)-antagonist and melanocyte-stimulating hormone (MSH) agonist activity in different behavioral paradigms. | ||
| M53286 | CART(62-76)(human, rat) | 5-HT Receptor |
| CART(62-76)(human,rat) is a neuropeptide (62-76 residues of the CART peptide) with neurotransmitter-like effects. | ||
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