| Quantity | 1 mg, 5 mg, 10 mg | 1 mg, 5 mg, 10 mg, 25 mg, 50 mg | 1 mg, 5 mg, 10 mg | 1 mg, 5 mg, 10 mg | 5 mg, 10 mg, 25 mg, 50 mg, 100 mg |
| Description | [S5K, F6Y, L9mL, M10Mox] neurokinin A (4–10) is a neuropeptide A analog and a peptide fragment of HY-P10746. [S5K, F6Y, L9mL, M10Mox] neurokinin A (4–10) is highly selective for mouse tachykinin receptors and human tachykinin receptor NK1R and has an in vivo half-life of 10.3 hours in [S5K, F6Y, L9mL, M10Mox] neurokinin A (4–10) is a neuropeptide A analog and a peptide fragment of HY-P10746. [S5K, F6Y, L9mL, M10Mox] neurokinin A (4–10) is highly selective for mouse tachykinin receptors and human tachykinin receptor NK1R and has an in vivo half-life of 10.3 hours in mice[1]... Read More | Argipressin (Arg8-vasopressin) binds to the V1, V2, V3-vascular arginine vasopressin receptor, with a Kd value of 1.31 nM in A7r5 rat aortic smooth muscle cells for V1 | BAM(8-22), a proteolytically cleaved product of proenkephalin A, is a potent activator of Mas-related G-protein-coupled receptors (Mrgprs), MrgprC11 and hMrgprX1, and induces scratching in mice in an Mrgpr-dependent manner[1] | Calcitonin (human) is a hypocalcemic hormone. Calcitonin can lower blood calcium levels and inhibit bone resorption. Calcitonin can be used in hypercalcemia or osteoporosis research[1][2][3] | Vapreotide is a neurokinin-1 (NK1) receptor antagonist, with an IC50 of 330 nM |