GH-1 inhibitors, classified within the realm of bioactive compounds, constitute a chemical category engineered to influence the function of growth hormone-1 (GH-1), also recognized as somatotropin or growth hormone. GH-1, a peptide hormone, is manufactured and discharged by the anterior pituitary gland situated in the brain. Its principal role is to encourage growth, cellular replication, and regeneration. GH-1's biological actions hinge upon its interaction with specific receptors on target cells, predominantly in the liver, where it stimulates the production of insulin-like growth factor-1 (IGF-1), a pivotal mediator of numerous physiological effects. GH-1 inhibitors are purposefully crafted to impede this process by either obstructing GH-1 from attaching to its receptors or inhibiting downstream signaling pathways.
Structurally, GH-1 inhibitors exhibit diverse forms, encompassing small molecules, peptides, or antibodies. Small molecule GH-1 inhibitors typically focus on the GH-1 receptor or molecules involved in subsequent signaling cascades, whereas peptide-based inhibitors may imitate fragments of the GH-1 molecule to compete for receptor binding. The primary aim of GH-1 inhibition revolves around regulating excessive or aberrant GH-1 secretion, as imbalances in GH-1 levels can lead to various medical conditions, such as gigantism (excessive GH-1 during childhood) or acromegaly (excessive GH-1 during adulthood). Furthermore, GH-1 inhibitors find utility in research contexts to delve into the intricate signaling pathways underlying growth hormone regulation, contributing to a deeper comprehension of growth-related disorders.
| Product Name | CAS # | Catalog # | QUANTITY | Price | Citations | RATING |
|---|---|---|---|---|---|---|
13C6-Lys octreotide tri(trifluoroacetate) | 83150-76-9 (unlabeled free base) | sc-477942 | 500 µg | $396.00 | ||
Octreotide is a somatostatin analog that binds to somatostatin receptors on pituitary cells. This inhibits GH secretion by the pituitary gland, reducing GH levels in the blood. | ||||||
Bromocriptine | 25614-03-3 | sc-337602A sc-337602B sc-337602 | 10 mg 100 mg 1 g | $57.00 $265.00 $567.00 | 4 | |
Bromocriptine is a dopamine receptor agonist that inhibits GH secretion by stimulating dopamine receptors on pituitary lactotrophs, reducing GH release. | ||||||
Cabergoline | 81409-90-7 | sc-203864 sc-203864A | 10 mg 50 mg | $300.00 $1055.00 | ||
Cabergoline, like bromocriptine, is a dopamine receptor agonist that inhibits GH secretion by acting on dopamine receptors and reducing pituitary GH release. | ||||||
Anamorelin | 249921-19-5 | sc-480157 | 10 mg | $260.00 | ||
Anamorelin is a selective ghrelin receptor agonist that activates the GHS-R1a receptor, stimulating GH release from the pituitary gland through the ghrelin pathway. | ||||||