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Gonadorelin

Gonadorelin

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Substance Overview and History

Gonadorelin, a synthetic decapeptide, functions as a gonadotropin-releasing hormone (GnRH) agonist. Comprising ten amino acids joined in sequence, including pyroglutamyl, histidyl, and glycinamide residues, it is synthesized using solid-phase peptide synthesis. Gonadorelin plays a pivotal role in stimulating the release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) from the anterior pituitary. Acting through transmembrane LHRH receptors on pituitary gonadotropic cells, gonadorelin triggers gonadotropin secretion. However, continuous administration induces desensitization, exerting a negative feedback effect. Clinically, gonadorelin is utilized to manage hypothalamic amenorrhea and to evaluate hypothalamic or pituitary function, reflecting its versatility as a hormone therapy agent.

References:

National Center for Biotechnology Information. "PubChem Compound Summary for CID 638793, Gonadorelin" PubChem

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FAQ
What is Gonadorelin?
Gonadorelin is a synthetic decapeptide that acts as a gonadotropin-releasing hormone (GnRH) agonist, stimulating the release of follicle-stimulating hormone (FSH) and luteinizing hormone (LH) from the anterior pituitary.
References:

National Center for Biotechnology Information. "PubChem Compound Summary for CID 638793, Gonadorelin" PubChem

How does Gonadorelin work?
Gonadorelin binds to luteinizing hormone-releasing hormone (LHRH) receptors on pituitary gonadotropic cells, promoting the synthesis and secretion of gonadotropins.
References:

National Center for Biotechnology Information. "PubChem Compound Summary for CID 638793, Gonadorelin" PubChem

What is the structure of Gonadorelin?
Gonadorelin is a decapeptide comprising ten amino acids, including pyroglutamyl, histidyl, tryptophyl, seryl, and glycinamide residues, linked in sequence.
References:

National Center for Biotechnology Information. "PubChem Compound Summary for CID 638793, Gonadorelin" PubChem