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GPCR/G Protein
GnRH Receptor

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GnRH Receptor

Chemical Structure Cat. No. Product Name CAS No.
Opigolix Chemical Structure
BCP36620 Opigolix 912587-25-8
Opigolix, also known as ASP1707, is a small-molecule, non-peptide, orally active gonadotropin-releasing hormone antagonist (GnRH antagonist).
Alarelin Acetate Chemical Structure
BCP27725 Alarelin Acetate 79561-22-1
Alarelin acetate is a synthetic GnRH agonist.
Histrelin Chemical Structure
BCP27657 Histrelin 76712-82-8
Histrelin is a nonapeptide analog of GnRH (gonadotropin-releasing hormone) with added potency. When present in the bloodstream, it can act on gonadotropes. Histrelin can stimulate these cells to release luteinizing hormone and follicle-stimulating hormone. Histrelin is considered a GnRH agonist. It can be used for the treatment of menstruation disorders.
Abarelix Chemical Structure
BCP27629 Abarelix 183552-38-7
Abarelix is a potent gonadotrophin-releasing hormone (GnRH) antagonist, used for prostate cancer treatment.
Linzagolix choline Chemical Structure
BCP30450 Linzagolix choline 1321816-57-2
Linzagolix choline is a small-molecule, non-peptide, orally active gonadotropin-releasing hormone antagonist (GnRH antagonist).
Linzagolix Chemical Structure
BCP30444 Linzagolix 935283-04-8
Linzagolix is a gonadotrophin releasing hormone (GnRH) antagonist.
Histrelin Acetate Chemical Structure
BCP19027 Histrelin Acetate 220810-26-4
Histrelin acetate is a nonapeptide analog of gonadotropin-releasing hormone (GnRH) with added potency.
Fertirelin acetate Chemical Structure
BCP19026 Fertirelin acetate 66002-66-2
Fertirelin Acetate is a gonadotropin-releasing hormone (GnRH) agonists that induces estrus in dogs and cats .
Nafarelin Acetate Chemical Structure
BCP19032 Nafarelin Acetate 86220-42-0
Nafarelin Acetate is the acetate salt form of nafarelin, a modified synthetic porcine luteinizing hormone (LH)-releasing hormone peptide analog, with gonadotropin-releasing hormone (GnRH) agonist activity.
Relugolix Chemical Structure
BCP21587 Relugolix 737789-87-6
Relugolix is an orally available, non-peptide gonadotropin-releasing hormone (GnRH or luteinizing hormone-releasing hormone (LHRH)) antagonist, with potential antineoplastic activity.
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