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Gonadorelin

SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS

Also known as: fertagyl, gonadorelin acetate, gonadorelin diacetate tetrahydrate, gonadorelin HCl, gonadorelin hydrochloride, hypocrine, Luteinizing hormone-releasing factor (swine)

OfmFDA approvedATC H01CA01ATC V04CM01

Data last refreshed: (DrugCentral release 2024-11-01)

Key facts

Gonadorelin is an ofm drug catalogued in DrugCentral. It was first approved by the FDA in 1982. DrugCentral lists 3 molecular targets, including Lhcgr, Gnrhr and GNRHR. Recorded indications include Amenorrhea and Diagnostic Test for Gonadotropin Deficiency.

  • Approval status: ofm (first approved 1982 by the FDA).
  • Molecular targets: Lhcgr, Gnrhr and GNRHR (3 listed in DrugCentral).
  • Indications: Amenorrhea and Diagnostic Test for Gonadotropin Deficiency.
  • ATC code: H01CA01 (Gonadotropin-releasing hormones).
  • Molecular formula: C55H75N17O13; molecular weight 1182.31 g/mol.

Indications & contraindications

Drug–disease relationships curated by DrugCentral (OMOP / SNOMED concepts).

Indications (2)

  • Amenorrhea
  • Diagnostic Test for Gonadotropin Deficiency

Mechanism & targets

Molecular targets (3)

TargetGeneActionActivity
Lutropin-choriogonadotropic hormone receptorLhcgrunknownKi 8.90
Gonadotropin-releasing hormone receptorGnrhrunknownIC50 8.70
Gonadotropin-releasing hormone receptorGNRHRagonistIC50 8.00

Regulatory approvals (1)

DateAgencyMarketed asApplicantOrphan
1982-09-30FDA——

ATC classification

ATC codeTherapeutic hierarchy
H01CA01SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS › PITUITARY AND HYPOTHALAMIC HORMONES AND ANALOGUES › HYPOTHALAMIC HORMONES › Gonadotropin-releasing hormones
V04CM01VARIOUS › DIAGNOSTIC AGENTS › OTHER DIAGNOSTIC AGENTS › Tests for fertility disturbances

Reported adverse-event signals

Strongest FDA FAERS disproportionality signals (log-likelihood ratio). A signal is a statistical association in spontaneous reports, not proof that the drug causes the event.

MedDRA termLLR
Metastases to bone202.0
Neutropenia197.7
Ovarian hyperstimulation syndrome133.3
Malignant neoplasm progression115.2
Carcinoembryonic antigen increased78.7
Carbohydrate antigen 15-3 increased61.5
Metastases to lymph nodes55.9
Hot flush54.9
Alanine aminotransferase increased54.7
Bone lesion51.6
Metastases to liver51.3
Radiation fibrosis - lung50.5

Chemical structure

Full physicochemical, ADMET and 3D-structure analysis of Gonadorelin is on its molecule page.

Molecular formulaC55H75N17O13
Molecular weight1182.31 g/mol
CAS number33515-09-2
InChIKeyXLXSAKCOAKORKW-AQJXLSMYSA-N
PubChem CID638793
CC(C)C[C@H](NC(=O)CNC(=O)[C@H](CC1=CC=C(O)C=C1)NC(=O)[C@H](CO)NC(=O)[C@H](CC1=CNC2=C1C=CC=C2)NC(=O)[C@H](CC1=CNC=N1)NC(=O)[C@@H]1CCC(=O)N1)C(=O)N[C@@H](CCCNC(N)=N)C(=O)N1CCC[C@H]1C(=O)NCC(N)=O

Frequently asked questions

Answers are generated from the structured data on this page, not written by hand.

What is Gonadorelin used for?

DrugCentral lists the following indications for Gonadorelin: Amenorrhea and Diagnostic Test for Gonadotropin Deficiency.

How does Gonadorelin work?

Its molecular targets in DrugCentral include Lhcgr, Gnrhr and GNRHR (agonist).

When was Gonadorelin first approved?

Gonadorelin was first approved by the FDA in 1982.

What is the chemical formula of Gonadorelin?

Gonadorelin has the molecular formula C55H75N17O13 and a molecular weight of 1182.31 g/mol.

Browse: all drugs starting with G · drug guides by category · protein targets A–Z.

Sources

How this page is built: methodology · editorial policy & corrections.

For research and educational use only — not medical advice. This page is compiled automatically from public databases. It is not written or reviewed by a clinician. Do not start, stop or change any treatment based on it; consult a qualified healthcare professional. Spotted an error? See our corrections policy or email hello@molforge.ai.

Quick facts

StatusOFM
First approval1982-09-30
AgencyFDA
Targets3
Indications2
FormulaC55H75N17O13
DrugCentral ID2958
Interactive profile