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)
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)
| Target | Gene | Action | Activity |
|---|---|---|---|
| Lutropin-choriogonadotropic hormone receptor | Lhcgr | unknown | Ki 8.90 |
| Gonadotropin-releasing hormone receptor | Gnrhr | unknown | IC50 8.70 |
| Gonadotropin-releasing hormone receptor | GNRHR | agonist | IC50 8.00 |
Regulatory approvals (1)
| Date | Agency | Marketed as | Applicant | Orphan |
|---|---|---|---|---|
| 1982-09-30 | FDA | — | — |
ATC classification
| ATC code | Therapeutic hierarchy |
|---|---|
H01CA01 | SYSTEMIC HORMONAL PREPARATIONS, EXCL. SEX HORMONES AND INSULINS › PITUITARY AND HYPOTHALAMIC HORMONES AND ANALOGUES › HYPOTHALAMIC HORMONES › Gonadotropin-releasing hormones |
V04CM01 | VARIOUS › 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 term | LLR |
|---|---|
| Metastases to bone | 202.0 |
| Neutropenia | 197.7 |
| Ovarian hyperstimulation syndrome | 133.3 |
| Malignant neoplasm progression | 115.2 |
| Carcinoembryonic antigen increased | 78.7 |
| Carbohydrate antigen 15-3 increased | 61.5 |
| Metastases to lymph nodes | 55.9 |
| Hot flush | 54.9 |
| Alanine aminotransferase increased | 54.7 |
| Bone lesion | 51.6 |
| Metastases to liver | 51.3 |
| Radiation fibrosis - lung | 50.5 |
Chemical structure
Full physicochemical, ADMET and 3D-structure analysis of Gonadorelin is on its molecule page.
| Molecular formula | C55H75N17O13 |
|---|---|
| Molecular weight | 1182.31 g/mol |
| CAS number | 33515-09-2 |
| InChIKey | XLXSAKCOAKORKW-AQJXLSMYSA-N |
| PubChem CID | 638793 |
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
- DrugCentral drug card 2958 — structure, indications, targets, approvals, pharmacologic classes (CC BY-SA 4.0)
- ChEMBL CHEMBL1007 — compound record and bioactivity
- PubChem CID 638793 — chemical identifiers
- DrugBank DB00644 — drug record
- FDA UNII 9O7312W37G — substance identity
- DailyMed: FDA labels for Gonadorelin — current prescribing information (label search)
- UniProt P30968 (GNRHR) — target protein
- FDA Adverse Event Reporting System (openFDA FAERS) — adverse-event signals, as aggregated by DrugCentral
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