Quinagolide
drug drugOn this page
Also known as Quinagolida
Summary
Quinagolide (CHEMBL2218861) is an approved small molecule (ATC G02CB04); indicated across 1 condition including ovarian hyperstimulation syndrome.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: G02CB04
- Indications: 1 condition
- Clinical trials: 3
- Chemistry: 395.6 Da · C20H33N3O3S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL2218861 |
| Name | Quinagolide |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 55645 |
| ATC | G02CB04 |
| Molecular formula | C20H33N3O3S |
| Molecular weight | 395.6 |
| InChIKey | GDFGTRDCCWFXTG-UHFFFAOYSA-N |
SMILES: CCCN1CC(CC2C1CC3=C(C2)C(=CC=C3)O)NS(=O)(=O)N(CC)CC
IUPAC name: 3-(diethylsulfamoylamino)-6-hydroxy-1-propyl-3,4,4a,5,10,10a-hexahydro-2H-benzo[g]quinoline
Also known as: Quinagolida, Quinagolide, QUINAGOLIDE, quinagolide
Parent form; salt/anhydrous children: CHEMBL5316219
Patent coverage: 41 distinct patent families (86 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 73 (85%) of the total. Mentions count patents naming the compound (not distinct inventions), so promiscuous / reference molecules inflate the mention figure — families are the dedup metric.
Targets
Targets
Broader ChEMBL bioactivity targets: 18 (assay-derived). Sample: 5-hydroxytryptamine receptor 2B, Adrenergic receptor alpha-1, Alpha-2C adrenergic receptor, Alpha-2B adrenergic receptor, D(1A) dopamine receptor, Adrenergic receptor alpha-2, Serotonin (5-HT) receptor, Dopamine receptor, 5-hydroxytryptamine receptor 1A, D(2) dopamine receptor, Sodium-dependent noradrenaline transporter, 5-hydroxytryptamine receptor 2A, Alpha-1A adrenergic receptor, Histamine H1 receptor, D(3) dopamine receptor, Kappa-type opioid receptor, Voltage-gated inwardly rectifying potassium channel KCNH2, Nuclear receptor subfamily 1 group I member 2.
Bioactivity
ChEMBL activities: 32 potent at pChembl ≥ 5 of 37 total. Top 100 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| DRD3 | 8.55 | AC50 | 2.8 | nM | CHEMBL_ACT_25193307 |
| DRD2 | 7.82 | AC50 | 15.2 | nM | CHEMBL_ACT_25140108 |
| P20288 | 7.72 | IC50 | 19 | nM | CHEMBL_ACT_483401 |
| P20288 | 7.32 | IC50 | 48 | nM | CHEMBL_ACT_431525 |
| P20288 | 7.32 | IC50 | 48 | nM | CHEMBL_ACT_499772 |
| P20288 | 7.12 | IC50 | 75 | nM | CHEMBL_ACT_483402 |
| DRD1 | 6.82 | AC50 | 150 | nM | CHEMBL_ACT_25180304 |
| P20288 | 6.72 | IC50 | 190 | nM | CHEMBL_ACT_431526 |
| P20288 | 6.72 | IC50 | 190 | nM | CHEMBL_ACT_499773 |
| HTR2B | 6.49 | AC50 | 324.1 | nM | CHEMBL_ACT_25164046 |
| ADRA1A | 6.35 | AC50 | 450 | nM | CHEMBL_ACT_25229635 |
| HTR1A | 5.96 | AC50 | 1100 | nM | CHEMBL_ACT_25216807 |
| OPRK1 | 5.77 | AC50 | 1700 | nM | CHEMBL_ACT_25129226 |
| P08909 | 5.64 | IC50 | 2300 | nM | CHEMBL_ACT_483403 |
| NR1I2 | 5.57 | AC50 | 2700 | nM | CHEMBL_ACT_25188028 |
| HRH1 | 5.55 | AC50 | 2800 | nM | CHEMBL_ACT_25212285 |
| P08909 | 5.5 | IC50 | 3200 | nM | CHEMBL_ACT_483404 |
| HTR2B | 5.44 | AC50 | 3666 | nM | CHEMBL_ACT_25228500 |
| P08909 | 5.34 | IC50 | 4600 | nM | CHEMBL_ACT_431528 |
| P08909 | 5.34 | IC50 | 4600 | nM | CHEMBL_ACT_499775 |
| P08909 | 5.29 | IC50 | 5100 | nM | CHEMBL_ACT_431527 |
| P08909 | 5.29 | IC50 | 5100 | nM | CHEMBL_ACT_499774 |
| HTR2A | 5.25 | AC50 | 5600 | nM | CHEMBL_ACT_25224975 |
| P19328 | 5.25 | IC50 | 5600 | nM | CHEMBL_ACT_431529 |
| P19328 | 5.25 | IC50 | 5600 | nM | CHEMBL_ACT_499776 |
| P15823 | 5.22 | IC50 | 6000 | nM | CHEMBL_ACT_483406 |
| KCNH2 | 5.19 | AC50 | 6500 | nM | CHEMBL_ACT_25117543 |
| HTR2A | 5.19 | AC50 | 6400 | nM | CHEMBL_ACT_25226128 |
| NR1I2 | 5.14 | AC50 | 7200 | nM | CHEMBL_ACT_25224230 |
| P19328 | 5.13 | IC50 | 7400 | nM | CHEMBL_ACT_483405 |
| P15823 | 5.11 | IC50 | 7800 | nM | CHEMBL_ACT_431530 |
| P15823 | 5.11 | IC50 | 7800 | nM | CHEMBL_ACT_499777 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
1 disease in clinical trials (phase 1–3, investigational — not approved indications). Highest ChEMBL trial phase per disease; a non-cancer approved use is occasionally logged at phase 3 here.
| Disease (in trials) | Phase | MONDO | EFO |
|---|---|---|---|
| ovarian hyperstimulation syndrome | 2 | MONDO:0011972 | MONDO:0011972 |
Clinical trials
Total trials: 3.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE2 | 3 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00665041 | PHASE2 | COMPLETED | Tolerability of Quinagolide in a Dose-titration Regimen in Oocyte Donors at Risk of Developing Ovarian Hyperstimulation Syndrome |
| NCT03692403 | PHASE2 | COMPLETED | Randomized Trial Assessing Quinagolide Vaginal Ring for Endometriosis-related Pain |
| NCT03749109 | PHASE2 | COMPLETED | Quinagolide Vaginal Ring on Lesion Reduction Assessed by MRI in Women With Endometriosis/Adenomyosis |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No PharmGKB pharmacogenomic data curated for this drug.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- In clinical trials for: ovarian hyperstimulation syndrome