Ensitrelvir
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Also known as S-217622
Summary
Ensitrelvir (CHEMBL5183847) is a phase-3 clinical-stage small molecule (ATC J05AE16); indicated across 5 conditions including severe acute respiratory syndrome and viral infectious disease.
At a glance
- Status: Max clinical phase 3 (not approved)
- Modality: Small molecule
- ATC class: J05AE16
- Indications: 5 conditions
- Clinical trials: 7
- Chemistry: 531.9 Da · C22H17ClF3N9O2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL5183847 |
| Name | Ensitrelvir |
| Type | Small molecule |
| Max phase | 3 |
| FDA approved | no |
| PubChem CID | 162533924 |
| ATC | J05AE16 |
| Molecular formula | C22H17ClF3N9O2 |
| Molecular weight | 531.9 |
| InChIKey | QMPBBNUOBOFBFS-UHFFFAOYSA-N |
SMILES: CN1C=C2C=C(C(=CC2=N1)Cl)NC3=NC(=O)N(C(=O)N3CC4=CC(=C(C=C4F)F)F)CC5=NN(C=N5)C
IUPAC name: 6-[(6-chloro-2-methylindazol-5-yl)amino]-3-[(1-methyl-1,2,4-triazol-3-yl)methyl]-1-[(2,4,5-trifluorophenyl)methyl]-1,3,5-triazine-2,4-dione
Also known as: Ensitrelvir, S-217622, ENSITRELVIR
Parent form; salt/anhydrous children: CHEMBL5185221
Patent coverage: 65 distinct patent families (102 SureChEMBL compound mentions), from 3 matched compound structure(s). One matched structure accounts for 74 (73%) 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
Primary targets (GtoPdb curated mechanism): the Cancer dependency column is the DepMap CRISPR fitness signal (% of screened cell lines dependent on the target).
| Gene | Target | Action | pAffinity | Cancer dependency | UniProt |
|---|---|---|---|---|---|
| CoV 3C-like (main) protease | Inhibition | 7.89 |
Broader ChEMBL bioactivity targets: 1 (assay-derived). Sample: Replicase polyprotein 1ab.
Bioactivity
ChEMBL activities: 3 potent at pChembl ≥ 5 of 3 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| P0DTD1 | 10.89 | IC50 | 0.01 | nM | CHEMBL_ACT_24695396 |
| P0DTD1 | 8.22 | Kd | 6 | nM | CHEMBL_ACT_29060402 |
| P0DTD1 | 8 | IC50 | 10 | nM | CHEMBL_ACT_24771740 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
5 indications (0 at ChEMBL trial phase 4). Phase below is the highest clinical-trial phase recorded for this drug against each disease — not the molecule’s overall approval status (that is in the Summary).
| Indication | Trial phase | MONDO | EFO |
|---|---|---|---|
| severe acute respiratory syndrome | 3 | MONDO:0005091 | MONDO:0100096 |
| viral infectious disease | 3 | MONDO:0005108 | EFO:0000763 |
| liver disorder | 1 | MONDO:0005154 | EFO:0001421 |
| kidney disorder | 1 | MONDO:0005240 | EFO:0003086 |
1 further indication record had no mapped disease name (EFO/MeSH-only) or were duplicates, and are omitted.
Clinical trials
Total trials: 7.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE1 | 3 |
| PHASE3 | 2 |
| PHASE2 | 2 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT05305547 | PHASE3 | COMPLETED | A Study to Compare S-217622 With Placebo in Non-Hospitalized Participants With COVID-19 |
| NCT05897541 | PHASE3 | COMPLETED | Phase 3 Study of S-217622 in Prevention of Symptomatic SARS-CoV-2 Infection |
| NCT05041907 | PHASE2 | RECRUITING | Finding Treatments for COVID-19: A Trial of Antiviral Pharmacodynamics in Early Symptomatic COVID-19 (PLATCOV) |
| NCT06161688 | PHASE2 | ACTIVE_NOT_RECRUITING | Ensitrelvir for Viral Persistence and Inflammation in People Experiencing Long COVID |
| NCT05363215 | PHASE1 | COMPLETED | A Study to Assess S-217622 in Participants With Renal Impairment and Healthy Participants |
| NCT05409911 | PHASE1 | COMPLETED | A Study to Assess S-217622 in Participants With Mild and Moderate Hepatic Impairment and Healthy Control Participants |
| NCT06775730 | PHASE1 | COMPLETED | A Drug-Drug Interaction Study of S-217622 With Combined Oral Contraceptives in Healthy Adult Female Participants |
Clinical evidence (CIViC)
No CIViC predictive evidence (expected for non-precision-medicine drugs).
Pharmacology
Pharmacogenomics
No CPIC/DPWG dosing guideline or drug-level clinical/variant annotations in PharmGKB for this molecule.
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).