Methyclothiazide
drugOn this page
Also known as AquatensenEnduronMethyclothiazide component of enduronylMethyclothiazide component of eutronMeticlotiazidaNSC-110431SID92764517SID50112700SID144206003METHYLCLOTHIAZIDESID170465243MethyclothiazideÊMethyclothiazideÂ
Summary
Methyclothiazide (CHEMBL1577) is an approved small molecule (ATC C03AA08); indicated across 1 condition including cardiovascular disorder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: C03AA08
- Indications: 1 condition
- Clinical trials: 1
- Chemistry: 360.2 Da · C9H11Cl2N3O4S2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1577 |
| Name | Methyclothiazide |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 4121 |
| ATC | C03AA08 |
| Molecular formula | C9H11Cl2N3O4S2 |
| Molecular weight | 360.2 |
| InChIKey | CESYKOGBSMNBPD-UHFFFAOYSA-N |
SMILES: CN1C(NC2=CC(=C(C=C2S1(=O)=O)S(=O)(=O)N)Cl)CCl
IUPAC name: 6-chloro-3-(chloromethyl)-2-methyl-1,1-dioxo-3,4-dihydro-1lambda6,2,4-benzothiadiazine-7-sulfonamide
Also known as: Aquatensen, Enduron, Methyclothiazide, Methyclothiazide component of enduronyl, Methyclothiazide component of eutron, Meticlotiazida, NSC-110431, METHYCLOTHIAZIDE, SID92764517, SID50112700, methyclothiazide, SID144206003
Patent coverage: 2,269 distinct patent families (7,322 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 7,284 (99%) 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: 2 (assay-derived). Sample: Muscarinic acetylcholine receptor M1, Alpha-1A adrenergic receptor.
Bioactivity
No ChEMBL bioactivity rows at pChembl ≥ 5 (expected for biologics / antibodies).
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
1 indication (1 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 |
|---|---|---|---|
| cardiovascular disorder | 4 | MONDO:0004995 | EFO:0000319 |
Clinical trials
Total trials: 1.
Phase distribution
| Phase | Trials |
|---|---|
| PHASE4 | 1 |
Top trials by phase / activity
| NCT | Phase | Status | Title |
|---|---|---|---|
| NCT00208442 | PHASE4 | COMPLETED | A Randomised Single Centre Study to Compare the Long-term Wear Characteristics of Marathon™ and Enduron™ Polyethylene Cup Liners in Primary Total Hip Replacement |
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).
Related Atlas pages
- Diseases: cardiovascular disorder