Sulfamethizole
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Also known as MicrosulMethazolNSC-757327ProklarSulfamethizolSulfametizolSulphamethylthiadiazoleThiosulfilTetracidUrolucosilSulfamethiazoleSID17389528SID856011SID11112301SID144203976SID174006999SID170465369SID144208233
Summary
Sulfamethizole (CHEMBL1191) is an approved small-molecule antimicrobial agent (ATC S01AB01); indicated across 3 conditions including bacterial infectious disease and eye infectious disorder.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: S01AB01 (+3 more)
- Indications: 3 conditions
- Chemistry: 270.3 Da · C9H10N4O2S2
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL1191 |
| Name | Sulfamethizole |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 5328 |
| ChEBI | CHEBI:9331 |
| ATC | S01AB01, D06BA04, J01EB02, B05CA04 |
| Molecular formula | C9H10N4O2S2 |
| Molecular weight | 270.3 |
| InChIKey | VACCAVUAMIDAGB-UHFFFAOYSA-N |
SMILES: CC1=NN=C(S1)NS(=O)(=O)C2=CC=C(C=C2)N
IUPAC name: 4-amino-N-(5-methyl-1,3,4-thiadiazol-2-yl)benzenesulfonamide
ChEBI definition: A sulfonamide consisting of a 1,3,4-thiadiazole nucleus with a methyl substituent at C-5 and a 4-aminobenzenesulfonamido group at C-2.
Pharmacological roles (ChEBI): antimicrobial agent, EC 2.5.1.15 (dihydropteroate synthase) inhibitor, antiinfective agent, drug allergen.
Also known as: Microsul, Methazol, NSC-757327, Proklar, Sulfamethizol, Sulfamethizole, Sulfametizol, Sulphamethylthiadiazole, Thiosulfil, Tetracid, Urolucosil, Sulfamethiazole
Patent coverage: 5,085 distinct patent families (16,793 SureChEMBL compound mentions), from 1 matched compound structure(s). 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: 4 (assay-derived). Sample: Prelamin-A/C, Beta-lactamase, Aldehyde dehydrogenase 1A1, Lethal factor.
Bioactivity
ChEMBL activities: 1 potent at pChembl ≥ 5 of 4 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| LMNA | 5.35 | Potency | 4467 | nM | CHEMBL_ACT_3652140 |
Target pathways
No target-pathway data for this drug (no mapped target genes).
Indications & clinical
Indications
3 indications (2 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 |
|---|---|---|---|
| bacterial infectious disease | 4 | MONDO:0005113 | EFO:0000771 |
| eye infectious disorder | 4 | MONDO:0043885 | EFO:1001888 |
| osteomyelitis | 0 | MONDO:0005246 | EFO:0003102 |
Clinical trials
Total trials: 0.
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).