Sulfapyridine
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Also known as Concord 693CoccoclaseDagenanEubasinNSC-41791NSC-4753PiridazolSulfapiridinaSulfanilamidopyridineSID26746948SID855656SID11112302SID174006222SID144203977SID170464707
Summary
Sulfapyridine (CHEMBL700) is an approved small-molecule antiinfective agent (ATC J01EB04); indicated across 1 condition including bacterial infectious disease.
At a glance
- Status: Approved (max clinical phase 4)
- Modality: Small molecule
- ATC class: J01EB04
- Indications: 1 condition
- Chemistry: 249.29 Da · C11H11N3O2S
Identifiers
Drug identity and classification
| Field | Value |
|---|---|
| ChEMBL ID | CHEMBL700 |
| Name | Sulfapyridine |
| Type | Small molecule |
| Max phase | 4 |
| FDA approved | no |
| PubChem CID | 5336 |
| ChEBI | CHEBI:132842 |
| ATC | J01EB04 |
| Molecular formula | C11H11N3O2S |
| Molecular weight | 249.29 |
| InChIKey | GECHUMIMRBOMGK-UHFFFAOYSA-N |
SMILES: C1=CC=NC(=C1)NS(=O)(=O)C2=CC=C(C=C2)N
IUPAC name: 4-amino-N-pyridin-2-ylbenzenesulfonamide
ChEBI definition: A sulfonamide consisting of pyridine with a 4-aminobenzenesulfonamido group at the 2-position.
Pharmacological roles (ChEBI): antiinfective agent, dermatologic drug, drug allergen.
Also known as: Concord 693, Coccoclase, Dagenan, Eubasin, NSC-41791, NSC-4753, Piridazol, Sulfapiridina, Sulfapyridine, Sulfanilamidopyridine, sulfapyridine, SID26746948
Parent form; salt/anhydrous children: CHEMBL2105500
Patent coverage: 2,219 distinct patent families (6,755 SureChEMBL compound mentions), from 2 matched compound structure(s). One matched structure accounts for 6,742 (100%) 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: 5 (assay-derived). Sample: Survival motor neuron protein, 4’-phosphopantetheinyl transferase ffp, Ferritin light chain, Beta-lactamase, Cruzipain.
Bioactivity
ChEMBL activities: 3 potent at pChembl ≥ 5 of 5 total. Top 30 by potency (10 = 0.1 nM, 6 = 1 µM):
| Target | pChembl | Type | Value | Unit | Activity ID |
|---|---|---|---|---|---|
| Q9F4F7 | 6.2 | Potency | 631 | nM | CHEMBL_ACT_4372660 |
| P25779 | 5.6 | Potency | 2512 | nM | CHEMBL_ACT_3992268 |
| P02791 | 5.2 | Potency | 6310 | nM | CHEMBL_ACT_4477834 |
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 |
|---|---|---|---|
| bacterial infectious disease | 4 | MONDO:0005113 | EFO:0000771 |
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, but PharmGKB curates 0 clinical and 10 variant annotation(s) for this drug (gene-keyed; see PharmGKB).
Related molecules
Related molecules
No competitor molecules sharing a primary target (ChEMBL phase ≥2 or PubChem drug-class).
Related Atlas pages
- Diseases: bacterial infectious disease