sulfisoxazole diolamine
An organoammonium salt obtained by combining equimolar amounts of sulfisoxazole and diethanolamine. It has antibiotic activity against a wide range of gram-negative and gram-positive organisms.
Machine-generated and unreviewed. Identity, structure and cross-references come straight from ChEBI's and CARD's own data; no curator has signed off on this record yet.
Classification
Chemical structure
| Molecular formula | C11H13N3O3S.C4H11NO2 |
|---|---|
| Charge | 0 |
| Average mass | 372.447 Da |
| Monoisotopic mass | 372.14674 Da |
| Source | ChEBI |
| InChIKey | FEPTXVIRMZIGFY-UHFFFAOYSA-N |
Cc1noc(NS(=O)(=O)c2ccc(N)cc2)c1C.OCCNCCO
InChI=1S/C11H13N3O3S.C4H11NO2/c1-7-8(2)13-17-11(7)14-18(15,16)10-5-3-9(12)4-6-10;6-3-1-5-2-4-7/h3-6,14H,12H2,1-2H3;5-7H,1-4H2
Also called
- 4-amino-N-(3,4-dimethyl-1,2-oxazol-5-yl)benzene-1-sulfonamide--2,2'-azanediyldi(ethan-1-ol) (1/1)
- Sulfafurazol 2,2'-imidodiethanol
- Sulfafurazole diolamine
- sulfisoxazole diethanolamine
Cross-references
- cas:4299-60-9
- reaxys:14856872
Drug registries
Activity roles
- antibacterial drug
CHEBI:36047
Source concepts
| Source | Native ID | Label | Minted CURIE | Version |
|---|---|---|---|---|
| CHEBI | CHEBI:88263 |
sulfisoxazole diolamine | antibioticmech:chebi-6baa7df085 |
2026-08-30 |
Mechanism summary
- Clinical status
- APPROVED
Curation history
-
SEEDED_FROM_SOURCES
Seeded from data/raw/ inventories (CHEBI)
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories
-
RESEEDED_FROM_SOURCES
Re-seeded from updated data/raw/ inventories