Compound ID | 2080
Synonym(s): Sulfaperin
Class: Antibacterial sulfonamide (sulfa drug)
Spectrum of activity: | Gram-positive & Gram-negative |
Details of activity: | Sulphonamides are structural analogues of p-aminobenzoic acid and act as competitive inhibitors (and alternate substrates) of dihydropteroate synthase (DHPS) to block the synthesis of folic acid. Primarily bacteriostatic; rapid emergence of resistance. |
Description: | Synthetic sufanilamide derivative; long-acting (~7 days). |
Year first mentioned: | 1946 |
Development status: | Discontinued |
Chemical structure(s): | |
Canonical SMILES: | CC1=CN=C(N=C1)NS(=O)(=O)C2=CC=C(C=C2)N |
Isomeric SMILES: | CC1=CN=C(N=C1)NS(=O)(=O)C2=CC=C(C=C2)N |
InChI: | InChI=1S/C11H12N4O2S/c1-8-6-13-11(14-7-8)15-18(16,17)10-4-2-9(12)3-5-10/h2-7H,12H2,1H3,(H,13,14,15) |
InChI Key: | DZQVFHSCSRACSX-UHFFFAOYSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/68933 |
External links: | |
Guide to Pharmacology: | sulfaperin |
Main Source: | https://pubmed.ncbi.nlm.nih.gov/7447603/ |