Compound ID | 2084
Synonym(s): Marfanil | sulfamylon | ambamide | Homosulfanilamide
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: Topical use in burn infections. |
Year first mentioned: | 1948 |
Development status: | Approved, off-patent |
Chemical structure(s): | |
Canonical SMILES: | C1=C(C=CC(=C1)S(=O)(=O)N)CN |
Isomeric SMILES: | C1=CC(=CC=C1CN)S(=O)(=O)N |
InChI: | InChI=1S/C7H10N2O2S/c8-5-6-1-3-7(4-2-6)12(9,10)11/h1-4H,5,8H2,(H2,9,10,11) |
InChI Key: | TYMRLRRVMHJFTF-UHFFFAOYSA-N |
Structure link: | https://pubchem.ncbi.nlm.nih.gov/compound/3998 |
External links: | |
Guide to Pharmacology: | mafenide |
Main Source: | https://pubmed.ncbi.nlm.nih.gov/5576444/ |
Citation: | https://pubmed.ncbi.nlm.nih.gov/35143154/ |