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Renoquid: Full Drug Profile

Medically reviewed by Min Clinic Staff | Updated: January 2026

Renoquid - General Information

Renoquid is a short-acting sulfonamide. The sulfonamides are synthetic bacteriostatic antibiotics with a wide spectrum against most gram-positive and many gram-negative organisms. However, many strains of an individual species may be resistant. Sulfonamides inhibit multiplication of bacteria by acting as competitive inhibitors of p-aminobenzoic acid in the folic acid metabolism cycle. Bacterial sensitivity is the same for the various sulfonamides, and resistance to one sulfonamide indicates resistance to all. Most sulfonamides are readily absorbed orally. However, parenteral administration is difficult, since the soluble sulfonamide salts are highly alkaline and irritating to the tissues. The sulfonamides are widely distributed throughout all tissues. High levels are achieved in pleural, peritoneal, synovial, and ocular fluids. Although these drugs are no longer used to treat meningitis, CSF levels are high in meningeal infections.
Renoquid is a competitive inhibitor of the enzyme dihydropteroate synthetase. It inhibits bacterial synthesis of of dihydrofolic acid by preventing the condensation of the pteridine with para-aminobenzoic acid (PABA), a substrate of the enzyme dihydropteroate synthetase. The inhibited reaction is necessary in these organisms for the synthesis of folic acid.

 

Pharmacology of Renoquid

Renoquid is a short-acting sulfonamide. The sulfonamides are synthetic bacteriostatic antibiotics with a wide spectrum against most gram-positive and many gram-negative organisms. However, many strains of an individual species may be resistant. Sulfonamides inhibit multiplication of bacteria by acting as competitive inhibitors of p-aminobenzoic acid in the folic acid metabolism cycle. Bacterial sensitivity is the same for the various sulfonamides, and resistance to one sulfonamide indicates resistance to all. Most sulfonamides are readily absorbed orally. However, parenteral administration is difficult, since the soluble sulfonamide salts are highly alkaline and irritating to the tissues. The sulfonamides are widely distributed throughout all tissues. High levels are achieved in pleural, peritoneal, synovial, and ocular fluids. Although these drugs are no longer used to treat meningitis, CSF levels are high in meningeal infections. Their antibacterial action is inhibited by pus.

 

Additional information about Renoquid

Renoquid Indication

Used orally in the treatment of acute urinary tract infections.

Mechanism Of Action
Renoquid is a competitive inhibitor of the enzyme dihydropteroate synthetase. It inhibits bacterial synthesis of of dihydrofolic acid by preventing the condensation of the pteridine with para-aminobenzoic acid (PABA), a substrate of the enzyme dihydropteroate synthetase. The inhibited reaction is necessary in these organisms for the synthesis of folic acid.
Generic Name
Sulfacytine
Synonyms
1-ethyl N4-sulfanilylcytosin; 1-ethyl-N-sulfanilylcytosine; N-sulfanilyl-l-ethylcytosine; Sulfacitina [inn-spanish]; Sulfacitinum [inn-latin]
Drug Category
Anti-Infective Agents, Urinary; Sulfonamides
Drug Type
Small Molecule; Approved
Other Brand Names containing Sulfacytine
Renoquid;
Absorption
Well absorbed following oral administration.
Dosage Forms of Renoquid
Tablet Oral
Chemical IUPAC Name
4-amino-N-(1-ethyl-2-oxopyrimidin-4-yl)benzenesulfonamide
Chemical Formula
C12H14N4O3S
Organisms Affected
Bacteria