Probenecid drug data and news

Probenecid drug data, resources, and news articles (when available). Onconews.org provides news on cancer research. This section, which includes profiles on medicines that may or not be cancer-related is in beta form. If things run smoothly we will be releasing a new format late in the summer of 2006.

Generic name Probenecid
Brand Names/Synonyms Apurina; Benecid; Benemid; Benuryl; Col-Probenecid; Colbenemid; Ethamide; Polycillin-Prb; Principen W/ Probenecid; Probalan; Probampacin; Probecid; Proben; Proben-C; Probenecid; Probenecid Acid; Probenecid W/ Colchicine; Probenecid and Colchicine; Probenemid; Probexin; Prolongine; Synergid R; Tubophan; Uricosid
Indication For the treatment of gout and high levels of uric acid in the blood
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Description Not Available
Pharmacology Probenecid is a uricosuric and renal tubular blocking agent and is used in combination with colchicine to treat chronic gouty arthritis when complicated by frequent, recurrent acute attacks of gout. It inhibits the tubular reabsorption of urate, thus increasing the urinary excretion of uric acid and decreasing serum urate levels. Effective uricosuria reduces the miscible urate pool, retards urate deposition, and promotes resorption of urate deposits.
Mechanism Of Action Probenecid inhibits the tubular reabsorption of urate, thus increasing the urinary excretion of uric acid and decreasing serum urate levels.
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Dosage Forms TABLET
Drug_Category Uricosuric Agents; ATC:M04AB01
Absorption Not Available
Interactions Interactions for Probenecid:

When probenecid is used to elevate plasma concentrations of penicillin, or other beta-lactams, or when such drugs are given to patients taking probenecid therapeutically, high plasma concentrations of the other drug may increase the incidence of adverse reactions associated with that drug. In the case of penicillin, or other beta-lactams, psychic disturbances have been reported.

The use of salicylates antagonizes the uricosuric action of probenecid . The uricosuric action of probenecid is also antagonized by pyrazinamide.

Probenecid produces an insignificant increase in free sulfonamide plasma concentrations but a significant increase in total sulfonamide plasma levels. Since probenecid decreases the renal excretion of conjugated sulfonamides, plasma concentrations of the latter should be determined from time to time when a sulfonamide and probenecid and colchicine are co-administered for prolonged periods. Probenecid may prolong or enhance the action of oral sulfonylureas and thereby increase the risk of hypoglycemia.

It has been reported that patients receiving probenecid require significantly less thiopental for induction of anesthesia. In addition, ketamine and thiopental anesthesia were significantly prolonged in rats receiving probenecid.

The concomitant administration of probenecid increases the mean plasma elimination half-life of a number of drugs which can lead to increased plasma concentrations. These include agents such as indomethacin, acetaminophen, naproxen, ketoprofen, meclofenamate, lorazepam, and rifampin. Although the clinical significance of this observation has not been established, a lower dosage of the drug may be required to produce a therapeutic effect, and increases in dosage of the drug in question should be made cautiously and in small increments when probenecid is being co-administrated. Although specific instances of toxicity due to this potential interaction have not been observed to date, physicians should be alert to this possibility.

Probenecid given concomitantly with sulindac had only a slight effect on plasma sulfide levels, while plasma levels of sulindac and sulfone were increased. Sulindac was shown to produce a modest reduction in the uricosuric action of probenecid, which probably is not significant under most circumstances.

In animals and in humans, probenecid has been reported to increase plasma concentrations of methotrexate .

Falsely high readings for theophylline have been reported in an in vitro study, using the Schack and Waxler technique, when therapeutic concentrations of theophylline and probenecid were added to human plasma.

Toxicity Not Available
Organisms Affected Humans and other mammals
Chemical IUPAC Name 4-(dipropylsulfamoyl)benzoicacid
Chemical Formula C13H19NO4S
Molecular Weight 285.36 g/mol
Smiles String CCCN(CCC)S(=O)(=O)C1=CC=C(C=C1)C(=O)O
Melting Point 195 °C
Water Solubility 27.1 mg/L
State Solid
LogP/Hphobicity 2.324
Isoelectric Point 3.4
Biotransformation Not Available
Half Life 6-12 hours
Protein Binding [%] 75-95%
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Drug Reference http://www.drugs.com/cons/Probenecid.html
http://www.rxlist.com/cgi/generic/colbenemid.htm
Drug Type Approved Drug
Accession No APRD00167
CAS Registry Number 57-66-9
KEGG Compound ID C07372
PubChem ID SID:9576
PharmGKB ID PA451106
SwissProt ID Not Available
GenBank ID Not Available
Drug ID Number [DIN] 294926

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