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Chemistry

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Also known as: 57-66-9, 4-(dipropylsulfamoyl)benzoic acid, Benemid, Probenecid acid, Probecid, Probalan
Molecular Formula
C13H19NO4S
Molecular Weight
285.36  g/mol
InChI Key
DBABZHXKTCFAPX-UHFFFAOYSA-N
FDA UNII
PO572Z7917

Probenecid
The prototypical uricosuric agent. It inhibits the renal excretion of organic anions and reduces tubular reabsorption of urate. Probenecid has also been used to treat patients with renal impairment, and, because it reduces the renal tubular excretion of other drugs, has been used as an adjunct to antibacterial therapy.
1 2D Structure

Probenecid

2 Identification
2.1 Computed Descriptors
2.1.1 IUPAC Name
4-(dipropylsulfamoyl)benzoic acid
2.1.2 InChI
InChI=1S/C13H19NO4S/c1-3-9-14(10-4-2)19(17,18)12-7-5-11(6-8-12)13(15)16/h5-8H,3-4,9-10H2,1-2H3,(H,15,16)
2.1.3 InChI Key
DBABZHXKTCFAPX-UHFFFAOYSA-N
2.1.4 Canonical SMILES
CCCN(CCC)S(=O)(=O)C1=CC=C(C=C1)C(=O)O
2.2 Other Identifiers
2.2.1 UNII
PO572Z7917
2.3 Synonyms
2.3.1 MeSH Synonyms

1. Benecid

2. Benemid

3. Benuryl

4. Pro-cid

5. Probecid

6. Probenecid Weimer

2.3.2 Depositor-Supplied Synonyms

1. 57-66-9

2. 4-(dipropylsulfamoyl)benzoic Acid

3. Benemid

4. Probenecid Acid

5. Probecid

6. Probalan

7. Benecid

8. Probenemid

9. Benuryl

10. Probexin

11. Prolongine

12. Tubophan

13. Uricosid

14. Apurina

15. P-(dipropylsulfamoyl)benzoic Acid

16. Proben

17. Synergid R

18. Probenecidum

19. Probenecida

20. Probenecide

21. 4-[(dipropylamino)sulfonyl]benzoic Acid

22. 4-((dipropylamino)sulfonyl)benzoic Acid

23. 4-(di-n-propylsulfamoyl)benzoesaeure

24. 4-(n,n-dipropylsulfamoyl)benzoesaeure

25. Nci-c56097

26. Benzoic Acid, 4-[(dipropylamino)sulfonyl]-

27. Benzoic Acid, P-(dipropylsulfamoyl)-

28. Probenate

29. 4-(n,n-dipropylsulfamoyl)benzoic Acid

30. P-(dipropylsulfamyl)benzoic Acid

31. Benzoic Acid, 4-((dipropylamino)sulfonyl)-

32. Nsc 18786

33. Chebi:8426

34. Probenecid (benemid)

35. Nsc-18786

36. Chembl897

37. Mls000028496

38. 4-dipropylsulfamoyl-benzoic Acid

39. Benemide

40. Probenid

41. Robenecid

42. Polycillin-brb

43. Po572z7917

44. Cas-57-66-9

45. Probenicid

46. Ncgc00016251-08

47. Smr000058280

48. Dsstox_cid_1188

49. Dsstox_rid_75998

50. Dsstox_gsid_21188

51. Probenecide [inn-french]

52. Probenecidum [inn-latin]

53. Probenecida [inn-spanish]

54. Benemid (tn)

55. Ccris 3643

56. Hsdb 3387

57. Sr-01000003108

58. Einecs 200-344-3

59. Mfcd00038402

60. Brn 2815775

61. Ai3-50078

62. Unii-po572z7917

63. Probenecid [usp:inn:ban:jan]

64. Prestwick_809

65. Spectrum_000834

66. Colbenemid (salt/mix)

67. Opera_id_677

68. Probenecid [mi]

69. Probenecid [inn]

70. Probenecid [jan]

71. Prestwick0_000542

72. Prestwick1_000542

73. Prestwick2_000542

74. Prestwick3_000542

75. Spectrum2_001294

76. Spectrum3_000554

77. Spectrum4_000486

78. Spectrum5_001419

79. Probenecid [hsdb]

80. Benemid; Benecid; Benuryl

81. Epitope Id:180853

82. Probenecid [mart.]

83. Schembl3663

84. Polycillin-prb (salt/mix)

85. Probenecid [usp-rs]

86. Probenecid [who-dd]

87. Probenecid [who-ip]

88. Bidd:pxr0092

89. Oprea1_416955

90. Wln: Qvr Dswn3&3

91. Bspbio_000583

92. Bspbio_002227

93. Kbiogr_000971

94. Kbioss_001314

95. Mls001076472

96. Bidd:gt0626

97. Divk1c_000056

98. Spectrum1500502

99. Spbio_001327

100. Spbio_002504

101. Bpbio1_000643

102. Gtpl4357

103. Probenecid (jp17/usp/inn)

104. Zinc1982

105. Dtxsid9021188

106. Probenecid [ep Impurity]

107. Probenecid [orange Book]

108. Hms500c18

109. Kbio1_000056

110. Kbio2_001314

111. Kbio2_003882

112. Kbio2_006450

113. Kbio3_001727

114. Amy8947

115. Probenecid [ep Monograph]

116. Probenecid [usp Impurity]

117. Ninds_000056

118. Hms1569n05

119. Hms1920j22

120. Hms2092c03

121. Hms2096n05

122. Hms2233n05

123. Hms3259g04

124. Hms3369l18

125. Hms3652o17

126. Hms3713n05

127. Hms3743e07

128. Hms3885i18

129. P-(dipropylsulfamoyl) Benzoic Acid

130. Pharmakon1600-01500502

131. Probenecid [usp Monograph]

132. Albb-025846

133. Bcp21785

134. Hy-b0545

135. Nsc18786

136. Probenecidum [who-ip Latin]

137. Str06053

138. Proben-c Component Probenecid

139. Tox21_110328

140. Tox21_202110

141. Tox21_302928

142. Bdbm50206509

143. Ccg-39232

144. Nsc757292

145. S4022

146. Stl229614

147. Colbenemid Component Probenecid

148. 4-dipropylsulfamoyl-benzoic Acid Anion

149. Akos000165123

150. Probampacin Component Probenecid

151. Tox21_110328_1

152. Ac-2023

153. Db01032

154. Hc 5006

155. Nc00530

156. Nsc-757292

157. Sb17360

158. Idi1_000056

159. Probenecid Component Of Proben-c

160. Ncgc00016251-01

161. Ncgc00016251-02

162. Ncgc00016251-03

163. Ncgc00016251-04

164. Ncgc00016251-05

165. Ncgc00016251-06

166. Ncgc00016251-07

167. Ncgc00016251-09

168. Ncgc00016251-10

169. Ncgc00016251-13

170. Ncgc00016251-17

171. Ncgc00023829-03

172. Ncgc00023829-04

173. Ncgc00023829-05

174. Ncgc00023829-06

175. Ncgc00023829-07

176. Ncgc00256441-01

177. Ncgc00259659-01

178. Probenecid Component Of Colbenemid

179. Bp166195

180. Col-probenecid Component Probenecid

181. Probenecid Component Of Probampacin

182. 4-(n,n-dipropylaminosulphonyl)benzoic Acid

183. Sbi-0051492.p003

184. 4-dipropylsulfamoyl-benzoic Acid(probenecid)

185. Ab00052080

186. P1975

187. Probenecid Component Of Col-probenecid

188. Sw196943-3

189. En300-69677

190. C07372

191. D00475

192. D92177

193. Ab00052080_15

194. Ab00052080_16

195. 038p402

196. Q900898

197. Q-201621

198. Sr-01000003108-2

199. Sr-01000003108-3

200. Brd-k95237249-001-05-9

201. Brd-k95237249-001-15-8

202. Z53037954

203. Probenecid, European Pharmacopoeia (ep) Reference Standard

204. Probenecid, United States Pharmacopeia (usp) Reference Standard

2.4 Create Date
2005-03-25
3 Chemical and Physical Properties
Molecular Weight 285.36 g/mol
Molecular Formula C13H19NO4S
XLogP33.2
Hydrogen Bond Donor Count1
Hydrogen Bond Acceptor Count5
Rotatable Bond Count7
Exact Mass285.10347926 g/mol
Monoisotopic Mass285.10347926 g/mol
Topological Polar Surface Area83.1 Ų
Heavy Atom Count19
Formal Charge0
Complexity374
Isotope Atom Count0
Defined Atom Stereocenter Count0
Undefined Atom Stereocenter Count0
Defined Bond Stereocenter Count0
Undefined Bond Stereocenter Count0
Covalently Bonded Unit Count1
4 Drug and Medication Information
4.1 Drug Information
1 of 4  
Drug NameProbalan
PubMed HealthProbenecid (By mouth)
Drug ClassesAntigout
Drug LabelProbenecid is a uricosuric and renal tubular transport blocking agent.The chemical name for probenecid is 4-[(dipropylamino) sulfonyl] benzoic acid (molecular weight 285.37). It has the following structural formula:C13H19NO4SProbenecid, USP is a whit...
Active IngredientProbenecid
Dosage FormTablet
RouteOral
Strength500mg
Market StatusPrescription
CompanyLannett

2 of 4  
Drug NameProbenecid
Active IngredientProbenecid
Dosage FormTablet
RouteOral
Strength500mg
Market StatusPrescription
CompanyWatson Labs; Mylan

3 of 4  
Drug NameProbalan
PubMed HealthProbenecid (By mouth)
Drug ClassesAntigout
Drug LabelProbenecid is a uricosuric and renal tubular transport blocking agent.The chemical name for probenecid is 4-[(dipropylamino) sulfonyl] benzoic acid (molecular weight 285.37). It has the following structural formula:C13H19NO4SProbenecid, USP is a whit...
Active IngredientProbenecid
Dosage FormTablet
RouteOral
Strength500mg
Market StatusPrescription
CompanyLannett

4 of 4  
Drug NameProbenecid
Active IngredientProbenecid
Dosage FormTablet
RouteOral
Strength500mg
Market StatusPrescription
CompanyWatson Labs; Mylan

4.2 Therapeutic Uses

Renal Agents; Uricosuric Agents

National Library of Medicine's Medical Subject Headings online file (MeSH, 1999)


IT HAS BEEN WIDELY USED IN LAB & CLINICAL INVESTIGATION OF EXCRETION OF A NUMBER OF SUBSTANCES. ... IT IS POTENT INHIBITOR OF CERTAIN GLYCINE CONJUGASES. HOWEVER, ITS THERAPEUTIC APPLICATIONS HAVE BEEN LIMITED PRINCIPALLY TO MODIFICATION OF RENAL EXCRETION OF PENICILLIN & URIC ACID.

Goodman, L.S., and A. Gilman. (eds.) The Pharmacological Basis of Therapeutics. 5th ed. New York: Macmillan Publishing Co., Inc., 1975., p. 862


... URICOSURIC AGENT FOR TREATMENT OF GOUT & GOUTY ARTHRITIS. ... /SRP: THEORETICAL (BUT NOT PRACTICAL) USE/ AS ADJUVANT THERAPY WITH PENICILLIN G, O OR V OR WITH AMPICILLIN, METHICILLIN, OXACILLIN, CLOXACILLIN, OR NAFCILLIN, FOR ELEVATION & PROLONGATION OF PENICILLIN PLASMA LEVELS BY ... ROUTE ANTIBIOTIC IS GIVEN.

Osol, A. and J.E. Hoover, et al. (eds.). Remington's Pharmaceutical Sciences. 15th ed. Easton, Pennsylvania: Mack Publishing Co., 1975., p. 873


ITS SUPPRESSION OF RENAL CLEARANCE OF PHENOLSULFONPHTHALEIN (PHENOL RED) IS OF SIGNIFICANCE IN APPLICATION OF THAT KIDNEY EXCRETION TEST AS CLINICAL GUIDE TO EFFECTIVENESS OF PROBENECID. ... /IT/ IS WELL TOLERATED /BY MOST PATIENTS ... .

Osol, A. and J.E. Hoover, et al. (eds.). Remington's Pharmaceutical Sciences. 15th ed. Easton, Pennsylvania: Mack Publishing Co., 1975., p. 873


For more Therapeutic Uses (Complete) data for PROBENECID (12 total), please visit the HSDB record page.


4.3 Drug Warning

SINCE ... /1955/ A SINGLE FATALITY HAS BEEN ATTRIBUTED TO HYPERSENSITIVITY TO PROBENECID. IN THIS PATIENTS, JAUNDICE, ASTHMA, SKIN RASH & EOSINOPHILIA PRECEDEDMASSIVE HEPATIC NECROSIS. PATHOLOGY RESEMBLED FEW REPORTED CASES OF HEPATIC NECROSIS FROM SULFONAMIDES.

Gosselin, R.E., R.P. Smith, H.C. Hodge. Clinical Toxicology of Commercial Products. 5th ed. Baltimore: Williams and Wilkins, 1984., p. II-405


USE OF PROBENECID & COLCHICINE IN TABLET COMBINATION (COLBENEMID) SHOULD BE AVOIDED IN TREATMENT OF INITIAL ATTACK OF GOUT, SINCE ACUTE LOWERING OF URIC ACID LEVEL MAY PERPETUATE ATTACK. RATIONALE FOR LONG TERM THERAPY ... IS QUESTIONABLE.

Miller, R. R., and D. J. Greenblatt. Handbook of Drug Therapy. New York: Elsevier North Holland, 1979., p. 482


CAUTION IS WARRANTED WHEN PROBENECID IS GIVEN TO ACHIEVE HIGHER SERUM PENICILLIN LEVELS, SINCE THE CAUSE OF SUBSEQUENT DRUG RASH WILL BE DIFFICULT TO INTERPRET.

Miller, R. R., and D. J. Greenblatt. Handbook of Drug Therapy. New York: Elsevier North Holland, 1979., p. 482


SOME DEGREE OF GI IRRITATION IS EXPERIENCED BY AT LEAST 2% OF PATIENTS; INCIDENCE IS CONSIDERABLY HIGHER AFTER LARGE DOSES. CAUTION IS ADVISED IN ADMINISTERING PROBENECID IN PATIENTS WITH HISTORY OF PEPTIC ULCER. MOST REPORTS PLACE INCIDENCE OF HYPERSENSITIVITY REACTIONS, USUALLY MILD SKIN RASHES, BETWEEN 2 & 4%.

Gilman, A.G., T.W. Rall, A.S. Nies and P. Taylor (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 8th ed. New York, NY. Pergamon Press, 1990., p. 746


For more Drug Warnings (Complete) data for PROBENECID (11 total), please visit the HSDB record page.


4.4 Drug Indication

For the reduction of serum uric acid concentrations in chronic gouty arthritis and tophaceous gout in patients with frequent disabling gout attacks. Has also been effectively used to promote uric acid excretion in hyperuricemia secondary to the administration of thiazide and related diuretics.


5 Pharmacology and Biochemistry
5.1 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 reabsorption of urate at the proximal convoluted tubule, 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. At the proximal and distal tubles, probenecid competitively inhibits the secretion of many weak organic acids including penicillins, most cephalosporins, and some other -lactam antibiotics. This results in an increase in the plasma concentrations of acidic drugs eliminated principally by renal secretion, but only a slight increase if the drug is eliminated mainly by filtration. Thus, the drug can be used for therapeutic advantages to increase concentrations of certain -lactam antibiotics in the treatment of gonorrhea, neurosyphilis, or pelvic inflammatory disease (PID).


5.2 MeSH Pharmacological Classification

Uricosuric Agents

Gout suppressants that act directly on the renal tubule to increase the excretion of uric acid, thus reducing its concentrations in plasma. (See all compounds classified as Uricosuric Agents.)


Adjuvants, Pharmaceutic

Agents that aid or increase the action of the principle drug (DRUG SYNERGISM) or that affect the absorption, mechanism of action, metabolism, or excretion of the primary drug (PHARMACOKINETICS) in such a way as to enhance its effects. (See all compounds classified as Adjuvants, Pharmaceutic.)


5.3 ATC Code

M - Musculo-skeletal system

M04 - Antigout preparations

M04A - Antigout preparations

M04AB - Preparations increasing uric acid excretion

M04AB01 - Probenecid


5.4 Absorption, Distribution and Excretion

Route of Elimination

Excreted principally in the urine as monoacyl glucuronide and unchanged drug. Alkalinization of urine increases renal probenecid excretion.


PROBENECID IS COMPLETELY ABSORBED AFTER ORAL ADMIN. PEAK PLASMA CONCN ARE REACHED IN 2-4 HR. THE HALF-LIFE OF THE DRUG IN PLASMA IS DOSE DEPENDENT AND VARIES FROM LESS THAN 5 HR TO MORE THAN 8 HR.

Gilman, A.G., T.W. Rall, A.S. Nies and P. Taylor (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 8th ed. New York, NY. Pergamon Press, 1990., p. 746


BETWEEN 85 & 95% OF DRUG IS BOUND TO PLASMA ALBUMIN, LARGELY TO ALBUMIN. SMALL UNBOUND PORTION GAINS ACCESS TO GLOMERULAR FILTRATE; A MUCH LARGER PORTION IS ACTIVELY SECRETED BY PROXIMAL TUBULE.

Gilman, A.G., T.W. Rall, A.S. Nies and P. Taylor (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 8th ed. New York, NY. Pergamon Press, 1990., p. 746


IN SPITE OF ITS LOW PKA (3.4), HIGH LIPID SOLUBILITY OF UNDISSOCIATED FORM RESULTS IN VIRTUALLY COMPLETE ABSORPTION BY BACK DIFFUSION UNLESS URINE IS MARKEDLY ALKALINE. SMALL AMOUNT OF PROBENECID GLUCURONIDE APPEARS IN URINE.

Gilman, A.G., T.W. Rall, A.S. Nies and P. Taylor (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 8th ed. New York, NY. Pergamon Press, 1990., p. 746


... /ORG ACID CMPD SUCH AS PROBENECID /ARE/ NOT TAKEN UP SO AVIDLY BY /PARENCHYMATOUS OR RETICULO-ENDOTHELIAL TISSUES/ & EXHIBIT HIGHER PLASMA CONCN ... .

LaDu, B.N., H.G. Mandel, and E.L. Way. Fundamentals of Drug Metabolism and Disposition. Baltimore: Williams and Wilkins, 1971., p. 372


For more Absorption, Distribution and Excretion (Complete) data for PROBENECID (8 total), please visit the HSDB record page.


5.5 Metabolism/Metabolites

YIELDS P-DIPROPYLSULFAMOYLBENZOYL-BETA-D-GLUCURONIC ACID; P-(2-HYDROXYPROPYL N-PROPYLSULFAMOYL) BENZOIC ACID; P-(3-HYDROXYPROPYL N-PROPYLSULFAMOYL) BENZOIC ACID; & P-PROPYLSULFAMOYLBENZOIC ACID IN MAN. /FROM TABLE/

Goodwin, B.L. Handbook of Intermediary Metabolism of Aromatic Compounds. New York: Wiley, 1976., p. D-100


STRUCTURES OF ALL OF METAB OF PROBENECID IN RAT BILE & HUMAN URINE HAVE BEEN ELUCIDATED. PROPIONIC ACID HAS NOW BEEN IDENTIFIED AS ANOTHER PROBENECID METAB. MAJOR METABOLIC PATHWAYS INVOLVE SIDE-CHAIN OXIDATION & GLUCURONIDE CONJUGATION ... .

The Chemical Society. Foreign Compound Metabolism in Mammals Volume 3. London: The Chemical Society, 1975., p. 288


... BETA-GLUCURONIDES OF 2- & 3-HYDROXYLATED METAB & ACYL GLUCURONIDE OF PROBENECID PER SE HAVE NOW BEEN IDENTIFIED. ... THERE IS CONSIDERABLE SPECIES DIFFERENCE IN METABOLISM. IN RATS & MONKEYS OXIDATION IS FAVORED. ... IN DOGS CONJUGATION ... /IS/ MAJOR PATHWAY, WHEREAS IN MAN, OXIDATIVE ... PATHWAY ... IS AS IMPORTANT AS GLUCURONIDATION.

The Chemical Society. Foreign Compound Metabolism in Mammals Volume 3. London: The Chemical Society, 1975., p. 288


CHRONIC ADMIN OF DRUGS NOT ONLY STIMULATES METAB OF OTHER CMPD, BUT IN SOME INSTANCES PHARMACOLOGICAL OR TOXIC EFFECT OF A DRUG WHEN GIVEN CHRONICALLY, DIMINISHES, BECAUSE IT STIMULATES ITS OWN METABOLISM EXAMPLE OF DRUG THAT EXERT THIS EFFECT IN DOGS ... /IS/ ... PROBENECID ... .

LaDu, B.N., H.G. Mandel, and E.L. Way. Fundamentals of Drug Metabolism and Disposition. Baltimore: Williams and Wilkins, 1971., p. 258


For more Metabolism/Metabolites (Complete) data for PROBENECID (6 total), please visit the HSDB record page.


5.6 Biological Half-Life

6-12 hours


THE HALF-LIFE OF /PROBENECID/ IN PLASMA IS DOSE DEPENDENT AND VARIES FROM LESS THAN 5 HR TO MORE THAN 8 HR ... .

Gilman, A.G., T.W. Rall, A.S. Nies and P. Taylor (eds.). Goodman and Gilman's The Pharmacological Basis of Therapeutics. 8th ed. New York, NY. Pergamon Press, 1990., p. 746


Following oral administration of 2 g of probenecid, plasma half-life of the drug ranges from 4-17 hr; the half-life decreases as the dose decreases from 2 g to 500 mg.

McEvoy, G.K. (ed.). American Hospital Formulary Service - Drug Information 93. Bethesda, MD: American Society of Hospital Pharmacists, Inc., 1993 (Plus Supplements, 1993)., p. 1652


5.7 Mechanism of Action

Probenecid inhibits the tubular reabsorption of urate, thus increasing the urinary excretion of uric acid and decreasing serum urate levels. Probenecid may also reduce plasma binding of urate and inhibit renal secretion of uric acid at subtherapeutic concentrations. The mechanism by which probenecid inhibits renal tubular transport is not known, but the drug may inhibit transport enzymes that require a source of high energy phosphate bonds and/or nonspecifically interfere with substrate access to protein receptor sites on the kidney tubules.


IN HIGHER DOSES THAN ARE REQUIRED FOR URICOSURIC EFFECT, PROBENECID ALSO INHIBITS TRANSPORT OF ORG ACIDS AT OTHER SITES, IE, TRANSPORT SYSTEM THAT REMOVES ORG ACIDS FROM CEREBROSPINAL FLUID.

Goodman, L.S., and A. Gilman. (eds.) The Pharmacological Basis of Therapeutics. 5th ed. New York: Macmillan Publishing Co., Inc., 1975., p. 862


IT INHIBITS TUBULAR REABSORPTION OF URATE, THUS INCR URINARY EXCRETION OF URIC ACID & DECR SERUM URIC ACID LEVELS.

Osol, A. and J.E. Hoover, et al. (eds.). Remington's Pharmaceutical Sciences. 15th ed. Easton, Pennsylvania: Mack Publishing Co., 1975., p. 873


Probenecid is a renal tubular blocking agent. The drug competitively inhibits active reabsorption of uric acid at the proximal convoluted tubule, thus promoting urinary excretion of uric acid and reducing serum urate concentrations. Probenecid may reduce plasma protein binding of urate and, in subtherapeutic doses, may inhibit renal secretion of uric acid. In healthy individuals, probenecid has no effect on the glomerular filtration rate or on the tubular reabsorption of normal urinary constituents such as glucose, arginine, urea, sodium, potassium, chloride, or phosphate.

McEvoy, G.K. (ed.). American Hospital Formulary Service - Drug Information 93. Bethesda, MD: American Society of Hospital Pharmacists, Inc., 1993 (Plus Supplements, 1993)., p. 1651


At the proximal and distal tubules, probenecid competitively inhibits the secretion of many weak organic acids including penicillins, most cephalosporins, and some other beta-lactam antibiotics. In general, the net effect of probenecid on the plasma concentration of weak acids depends on the ratio of the amount of organic acid secreted by the kidneys to that amount filtered at the glomeruli. Thus, probenecid substantially increases plasma concentrations of acidic drugs eliminated principally by renal secretion, but increases plasma concentrations only slightly if the drug is eliminated mainly by filtration. Plasma concentrations of penicillins are often more than doubled by probenecid; the concentration of penicillin in the CSF is also increased. Probenecid also substantially increases plasma concentrations of most cephalosporins and some other beta-lactam antibiotics. In addition, half-lives of the penicillins and cephalosporins are prolonged and their volumes of distribution may be reduced by probenecid. ... The cellular mechanism(s) responsible for the inhibition of renal tubular transport by probenecid is not known. The drug may inhibit transport enzymes that require a source of high energy phosphate bonds and/or nonspecifically interfere with substrate access to protein receptor sites on the kidney tubules.

McEvoy, G.K. (ed.). American Hospital Formulary Service - Drug Information 93. Bethesda, MD: American Society of Hospital Pharmacists, Inc., 1993 (Plus Supplements, 1993)., p. 1652


CSF concentrations of 5-hydroxyindoleacetic acid, homovanillic acid, cyclic adenosine monophosphate, and 4-hydroxy-3-methoxyphenylglycol are elevated following administration of probenecid. It has been proposed that probenecid blocks the active transport of these organic acids from the CSF into blood. Probenecid-induced elevations of homovanillic acid (a dopamine metabolite) in the CSF of patients with parkinsonian syndrome and of 5-hydroxyindoleacetic acid(a metabolite of serotonin) in the CSF of mentally depressed patients are substantially lower than those in healthy patients.

McEvoy, G.K. (ed.). American Hospital Formulary Service - Drug Information 93. Bethesda, MD: American Society of Hospital Pharmacists, Inc., 1993 (Plus Supplements, 1993)., p. 1652


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A. KIDWAI MARG,,WA DALA,","city":"MUMBAI,MAHARASHTRA","supplier":"TEVA API","supplierCountry":"ISRAEL","foreign_port":"NA","customer":"SIGMA LABORATORIES PRIVATE ","customerCountry":"INDIA","quantity":"701.65","actualQuantity":"701.65","unit":"KGS","unitRateFc":"380","totalValueFC":"272466.1","currency":"USD","unitRateINR":"31749","date":"03-Jan-2023","totalValueINR":"22276685.85","totalValueInUsd":"272466.1","indian_port":"BOMBAY AIR","hs_no":"29359090","bill_no":"4017654","productDescription":"API","marketType":"LESS REGULATED MARKET","country":"ISRAEL","selfForZScoreResived":"Pharma Grade","supplierPort":"NA","supplierAddress":"","customerAddress":"SIGMA HOUSE, R. A. KIDWAI MARG,,WA DALA,"},{"dataSource":"API Import","activeIngredients":"","year":"2023","qtr":"Q2","strtotime":1684348200,"product":"PROBENECID","address":"12TH FLOOR, COMMERZ IIINTERNATIO NAL BUSNESS PARK,OBEROI GARDEN CITY","city":"MUMBAI","supplier":"CHEMICAL INDUSTRIES ASSOCIATION","supplierCountry":"ISRAEL","foreign_port":"HAIFA","customer":"TEVA PHARMACEUTICAL INDUSTRIES","customerCountry":"INDIA","quantity":"1437.60","actualQuantity":"1437.6","unit":"KGS","unitRateFc":"180","totalValueFC":"311713.3","currency":"USD","unitRateINR":"17841.6","date":"18-May-2023","totalValueINR":"25649084.16","totalValueInUsd":"311713.3","indian_port":"JNPT","hs_no":"29359090","bill_no":"0","productDescription":"API","marketType":"LESS REGULATED MARKET","country":"Israel","selfForZScoreResived":"Pharma Grade","supplierPort":"HAIFA","supplierAddress":"","customerAddress":"12TH FLOOR, COMMERZ IIINTERNATIO NAL BUSNESS PARK,OBEROI GARDEN CITY"},{"dataSource":"API Import","activeIngredients":"","year":"2023","qtr":"Q4","strtotime":1696617000,"product":"PROBENECID 770A23070","address":"21-22, KALPATARU SQUARE, KONDIVITA","city":"ANDHERI (E), MUMBAI,MAHARASHTRA","supplier":"CHEMICAL INDUSTRIES ASSOCIATION","supplierCountry":"ISRAEL","foreign_port":"TEL AVIV YAFO","customer":"TEVA PHARMACEUTICAL INDUSTRIES","customerCountry":"INDIA","quantity":"150.00","actualQuantity":"150","unit":"KGS","unitRateFc":"460","totalValueFC":"83716","currency":"USD","unitRateINR":"46450.8","date":"07-Oct-2023","totalValueINR":"6967620","totalValueInUsd":"83716","indian_port":"Bombay Air","hs_no":"29359090","bill_no":"8198729","productDescription":"API","marketType":"LESS REGULATED MARKET","country":"ISRAEL","selfForZScoreResived":"Pharma Grade","supplierPort":"TEL AVIV YAFO","supplierAddress":"Teva Tech site Neot Hovav Eco-Industrial Park, Emek Sara P.O. 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Box 2049 Be\\'er Sheva, 8412316, Israel","customerAddress":"21-22, KALPATARU SQUARE, KONDIVITA"}]
13-Jan-2021
11-Oct-2024
KGS
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