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Details

Stereochemistry ACHIRAL
Molecular Formula C13H19NO4S
Molecular Weight 285.359
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PROBENECID

SMILES

CCCN(CCC)S(=O)(=O)C1=CC=C(C=C1)C(O)=O

InChI

InChIKey=DBABZHXKTCFAPX-UHFFFAOYSA-N
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)

HIDE SMILES / InChI
Molecular Formula C13H19NO4S
Molecular Weight 285.359
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
86413
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:21:18 UTC 2023
Edited
by admin
on Fri Dec 15 15:21:18 UTC 2023
Record UNII
PO572Z7917
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
PROBENECID
EP   HSDB   INN   JAN   MART.   MI   ORANGE BOOK   USP   USP-RS   VANDF   WHO-DD   WHO-IP  
INN  
Official Name English
PROBENECID [USP-RS]
Common Name English
PROBAMPACIN COMPONENT PROBENECID
Common Name English
PROBENECID [ORANGE BOOK]
Common Name English
PROBENECID [MART.]
Common Name English
PROBENECID [USP IMPURITY]
Common Name English
PROBENECID [EP MONOGRAPH]
Common Name English
PROBENECID [USP MONOGRAPH]
Common Name English
PROBENATE
Common Name English
BENZOIC ACID, 4-((DIPROPYLAMINO)SULFONYL)-
Common Name English
PROBENECID [JAN]
Common Name English
PROBENECID COMPONENT OF COLBENEMID
Common Name English
probenecid [INN]
Common Name English
PROBENECID COMPONENT OF PROBAMPACIN
Common Name English
PROBENECID COMPONENT OF COL-PROBENECID
Common Name English
P-(DIPROPYLSULFAMOYL)BENZOIC ACID
Common Name English
PROBENECID [MI]
Common Name English
BENEMID
Brand Name English
PROBENECID [HSDB]
Common Name English
PROBENECID COMPONENT OF PROBEN-C
Common Name English
NSC-18786
Code English
PROBENECID [WHO-IP]
Common Name English
Probenecid [WHO-DD]
Common Name English
PROBENECIDUM [WHO-IP LATIN]
Common Name English
PROBENECID [EP IMPURITY]
Common Name English
PROBEN-C COMPONENT PROBENECID
Common Name English
COL-PROBENECID COMPONENT PROBENECID
Common Name English
COLBENEMID COMPONENT PROBENECID
Common Name English
PROBALAN
Brand Name English
Classification Tree Code System Code
NCI_THESAURUS C921
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
LIVERTOX NBK548599
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
WHO-ATC M04AB01
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
WHO-VATC QM04AB01
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
Code System Code Type Description
DAILYMED
PO572Z7917
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
IUPHAR
4357
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
LACTMED
Probenecid
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
HSDB
3387
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
MERCK INDEX
m9142
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY Merck Index
EVMPD
SUB10053MIG
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
ChEMBL
CHEMBL897
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
EPA CompTox
DTXSID9021188
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
WIKIPEDIA
Probenecid
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
CAS
57-66-9
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
RS_ITEM_NUM
1563003
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
DRUG CENTRAL
2268
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
MESH
D011339
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
NSC
18786
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
RXCUI
8698
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY RxNorm
SMS_ID
100000081091
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
WHO INTERNATIONAL PHARMACOPEIA
PROBENECID
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY Description: A white or almost white, crystalline powder; odourless. Solubility: Practically insoluble in water; soluble in 25 parts of ethanol (~750 g/l) TS and in 12 parts of acetone R; soluble in dilutesolutions of alkali hydroxides. Category: Antigout drug. Storage: Probenecid should be kept in a well-closed container. Definition: Probenecid contains not less than 98.0% and not more than 101.0% of C13H19NO4S, calculated with reference to thedried substance.
FDA UNII
PO572Z7917
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
CHEBI
8426
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
INN
563
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
DRUG BANK
DB01032
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
NCI_THESAURUS
C772
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
ECHA (EC/EINECS)
200-344-3
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
PUBCHEM
4911
Created by admin on Fri Dec 15 15:21:18 UTC 2023 , Edited by admin on Fri Dec 15 15:21:18 UTC 2023
PRIMARY
Related Record Type Details
OAT-3
TRANSPORTER -> INHIBITOR
OAT-2
TRANSPORTER -> INHIBITOR
OAT-1
TARGET -> INHIBITOR
OAT-3
TARGET -> INHIBITOR
OATP-8
TRANSPORTER -> INHIBITOR
OATL-4
TARGET -> INHIBITOR
Primary target.
Structure of PIVAMPICILLIN PROBENATE
SALT/SOLVATE -> PARENT
OATL-4
TRANSPORTER -> INHIBITOR
OAT-1
TRANSPORTER -> INHIBITOR
OAT-4
TRANSPORTER -> INHIBITOR
MONOCARBOXYLATE TRANSPORTER 6
TRANSPORTER -> SUBSTRATE
Related Record Type Details
Structure of PROBENECID GLYCINE CONJUGATE
METABOLITE -> PARENT
Structure of 4-((PROPYLAMINO)SULFONYL)BENZOIC ACID
METABOLITE -> PARENT
Structure of BENZOIC ACID, 4-(((3-HYDROXYPROPYL)PROPYLAMINO)SULFONYL)-
METABOLITE -> PARENT
Related Record Type Details
Structure of 4-(DIPROPYLSULFAMOYL)-N,N-DIPROPYLBENZAMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 4-SULFOBENZOIC ACID
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of ETHYL 4-(DIPROPYLSULFAMOYL)BENZOATE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of DITOLAMIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Related Record Type Details
Structure of PROBENECID
ACTIVE MOIETY
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