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Details

Stereochemistry ACHIRAL
Molecular Formula C15H13N3O4S
Molecular Weight 331.346
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of PIROXICAM

SMILES

CN1C(C(=O)NC2=CC=CC=N2)=C(O)C3=C(C=CC=C3)S1(=O)=O

InChI

InChIKey=QYSPLQLAKJAUJT-UHFFFAOYSA-N
InChI=1S/C15H13N3O4S/c1-18-13(15(20)17-12-8-4-5-9-16-12)14(19)10-6-2-3-7-11(10)23(18,21)22/h2-9,19H,1H3,(H,16,17,20)

HIDE SMILES / InChI
Molecular Formula C15H13N3O4S
Molecular Weight 331.346
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Unknown
123738
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:49:53 UTC 2023
Edited
by admin
on Fri Dec 15 15:49:53 UTC 2023
Record UNII
13T4O6VMAM
Record Status Validated (UNII)
Record Version
  • Download
Related Record Type
Name Type Language
PIROXICAM
EP   INN   MART.   MI   ORANGE BOOK   USAN   USP   USP-RS   VANDF   WHO-DD  
INN   USAN  
Official Name English
4-HYDROXY-2-METHYL-N-2-PYRIDINYL-2H-1,2-BENZOTHIAZINE-3-CARBOXAMIDE 1,1-DIOXIDE
Systematic Name English
piroxicam [INN]
Common Name English
PIROXICAM [MI]
Common Name English
FELDENE
Brand Name English
PIROXICAM [EP MONOGRAPH]
Common Name English
NSC-666076
Code English
PIROXICAM [JAN]
Common Name English
PIROXICAM [USP-RS]
Common Name English
2H-1,2-BENZOTHIAZINE-3-CARBOXAMIDE, 4-HYDROXY-2-METHYL-N-2-PYRIDINYL-, 1,1-DIOXIDE
Systematic Name English
CP-16171
Code English
PIROXICAM [VANDF]
Common Name English
PIROXICAM ANHYDROUS
Common Name English
CP-16,171
Code English
PIROXICAM [USP MONOGRAPH]
Common Name English
PIROXICAM [USAN]
Common Name English
PIROXICAM [MART.]
Common Name English
PIROXICAM [ORANGE BOOK]
Common Name English
Piroxicam [WHO-DD]
Common Name English
Classification Tree Code System Code
WHO-VATC QM01AC01
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
WHO-VATC QS01BC06
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
NDF-RT N0000175722
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
WHO-ATC S01BC06
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
NCI_THESAURUS C1915
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
NCI_THESAURUS C1323
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
WHO-ATC M01AC01
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
WHO-ATC M02AA07
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
NDF-RT N0000000160
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
NDF-RT N0000175721
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
WHO-VATC QM02AA07
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
LIVERTOX NBK548425
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
Code System Code Type Description
DRUG CENTRAL
2210
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
DRUG BANK
DB00554
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
CHEBI
8249
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
FDA UNII
13T4O6VMAM
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
RXCUI
8356
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
MERCK INDEX
m8889
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY Merck Index
EPA CompTox
DTXSID5021170
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
RS_ITEM_NUM
1544508
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
CAS
36322-90-4
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
IUPHAR
7273
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
ECHA (EC/EINECS)
252-974-3
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
NSC
666076
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
PUBCHEM
54676228
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
RXCUI
68115
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
ALTERNATIVE
SMS_ID
100000092492
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
EVMPD
SUB127114
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
LACTMED
Piroxicam
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
EVMPD
SUB09936MIG
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
WIKIPEDIA
PIROXICAM
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
INN
3713
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
ChEMBL
CHEMBL527
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
NCI_THESAURUS
C751
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
MESH
D010894
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
DAILYMED
13T4O6VMAM
Created by admin on Fri Dec 15 15:49:53 UTC 2023 , Edited by admin on Fri Dec 15 15:49:53 UTC 2023
PRIMARY
Related Record Type Details
OAT-3
TRANSPORTER -> INHIBITOR
OAT-2
TRANSPORTER -> INHIBITOR
Structure of PIROXICAM
BASIS OF STRENGTH->SUBSTANCE
ASSAY (TITRATION)
EP
OAT-4
TRANSPORTER -> INHIBITOR
Structure of PIROXICAM OLAMINE
SALT/SOLVATE -> PARENT
Structure of PIROXICAM
BASIS OF STRENGTH->SUBSTANCE
ASSAY (HPLC)
USP
OAT-1
TRANSPORTER -> INHIBITOR
PLASMA PROTEIN FRACTION (HUMAN)
BINDER->LIGAND
BINDING
PIROXICAM BETADEX
SUB_CONCEPT->SUBSTANCE
Structure of PIROXICAM MONOHYDRATE
SOLVATE->ANHYDROUS
Structure of PIROXICAM MONOHYDRATE
SALT/SOLVATE -> PARENT
Related Record Type Details
Structure of 2H-1,2-BENZOTHIAZINE-3-CARBOXYLIC ACID, 4-HYDROXY-2-METHYL-, 1,1-DIOXIDE
METABOLITE -> PARENT
Structure of 6H,7H-PYRIDO(2',1':2,3)PYRIMIDO(5,4-C)(1,2)BENZOTHIAZIN-7-ONE, 6-METHYL-, 5,5-DIOXIDE
METABOLITE -> PARENT
Structure of 5'-HYDROXYPIROXICAM
METABOLITE -> PARENT
Structure of 6H,7H-PYRIDO(2',1':2,3)PYRIMIDO(5,4-C)(1,2)BENZOTHIAZIN-7-ONE, 6-METHYL-, 5,5-DIOXIDE
PARENT -> METABOLITE
Related Record Type Details
Structure of SACCHARIN N-(2-ACETIC ACID METHYL ESTER)
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 1-METHYLETHYL 4-HYDROXY-2H-1,2-BENZOTHIAZINE-3-CARBOXYLATE 1,1-DIOXIDE
IMPURITY -> PARENT
UNSPECIFIED
EP
Structure of DESMETHYL PIROXICAM
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of METHYL 4-HYDROXY-2-METHYL-2H-1,2-BENZOTHIAZINE-3-CARBOXYLATE 1,1-DIOXIDE
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of Methyl 4-hydroxy-2H-1,2-benzothiazine-3-carboxylate 1,1-dioxide
IMPURITY -> PARENT
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of SACCHARIN N-(2-ACETIC ACID ETHYL ESTER)
IMPURITY -> PARENT
UNSPECIFIED
EP
Structure of DESPYRIDYL PIROXICAM
IMPURITY -> PARENT
UNSPECIFIED
EP
Structure of 2-AMINOPYRIDINE
IMPURITY -> PARENT
For the calculation of contents, multiply the peak areas by 0.6
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
Structure of 4-HYDROXY-2-METHYL-2H-1,2-BENZOTHIAZINE-3-CARBOXYLIC ACID ETHYLESTER 1,1-DIOXIDE
IMPURITY -> PARENT
UNSPECIFIED
EP
Structure of SACCHARIN N-(2-ACETIC ACID ISOPROPYL ESTER)
IMPURITY -> PARENT
UNSPECIFIED
EP
Structure of ISOPROPYL-4-HYDROXY-2-METHYL-2H-1,2-BENZOTHIAZINE-3-CARBOXYLATE-1,1-DIOXIDE
IMPURITY -> PARENT
UNSPECIFIED
EP
Structure of ETHYL 4-HYDROXY-2H-1,2-BENZOTHIAZINE-3-CARBOXYLATE 1,1-DIOXIDE
IMPURITY -> PARENT
UNSPECIFIED
EP
Related Record Type Details
Structure of PIROXICAM
ACTIVE MOIETY
Name Property Type Amount Referenced Substance Defining Parameters References
Volume of Distribution PHARMACOKINETIC
Biological Half-life PHARMACOKINETIC
NIH
NCATS
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