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Details

Stereochemistry ACHIRAL
Molecular Formula C12H15N3O
Molecular Weight 217.267
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of NORAMIDOPYRINE

SMILES

CNC1=C(C)N(C)N(C1=O)C2=CC=CC=C2

InChI

InChIKey=JILCEWWZTBBOFS-UHFFFAOYSA-N
InChI=1S/C12H15N3O/c1-9-11(13-2)12(16)15(14(9)3)10-7-5-4-6-8-10/h4-8,13H,1-3H3

HIDE SMILES / InChI

Molecular Formula C12H15N3O
Molecular Weight 217.267
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Population pharmacokinetic analysis of the active product of dipyrone.
2010-12
Investigation of the microbial degradation of phenazone-type drugs and their metabolites by natural biofilms derived from river water using liquid chromatography/tandem mass spectrometry (LC-MS/MS).
2010-08
Scavenging activity of aminoantipyrines against hydroxyl radical.
2010-06
Quantification of 4-methylaminoantipyrine, the active metabolite of dipyrone, in human plasma.
2009-05
Treatment of postherpetic neuralgia: focus on pregabalin.
2009
Photodegradation study of three dipyrone metabolites in various water systems: identification and toxicity of their photodegradation products.
2008-05
Pyrazolinone analgesics prevent the antiplatelet effect of aspirin and preserve human platelet thromboxane synthesis.
2008-01
Clinical review: Drug metabolism and nonrenal clearance in acute kidney injury.
2008
[Analysis of three metabolite residues of dipyrone in bovine muscle and pork muscle using high performance liquid chromatography].
2007-11
[Favorable outcome of acute porphyric neuropathy after treatment with heme arginate].
2007-11
Dipyrone elicits substantial inhibition of peripheral cyclooxygenases in humans: new insights into the pharmacology of an old analgesic.
2007-08
Solid-phase extraction followed by liquid chromatography-time-of-flight-mass spectrometry to evaluate pharmaceuticals in effluents. A pilot monitoring study.
2007-07
Inhibition of cyclooxygenases by dipyrone.
2007-06
[Drug-induced agranulocytosis in rheumatology. A retrospective study of 12 cases].
2007-04-23
Simultaneous determination of residues of dipyrone and its major metabolites in milk, bovine muscle, and porcine muscle by liquid chromatography/mass spectrometry.
2005-04-30
Characterization of the role of physicochemical factors on the hydrolysis of dipyrone.
2004-05-28
Effect of metamizol on promyelocytic and terminally differentiated granulocytic cells. Comparative analysis with acetylsalicylic acid and diclofenac.
2003-01-15
Allergic cholestatic hepatitis and exanthema induced by metamizole: verification by lymphocyte transformation test.
2002-12
Bioavailability of two metamizole (dipyrone) solutions as single doses of 2 g versus metamizole capsules.
2002-07
Benzydamine: an alternative nonsteroidal anti-inflammatory drug in patients with nimesulide-induced urticaria.
2002-05
Retrospective analysis of drug-induced urticaria and angioedema: a survey of 2287 patients.
2001-11
Limited-sampling strategy models for estimating the pharmacokinetic parameters of 4-methylaminoantipyrine, an active metabolite of dipyrone.
2001-11
Impairment of the metabolism of dipyrone in asymptomatic carriers of the hepatitis-B virus does not occur in rapid acetylators.
2001-09
Acute hepatitis due to ketoprofen.
1991-06
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:52:12 GMT 2025
Edited
by admin
on Mon Mar 31 18:52:12 GMT 2025
Record UNII
NER31DE951
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NORAMIDOPYRINE
WHO-DD  
Common Name English
NORAMINOPYRINE
Preferred Name English
1,5-DIMETHYL-4-METHYLAMINO-2-PHENYL-1,2-DIHYDRO-3H-PYRAZOL-3-ONE
Systematic Name English
Noramidopyrine [WHO-DD]
Common Name English
N-METHYL-4-AMINOPHENAZONE
Systematic Name English
N-METHYLAMINOPHENAZONE
Systematic Name English
4-Methylaminoantipyrine
Common Name English
METAMIZOLE SODIUM MONOHYDRATE IMPURITY C [EP IMPURITY]
Common Name English
Code System Code Type Description
CAS
519-98-2
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
PRIMARY
FDA UNII
NER31DE951
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
PRIMARY
EVMPD
SUB14664MIG
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
PRIMARY
CHEBI
73261
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
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EPA CompTox
DTXSID80199865
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
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MESH
C008667
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
PRIMARY
PUBCHEM
10618
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-281-3
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
PRIMARY
SMS_ID
100000080001
Created by admin on Mon Mar 31 18:52:12 GMT 2025 , Edited by admin on Mon Mar 31 18:52:12 GMT 2025
PRIMARY
Related Record Type Details
PRODRUG -> METABOLITE ACTIVE
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PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP
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ACTIVE MOIETY