CHEBI:160246 - aminophenazone

ChEBI IDCHEBI:160246
ChEBI Nameaminophenazone
Stars
DefinitionA pyrazolone that is 1,2-dihydro-3H-pyrazol-3-one substituted by a dimethylamino group at position 4, methyl groups at positions 1 and 5 and a phenyl group at position 2. It exhibits analgesic, anti-inflammatory, and antipyretic properties.
Last Modified22 February 2017
DownloadsMolfile
FormulaC13H17N3O
Net Charge0
Average Mass231.299
Monoisotopic Mass231.13716
SMILESCc1c(N(C)C)c(=O)n(-c2ccccc2)n1C
InChIInChI=1S/C13H17N3O/c1-10-12(14(2)3)13(17)16(15(10)4)11-8-6-5-7-9-11/h5-9H,1-4H3
InChIKeyRMMXTBMQSGEXHJ-UHFFFAOYSA-N
Wikipedia
Roles Classification
Chemical Roles:
environmental contaminant  Any minor or unwanted substance introduced into the environment that can have undesired effects.
Bronsted base  A molecular entity capable of accepting a hydron from a donor (Brønsted acid).
Biological Roles:
xenobiotic  A xenobiotic (Greek, xenos "foreign"; bios "life") is a compound that is foreign to a living organism. Principal xenobiotics include: drugs, carcinogens and various compounds that have been introduced into the environment by artificial means.
non-narcotic analgesic  A drug that has principally analgesic, antipyretic and anti-inflammatory actions. Non-narcotic analgesics do not bind to opioid receptors.
Applications:
non-narcotic analgesic  A drug that has principally analgesic, antipyretic and anti-inflammatory actions. Non-narcotic analgesics do not bind to opioid receptors.
antipyretic  A drug that prevents or reduces fever by lowering the body temperature from a raised state. An antipyretic will not affect the normal body temperature if one does not have fever. Antipyretics cause the hypothalamus to override an interleukin-induced increase in temperature. The body will then work to lower the temperature and the result is a reduction in fever.
non-steroidal anti-inflammatory drug  An anti-inflammatory drug that is not a steroid. In addition to anti-inflammatory actions, non-steroidal anti-inflammatory drugs have analgesic, antipyretic, and platelet-inhibitory actions. They act by blocking the synthesis of prostaglandins by inhibiting cyclooxygenase, which converts arachidonic acid to cyclic endoperoxides, precursors of prostaglandins.
ChEBI Ontology
Outgoing Relation(s)
aminophenazone (CHEBI:160246) has role antipyretic (CHEBI:35493)
aminophenazone (CHEBI:160246) has role environmental contaminant (CHEBI:78298)
aminophenazone (CHEBI:160246) has role non-narcotic analgesic (CHEBI:35481)
aminophenazone (CHEBI:160246) has role non-steroidal anti-inflammatory drug (CHEBI:35475)
aminophenazone (CHEBI:160246) has role xenobiotic (CHEBI:35703)
aminophenazone (CHEBI:160246) is a pyrazolone (CHEBI:83328)
aminophenazone (CHEBI:160246) is a tertiary amino compound (CHEBI:50996)
IUPAC Name 
4-(dimethylamino)-1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one
INNs  Source
aminofenazonaChemIDplus
aminophenazoneKEGG DRUG
aminophenazonumChemIDplus
Synonyms  Source
1,5-Dimethyl-4-dimethylamino-2-phenyl-3-pyrazoloneChemIDplus
1-Phenyl-2,3-dimethyl-4-(dimethylamino)-5-pyrazoloneNIST Chemistry WebBook
1-Phenyl-2,3-dimethyl-4-dimethylaminopyrazol-5-oneChemIDplus
2,3-Dimethyl-4-dimethylamino-1-phenyl-5-pyrazoloneChemIDplus
3-Keto-1,5-dimethyl-4-dimethylamino-2-phenyl-2,3-dihydropyrazoleChemIDplus
4-(Dimethylamino)-1,2-dihydro-1,5-dimethyl-2-phenyl-3H-pyrazol-3-oneChemIDplus
Manual XrefsDatabases
171DrugCentral
AminophenazoneWikipedia
C07539KEGG COMPOUND
D00556KEGG DRUG
DB01424DrugBank
HMDB0015493HMDB
LSM-20000LINCS
Registry NumbersSources
Gmelin:103164Gmelin
Reaxys:222626Reaxys
CAS:58-15-1ChemIDplus
CAS:58-15-1NIST Chemistry WebBook
CAS:58-15-1KEGG DRUG
CAS:58-15-1KEGG COMPOUND
CAS:58-15-1DrugBank
Citations