Aminophenazone

Aminophenazone
INN: aminophenazone

Clinical data
AHFS/Drugs.com	International Drug Names
ATC code	N02BB03 (WHO)
Pharmacokinetic data
Metabolism	N-demethylation
Identifiers
IUPAC name 4-Dimethylamino-1,5-dimethyl-2-phenylpyrazol-3-one
CAS Number	58-15-1 Y
PubChem CID	6009
DrugBank	DB01424 Y
ChemSpider	5787 Y
UNII	01704YP3MO
KEGG	D00556 Y
ChEBI	CHEBI:160246 Y
ChEMBL	ChEMBL288470 Y
CompTox Dashboard (EPA)	DTXSID7020504
ECHA InfoCard	100.000.332
Chemical and physical data
Formula	C13H17N3O
Molar mass	231.29358 g·mol−1
3D model (JSmol)	Interactive image
SMILES O=C2\C(=C(/N(N2c1ccccc1)C)C)N(C)C
InChI InChI=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 Y Key:RMMXTBMQSGEXHJ-UHFFFAOYSA-N Y
(verify)

Aminophenazone (or aminopyrine, amidopyrine, Pyramidon) is a non-narcotic analgesic substance. It is a pyrazolone and a derivative of phenazone, which also has anti-inflammatory and antipyretic properties. While inexpensive and effective, especially in the treatment of rheumatism, the drug carries a serious risk of severe and sometimes fatal side effects, including agranulocytosis. While its production and use have been banned in many countries, including France, Thailand, Indian and Japan, it is still sometimes used in the developing world.

A breath test with ¹³C-labeled aminopyrine has been used as a non-invasive measure of cytochrome P-450 metabolic activity in liver function tests. It is also used in measuring the total body water in the human body system.

History

Aminophenazone was first synthesized by Friedrich Stolz and Ludwig Knorr in the late nineteenth century, and sold as an anti-fever medicine known as Pyramidon by Hoechst AG from 1897 until its eventual replacement by the safer propyphenazone molecule.

Symptoms

Symptoms of exposure to this compound include:

• allergic reactions
• strong spasmolytic effect on smooth muscle of peripheral blood vessels
• irritability
• palsy
• copious sweating
• dilated pupils
• sharp drop then rise in body temperature
• dysuria
• dyspnea
• anxiety
• rectal tenesmus
• urinary frequency
• intermittent fever
• fatty infiltration of the liver
• heart muscle degeneration
• death due to circulatory failure following cardiovascular collapse

Agranulocytosis often occurs. Ingestion may cause central nervous system stimulation, vomiting, convulsions, cyanosis, tinnitus, leukopenia, kidney damage and coma. Ingestion may also lead to nausea, mental disturbances, methemoglobinemia, chocolate-colored blood, dizziness, epigastric pain, difficulty in hearing, thready pulse and liver damage.

Other symptoms reported via ingestion include hemolytic anemia, porphyria and severe gastrointestinal bleeding. Bone marrow depression also occurs. Rare eye effects include acute transient myopia.

Chronic symptoms include:

• anorexia
• edema
• oliguria
• urticaria
• hypersensitivity
• aplastic anemia
• sore throat
• fever
• pharyngeal membrane
• jaundice enlargement of the liver and spleen
• exfoliative dermatitis
• gastric or duodenal erosion with perforation or bleeding
• adrenal necrosis
• thrombocytopenic purpura
• acute leukemia

When heated to decomposition this compound emits toxic fumes of nitrogen oxides.

Metabolism

Amidopyrine is metabolized by demethylation and acetylation. Amidopirina metabolites are 4-aminoantipyrine, metilaminoantipirin, rubazonovaya and metilrubazonovaya acid. These acids have a reddish color. At high amidopirine doses, urine can have a reddish brown coloration, due to the presence in the urine of these acid markers.