イソプロピルアンチピリン
Wikipedia preview
出典(authority):フリー百科事典『ウィキペディア(Wikipedia)』「2016/05/26 15:54:20」(JST)
[Wiki en表示]
Propyphenazone
|
Systematic (IUPAC) name |
1,5-Dimethyl-2-phenyl-4-propan-2-yl-pyrazol-3-one
|
Clinical data |
AHFS/Drugs.com |
International Drug Names |
Administration |
Oral |
Identifiers |
CASRN |
479-92-5 N |
ATC code |
N02BB04 (WHO) |
PubChem |
CID 3778 |
ChemSpider |
3646 Y |
UNII |
OED8FV75PY Y |
ChEBI |
CHEBI:135538 Y |
ChEMBL |
CHEMBL28318 Y |
Chemical data |
Formula |
C14H18N2O |
Molar mass |
230.306 g/mol |
SMILES
-
O=C2\C(=C(/N(N2c1ccccc1)C)C)C(C)C
|
InChI
-
InChI=1S/C14H18N2O/c1-10(2)13-11(3)15(4)16(14(13)17)12-8-6-5-7-9-12/h5-10H,1-4H3 Y
-
Key:PXWLVJLKJGVOKE-UHFFFAOYSA-N Y
|
NY (what is this?) (verify) |
Propyphenazone is a derivative of phenazone[1] with similar analgesic and antipyretic effects.
Adverse effects of propyphenazone
There have been case reports describing risk of acute inferior myocardial infarction with low atrial rhythm due to propyphenazone (Kounis syndrome).[2][citation needed]
Countries that have banned propyphenazone
Excerpt from WHO comments:
-
- “Propyphenazone, a pyrazolone derivative with anti-inflammatory, analgesic and antipyretic activity, was introduced in 1951 for the treatment of rheumatic disorders. As it is structurally related to aminophenazone it has been associated with severe blood dyscrasias. However, it cannot be transformed into potentially carcinogenic nitrosamines and has therefore been widely used as a replacement drug for aminophenazone. In certain countries, products containing propyphenazone have now been restricted in their indications, whereas in others they are still available, sometimes as over-the-counter preparations.”[3]
- Sri Lanka[4]
- South Korea[4] - as reported by PharmAsia News in 2009:
-
- “Amid rising claims that it isn't moving fast enough to counter public concern over the safety of OTC painkillers, Korea FDA has banned Bayer Korea's painkiller Saridon-A, Samjin Pharm's Geworin and 26 other products from being prescribed or sold over the counter to those under 15 years of age.”[5]
- Malaysia[4]
- Thailand[4]
- Turkey - production and sale banned in January 1986 due to incidence of severe adverse reactions.[3]
- India- Still in use. Saridon tablets contain 150 mg/tablet.
References
- ^ Göres, E.; Kossowicz, J.; Schneider, H. G. (2004). "Propyphenazone. Pharmacology and use" [Propyphenazone. Pharmacology and use]. Medizinische Monatsschrift für Pharmazeuten (in German) 27 (3): 72–76. PMID 15032249.
- ^ Akyel, A.; Alsancak, Y.; Yayla, Ç. R.; Şahinarslan, A.; Özdemir, M. (2011). "Acute inferior myocardial infarction with low atrial rhythm due to propyphenazone: Kounis syndrome". International Journal of Cardiology 148 (3): 352–353. doi:10.1016/j.ijcard.2010.05.038. PMID 20541820.
- ^ a b Consolidated List of Products whose Consumption and/or Sale have been Banned, Withdrawn, Severely Restricted or not Approved by Governments, Twelfth Issue (pdf). New York: Department of Economic and Social Affairs of the United Nations Secretariat. 2005. p. 232.
- ^ a b c d "Multi-Country Survey On Banned And Restricted Pharmaceuticals". Health Action International Asia Pacific. August 2008. p. 7.
- ^ "Bayer’s Saridon-A Among 28 Painkillers Banned To Those Under 15 In Korea". PharmAsia News. 2009-03-12.
English Journal
- Determination of selected pharmaceuticals in tap water and drinking water treatment plant by high-performance liquid chromatography-triple quadrupole mass spectrometer in Beijing, China.
- Cai MQ1, Wang R, Feng L, Zhang LQ.
- Environmental science and pollution research international.Environ Sci Pollut Res Int.2015 Feb;22(3):1854-67. doi: 10.1007/s11356-014-3473-8. Epub 2014 Sep 9.
- A simultaneous determination method of 14 multi-class pharmaceuticals using solid-phase extraction (SPE) followed by high-performance liquid chromatography-tandem mass spectrometer (HPLC-MS/MS) was established to measure the occurrence and distribution of these pharmaceuticals in tap water and a dri
- PMID 25196960
- Fundamental properties of a touchable high-power pulsed microplasma jet and its application as a desorption/ionization source for ambient mass spectrometry.
- Iwai T1, Kakegawa K, Okumura K, Kanamori-Kataoka M, Miyahara H, Seto Y, Okino A.
- Journal of mass spectrometry : JMS.J Mass Spectrom.2014 Jun;49(6):522-8. doi: 10.1002/jms.3368.
- Plasma-based ambient desorption/ionization mass spectrometry (ADI-MS) has attracted considerable attention in many fields because of its capacity for direct sample analyses. In this study, a high-power pulsed microplasma jet (HPPMJ) was developed and investigated as a new plasma desorption/ionizatio
- PMID 24913404
- Clinical features of immediate hypersensitivity to isopropylantipyrine.
- Hwang EK1, Nam YH, Jin HJ, Shin YS, Ye YM, Park HS.
- Allergy, asthma & immunology research.Allergy Asthma Immunol Res.2013 Jan;5(1):55-8. doi: 10.4168/aair.2013.5.1.55. Epub 2012 Aug 29.
- Hypersensitivities induced by isopropylantipyrine (IPA), a pyrazolone derivative within the wider family of non-steroidal anti-inflammatory drugs (NSAIDs), are rarely reported. We characterized the clinical features of 12 patients with IPA-induced hypersensitivity. Twelve patients with immediate hyp
- PMID 23277879
Japanese Journal
- 症例 イソプロピルアンチピリンによる蕁麻疹型薬疹の1例
- Drug-induced hepatitis with hepatic granuloma due to saridon
- ABE MASANORI,KUMAGI TERU,NAKANISHI SEIJI,YAMAGAMI TAKASHI,MICHITAKA KOJIRO,ABE KAYO,OKURA IZUMI,YAMASHITA HARUHIKO,HORIIKE NORIO,ONJI MORIKAZU
- Journal of gastroenterology 37(12), 1068-1072, 2002-12-01
- NAID 10013893850
Related Links
- Isopropylantipyrine. C14H18N2O: 230.31. 4 - Isopropyl - 2, 3 - dimethyl - 1 - phenyl - 3 - pyrazolin - 5 - one. CAS Registry Number : Space: , Ball&Stick: , Stick: , Dots On: Rotation On: , Rotation Off: , Reset: ...
Related Pictures
★リンクテーブル★
[★]
- 英
- isopropylantipyrine
- ラ
- isopropylantipyrinum
- 同
- プロピフェナゾン propyphenazone、イソプロピルフェナゾン isopropylphenazone
- 商
- SG配合、クリアミン配合、ヨシピリン
- 関
- 非ステロイド性抗炎症薬