Propyphenazone
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Propyphenazone
structure -
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CAS No:
479-92-5
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Formula:
C14H18N2O
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Chemical Name:
Propyphenazone
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Synonyms:
3H-Pyrazol-3-one,1,2-dihydro-1,5-dimethyl-4-(1-methylethyl)-2-phenyl-;Antipyrine,4-isopropyl-;1,2-Dihydro-1,5-dimethyl-4-(1-methylethyl)-2-phenyl-3H-pyrazol-3-one;Isopropylantipyrine;4-Isopropyl-2,3-dimethyl-1-phenyl-3-pyrazolin-5-one;Isopropylphenazone;Larodon;1-Phenyl-2,3-dimethyl-4-isopropyl-3-pyrazolin-5-one;1-Phenyl-2,3-dimethyl-4-isopropylpyrazol-5-one;Propyphenazone;4-Isopropylantipyrine;1,2-Dihydro-1,5-dimethyl-2-phenyl-4-isopropyl-3H-pyrazol-3-one;Isopropylantipyrin;Isopropyrine;Propyfenazone;Arantil P;Isopropchin;4-Isopropylphenazone;Budirol;Eufibron;Cibalgina;Causyth;1,5-Dimethyl-2-phenyl-4-propan-2-ylpyrazol-3-one;128065-64-5;12542-35-7;88205-06-5
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CAS No:
Description
Propyphenazone is a pyrazolone derivative with anti-inflammatory, analgesic and antipyretic activity, Propyphenazone-based analogues as prodrugs and selective cyclooxygenase-2 inhibitors.Target:COX-2Propyphenazone is structurally related to aminophenazone it has been associated with severe blood dyscrasias. Propyphenazone is introduced for the treatment of rheumatic disorders.
Propyphenazone is a pyrazolone derivative that is antipyrine substituted at C-4 by an isopropyl group. It has a role as a non-steroidal anti-inflammatory drug, a non-narcotic analgesic and a peripheral nervous system drug. It derives from an antipyrine.
Propyphenazone Basic Attributes
230.31
230.31
207-539-2
OED8FV75PY
DTXSID6023529
N - Nervous system
2933199090
Characteristics
23.6
1.74
1.1±0.1 g/cm3
103 °C
319.0±25.0 °C at 760 mmHg
123.8±15.5 °C
1.556
743.6g/L(25.35 ºC)
Refrigerator
150 Ų [M+H]+ [CCS Type: TW]
Safety Information
NONH for all modes of transport
3
36/37/38-22
26-36/37/39
CD2800000
Xn
Stable. Incompatible with strong oxidizing agents.
P301 + P312 + P330
H302
Drug Information
Anti-inflammatory agents that are non-steroidal in nature. In addition to anti-inflammatory actions, they 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. Inhibition of prostaglandin synthesis accounts for their analgesic, antipyretic, and platelet-inhibitory actions; other mechanisms may contribute to their anti-inflammatory effects. (See all compounds classified as Anti-Inflammatory Agents, Non-Steroidal.)
4-isopropyl-2,3-dimethyl-1-phenyl-3-pyrazoline-5-one
Propyphenazone Use and Manufacturing
Analgesic; antipyretic; anti-inflammatory.
3H-Pyrazol-3-one, 1,2-dihydro-1,5-dimethyl-4-(1-methylethyl)-2-phenyl-: INACTIVE
Pharmaceuticals
Computed Properties
Molecular Weight:230.31
XLogP3:1.7
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:230.141913202
Monoisotopic Mass:230.141913202
Topological Polar Surface Area:23.6
Heavy Atom Count:17
Complexity:340
Covalently-Bonded Unit Count:1
Compound Is Canonicalized:Yes
Drug Function and Efficacy
Inhibits prostaglandin synthesis and has antipyretic and analgesic effects
Registered Holders
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Zhejiang Haisen Pharmaceutical Co., Ltd.
Active
China
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Shandong Xinhua Pharmaceutical Company Limited
Active
China
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SHANDONG XINHUA PHARMACEUTICAL CO., LTD.
Active
European Union
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