Ramifenazone

For research use only. Not for therapeutic Use.

  • CAT Number: I003328
  • CAS Number: 3615-24-5
  • Molecular Formula: C14H19N3O
  • Molecular Weight: 245.32
  • Purity: ≥95%
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Ramifenazone(CAT: I003328), also known as RGH-2202, is a pharmaceutical compound that exhibits a wide range of pharmacological properties. It acts as an anti-inflammatory and analgesic agent, with reported activity in inhibiting prostaglandin synthesis. Ramifenazone has also shown antioxidant effects, potentially contributing to its anti-inflammatory properties. Furthermore, it displays antiplatelet activity by inhibiting platelet aggregation. The compound has been investigated for its potential therapeutic applications in the treatment of various conditions, including rheumatoid arthritis, osteoarthritis, and pain management.


Catalog Number I003328
CAS Number 3615-24-5
Synonyms

Isopyrin; Isopirina

Molecular Formula C14H19N3O
Purity ≥95%
Target Bacterial
Solubility 10 mM in DMSO
Storage Store at -20°C
IUPAC Name 1,5-dimethyl-2-phenyl-4-(propan-2-ylamino)pyrazol-3-one
InChI InChI=1S/C14H19N3O/c1-10(2)15-13-11(3)16(4)17(14(13)18)12-8-6-5-7-9-12/h5-10,15H,1-4H3
InChIKey XOZLRRYPUKAKMU-UHFFFAOYSA-N
SMILES CC1=C(C(=O)N(N1C)C2=CC=CC=C2)NC(C)C
Reference

<p style=”/line-height:25px/”>
<span style=”font-family:arial,helvetica,sans-serif;”><span style=”font-size:12px;”><span style=”color:#000000;”>1.<span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Dowling, Geraldine, and Edward Malone. &quot;Analytical strategy for the confirmatory analysis of the non-steroidal anti-inflammatory drugs firocoxib, propyphenazone, ramifenazone and piroxicam in bovine plasma by liquid chromatography tandem mass spectrometry.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Journal of pharmaceutical and biomedical analysis</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;56.2 (2011): 359-365.<br />
2.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Nehra, Bhupender, et al. &quot;Recent advancements in the development of bioactive pyrazoline derivatives.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>European Journal of Medicinal Chemistry</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;(2020): 112666.</span><br />
<span style=”text-decoration: none; line-height: 18px; font-variant-ligatures: normal; orphans: 2; text-align: justify; widows: 2;”>3.</span><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>Kumar, R. Surendra, et al. &quot;Anti-inflammatory and antimicrobial activities of novel pyrazole analogues.&quot;&nbsp;</span><i style=”font-family: Arial, sans-serif; font-size: 13px; font-variant-ligatures: normal; orphans: 2; widows: 2;”>Saudi journal of biological sciences</i><span style=”font-variant-ligatures: normal; orphans: 2; widows: 2;”>&nbsp;23.5 (2016): 614-620.</span></span></span></span><br />
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