Imrecoxib

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Company Name: ZHENGZHOU JIUYI TIME NEW MATERIALS CO,.LTD
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Products Intro: Product Name:Imrecoxib
CAS:395683-14-4
Purity:99% Package:100kg;2USD|10kg;4USD|1kg;5USD
Company Name: TargetMol Chemicals Inc.
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Products Intro: Product Name:Imrecoxib
CAS:395683-14-4
Purity:99.94% Package:25mg;29.00;USD|50mg; Remarks:REAGENT;FOR LABORATORY USE ONLY
Company Name: Dideu Industries Group Limited
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Products Intro: Product Name:Imrecoxib
CAS:395683-14-4
Purity:99.9% Package:1g;1.1USD Remarks:FDA GMP CEP Approved Manufacturer
Company Name: Hangzhou Huarong Pharm Co., Ltd.
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Products Intro: Product Name:2H-Pyrrol-2-one,1,5-dihydro-3-(4-methylphenyl)-4-[4-(methylsulfonyl)phenyl]-1-propyl-
CAS:395683-14-4
Purity:0.99 Package:10MG,50MG,100MG,1G
Company Name: SUZHOU SENFEIDA CHEMICAL CO.,LTD
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Products Intro: Product Name:Imrecoxib
CAS:395683-14-4
Purity:0.99 Package:25KG

Imrecoxib manufacturers

  • Imrecoxib
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  • $29.00 / 25mg
  • 2026-04-21
  • CAS:395683-14-4
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  • Purity: 99.94%
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  • Imrecoxib
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  • $2.00 / 100kg
  • 2026-04-17
  • CAS:395683-14-4
  • Min. Order: 1kg
  • Purity: 99%
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  • Imrecoxib
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  • $0.00 / 25kg
  • 2025-12-01
  • CAS:395683-14-4
  • Min. Order: 1kg
  • Purity: 98%
  • Supply Ability: 1000kg
Imrecoxib Basic information
Product Name:Imrecoxib
Synonyms:Imrecoxib;2H-Pyrrol-2-one, 1,5-dihydro-3-(4-methylphenyl)-4-[4-(methylsulfonyl)phenyl]-1-propyl-;Imrecoxib USP/EP/BP;BAP 909,Cyclooxygenase,Inhibitor,COX,Imrecoxib,inhibit,BAP909;Imrecoxib, 10 mM in DMSO;Imrecoxib (BAP-909);4-(4-(Methylsulfonyl)phenyl)-1-propyl-3-(p-tolyl)-1,5-dihydro-2H-pyrrol-2-one;Airixib
CAS:395683-14-4
MF:C21H23NO3S
MW:369.48
EINECS:
Product Categories:
Mol File:395683-14-4.mol
Imrecoxib Structure
Imrecoxib Chemical Properties
Boiling point 604.1±55.0 °C(Predicted)
density 1+-.0.06 g/cm3(Predicted)
storage temp. Store at -20°C
solubility DMSO: 100 mg/mL (270.65 mM)
pka-2.25±0.60(Predicted)
form Solid
color White to off-white
InChIInChI=1S/C21H23NO3S/c1-4-13-22-14-19(16-9-11-18(12-10-16)26(3,24)25)20(21(22)23)17-7-5-15(2)6-8-17/h5-12H,4,13-14H2,1-3H3
InChIKeyAXMZZGKKZDJGAZ-UHFFFAOYSA-N
SMILESN1(CCC)CC(C2=CC=C(S(C)(=O)=O)C=C2)=C(C2=CC=C(C)C=C2)C1=O
CAS DataBase Reference395683-14-4
Safety Information
MSDS Information
Imrecoxib Usage And Synthesis
UsesImrecoxib (BAP-909) is a novel and selective cyclooxygenase 2 (COX-2) inhibitor with an IC50 value of 18 nM, it also inhibits COX1- activity with an IC50 value of 115 nM. Imrecoxib (BAP-909) has anti-inflammatory effect[1].
Clinical UseImrecoxib, a new non-steroid anti-inflammtory drug (NSAID), was launched in China with the trade name of Hengyang® for the treatment of osteoarthritis in 2012. It was originally designed and synthesized by Guo and co-workers at the Institute of Materia Medica (IMM) of the Chinese Academy of Medical Sciences in collaboration with Hengrui Pharmaceuticals. Imrecoxib, which is a moderately selective COX-2 inhibitor (with IC50 values against COX-1 and COX-2 being 115 ± 28 nM and 18 4 nM, respectively).
SynthesisImrecoxib has had two synthetic routes reported across several publications. The most likely process-scale route to this drug is described in the scheme, which began with 2-bromo-4'-(methylsulfonyl)-acetophenone (84) and p-tolylacetic acid (85) as starting materials. In the presence of base, |á-bromoketone 84 was treated with acid 85 which resulted in lactone 86 in 72% yield across the two-step sequence. Exposure of lactone 86 with propylamine triggered a ring-opening-ring closing reaction, which resulted in imrecoxib (XIII) directly in 85% yield.

Synthesis_395683-14-4

in vivo

Imrecoxib (BAP-909) (gastrointestinal administration; 5-20 mg/kg; 1 hour before carrageenan injection) inhibits carrageenan-induced acute inflammation, and the inhibitory effect is maximal at 4 hours[1]. Imrecoxib (BAP-909) (gastrointestinal administration; 5-20 mg/kg; started on day 7; 26 days) diminishes the secondary paw swelling and inhibits heat-inactivated BCG induced-inflammtory polyarthritis[1].

Animal Model:Rat carrageenan-induced edema model[1]
Dosage:5 mg/kg, 10 mg/kg, 20 mg/kg
Administration:Gastrointestinal administration; 5-20 mg/kg; 1 hour before carrageenan injection
Result:Inhibited the edema response with different doses.
Animal Model:Rat adjuvant-induced arthritis (AIA) model[1]
Dosage:5 mg/kg, 10 mg/kg, 20 mg/kg
Administration:Gastrointestinal administration; 5-20 mg/kg; started on day 7; 26 days
Result:Inhibited adjuvant-induced chronic inflammation at the doses of 10 and 20 mg/kg.
IC 50Human COX-1: 115 nM (IC50); Human COX-2: 18 nM (IC50)
References[1] Chen XH, et al. Imrecoxib: a novel and selective cyclooxygenase 2 inhibitor with anti-inflammatory effect. Acta Pharmacol Sin. 2004 Jul;25(7):927-31. PMID:15210067
Imrecoxib Preparation Products And Raw materials
Tag:Imrecoxib(395683-14-4) Related Product Information
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