Basic information Safety Supplier Related
ChemicalBook >  Product Catalog >  API >  Antipyretic analgesics >  Nonsteroidal Anti-Inflammatory Drugs (NSAIDS) >  Loxoprofen sodium

Loxoprofen sodium

Basic information Safety Supplier Related

Loxoprofen sodium Basic information

Product Name:
Loxoprofen sodium
Synonyms:
  • alpha-methyl-4-((2-oxocyclopentyl)methyl)benzeneacetatesodiumsaltdihydrate
  • benzeneaceticacid,alpha-methyl-4-((2-oxocyclopentyl)methyl)-,sodiumsalt,di
  • cs-600
  • loxoprofensodium(patented-nosupply)
  • Loxoprofen sodium dihydrate, >=99%
  • Sodium 2-(4-((2-oxocyclopentyl)methyl)phenyl)propanoate
  • sodium 2-[4-[(2-oxocyclopentyl)methyl]phenyl]propanoate dihydrate
  • 2-{4-[(2-Oxocyclopentyl)methyl]phenyl}propanoic acid sodium salt
CAS:
80382-23-6
MF:
C15H19NaO3
MW:
270.3
EINECS:
1806241-263-5
Product Categories:
  • Analgesics
  • Aromatics
  • Inhibitors
  • Intermediates & Fine Chemicals
  • Pharmaceuticals
  • Antipyretic analgesics
  • Other APIs
  • APIS
  • 80382-23-6
Mol File:
80382-23-6.mol
More
Less

Loxoprofen sodium Chemical Properties

storage temp. 
Inert atmosphere,Room Temperature
solubility 
DMSO: soluble
form 
A solid
color 
White to off-white
InChI
InChI=1S/C15H18O3.Na.H/c1-10(15(17)18)12-7-5-11(6-8-12)9-13-3-2-4-14(13)16;;/h5-8,10,13H,2-4,9H2,1H3,(H,17,18);;
InChIKey
ALZXNWUYLUBHJL-UHFFFAOYSA-N
SMILES
C(C1CCCC1=O)C1C=CC(C(C)C(=O)O)=CC=1.[NaH]
CAS DataBase Reference
80382-23-6(CAS DataBase Reference)
More
Less

Loxoprofen sodium Usage And Synthesis

Description

Loxoprofen sodium i s an antiinflammatory/analgesic agent useful in the management of rheumatoid arthritis and related disorders. It is converted in vivo to the corresponding trans-hydroxycyclopentane analog, through which it appears to exert its activity.

Originator

Sankyo (Japan)

Uses

anti-inflammatory

Definition

ChEBI: A hydrate that is the dihydrate form of loxoprofen sodium. The parent acid, loxoprofen, is a prodrug that is rapidly converted to its active trans-alcohol metabolite following oral administration.

brand name

LOXONIN

Mechanism of action

As most NSAIDs, loxoprofen is a non-selective cyclooxygenase inhibitor, and works by reducing the synthesis of prostaglandins from arachidonic acid.

Side effects

Adverse effects include anorexia, nausea, vomiting, bleeding, anemia, diarrhea, and constipation.

Synthesis

68767-14-6

80382-23-6

General procedure for the synthesis of sodium 2-(4-((2-oxocyclopentyl)methyl)phenyl)propionate from 2-(4-((2-oxocyclopentyl)methyl)phenyl)propionic acid: 2-(4-((2-oxocyclopentyl)methyl)phenyl)propionic acid and methanol were added into a round-bottomed flask, and 1 equivalent of aqueous sodium hydroxide was added to the above solution drop by drop, and the reaction was stirred for 1 hour at room temperature. Upon completion of the reaction, a decompression distillation was carried out at 50-55°C to remove the solvent. Subsequently, a 5% aqueous solution of ethyl acetate was added to the residue, heated until dissolved and then slowly cooled to room temperature. Crystallization was induced by the addition of crystal seeds during cooling and stirring was continued for 5-6 hours at 0-5°C until a suspension was formed. Finally, the solid was collected by filtration to give loxoprofen sodium dihydrate in 95% yield and 99.1% HPLC purity.

References

[1] Journal of Medicinal Chemistry, 2010, vol. 53, # 21, p. 7879 - 7882
[2] Patent: CN107176942, 2017, A. Location in patent: Paragraph 0067; 0068; 0069
[3] Patent: CN108440274, 2018, A. Location in patent: Paragraph 0076; 0077; 0078; 0079; 0080

Loxoprofen sodiumSupplier

Wuhan Penglei Biological Technology Co., Ltd. Gold
Tel
18672616696
Email
229092275@qq.com
Beijing ECom Technology Co., Ltd. Gold
Tel
17710328343
Email
3004011422@qq.com
Wuhan haorong Biotechnology Co., Ltd Gold
Tel
13217229939
Email
773651767@qq.com
Huzhou Qingliu Silicate Biotechnology Co., Ltd Gold
Tel
13626726938
Email
15952452933@163.cn
J & K SCIENTIFIC LTD.
Tel
18210857532; 18210857532
Email
jkinfo@jkchemical.com