Loxoprofen Sodium CAS NO.80382-23-6

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Loxoprofen Sodium CAS NO.80382-23-6
Details
Additives; antipyretic and analgesic; phenylpropionic acid non-steroidal anti-inflammatory drugs JP/KP GMP
Category
Loxoprofen APIs
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Description

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:

C15H17NaO3

MW:

268.283

EINECS:

1806241-263-5

Physical and Chemical Properties

Melting point

Null

Boiling point

417.9ºC at 760 mmHg

Storage Condition

2-8° CInert atmosphere,Room Temperature

Flash Point 220.7℃

Form

Null

Solubility

Null

Usage

Descripyion 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.

Uses

Used as an anti-inflammatory and analgesic

 

After oral administration of Le Song, it is quickly absorbed in the gastrointestinal tract, and appears in the blood in the form of loxoprofen sodium and anti-OH metabolites (active metabolites), and is distributed in the liver, kidneys, and kidneys in higher concentrations. In the plasma. The peak time after oral administration of 60 mg of Lepine for healthy adults is 30 minutes for the original drug, and about 50 minutes for the active metabolite. The protein binding rate of the original product is 97. Chemicalbook 0%, and the protein binding rate of the active metabolite is 92.8%. Part of the glucuronic acid conjugate or hydroxylated glucuronic acid conjugate is mainly excreted quickly through urine, and about 50% of it is excreted within 8 hours after oral administration. Oral for 5 consecutive days, no accumulation. The half-life of the original product is 1.2h, and the half-life of the active metabolite is 1.3h.

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