XILVEPYQJIOVNB-ZEJCXXMWSA-N

XILVEPYQJIOVNB-ZEJCXXMWSA-N Suppliers list
Company Name: Energy Chemical  
Tel: 021-58432009 400-005-6266
Email: marketing1@energy-chemical.com
Products Intro: Product Name:Etofenamate-d4
CAS:1329837-73-1
Purity:NULL Package:10mg;1mg Remarks:NULL
Company Name: ChemeGen 中国  
Tel: 18818260767
Email: sales@chemegen.com
Products Intro: Product Name:Etofenamate-d4
CAS:1329837-73-1
Purity:98% Package:10 mg;50 mg;100 mg;500 mg;1 g;5 g;10 g
Company Name: Shanghai Yiyan Biotechnology Co. , Ltd.  
Tel: 021-69985186 13611928337
Email: 3427709316@qq.com
Products Intro: Product Name:Etofenamate-d4
CAS:1329837-73-1
Company Name: Shanghai Yifei Biotechnology Co. , Ltd.  
Tel: 021-65675885 18964387627
Email: customer_service@efebio.com
Products Intro: Product Name:Etofenamate-d4
CAS:1329837-73-1
Purity:>95% Package:5mg
Company Name: Hubei Qingbei Yunyan Pharmaceutical Technology Co., Ltd  
Tel: 18162595016
Email: 3287908757@qq.com
Products Intro: Product Name:Ibudilast Impurity 1
CAS:1329837-73-1
Purity:95%+HPLC Package:10mg;25mg;50mg;100mg;200mg
XILVEPYQJIOVNB-ZEJCXXMWSA-N Basic information
Product Name:XILVEPYQJIOVNB-ZEJCXXMWSA-N
Synonyms:XILVEPYQJIOVNB-ZEJCXXMWSA-N
CAS:1329837-73-1
MF:C18H14D4F3NO4
MW:373.359676712
EINECS:
Product Categories:
Mol File:1329837-73-1.mol
XILVEPYQJIOVNB-ZEJCXXMWSA-N Structure
XILVEPYQJIOVNB-ZEJCXXMWSA-N Chemical Properties
storage temp. Store at -20°C
solubility Acetonitrile: soluble,Methanol: soluble
form An oil
Safety Information
MSDS Information
XILVEPYQJIOVNB-ZEJCXXMWSA-N Usage And Synthesis
UsesMedication used to alleviate joint and muscle pain.
Biological ActivityEtofenamate-d4 is intended for use as an internal standard for the quantification of etofenamate by GC- or LC-MS. Etofenamate is a non-steroidal anti-inflammatory drug (NSAID) and diethylene glycol ester form of flufenamic acid that has anti-inflammatory and analgesic activities.1,2 It inhibits lipoxygenase isolated from guinea pig leukocytes (IC50 = 5.3 μM) and the production of prostaglandin E2 in stimulated rat peritoneal macrophages.2 In vivo, etofenamate reduces acetic acid-induced vascular permeability in mice and UV-induced erythema in guinea pigs in a dose-dependent manner at doses ranging from 40-320 and 5-20 mg/kg, respectively.1 Etofenamate (40 mg/kg per day for 21 days) inhibits inflammation in a rat model of adjuvant-induced arthritis. It also decreases the pain response in a silver nitrate-induced rat model of arthritis and the acetic acid-induced writhing test in mice, indicating analgesic activity. Formulations containing etofenamate have been used in the treatment of osteoarthritis.
References1.Nakamura, H., Motoyoshi, S., Imazu, C., et al.Anti-inflammatory, analgesic and anti-pyretic activities of a non-steroidal anti-inflammatory drug, etofenamate, in experimental animalsNihon Yakurigaku Zasshi.80(2)125-135(1982) 2.Nakamura, H., Motoyoshi, S., Ishii, K., et al.The mode of anti-inflammatory action of a topical non-steroidal anti-inflammatory drug, etofenamateNihon Yakurigaku Zasshi.89(1)15-24(1987)
XILVEPYQJIOVNB-ZEJCXXMWSA-N Preparation Products And Raw materials
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