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(2S)-2-(4-isobutylphenyl)propionic acid 2-methylaminoethyl ester is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

1385022-07-0

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1385022-07-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1385022-07-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,8,5,0,2 and 2 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 1385022-07:
(9*1)+(8*3)+(7*8)+(6*5)+(5*0)+(4*2)+(3*2)+(2*0)+(1*7)=140
140 % 10 = 0
So 1385022-07-0 is a valid CAS Registry Number.

1385022-07-0Downstream Products

1385022-07-0Relevant academic research and scientific papers

In vitro and in vivo investigation of dexibuprofen derivatives for CNS delivery

Xuan, Zhang,Xing, Liu,Tao, Gong,Xun, Sun,Zhang, Zhi-Rong

, p. 279 - 288 (2012/07/01)

Aim:Dexibuprofen, the S(+)-isomer of ibuprofen, is an effective therapeutic agent for the treatment of neurodegenerative disorders. However, its clinical use is hampered by a limited brain distribution. The aim of this study was to design and synthesize brain-targeting dexibuprofen prodrugs and to evaluate their brain-targeting efficiency using biodistribution and pharmacokinetic analysis.Methods:In vitro stability, biodistribution and pharmacokinetic studies were performed on male Sprague-Dawley rats. The concentrations of dexibuprofen in biosamples, including the plasma, brain, heart, liver, spleen, lung, and kidney, were measured using high pressure lipid chromatography (HPLC). The pharmacokinetic parameters of the drug in the plasma and tissues were calculated using obtained data and statistics.Results:Five dexibuprofen prodrugs that were modified to contain ethanolamine-related structures were designed and synthesized. Their chemical structures were confirmed using 1 H NMR, 13 C NMR, IR, and HRMS. In the biodistribution study, 10min after intravenous administration of dexibuprofen (11.70 mg/kg) and its prodrugs (the dose of each compound was equivalent to 11.70 mg/kg of dexibuprofen) in male Sprague-Dawley rats, the dexibuprofen concentrations in the brain and plasma were measured. The C brain /C plasma ratios of prodrugs 1, 2, 3, 4, and 5 were 17.0-, 15.7-, 7.88-, 9.31-, and 3.42-fold higher than that of dexibuprofen, respectively (P0.01). Thus, each of the prodrugs exhibited a significantly enhanced brain distribution when compared with dexibuprofen. In the pharmacokinetic study, prodrug 1 exhibited a brain-targeting index of 11.19 {DTI=(AUC brain /AUC plasma) 1 /(AUC brain /AUC plasma) dexibuprofen }.Conclusion:The ethanolamine-related structures may play an important role in transport across the brain blood barrier.

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