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N-(tert-butyloxycarbonyl)-Nε-(benzyloxycarbonyl)-L-lysinyl-1H,1H,2H,2H-perfluorooctylamide is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

887760-22-7

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887760-22-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 887760-22-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,7,7,6 and 0 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 887760-22:
(8*8)+(7*8)+(6*7)+(5*7)+(4*6)+(3*0)+(2*2)+(1*2)=227
227 % 10 = 7
So 887760-22-7 is a valid CAS Registry Number.

887760-22-7Downstream Products

887760-22-7Relevant academic research and scientific papers

Fluorinated amphiphilic amino acid derivatives as antioxidant carriers: A new class of protective agents

Ortial, Stéphanie,Durand, Grégory,Poeggeler, Burkhard,Polidori, Ange,Pappolla, Miguel A.,B?ker, Jutta,Hardeland, Rüdiger,Pucci, Bernard

, p. 2812 - 2820 (2007/10/03)

The use of classical antioxidants is limited by their low bioavailabilities, and therefore, high doses are usually required to display significant protective activity. In a recent article (J. Med. Chem. 2003, 46, 5230) we showed that the ability of the α-phenyl-N-tert-butylnitrone (PBN) to restore the viability of ATPase-deficient human skin fibroblasts was greatly enhanced by grafting it on a fluorinated amphiphilic carrier. With the aim of extending this concept to other antioxidants, we present here the design, the synthesis, and the physicochemical measurements of a new series of fluorinated amphiphilic antioxidant derivatives. The hydroxyl radical scavenging activity and the radical reducing potency of these newly designed compounds were respectively demonstrated in an ABTS competition and an ABTS.+ reduction assay. We also showed that the protective effects of amphiphilic antioxidants derived from PBN, Trolox (6-hydroxy-2,5,7,8-tetramethylchroman-2- carboxylic acid) or lipoic acid (5-[1,2]-dithiolan-3-ylpentanoic acid) in primary cortical mixed cell cultures exposed to oxidotoxins are greatly improved compared to their parent compounds in the following rank-order: (1) PBN, (2) Trolox, and (3) lipoic acid. In contrast, the protective activity of indole-3-propionic acid was slightly decreased by grafting it on the amphiphilic carrier. Similar observations were made in in vivo experiments using aquatic invertebrate microorganisms, called rotifers, which were exposed to lethal concentrations of nonselective (H2O2) and mitochondria-selective (doxorubicin) oxidotoxins. The conclusion of these studies is that fluorinated amphiphilic PBN, Trolox, and lipoic acid derivatives exhibit very potent protective activities in in vitro and in vivo experiments. The findings demonstrated herein therefore strongly suggest that the amphiphilic character enhances the bioavailability of the antioxidants and allows for a selective targeting of mitochondria.

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