Literature DB >> 5579257

New synthetic phosphinate analogues of lecithin.

A F Rosenthal, S V Chodsky.   

Abstract

The chemical syntheses of two new, completely nonhydrolyzable phosphinate analogues of lecithin are described. These have the structures ROCH(2)CH(OR)CH(2)CH(2)P(O)(O(-))CH(2)CH(2)N(+)(CH(3))(3) and ROCH(2)CH(OR')CH(2)P(O)(O(-))CH(2)CH(2)CH(2)N(+)(CH(3))(3), where R = C(18)H(37) and R' = C(16)H(33); each is thus isosteric with lecithin on either side of the phosphorus function. The infrared spectra of these compounds undergo unexpected changes under mild acid, base, or adsorptive treatment. These are discussed and compared with related lecithin analogues, including the simple phosphinate C(18)H(37)P(O)(O(-))CH(2)CH(2)N(+)(CH(3))(3), whose synthesis is also reported.

Entities:  

Mesh:

Substances:

Year:  1971        PMID: 5579257

Source DB:  PubMed          Journal:  J Lipid Res        ISSN: 0022-2275            Impact factor:   5.922


  1 in total

1.  Inhibition of phospholipase C by isosteric phosphinic acid analogues of lecithin.

Authors:  A F Rosenthal; S V Chodsky
Journal:  Lipids       Date:  1974-02       Impact factor: 1.880

  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.