Literature DB >> 32127260

Study on structure-activity relationship of vitamin K derivatives: Conversion of the naphthoquinone part into another aromatic ring and evaluation of their neuronal differentiation-inducing activity.

Hiroshi Yoshimura1, Yoshihisa Hirota2, Seiya Soda1, Mayu Okazeri3, Yuta Takagi3, Atsuko Takeuchi4, Chisato Tode4, Maya Kamao5, Naomi Osakabe6, Yoshitomo Suhara7.   

Abstract

We synthesized novel vitamin K derivatives by converting the naphthoquinone group to benzene derivatives and benzoquinone. We evaluated their neuronal differentiation activities to investigate the effect of the quinone moiety on this process. We observed that the 1,4-quinone as well as the side chain part play important roles in neuronal differentiation. We also performed QSAR analysis to predict the compounds which would have higher differentiation activity.
Copyright © 2020 The Authors. Published by Elsevier Ltd.. All rights reserved.

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Keywords:  Neural differentiation; Neuron; Structure-activity relationship; Vitamin K

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Year:  2020        PMID: 32127260     DOI: 10.1016/j.bmcl.2020.127059

Source DB:  PubMed          Journal:  Bioorg Med Chem Lett        ISSN: 0960-894X            Impact factor:   2.823


  1 in total

1.  Naturally occurring UBIAD1 mutations differentially affect menaquinone biosynthesis and vitamin K-dependent carboxylation.

Authors:  Xuejie Chen; Natsuko Furukawa; Da-Yun Jin; Yizhou Liu; Darrel W Stafford; Craig M Williams; Yoshitomo Suhara; Jian-Ke Tie
Journal:  FEBS J       Date:  2021-12-01       Impact factor: 5.622

  1 in total

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