Literature DB >> 17971741

Cerebrosides from the roots of Serratula chinensis.

Tiejun Ling1, Tao Xia, Xiaochun Wan, Daxiang Li, Xiaoyi Wei.   

Abstract

A new cerebroside, 1-O-beta-D-glucopyranosyl-(2S,3R,8E)-2-[(2'R)-2-hydroxy- palmitoylamino]-8-octadecene-1,3-diol, along with aralia cerebroside and 1-O-beta-D- glucopyranosyl-(2S,3S,4R,8E)-2-[(2'R)-2-hydroxybehenoylamino]-8-octadecene-1,3,4-triol were isolated from the roots of Serratula chinensis S. Moore. The structure of the new cerebroside was established by spectroscopic and chemical means. Occurrence of cerebrosides in Serratula is reported here for the first time.

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Year:  2006        PMID： 17971741      PMCID： PMC6148527          DOI： 10.3390/11090677

Source DB:  PubMed          Journal:  Molecules        ISSN： 1420-3049            Impact factor:   4.411


  6 in total

1.  Isolation of a new cerebroside from the root bark of aralia elata

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Journal:  J Nat Prod       Date:  1999-07       Impact factor: 4.050

Review 2.  The cerebrosides.

Authors:  R X Tan; J H Chen
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3.  Sphingolipids and glycerolipids. I. Chemical structures and ionophoretic activities of soya-cerebrosides I and II from soybean.

Authors:  H Shibuya; K Kawashima; M Sakagami; H Kawanishi; M Shimomura; K Ohashi; I Kitagawa
Journal:  Chem Pharm Bull (Tokyo)       Date:  1990-11       Impact factor: 1.645

4.  New bioactive cerebrosides from Arisaema amurense.

Authors:  J H Jung; C O Lee; Y C Kim; S S Kang
Journal:  J Nat Prod       Date:  1996-03       Impact factor: 4.050

5.  Cyclooxygenase-2 inhibitory cerebrosides from phytolaccae radix.

Authors:  S S Kang; J S Kim; K H Son; H P Kim; H W Chang
Journal:  Chem Pharm Bull (Tokyo)       Date:  2001-03       Impact factor: 1.645

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Authors:  R Yamauchi; K Aizawa; T Inakuma; K Kato
Journal:  J Agric Food Chem       Date:  2001-02       Impact factor: 5.279
  6 in total
  5 in total

1.  Chloroform fraction of Serratulae chinensis S. Moore suppresses proliferation and induces apoptosis via the phosphatidylinositide 3-kinase/Akt pathway in human gastric cancer cells.

Authors:  Qiaoyan Cai; Jing Lin; Ling Zhang; Shan Lin; Jun Peng
Journal:  Oncol Lett       Date:  2018-03-28       Impact factor: 2.967

Review 2.  Use of Bodipy-labeled sphingolipid and cholesterol analogs to examine membrane microdomains in cells.

Authors:  David L Marks; Robert Bittman; Richard E Pagano
Journal:  Histochem Cell Biol       Date:  2008-09-27       Impact factor: 4.304

3.  Separation and Identification of Four New Compounds with Antibacterial Activity from Portulaca oleracea L.

Authors:  Xia Lei; Jianmin Li; Bin Liu; Ning Zhang; Haiyang Liu
Journal:  Molecules       Date:  2015-09-10       Impact factor: 4.411

Review 4.  Phytoecdysteroids: Distribution, Structural Diversity, Biosynthesis, Activity, and Crosstalk with Phytohormones.

Authors:  Yamshi Arif; Priyanka Singh; Andrzej Bajguz; Shamsul Hayat
Journal:  Int J Mol Sci       Date:  2022-08-04       Impact factor: 6.208

5.  Two new sphingolipids from the leaves of Piper betle L.

Authors:  Duo-Zhi Chen; Hua-Bin Xiong; Kai Tian; Jun-Ming Guo; Xiang-Zhong Huang; Zhi-Yong Jiang
Journal:  Molecules       Date:  2013-09-12       Impact factor: 4.411
  5 in total

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