Literature DB >> 27539922

Cephalotanins A-D, Four Norditerpenoids Represent Three Highly Rigid Carbon Skeletons from Cephalotaxus sinensis.

Jin-Biao Xu1, Yao-Yue Fan1, Li-She Gan2, Yu-Bo Zhou1, Jia Li1, Jian-Min Yue3.   

Abstract

Four polycyclic norditerpenoids, cephalotanins A-D (1-4) representing three unprecedented carbon skeletons with highly rigid ring systems, were isolated from Cephalotaxus sinensis and structurally characterized by a combination of various methods. Compounds 1 and 2 are new skeletal norditerpenoid trilactones, while 3 and 4 are two norditerpenoids featuring different new carbon skeletons. Biosynthetic pathways for 1-4 were proposed by involving diverse and very fascinating chemical events with the coexisting cephalotane troponoids as the precursors. Compound 1 exhibited good NF-κB inhibition with an IC50 value of 4.12±0.61 μΜ.
© 2016 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

Entities:  

Keywords:  biosynthetic pathways; cephalotanins; cephalotaxus norditerpenoid; nf-κb inhibition; structural elucidation

Mesh:

Substances:

Year:  2016        PMID: 27539922     DOI: 10.1002/chem.201603373

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

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Review 2.  Natural Products Research in China From 2015 to 2016.

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3.  Trinorlabdane diterpenoid alkaloids featuring an unprecedented skeleton with anti-inflammatory and anti-viral activities from Forsythia suspensa.

Authors:  Wei Li; Lin Zhao; Li-Tong Sun; Ze-Ping Xie; Shu-Min Zhang; Xi-Dian Yue; Sheng-Jun Dai
Journal:  RSC Adv       Date:  2021-09-06       Impact factor: 4.036

  3 in total

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