Literature DB >> 25159309

Aromatic acid derivatives from the lateral roots of Aconitum carmichaelii.

Zhi-Bo Jiang1, Bing-Ya Jiang, Cheng-Gen Zhu, Qing-Lan Guo, Ying Peng, Xiao-Liang Wang, Sheng Lin, Jian-Gong Shi.   

Abstract

Seven new aromatic acid derivatives (1-7), together with five known analogs, were isolated from the lateral roots of Aconitum carmichaelii. Structures of the new compounds were determined by spectroscopic and chemical methods as 4-methyl ( - )-(R)-hydroxyeucomate (1), 4-butyl ( - )-(R)-hydroxyeucomate (2), 4-butyl-1-methyl (+)-(R)-2-O-(4'-hydroxy-3'-methoxybenzoyl)malate (3), 1-butyl-4-methyl (+)-(R)-2-O-(4'-hydroxy-3'-methoxybenzoyl)malate (4), dimethyl (+)-(R)-2-O-(4'-hydroxy-3'-methoxybenzoyl)malate (5), dimethyl (+)-(R)-2-O-(4'-hydroxybenzoyl)malate (6), and methyl ( ± )-3-(4'-hydroxy-3'-methoxyphenyl)-3-sulfopropionate (7), respectively. Compounds 1 and 2 are 2-benzylmalates (eucomate derivatives), 3-6 belong to 2-O-benzoylmalates, and 7 is a rare phenylpropionate containing a sulfonic acid group. The absolute configurations of eucomate derivatives were confirmed by X-ray crystallographic analysis of 4-methyl eucomate (11).

Entities:  

Keywords:  (R)-2-O-benzoylmalates; (R)-2-benzylmalates; Aconitumcarmichaelii; Ranunculaceae; methyl 3-(4′-hydroxy-3′-methoxyphenyl)-3-sulfopropionate

Mesh:

Substances:

Year:  2014        PMID: 25159309     DOI: 10.1080/10286020.2014.939585

Source DB:  PubMed          Journal:  J Asian Nat Prod Res        ISSN: 1028-6020            Impact factor:   1.569


  8 in total

1.  Chemical Constituents from the Roots and Rhizomes of Sophora tonkinensis and Their Effects on Proprotein Convertase Substilisin/Kexin Type 9 Expression.

Authors:  Pisey Pel; Hee-Sung Chae; Piseth Nhoek; Young-Mi Kim; Chae-Yeong An; Hunseung Yoo; Minseok Kang; Hyun Woo Kim; Young Hee Choi; Young-Won Chin
Journal:  ACS Omega       Date:  2022-06-08

Review 2.  Non-alkaloidal constituents from the genus Aconitum: a review.

Authors:  Tianpeng Yin; Hao Zhou; Le Cai; Zhongtao Ding
Journal:  RSC Adv       Date:  2019-04-02       Impact factor: 4.036

3.  Indole alkaloid sulfonic acids from an aqueous extract of Isatis indigotica roots and their antiviral activity.

Authors:  Lingjie Meng; Qinglan Guo; Yufeng Liu; Minghua Chen; Yuhuan Li; Jiandong Jiang; Jiangong Shi
Journal:  Acta Pharm Sin B       Date:  2017-04-29       Impact factor: 11.413

4.  Aromatic compounds from an aqueous extract of "ban lan gen" and their antiviral activities.

Authors:  Yufeng Liu; Minghua Chen; Qinglan Guo; Yuhuan Li; Jiandong Jiang; Jiangong Shi
Journal:  Acta Pharm Sin B       Date:  2016-11-08       Impact factor: 11.413

5.  C19-Diterpenoid alkaloid arabinosides from an aqueous extract of the lateral root of Aconitum carmichaelii and their analgesic activities.

Authors:  Qinglan Guo; Huan Xia; Xianhua Meng; Gaona Shi; Chengbo Xu; Chenggen Zhu; Tiantai Zhang; Jiangong Shi
Journal:  Acta Pharm Sin B       Date:  2018-03-27       Impact factor: 11.413

6.  Sulfur-enriched alkaloids from the root of Isatis indigotica.

Authors:  Qinglan Guo; Chengbo Xu; Minghua Chen; Sheng Lin; Yuhuan Li; Chenggen Zhu; Jiandong Jiang; Yongchun Yang; Jiangong Shi
Journal:  Acta Pharm Sin B       Date:  2018-08-23       Impact factor: 11.413

7.  Three pairs of alkaloid enantiomers from the root of Isatis indigotica.

Authors:  Yufeng Liu; Xiaoliang Wang; Minghua Chen; Sheng Lin; Li Li; Jiangong Shi
Journal:  Acta Pharm Sin B       Date:  2016-02-11       Impact factor: 11.413

8.  8,4'-Oxyneolignane glucosides from an aqueous extract of "ban lan gen" (Isatis indigotica root) and their absolute configurations.

Authors:  Lingjie Meng; Qinglan Guo; Yufeng Liu; Jiangong Shi
Journal:  Acta Pharm Sin B       Date:  2017-10-18       Impact factor: 11.413

  8 in total

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