Literature DB >> 19374387

Alkaloids from the roots of Stemona aphylla.

Pitchaya Mungkornasawakul1, Sukanda Chaiyong, Thanapat Sastraruji, Araya Jatisatienr, Chaiwat Jatisatienr, Stephen G Pyne, Alison T Ung, John Korth, Wilford Lie.   

Abstract

Three known compounds, stemofoline (1), (2'S)-hydroxystemofoline (2), and (11Z)-1',2'-didehydrostemofoline (3), along with two new alkaloids, stemaphylline (4) and stemaphylline-N-oxide (5), have been isolated from a root extract of Stemona aphylla. The structures of these alkaloids were determined on the basis of their spectroscopic data. The analysis of the crude dichloromethane extract by GC-MS in the EIMS mode showed the presence of alkaloids 1-4, the alkaloid 11, and stilbostemin R (12). The crude dichloromethane extract and 4 were tested for their comparative biological activities. The results of their acetylcholinesterase (AChE) inhibitory activities showed that the crude extract had higher activity than that of 4. The insecticidal properties of the crude extract and 4, using a topical application, showed that 4 had an activity similar to the positive control, methomyl, whereas the crude extract had much lower activity. Their antimicrobial activity against Escherichia coli ATCC 25922, Staphylococcus aureus ATCC 25923, Pseudomonas auruginosa ATCC 27853, and Candida albicans ATCC 90028 was weak (MIC 62.5-125 microg/mL, MBC 125-250 microg/mL, MFC 125 microg/mL) but much higher than that of the crude extract.

Entities:  

Mesh:

Substances:

Year:  2009        PMID: 19374387     DOI: 10.1021/np900030y

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  7 in total

1.  Total synthesis of stemaphylline N-oxide and related C9a-epimeric analogues.

Authors:  Michael L Schulte; Mark L Turlington; Sharangdhar S Phatak; Joel M Harp; Shaun R Stauffer; Craig W Lindsley
Journal:  Chemistry       Date:  2013-08-16       Impact factor: 5.236

2.  Asymmetric Formal Total Synthesis of the Stemofoline Alkaloids: The Evolution, Development and Application of a Catalytic Dipolar Cycloaddition Cascade.

Authors:  Charles S Shanahan; Chao Fang; Daniel H Paull; Stephen F Martin
Journal:  Tetrahedron       Date:  2013-09-09       Impact factor: 2.457

3.  Enantioselective formal total syntheses of didehydrostemofoline and isodidehydrostemofoline through a catalytic dipolar cycloaddition cascade.

Authors:  Chao Fang; Charles S Shanahan; Daniel H Paull; Stephen F Martin
Journal:  Angew Chem Int Ed Engl       Date:  2012-09-17       Impact factor: 15.336

Review 4.  Plant extracts as potential mosquito larvicides.

Authors:  Anupam Ghosh; Nandita Chowdhury; Goutam Chandra
Journal:  Indian J Med Res       Date:  2012-05       Impact factor: 2.375

5.  Stemofoline ethyl acetate solvate.

Authors:  Pitchaya Mungkornasawakul; Stephen G Pyne; Alison T Ung; Araya Jatisatienr; Anthony C Willis
Journal:  Acta Crystallogr Sect E Struct Rep Online       Date:  2009-07-18

6.  Stereocontrolled Total Synthesis of (-)-Stemaphylline.

Authors:  Ana Varela; Lennart K B Garve; Daniele Leonori; Varinder K Aggarwal
Journal:  Angew Chem Int Ed Engl       Date:  2017-01-18       Impact factor: 15.336

7.  Diastereo- and Enantioselective Access to Stereotriads through a Flexible Coupling of Substituted Aldehydes and Alkenes.

Authors:  Jing Li; Alexander Preinfalk; Nuno Maulide
Journal:  Angew Chem Int Ed Engl       Date:  2019-03-27       Impact factor: 15.336

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.