Literature DB >> 17939738

Biologically active aspidofractinine, rhazinilam, akuammiline, and vincorine alkaloids from Kopsia.

G Subramaniam1, Osamu Hiraku, Masahiko Hayashi, Takashi Koyano, Kanki Komiyama, Toh-Seok Kam.   

Abstract

Eleven new indole alkaloids, in addition to the previously reported rhazinal (1), and 14 other known alkaloids, were obtained from the Malayan Kopsia singapurensis, viz., kopsiloscines A-F (2-7), 16-epikopsinine (8), kopsilongine- N-oxide (9), 16-epiakuammiline (10), aspidophylline A (11), and vincophylline (12). The structures of these alkaloids were determined using NMR and MS analyses. Rhazinal (1), rhazinilam (17), and rhazinicine (18) showed appreciable cytotoxicity toward drug-sensitive as well as vincristine-resistant KB cells, while kopsiloscines A (2), B (3), and D (5) and aspidophylline A (11) were found to reverse drug-resistance in drug-resistant KB cells.

Entities:  

Mesh:

Substances:

Year:  2007        PMID: 17939738     DOI: 10.1021/np0703747

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


  12 in total

1.  Total synthesis of (+)-scholarisine A.

Authors:  Gregory L Adams; Patrick J Carroll; Amos B Smith
Journal:  J Am Chem Soc       Date:  2012-01-25       Impact factor: 15.419

2.  Synthesis of 3,3'-Disubstituted Indolenines Utilizing the Lewis Acid Catalyzed Alkylation of 2,3-Disubstituted Indoles with Trichloroacetimidates.

Authors:  Arijit A Adhikari; Léa Radal; John D Chisholm
Journal:  Synlett       Date:  2017-07-11       Impact factor: 2.454

3.  Exploration of the interrupted Fischer indolization reaction.

Authors:  Alex W Schammel; Ben W Boal; Liansuo Zu; Tehetena Mesganaw; Neil K Garg
Journal:  Tetrahedron       Date:  2010-06-26       Impact factor: 2.457

Review 4.  Synthesis of indole derivatives as prevalent moieties present in selected alkaloids.

Authors:  Majid M Heravi; Zahra Amiri; Kosar Kafshdarzadeh; Vahideh Zadsirjan
Journal:  RSC Adv       Date:  2021-10-15       Impact factor: 4.036

5.  Pardon the Interruption: A Modification of Fischer's Venerable Reaction for the Synthesis of Heterocycles and Natural Products.

Authors:  Robert B Susick; Lucas A Morrill; Elias Picazo; Neil K Garg
Journal:  Synlett       Date:  2017       Impact factor: 2.454

6.  Access to the akuammiline family of alkaloids: total synthesis of (+)-scholarisine A.

Authors:  Gregory L Adams; Patrick J Carroll; Amos B Smith
Journal:  J Am Chem Soc       Date:  2012-12-26       Impact factor: 15.419

7.  Direct, Enantioselective Synthesis of Pyrroloindolines and Indolines From Simple Indole Derivatives.

Authors:  Jane Ni; Haoxuan Wang; Sarah E Reisman
Journal:  Tetrahedron       Date:  2013-07-08       Impact factor: 2.457

8.  Understanding and Interrupting the Fischer Azaindolization Reaction.

Authors:  Bryan J Simmons; Marie Hoffmann; Pier Alexandre Champagne; Elias Picazo; Katsuya Yamakawa; Lucas A Morrill; K N Houk; Neil K Garg
Journal:  J Am Chem Soc       Date:  2017-10-12       Impact factor: 15.419

9.  Dialkylation of Indoles with Trichloroacetimidates to Access 3,3-Disubstituted Indolenines.

Authors:  Tamie Suzuki; Nilamber A Mate; Arijit A Adhikari; John D Chisholm
Journal:  Molecules       Date:  2019-11-15       Impact factor: 4.411

10.  Total synthesis of the akuammiline alkaloid picrinine.

Authors:  Joel M Smith; Jesus Moreno; Ben W Boal; Neil K Garg
Journal:  J Am Chem Soc       Date:  2014-03-12       Impact factor: 15.419

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.