Literature DB >> 12530851

Haouamines A and B: a new class of alkaloids from the ascidian Aplidium haouarianum.

Leda Garrido1, Eva Zubía, María J Ortega, Javier Salvá.   

Abstract

The chemical study of the ascidian Aplidium haouarianum has led to the isolation of the new metabolites haouamines A (1) and B (2) which belong to a novel class of alkaloids. The structure of 1 was established by interpretation of its spectroscopic data and those of the N-methyl derivative 3, and confirmed by X-ray crystallographic analysis. The structure of 2 was deduced by spectroscopic study of its peracetyl derivative 2a. In solution each haouamine exists as an unseparable mixture of two interconverting isomers derived by the presence of a highly strained 3-aza-[7]-paracyclophane moiety in their structures. Compound 1 exhibits a selective cytotoxic activity against the HT-29 human colon carcinoma cell line.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12530851     DOI: 10.1021/jo020487p

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  12 in total

1.  Use of a tandem Prins/Friedel-Crafts reaction in the construction of the indeno-tetrahydropyridine core of the haouamine alkaloids: formal synthesis of (-)-haouamine A.

Authors:  Erik Fenster; Charlie Fehl; Jeffrey Aubé
Journal:  Org Lett       Date:  2011-04-25       Impact factor: 6.005

2.  Formal total synthesis of the cytotoxic marine ascidian alkaloid haouamine A.

Authors:  Jeannie H Jeong; Steven M Weinreb
Journal:  Org Lett       Date:  2006-05-25       Impact factor: 6.005

3.  Total synthesis of haouamine A: the indeno-tetrahydropyridine core.

Authors:  Noah Z Burns; Mikkel Jessing; Phil S Baran
Journal:  Tetrahedron       Date:  2009-08-15       Impact factor: 2.457

Review 4.  Applications of Friedel-Crafts reactions in total synthesis of natural products.

Authors:  Majid M Heravi; Vahideh Zadsirjan; Pegah Saedi; Tayebeh Momeni
Journal:  RSC Adv       Date:  2018-12-03       Impact factor: 4.036

5.  Chemoselectivity: the mother of invention in total synthesis.

Authors:  Ryan A Shenvi; Daniel P O'Malley; Phil S Baran
Journal:  Acc Chem Res       Date:  2009-04-21       Impact factor: 22.384

6.  Scalable total synthesis and biological evaluation of haouamine A and its atropisomer.

Authors:  Noah Z Burns; Irina N Krylova; Rami N Hannoush; Phil S Baran
Journal:  J Am Chem Soc       Date:  2009-07-08       Impact factor: 15.419

Review 7.  Recent highlights in biosynthesis research using stable isotopes.

Authors:  Jan Rinkel; Jeroen S Dickschat
Journal:  Beilstein J Org Chem       Date:  2015-12-09       Impact factor: 2.883

8.  Nickel-Catalyzed C-3 Direct Arylation of Pyridinium Ions for the Synthesis of 1-Azafluorenes.

Authors:  Jean-Nicolas Desrosiers; Xudong Wei; Osvaldo Gutierrez; Jolaine Savoie; Bo Qu; Xingzhong Zeng; Heewon Lee; Nelu Grinberg; Nizar Haddad; Nathan K Yee; Frank Roschangar; Jinhua J Song; Marisa C Kozlowski; Chris H Senanayake
Journal:  Chem Sci       Date:  2016-05-19       Impact factor: 9.825

Review 9.  Natural Products Diversity of Marine Ascidians (Tunicates; Ascidiacea) and Successful Drugs in Clinical Development.

Authors:  Satheesh Kumar Palanisamy; N M Rajendran; Angela Marino
Journal:  Nat Prod Bioprospect       Date:  2017-01-17

Review 10.  Marine Natural Products from Tunicates and Their Associated Microbes.

Authors:  Chatragadda Ramesh; Bhushan Rao Tulasi; Mohanraju Raju; Narsinh Thakur; Laurent Dufossé
Journal:  Mar Drugs       Date:  2021-05-26       Impact factor: 5.118

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.