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Literature DB >> 8021654

Eudistomin U and isoeudistomin U, new alkaloids from the Caribbean ascidian Lissoclinum fragile.

A Badre¹, A Boulanger, E Abou-Mansour, B Banaigs, G Combaut, C Francisco.

Abstract

Chemical investigations of the Caribbean ascidian Lissoclinum fragile (Didemnidae) have resulted in the isolation of new alkaloids which we have designated eudistomin U [1] and isoeudistomin U [2]. Their structures were determined by spectrometric and chemical means.

Entities: Chemical Species

Mesh：

Substances：

Year: 1994 PMID： 8021654 DOI： 10.1021/np50106a016

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

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Cited

10 in total

1. Discovery and biological characterization of 1-(1H-indol-3-yl)-9H-pyrido[3,4-b]indole as an aryl hydrocarbon receptor activator generated by photoactivation of tryptophan by sunlight.

Authors: Silvia Diani-Moore; Yuliang Ma; Erin Labitzke; Hui Tao; J David Warren; Jared Anderson; Qiuying Chen; Steven S Gross; Arleen B Rifkind
Journal: Chem Biol Interact Date: 2011-06-22 Impact factor: 5.192

2. Room-temperature aromatization of tetrahydro-β-carbolines by 2-iodoxybenzoic acid: utility in a total synthesis of eudistomin U.

Authors: Joseph D Panarese; Stephen P Waters
Journal: Org Lett Date: 2010-09-17 Impact factor: 6.005

Review 3. 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

4. Efficient synthesis of eudistomin U and evaluation of its cytotoxicity.

Authors: Chad M Roggero; Jennifer M Giulietti; Seann P Mulcahy
Journal: Bioorg Med Chem Lett Date: 2014-05-27 Impact factor: 2.823

5. Three-step synthesis of an annulated β-carboline via palladium catalysis.

Authors: Seann P Mulcahy; Jonathan G Varelas
Journal: Tetrahedron Lett Date: 2013-11-27 Impact factor: 2.415

6. Synthesis of 1-substituted carbazolyl-1,2,3,4-tetrahydro- and carbazolyl-3,4-dihydro-β-carboline analogs as potential antitumor agents.

Authors: Ya-Ching Shen; Yao-To Chang; Chun-Ling Lin; Chia-Ching Liaw; Yao Haur Kuo; Lan-Chun Tu; Sheau Farn Yeh; Ji-Wang Chern
Journal: Mar Drugs Date: 2011-02-10 Impact factor: 6.085

Eudistomin U and isoeudistomin U, new alkaloids from the Caribbean ascidian Lissoclinum fragile.

1. Discovery and biological characterization of 1-(1H-indol-3-yl)-9H-pyrido[3,4-b]indole as an aryl hydrocarbon receptor activator generated by photoactivation of tryptophan by sunlight.

2. Room-temperature aromatization of tetrahydro-β-carbolines by 2-iodoxybenzoic acid: utility in a total synthesis of eudistomin U.

Review 3. Synthesis of indole derivatives as prevalent moieties present in selected alkaloids.

4. Efficient synthesis of eudistomin U and evaluation of its cytotoxicity.

5. Three-step synthesis of an annulated β-carboline via palladium catalysis.

6. Synthesis of 1-substituted carbazolyl-1,2,3,4-tetrahydro- and carbazolyl-3,4-dihydro-β-carboline analogs as potential antitumor agents.

7. An intramolecular inverse electron demand Diels-Alder approach to annulated α-carbolines.

8. Synthesis and Investigation of Tetrahydro-β-carboline Derivatives as Inhibitors of Plant Pathogenic Fungi.

Review 9. Recent Advances in the Synthesis of β-Carboline Alkaloids.

10. Bioactive compounds from the Red Sea marine sponge Hyrtios species.