Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Linh H. Mai"'
Autor:
Fei He, Linh H. Mai, Arlette Longeon, Brent R. Copp, Nadège Loaëc, Amandine Bescond, Laurent Meijer, Marie-Lise Bourguet-Kondracki
Publikováno v:
Marine Drugs, Vol 13, Iss 5, Pp 2617-2628 (2015)
Seven new adociaquinone derivatives, xestoadociaquinones A (1a), B (1b), 14-carboxy-xestoquinol sulfate (2) and xestoadociaminals A–D (3a, 3c, 4a, 4c), together with seven known compounds (5–11) were isolated from an Indonesian marine sponge Xest
Externí odkaz:
https://doaj.org/article/cc7a1e0c1d42437198d0b8423edf641b
Autor:
Germana Esposito, Linh H. Mai, Arlette Longeon, Alfonso Mangoni, Emilie Durieu, Laurent Meijer, Rob Van Soest, Valeria Costantino, Marie-Lise Bourguet-Kondracki
Publikováno v:
Marine Drugs, Vol 17, Iss 8, p 472 (2019)
Thirteen nitrogen-containing molecules (1a/1b and 2−12) were isolated from the Indonesian sponge Acanthostrongylophora ingens, highlighting the richness of this organism as a source of alkaloids. Their structures were elucidated using one- and two-
Externí odkaz:
https://doaj.org/article/3d765d314c3a41ec888eaa00942a6f5c
Autor:
Arlette Longeon, Marie-Lise Bourguet-Kondracki, Alfonso Mangoni, Laurent Meijer, Valeria Costantino, Rob W. M. Van Soest, Linh H. Mai, Roberta Teta, Germana Esposito
Publikováno v:
Journal of Natural Products. 79:2953-2960
The halogenated alkaloid chloromethylhalicyclamine B (1), together with the known natural compound halicyclamine B (2), was isolated from the extract of the sponge Acanthostrongylophora ingens. The structure of compound 1 was determined by spectrosco
Autor:
Valeria Costantino, Alfonso Mangoni, Linh H. Mai, Laurent Meijer, Arlette Longeon, Emilie Durieu, Rob W. M. Van Soest, Germana Esposito, Marie-Lise Bourguet-Kondracki
Publikováno v:
Marine drugs
Marine drugs, MDPI, 2019, 17 (8), pp.472. ⟨10.3390/md17080472⟩
Marine Drugs, Vol 17, Iss 8, p 472 (2019)
Marine drugs, 2019, 17 (8), pp.472. ⟨10.3390/md17080472⟩
Marine Drugs
Volume 17
Issue 8
Marine drugs, MDPI, 2019, 17 (8), pp.472. ⟨10.3390/md17080472⟩
Marine Drugs, Vol 17, Iss 8, p 472 (2019)
Marine drugs, 2019, 17 (8), pp.472. ⟨10.3390/md17080472⟩
Marine Drugs
Volume 17
Issue 8
Thirteen nitrogen-containing molecules (1a/1b and 2&ndash
12) were isolated from the Indonesian sponge Acanthostrongylophora ingens, highlighting the richness of this organism as a source of alkaloids. Their structures were elucidated using one-
12) were isolated from the Indonesian sponge Acanthostrongylophora ingens, highlighting the richness of this organism as a source of alkaloids. Their structures were elucidated using one-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b5ecb2f83561d3701a3c55727a02f988
https://hal-amu.archives-ouvertes.fr/hal-02396669
https://hal-amu.archives-ouvertes.fr/hal-02396669
Autor:
Nadège Loaëc, Laurent Meijer, Amandine Bescond, Arlette Longeon, Brent R. Copp, Marie-Lise Bourguet-Kondracki, Fei He, Linh H. Mai
Publikováno v:
Marine Drugs, Vol 13, Iss 5, Pp 2617-2628 (2015)
Marine Drugs
Volume 13
Issue 5
Pages 2617-2628
Marine Drugs
Volume 13
Issue 5
Pages 2617-2628
Seven new adociaquinone derivatives, xestoadociaquinones A (1a), B (1b), 14-carboxy-xestoquinol sulfate (2) and xestoadociaminals A–D (3a, 3c, 4a, 4c), together with seven known compounds (5–11) were isolated from an Indonesian marine sponge Xest
Autor:
Linh H. Mai, Cyril Poulain, Sylvie Michel, Vincent Dumontet, Guy G. Chabot, Lionel Quentin, Laila S. Espindola, Raphaël Grougnet, Brigitte Deguin, Hue T.B. Vo, Philippe Grellier
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2015, 93, pp.93-100. ⟨10.1016/j.ejmech.2015.01.012⟩
European Journal of Medicinal Chemistry, Elsevier, 2015, 93, pp.93-100. 〈10.1016/j.ejmech.2015.01.012〉
European Journal of Medicinal Chemistry, Elsevier, 2015, 93, pp.93-100. ⟨10.1016/j.ejmech.2015.01.012⟩
European Journal of Medicinal Chemistry, Elsevier, 2015, 93, pp.93-100. 〈10.1016/j.ejmech.2015.01.012〉
International audience; A series of 16 flavonoids were isolated and prepared from bud exudate of Gardenia urvillei and Gardenia oudiepe, endemic to New Caledonia. Most of them are rare polymethoxylated flavones. Some of these compounds showed noticea