نتایج جستجو برای: 3 alkylpyridine marine alkaloid analogs

تعداد نتایج: 1915457  

2007
Kin S. Lam Ginger Tsueng Katherine A. McArthur Scott S. Mitchell Barbara C. M. Potts Jianlin Xu

We examined the effects of halogens on the production of salinosporamide A (NPI-0052) by the obligate marine actinomycete Salinispora tropica NPS465, specifically the production of analogs containing halogens other than chlorine. Adding NaF, NaBr and NaI directly to the production medium prepared in seawater containing 3% NaCl did not induce the production of the corresponding analogs. Replacin...

2010
Kasım Cemal Güven Aline Percot Ekrem Sezik

This paper presents the alkaloids found in green, brown and red marine algae. Algal chemistry has interested many researchers in order to develop new drugs, as algae include compounds with functional groups which are characteristic from this particular source. Among these compounds, alkaloids present special interest because of their pharmacological activities. Alkaloid chemistry has been widel...

2013
Anna Carbone Barbara Parrino Paola Barraja Virginia Spanò Girolamo Cirrincione Patrizia Diana Armin Maier Gerhard Kelter Heinz-Herbert Fiebig

2,5-bis(3'-Indolyl)pyrroles, analogues of the marine alkaloid nortopsentin, were conveniently prepared through a three step procedure in good overall yields. Derivatives 1a and 1b exhibited concentration-dependent antitumor activity towards a panel of 42 human tumor cell lines with mean IC50 values of 1.54 μM and 0.67 μM, respectively. Investigating human tumor xenografts in an ex-vivo clonogen...

2010
Susu Zughaier Prasanthi Karna David Stephens Ritu Aneja

Noscapine, a plant-derived, non-toxic, over-the-counter antitussive alkaloid has tubulin-binding properties. Based upon the structural resemblance of noscapine to colchicine, a tubulin-binding anti-inflammatory drug, noscapine and its semi-synthetic brominated analogs were examined for in vitro anti-inflammatory activity. Brominated noscapine analogs were found to inhibit cytokine and chemokine...

Journal: :ACS chemical neuroscience 2011
John T Brogan Sydney L Stoops Brenda C Crews Lawrence J Marnett Craig W Lindsley

The first total synthesis of (+)-7-bromotrypargine, a β-carboline alkaloid from Ancornia sp. is reported. The synthesis proceeds in 9 steps, 8 steps longest linear sequence, in 36.9% overall yield. Biological characterization found that (+)-7-bromotrypargine is an H(3) antagonist, and a selective inhibitor of DAT and NET, without inhibiting SERT. Moreover, unlike electron rich congeners, (+)-7-...

Journal: :Biochemical and biophysical research communications 2008
Ulf Bickmeyer Achim Grube Karl-Walter Klings Matthias Köck

The alkaloid ageladine A, a pyrrole-imidazole alkaloid isolated from marine Agelas sponges shows fluorescence in the blue-green range during excitation with UV light with the highest absorption at 370 nm. The fluorescence of this alkaloid is pH dependent. Highest fluorescence is observed at pH 4, lowest at pH 9 with the largest fluorescence changes between pH 6 and 7. Ageladine A is brominated,...

2014
Cristina I. Canché Chay Rocío Gómez Cansino Clara I. Espitia Pinzón Rubén O. Torres-Ochoa Roberto Martínez

Caulerpin (1a), a bis-indole alkaloid from the marine algal Caulerpa sp., was synthesized in three reaction steps with an overall yield of 11%. The caulerpin analogues (1b-1g) were prepared using the same synthetic pathway with overall yields between 3% and 8%. The key reaction involved a radical oxidative aromatic substitution involving xanthate (3) and 3-formylindole compounds (4a-4g). All bi...

Journal: :Chemical and Pharmaceutical Bulletin 1983

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