Pleiocarpaman alkaloids
Pleiocarpaman alkaloids are a class of naturally occurring compounds derived from the Pleiocarpa plants, primarily found in certain regions of South America. These alkaloids exhibit a diverse range of biological activities, including potential anti-inflammatory, antifungal, and cytotoxic properties. Structurally, pleiocarpaman alkaloids feature complex molecular architectures characterized by multiple rings and functional groups such as amine moieties.
These compounds have attracted significant interest in the pharmaceutical and chemical research communities due to their promising pharmacological profiles. Ongoing studies are focused on elucidating their structural-activity relationships (SAR) with the aim of developing new therapeutic agents for various diseases, including cancer and inflammatory disorders. Further investigations into pleiocarpaman alkaloids may lead to the discovery of novel drugs or bioactive molecules.
The extraction and purification of these alkaloids from natural sources present significant challenges due to their complex structures and low yields, which necessitate advanced techniques such as HPLC (High-Performance Liquid Chromatography) and preparative TLC (Thin-Layer Chromatography). The study of pleiocarpaman alkaloids continues to be an active area of research in the field of natural product chemistry.
| Structure | Chemical Name | CAS | MF |
|---|---|---|---|
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2H-2,12-Methanoindolo[2,3-a]quinolizine-13-carboxylicacid, 3-ethylidene-1,3,4,6,7,12b-hexahydro-, methyl ester, (2R,3E,12bS,13S)- | 6393-66-4 | C20H22N2O2 |
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Pycnanthine; 14',15'-Dihydro, N4-oxide | 2229820-11-3 | C40H46N4O3 |
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Mavacurine; 21-Oxo, N-de-Me | 2016786-27-7 | C19H20N2O2 |
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Villalstonidine B | 1418133-12-6 | C42H50N4O5 |
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Villalstonine; 1-N-De-Me | 1422747-99-6 | C40H46N4O4 |
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Goniomedine A | 1392003-53-0 | C40H49N4O4 |
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Goniomedine A; N4-α-Oxide | 1428423-11-3 | C40H49N4O5 |
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Goniomedine B | 1392003-56-3 | C40H48N4O3 |
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C-Alkaloid Y | 6822-67-9 | C20H27N2O3 |
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(+) pleiocarpamine | 60325-74-8 | C20H22N2O2 |
Related Literature
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J. Zagora,M. Vosla?,L. Schreiberová,I. Schreiber Phys. Chem. Chem. Phys., 2002,4, 1284-1291
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Bruce Parkinson Energy Environ. Sci., 2010,3, 509-511
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Dan Yang,Yanping Zhou,Xianhong Rui,Jixin Zhu,Ziyang Lu,Eileen Fong,Qingyu Yan RSC Adv., 2013,3, 14960-14962
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Hui Liu,Deyong Su,Guolin Cheng,Jimin Xu,Xinyan Wang,Yuefei Hu Org. Biomol. Chem., 2010,8, 1899-1904
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