Structural Diversity and Biological Potential of Alkaloids from the Genus Hippeastrum, Amaryllidaceae: an Update

被引：1
|
作者：
Tallini, Luciana R. [1 ,2 ]
Giordani, Raquel B. [3 ]
de Andrade, Jean Paulo [4 ]
Bastida, Jaume [2 ]
Zuanazzi, Jose Angelo S. [1 ]
机构：
[1] Univ Fed Rio Grande do Sul, Fac Farm, Programa Posgrad Ciencias Farmaceut, BR-90610000 Porto Alegre, RS, Brazil
[2] Univ Barcelona, Fac Farm & Ciencies Alimentacio, Dept Biol Sanitat & Medi Ambient, Grp Productes Nat, Barcelona 08028, Spain
[3] Univ Fed Rio Grande do Norte, Dept Farm, BR-59012570 Natal, RN, Brazil
[4] Univ Talca, Inst Invest Interdisciplinaria, Vicerrectoria Acad, Campus Talca, Talca 3460000, Chile
来源：
REVISTA BRASILEIRA DE FARMACOGNOSIA-BRAZILIAN JOURNAL OF PHARMACOGNOSY | 2021年 / 31卷 / 05期
关键词：
Alzheimer's disease; Anti-inflammatory; Antitumoral; Antiparasitic; Cytotoxic; Isoquinoline alkaloids; ABSOLUTE-CONFIGURATION; INHIBITORY-ACTIVITIES; CYTOTOXIC ACTIVITIES; NARCICLASINE; CANCER; BIOSYNTHESIS; GALANTAMINE; LYCORINE; DRUG; HAEMANTHAMINE;
D O I：
10.1007/s43450-021-00211-z
中图分类号：
R914 [药物化学];
学科分类号：
100701 ;
摘要：
The subfamily Amaryllidoideae, Amaryllidaceae, presents an exclusive group of structures known as Amaryllidaceae alkaloids, which have a broad spectrum of biological activities. These plants are classified into 59 genera, including Hippeastrum Herb., which comprises approximately 60 species distributed mainly in South America, being widely used as ornamental plants due to the beauty of its flowers. This review presents an update about the alkaloid profiling of Hippeastrum extracts published between 2012 and 2021, as well as an approach to the biological potential of these compounds.
引用
收藏
页码：648 / 657
页数：10
相关论文
共 50 条
  • [1] Structural Diversity and Biological Potential of Alkaloids from the Genus Hippeastrum, Amaryllidaceae: an Update
    Luciana R. Tallini
    Raquel B. Giordani
    Jean Paulo de Andrade
    Jaume Bastida
    José Angelo S. Zuanazzi
    Revista Brasileira de Farmacognosia, 2021, 31 : 648 - 657
  • [2] Alkaloids from Hippeastrum morelianum Lem. (Amaryllidaceae)
    Giordani, Raquel B.
    de Andrade, Jean P.
    Verli, Hugo
    Dutilh, Julie H.
    Henriques, Amelia T.
    Berkov, Strahil
    Bastida, Jaume
    Zuanazzi, Jose Angelo S.
    MAGNETIC RESONANCE IN CHEMISTRY, 2011, 49 (10) : 668 - 672
  • [3] Chemistry and Biological Activity of Alkaloids from the Genus Lycoris (Amaryllidaceae)
    Cahlikova, Lucie
    Breiterova, Katerina
    Opletal, Lubomir
    MOLECULES, 2020, 25 (20):
  • [4] Alkaloids from Hippeastrum equestre Herb (Amaryllidaceae) .3.
    Pham, LH
    Grundemann, E
    Dopke, W
    PHARMAZIE, 1997, 52 (02): : 160 - 162
  • [5] Amaryllidaceae Alkaloids from Clivia miniata (Lindl.) Bosse (Amaryllidaceae): Isolation, Structural Elucidation, and Biological Activity
    Safratova, Marcela
    Kroustkova, Jana
    Maafi, Negar
    Suchankova, Daniela
    Vrabec, Rudolf
    Chlebek, Jakub
    Kunes, Jiri
    Opletal, Lubomir
    Bucar, Franz
    Cahlikova, Lucie
    PLANTS-BASEL, 2022, 11 (22):
  • [6] Isolation, Absolute Configuration and Cytotoxic Activities of Alkaloids from Hippeastrum goianum (Ravenna) Meerow (Amaryllidaceae)
    Lianza, Mariacaterina
    Verdan, Maria Helena
    de Andrade, Jean Paulo
    Poli, Ferruccio
    de Almeida, Larissa
    Costa-Lotufo, Leticia, V
    Cunha Neto, Alvaro
    Oliveira, Sarah C. C.
    Bastida, Jaume
    Batista, Andrea N. L.
    Batista, Joao M., Jr.
    Borges, Warley S.
    JOURNAL OF THE BRAZILIAN CHEMICAL SOCIETY, 2020, 31 (10) : 2135 - 2145
  • [7] Multitarget anti-parasitic activities of isoquinoline alkaloids isolated from Hippeastrum aulicum (Amaryllidaceae)
    Bessa, Carliani Dal Piero Betzel
    Feu, Amanda Eiriz
    de Menezes, Renata Priscila Barros
    Scotti, Marcus Tullius
    Lima, Julia Maria Godoi
    Lima, Marta Lopes
    Tempone, Andre Gustavo
    de Andrade, Jean Paulo
    Bastida, Jaume
    Borges, Warley de Souza
    PHYTOMEDICINE, 2024, 128
  • [8] Amaryllidaceae alkaloids from Hippeastrum X Hybridum CV. Ferrari, and preparation of vittatine derivatives as potential ligands for Alzheimer's disease
    Al Shammari, L.
    Hulcova, D.
    Marikova, J.
    Kucera, T.
    Safratova, M.
    Novakova, L.
    Schmidt, M.
    Pulkrabkova, L.
    Janousek, J.
    Soukup, O.
    Kunes, J.
    Opletal, L.
    Cahlikova, L.
    SOUTH AFRICAN JOURNAL OF BOTANY, 2021, 136 : 137 - 146
  • [9] Structural Diversity and Biological Activities of Indole Diketopiperazine Alkaloids from Fungi
    Ma, Yang-Min
    Liang, Xi-Ai
    Kong, Yang
    Jia, Bin
    JOURNAL OF AGRICULTURAL AND FOOD CHEMISTRY, 2016, 64 (35) : 6659 - 6671
  • [10] Two novel Amaryllidaceae alkaloids from Hippeastrum equestre Herb.:: 3-O-demethyltazettine and egonine
    Pham, LH
    Gründemann, E
    Wagner, J
    Bartoszek, M
    Döpke, W
    PHYTOCHEMISTRY, 1999, 51 (02) : 327 - 332
12345