Literature DB >> 33927787

Spermidine alkaloid and glycosidic constituents of Vietnamese Homalium cochinchinensis.

Ermias Mekuria Addo1, Yulin Ren1, Gerardo D Anaya-Eugenio1, Tran Ngoc Ninh2, Harinantenaina L Rakotondraibe1, Esperanza J Carcache de Blanco1, Djaja D Soejarto3,4, A Douglas Kinghorn1.   

Abstract

Phytochemical investigation of the aerial parts of Homalium cochinchinensis led to the isolation of secondary metabolites belonging to the spermidine alkaloid, glycoside, depsidone and phenol classes. Of the eleven secondary metabolites isolated in this study, two spermidine alkaloids, dovyalicins H (1) and I (2), which belong to a rare group among this class, and six glycosides (3-8) are previously undescribed. The structures of all new isolates were determined by interpretation of spectroscopic and spectrometric data. In this report, the structural elucidation of these unprecedented secondary metabolites (1-8) is described.

Entities:  

Keywords:  Homalium cochinchinensis; dovyalicins; glycosides; secondary metabolites; spermidine alkaloids

Year:  2021        PMID: 33927787      PMCID: PMC8078847          DOI: 10.1016/j.phytol.2021.04.002

Source DB:  PubMed          Journal:  Phytochem Lett        ISSN: 1874-3900            Impact factor:   1.873


  12 in total

1.  Cochinolide, a new gamma-alkylidene bicyclic butenolide with antiviral activity, and its beta-glucopyranoside from Homalium cochinchinensis.

Authors:  T Ishikawa; K Nishigaya; H Uchikoshi; I S Cheng
Journal:  J Nat Prod       Date:  1998-04       Impact factor: 4.050

2.  Caspase-Dependent Apoptosis in Prostate Cancer Cells and Zebrafish by Corchorusoside C from Streptocaulon juventas.

Authors:  Gerardo D Anaya-Eugenio; Ermias Mekuria Addo; Nathan Ezzone; Joshua M Henkin; Tran Ngoc Ninh; Yulin Ren; Djaja D Soejarto; A Douglas Kinghorn; Esperanza J Carcache de Blanco
Journal:  J Nat Prod       Date:  2019-05-23       Impact factor: 4.050

3.  Dovyalicin-type spermidine alkaloids from Dovyalis species.

Authors:  Bonnie Rasmussen; Aimee-Justine Nkurunziza; Matthias Witt; Hellen A Oketch-Rabah; Jerzy W Jaroszewski; Dan Staerk
Journal:  J Nat Prod       Date:  2006-09       Impact factor: 4.050

4.  Bioassay-guided isolation of constituents of Piper sarmentosum using a mitochondrial transmembrane potential assay.

Authors:  Li Pan; Susan Matthew; Daniel D Lantvit; Xiaoli Zhang; Tran Ngoc Ninh; Heebyung Chai; Esperanza J Carcache de Blanco; Djaja D Soejarto; Steven M Swanson; A Douglas Kinghorn
Journal:  J Nat Prod       Date:  2011-10-05       Impact factor: 4.050

5.  Heteronuclear two-bond correlation: suppressing heteronuclear three-bond or higher NMR correlations while enhancing two-bond correlations even for vanishing 2J(CH).

Authors:  Nils T Nyberg; Jens O Duus; Ole W Sørensen
Journal:  J Am Chem Soc       Date:  2005-05-04       Impact factor: 15.419

6.  Phenolic glucosides from Hasseltia floribunda.

Authors:  Enkhmaa Dagvadorj; Kamel H Shaker; Donald Windsor; Bernd Schneider; Wilhelm Boland
Journal:  Phytochemistry       Date:  2010-09-06       Impact factor: 4.072

7.  Isolation of salicin derivatives from Homalium cochinchinensis and their antiviral activities.

Authors:  Tsutomu Ishikawa; Kaori Nishigaya; Kazuko Takami; Hide Uchikoshi; Ih-Sheng Chen; Ian-Lih Tsai
Journal:  J Nat Prod       Date:  2004-04       Impact factor: 4.050

8.  A new class of spermidine-derived alkaloids.

Authors:  Dan Staerk; Matthias Witt; Hellen A Oketch-Rabah; Jerzy W Jaroszewski
Journal:  Org Lett       Date:  2003-08-07       Impact factor: 6.005

9.  Cytotoxic constituents from Penicillium concentricum, an endophytic fungus from Trichocolea tomentella.

Authors:  Gerardo D Anaya-Eugenio; Tehane Ali; Liva Harinantenaina Rakotondraibe; Esperanza Carcache de Blanco
Journal:  Anticancer Drugs       Date:  2019-04       Impact factor: 2.248

10.  Facile discrimination of aldose enantiomers by reversed-phase HPLC.

Authors:  Takashi Tanaka; Tatsuya Nakashima; Toshihisa Ueda; Kenji Tomii; Isao Kouno
Journal:  Chem Pharm Bull (Tokyo)       Date:  2007-06       Impact factor: 1.645

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.