Literature DB >> 16989522

Grandisines C-G, indolizidine alkaloids from the Australian rainforest tree Elaeocarpus grandis.

Peter L Katavic1, Debra A Venables, Paul I Forster, Gordon Guymer, Anthony R Carroll.   

Abstract

Five new indolizidine alkaloids, grandisines C, D, E, F, and G (4-8), and one known indolizidine alkaloid, (-)-isoelaeocarpiline (3), were isolated from the leaves of Elaeocarpus grandis and their structures determined by 1D and 2D NMR spectroscopy. Grandisine C (4) is isomeric with the known compound rudrakine (1). The absolute configuration of grandisine D (5) was deduced by its conversion to (-)-isoelaeocarpiline. Grandisine E (6) contains a novel tetracyclic ring system. Grandisine F (7) is the 14-amino analogue of grandisine C. Grandisine G (8) contains the novel combination of a piperidine attached to an indolizidine. Grandisines C, D, F, and G and (-)-isoelaeocarpiline showed receptor binding affinity for the human delta-opioid receptor with IC(50) values of 14.6, 1.65, 1.55, 75.4, and 9.9 microM, respectively.

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Year:  2006        PMID: 16989522     DOI: 10.1021/np060179c

Source DB:  PubMed          Journal:  J Nat Prod        ISSN: 0163-3864            Impact factor:   4.050


  2 in total

1.  A versatile enantioselective synthesis of azabicyclic ring systems: a concise total synthesis of (+)-grandisine D and unnatural analogues.

Authors:  Olugbeminiyi O Fadeyi; Timothy J Senter; Kristopher N Hahn; Craig W Lindsley
Journal:  Chemistry       Date:  2012-03-30       Impact factor: 5.236

2.  Antiulcer secondary metabolites from Elaeocarpus grandis, family Elaeocarpaceae, supported by in silico studies.

Authors:  Radwa Taher Mohie El-Dien; Sherif A Maher; Usama Ramadan Abdelmohsen; Asmaa M AboulMagd; Mostafa Ahmed Fouad; Mohamed Salah Kamel
Journal:  RSC Adv       Date:  2020-09-21       Impact factor: 4.036

  2 in total

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