Literature DB >> 33562248

Tedaniophorbasins A and B-Novel Fluorescent Pteridine Alkaloids Incorporating a Thiomorpholine from the Sponge Tedaniophorbas ceratosis.

Asadhawut Hiranrat1,2,3, Darren C Holland1,4, Wilawan Mahabusarakam2,3, John N A Hooper4,5, Vicky M Avery4,6, Anthony R Carroll1,4.   

Abstract

Two new fluorescent pteridine alkaloids, tedaniophorbasins A (1) and B (2), together with the known alkaloid N-methyltryptamine, were isolated, through application of mass directed purification, from the sponge Tedaniophorbas ceratosis collected from northern New South Wales, Australia. The structures of tedaniophorbasins A and B were deduced from the analysis of 1D/2D NMR and MS data and through application of 13C NMR DFT calculations. Tedaniophorbasin A possesses a novel 2-imino-1,3-dimethyl-2,3,7,8-tetrahydro-1H-[1,4]thiazino[3,2-g]pteridin-4(6H)-one skeleton, while tedaniophorbasin B is its 2-oxo derivative. The compounds show significant Stokes shifts (~14,000 cm-1) between excitation and emission wavelengths in their fluorescence spectra. The new compounds were tested for bioactivity against chloroquine-sensitive and chloroquine-resistant strains of the malaria parasite Plasmodium falciparum, breast and pancreatic cancer cell lines, and the protozoan parasite Trypanosoma brucei brucei but were inactive against all targets at 40 µM.

Entities:  

Keywords:  Tedaniophorbas ceratosis; fluorescence; malaria; pteridine alkaloids; sponge; tedaniophorbasin A

Mesh:

Substances:

Year:  2021        PMID: 33562248      PMCID: PMC7915533          DOI: 10.3390/md19020095

Source DB:  PubMed          Journal:  Mar Drugs        ISSN: 1660-3397            Impact factor:   5.118


  18 in total

1.  Property distributions: differences between drugs, natural products, and molecules from combinatorial chemistry.

Authors:  Miklos Feher; Jonathan M Schmidt
Journal:  J Chem Inf Comput Sci       Date:  2003 Jan-Feb

2.  Beyond DP4: an Improved Probability for the Stereochemical Assignment of Isomeric Compounds using Quantum Chemical Calculations of NMR Shifts.

Authors:  Nicolás Grimblat; María M Zanardi; Ariel M Sarotti
Journal:  J Org Chem       Date:  2015-12-10       Impact factor: 4.354

3.  Anti-prion and α-Synuclein Aggregation Inhibitory Sterols from the Sponge Lamellodysidea cf. chlorea.

Authors:  Laurence K Jennings; Dale W Prebble; Mingming Xu; Merrick G Ekins; Alan L Munn; George D Mellick; Anthony R Carroll
Journal:  J Nat Prod       Date:  2020-12-03       Impact factor: 4.050

4.  Pteridine-, thymidine-, choline- and imidazole-derived alkaloids from the Australian ascidian, Leptoclinides durus.

Authors:  Kathryn E Rudolph; Michelle S Liberio; Rohan A Davis; Anthony R Carroll
Journal:  Org Biomol Chem       Date:  2012-11-19       Impact factor: 3.876

Review 5.  Marine natural products.

Authors:  John W Blunt; Anthony R Carroll; Brent R Copp; Rohan A Davis; Robert A Keyzers; Michèle R Prinsep
Journal:  Nat Prod Rep       Date:  2018-01-16       Impact factor: 13.423

6.  High-Throughput in Silico Structure Validation and Revision of Halogenated Natural Products Is Enabled by Parametric Corrections to DFT-Computed 13C NMR Chemical Shifts and Spin-Spin Coupling Constants.

Authors:  Andrei G Kutateladze; D Sai Reddy
Journal:  J Org Chem       Date:  2017-03-24       Impact factor: 4.354

7.  Anti-prion Butenolides and Diphenylpropanones from the Australian Ascidian Polycarpa procera.

Authors:  Laurence K Jennings; Luke P Robertson; Kathryn E Rudolph; Alan L Munn; Anthony R Carroll
Journal:  J Nat Prod       Date:  2019-08-22       Impact factor: 4.050

8.  A guide to small-molecule structure assignment through computation of (¹H and ¹³C) NMR chemical shifts.

Authors:  Patrick H Willoughby; Matthew J Jansma; Thomas R Hoye
Journal:  Nat Protoc       Date:  2014-02-20       Impact factor: 13.491

9.  Orthoscuticellines A-E, β-Carboline Alkaloids from the Bryozoan Orthoscuticella ventricosa Collected in Australia.

Authors:  Guy Kleks; Sandra Duffy; Leonardo Lucantoni; Vicky M Avery; Anthony R Carroll
Journal:  J Nat Prod       Date:  2020-01-21       Impact factor: 4.050

10.  Lumazine peptides from the marine-derived fungus Aspergillus terreus.

Authors:  Minjung You; Lijuan Liao; Soo Hyun Hong; Wanki Park; Dah In Kwon; Jeeyeon Lee; Minsoo Noh; Dong-Chan Oh; Ki-Bong Oh; Jongheon Shin
Journal:  Mar Drugs       Date:  2015-03-12       Impact factor: 5.118

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.