Detalhe da pesquisa
1.
Chemical Investigation of the Calcareous Marine Sponge Pericharax heteroraphis, Clathridine-A Related Derivatives Isolation, Synthesis and Osteogenic Activity.
Mar Drugs
; 22(5)2024 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-38786586
2.
Isolation, Synthesis and Absolute Configuration of the Pericharaxins A and B, Epimeric Hydroxy-Polyene Glycerol Ethers from the Calcarean Sponge Pericharax heteroraphis.
Mar Drugs
; 20(10)2022 Oct 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-36286459
3.
Bioactive Bromotyrosine Derivatives from the Pacific Marine Sponge Suberea clavata (Pulitzer-Finali, 1982).
Mar Drugs
; 19(3)2021 Mar 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-33800819
4.
Quorum Sensing Inhibitory and Antifouling Activities of New Bromotyrosine Metabolites from the Polynesian Sponge Pseudoceratina n. sp.
Mar Drugs
; 18(5)2020 May 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-32455754
5.
New Antimalarial and Antimicrobial Tryptamine Derivatives from the Marine Sponge Fascaplysinopsis reticulata.
Mar Drugs
; 17(3)2019 Mar 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-30875899
6.
Chemical Diversity and Biological Activities of Marine Sponges of the Genus Suberea: A Systematic Review.
Mar Drugs
; 17(2)2019 Feb 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-30759850
7.
Chemistry and Biological Activities of the Marine Sponges of the Genera Mycale (Arenochalina), Biemna and Clathria.
Mar Drugs
; 16(6)2018 Jun 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-29912171
8.
Synergistic AML Cell Death Induction by Marine Cytotoxin (+)-1(R), 6(S), 1'(R), 6'(S), 11(R), 17(S)-Fistularin-3 and Bcl-2 Inhibitor Venetoclax.
Mar Drugs
; 16(12)2018 Dec 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-30572618
9.
Bioactive Bromotyrosine-Derived Alkaloids from the Polynesian Sponge Suberea ianthelliformis.
Mar Drugs
; 16(5)2018 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-29702602
10.
Orbicularisine: A Spiro-Indolothiazine Isolated from Gills of the Tropical Bivalve Codakia orbicularis.
J Nat Prod
; 80(5): 1693-1696, 2017 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28421754
11.
Unguiculin A and Ptilomycalins E-H, Antimalarial Guanidine Alkaloids from the Marine Sponge Monanchora unguiculata.
J Nat Prod
; 80(5): 1404-1410, 2017 05 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-28368118
12.
Remarkably high homoselectivity in [2 + 2] photodimerization of trans-cinnamic acids in multicomponent systems.
Photochem Photobiol Sci
; 15(9): 1115-1119, 2016 08 31.
Artigo
em Inglês
| MEDLINE | ID: mdl-27459036
13.
Cytotoxic Guanidine Alkaloids from a French Polynesian Monanchora n. sp. Sponge.
J Nat Prod
; 79(8): 1929-37, 2016 08 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-27419263
14.
Netamines O-S, Five New Tricyclic Guanidine Alkaloids from the Madagascar Sponge Biemna laboutei, and Their Antimalarial Activities.
Chem Biodivers
; 12(11): 1725-33, 2015 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-26567950
15.
Netamines H-N, tricyclic alkaloids from the marine sponge Biemna laboutei and their antimalarial activity.
J Nat Prod
; 77(4): 818-23, 2014 Apr 25.
Artigo
em Inglês
| MEDLINE | ID: mdl-24601655
16.
Elemental sulfur disproportionation in the redox condensation reaction between o-halonitrobenzenes and benzylamines.
Angew Chem Int Ed Engl
; 53(50): 13808-12, 2014 Dec 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-25296684
17.
Iron sulfide catalyzed redox/condensation cascade reaction between 2-amino/hydroxy nitrobenzenes and activated methyl groups: a straightforward atom economical approach to 2-hetaryl-benzimidazoles and -benzoxazoles.
J Am Chem Soc
; 135(1): 118-21, 2013 Jan 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-23249371
18.
Unprecedented biomimetic homodimerization of oroidin and clathrodin marine metabolites in the presence of HMPA or phosphonate salt tweezers.
J Nat Prod
; 76(5): 903-8, 2013 May 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-23654209
19.
Pipestelides A-C: cyclodepsipeptides from the Pacific marine sponge Pipestela candelabra.
J Nat Prod
; 75(4): 759-63, 2012 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-22364566
20.
Organic Matrix and Secondary Metabolites in Nacre.
Mar Biotechnol (NY)
; 24(5): 831-842, 2022 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-36057751