Detalhe da pesquisa
1.
Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts.
Bioorg Med Chem Lett
; 27(22): 4975-4978, 2017 11 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-29037945
2.
Bioconversion of 6-epi-Notoamide T Produces Metabolites of Unprecedented Structures in a Marine-derived Aspergillus sp.
Tetrahedron Lett
; 56(1): 247-251, 2015 Jan 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-25767298
3.
Corrigendum to "Enantioselective inhibitory abilities of enantiomers of notoamides against RANKL-induced formation of multinuclear osteoclasts" [Bioorg. Med. Chem. Lett. 27 (22) (2017) 4975-4978].
Bioorg Med Chem Lett
; 28(14): 2573, 2018 08 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-29903661
4.
Biochemical characterization of NotB as an FAD-dependent oxidase in the biosynthesis of notoamide indole alkaloids.
J Am Chem Soc
; 134(2): 788-91, 2012 Jan 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-22188465
5.
Fungal origins of the bicyclo[2.2.2]diazaoctane ring system of prenylated indole alkaloids.
J Nat Prod
; 75(4): 812-33, 2012 Apr 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-22502590
6.
Enantiomeric natural products: occurrence and biogenesis.
Angew Chem Int Ed Engl
; 51(20): 4802-36, 2012 May 14.
Artigo
em Inglês
| MEDLINE | ID: mdl-22555867
7.
Studies on the biosynthesis of the notoamides: synthesis of an isotopomer of 6-hydroxydeoxybrevianamide E and biosynthetic incorporation into notoamide J.
J Org Chem
; 76(15): 5954-8, 2011 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-21504234
8.
Notoamide E: Biosynthetic incorporation into notoamides C and D in cultures of Aspergillus versicolor NRRL 35600.
Tetrahedron Lett
; 52(16): 1987-1989, 2011 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-22140279
9.
Study on the biosynthesis of the notoamides: Pinacol-type rearrangement of the isoprenyl unit in deoxybrevianamide E and 6-hydroxydeoxybrevianamide E.
Tetrahedron Lett
; 52(51): 6923-6926, 2011 Dec 21.
Artigo
em Inglês
| MEDLINE | ID: mdl-22140281
10.
Genome-based characterization of two prenylation steps in the assembly of the stephacidin and notoamide anticancer agents in a marine-derived Aspergillus sp.
J Am Chem Soc
; 132(36): 12733-40, 2010 Sep 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20722388
11.
Synthesis of notoamide J: a potentially pivotal intermediate in the biosynthesis of several prenylated indole alkaloids.
J Org Chem
; 75(9): 2785-9, 2010 May 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-20359229
12.
Detection of VM55599 and preparaherquamide from Aspergillus japonicus and Penicillium fellutanum: biosynthetic implications.
J Nat Prod
; 71(9): 1574-8, 2008 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-18754595
13.
Synthesis and bioconversions of notoamide T: a biosynthetic precursor to stephacidin A and notoamide B.
Org Lett
; 15(1): 22-5, 2013 Jan 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23249380
14.
Comparative analysis of the biosynthetic systems for fungal bicyclo[2.2.2]diazaoctane indole alkaloids: the (+)/(-)-notoamide, paraherquamide and malbrancheamide pathways.
Medchemcomm
; 3(8): 987-996, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-23213353
15.
Biosynthetic studies of the notoamides: isotopic synthesis of stephacidin A and incorporation into notoamide B and sclerotiamide.
Org Lett
; 13(15): 3802-5, 2011 Aug 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-21714564
16.
Intramolecular chiral relay at stereogenic nitrogen. Synthesis and application of a new chiral auxiliary derived from (1R,2S)-norephedrine and acetone.
J Org Chem
; 69(3): 714-8, 2004 Feb 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-14750795