Detalhe da pesquisa
1.
Perturbation of the interactions of calmodulin with GRK5 using a natural product chemical probe.
Proc Natl Acad Sci U S A
; 116(32): 15895-15900, 2019 08 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31337679
2.
circDeep: deep learning approach for circular RNA classification from other long non-coding RNA.
Bioinformatics
; 36(1): 73-80, 2020 01 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-31268128
3.
Taichunins E-T, Isopimarane Diterpenes and a 20-nor-Isopimarane, from Aspergillus taichungensis (IBT 19404): Structures and Inhibitory Effects on RANKL-Induced Formation of Multinuclear Osteoclasts.
J Nat Prod
; 84(9): 2475-2485, 2021 09 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-34464116
4.
Molecular Basis for Spirocycle Formation in the Paraherquamide Biosynthetic Pathway.
J Am Chem Soc
; 142(5): 2244-2252, 2020 02 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-31904957
5.
Flavin-Dependent Monooxygenases NotI and NotI' Mediate Spiro-Oxindole Formation in Biosynthesis of the Notoamides.
Chembiochem
; 21(17): 2449-2454, 2020 09 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-32246875
6.
Structural basis of the Cope rearrangement and cyclization in hapalindole biogenesis.
Nat Chem Biol
; 14(4): 345-351, 2018 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-29531360
7.
Stereoselective Synthesis of Baulamycin A.
J Org Chem
; 85(5): 3812-3823, 2020 03 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-31970985
8.
Irpexine, an Isoindolinone Alkaloid Produced by Coculture of Endophytic Fungi, Irpex lacteus and Phaeosphaeria oryzae.
J Nat Prod
; 83(5): 1368-1373, 2020 05 22.
Artigo
em Inglês
| MEDLINE | ID: mdl-32301614
9.
Control of Stereoselectivity in Diverse Hapalindole Metabolites is Mediated by Cofactor-Induced Combinatorial Pairing of Stig Cyclases.
Angew Chem Int Ed Engl
; 59(21): 8166-8172, 2020 05 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-32052896
10.
Decoding cyclase-dependent assembly of hapalindole and fischerindole alkaloids.
Nat Chem Biol
; 13(5): 467-469, 2017 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-28288107
11.
Taichunins A-D, Norditerpenes from Aspergillus taichungensis (IBT 19404).
J Nat Prod
; 82(5): 1377-1381, 2019 05 24.
Artigo
em Inglês
| MEDLINE | ID: mdl-30995043
12.
Structural and stereochemical diversity in prenylated indole alkaloids containing the bicyclo[2.2.2]diazaoctane ring system from marine and terrestrial fungi.
Nat Prod Rep
; 35(6): 532-558, 2018 06 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-29632911
13.
Unveiling sequential late-stage methyltransferase reactions in the meleagrin/oxaline biosynthetic pathway.
Org Biomol Chem
; 16(35): 6450-6459, 2018 09 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-30141817
14.
Isolation of a new indoxyl alkaloid, Amoenamide B, from Aspergillus amoenus NRRL 35600: biosynthetic implications and correction of the structure of Speramide B.
Tetrahedron Lett
; 50(48): 4236-4240, 2018 Nov 28.
Artigo
em Inglês
| MEDLINE | ID: mdl-30765898
15.
Function and Structure of MalA/MalA', Iterative Halogenases for Late-Stage C-H Functionalization of Indole Alkaloids.
J Am Chem Soc
; 139(34): 12060-12068, 2017 08 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-28777910
16.
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
17.
Isolation of amoenamide A and five antipodal prenylated alkaloids from Aspergillus amoenus NRRL 35600.
Tetrahedron Lett
; 58(29): 2797-2800, 2017 Jul 19.
Artigo
em Inglês
| MEDLINE | ID: mdl-29622844
18.
Synthesis and Biochemical Evaluation of Biotinylated Conjugates of Largazole Analogues: Selective Class I Histone Deacetylase Inhibitors.
Isr J Chem
; 57(3-4): 319-330, 2017 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-30760938
19.
OxaD: A Versatile Indolic Nitrone Synthase from the Marine-Derived Fungus Penicillium oxalicum F30.
J Am Chem Soc
; 138(35): 11176-84, 2016 09 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-27505044
20.
Stereoselective Total Synthesis of (-)-Renieramycin T.
J Org Chem
; 81(10): 4039-47, 2016 05 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-27019081