Detalhe da pesquisa
1.
The renaissance of bacillosamine and its derivatives: pathway characterization and implications in pathogenicity.
Biochemistry
; 53(4): 624-38, 2014 Feb 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-24383882
2.
Biochemical analysis and structure determination of bacterial acetyltransferases responsible for the biosynthesis of UDP-N,N'-diacetylbacillosamine.
J Biol Chem
; 288(45): 32248-32260, 2013 Nov 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-24064219
3.
Biosynthesis of UDP-N,N'-diacetylbacillosamine in Acinetobacter baumannii: Biochemical characterization and correlation to existing pathways.
Arch Biochem Biophys
; 536(1): 72-80, 2013 Aug 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-23747578
4.
Monitoring GAPDH activity and inhibition with cysteine-reactive chemical probes.
RSC Chem Biol
; 3(7): 972-982, 2022 Jul 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-35866162
5.
Biochemical characterization of the O-linked glycosylation pathway in Neisseria gonorrhoeae responsible for biosynthesis of protein glycans containing N,N'-diacetylbacillosamine.
Biochemistry
; 50(22): 4936-48, 2011 Jun 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21542610
6.
Discovery of 2,4-bis-arylamino-1,3-pyrimidines as insulin-like growth factor-1 receptor (IGF-1R) inhibitors.
Bioorg Med Chem Lett
; 21(8): 2394-9, 2011 Apr 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-21414779
7.
Detection of an enzyme isomechanism by means of the kinetics of covalent inhibition.
Biochim Biophys Acta Proteins Proteom
; 1869(9): 140681, 2021 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-34087495
8.
Novel 2,3-dihydro-1,4-benzoxazines as potent and orally bioavailable inhibitors of tumor-driven angiogenesis.
J Med Chem
; 51(6): 1695-705, 2008 Mar 27.
Artigo
em Inglês
| MEDLINE | ID: mdl-18311900
9.
Identification of a peptide inhibitor for the histone methyltransferase WHSC1.
PLoS One
; 13(5): e0197082, 2018.
Artigo
em Inglês
| MEDLINE | ID: mdl-29742153
10.
Targeting Bacillosamine Biosynthesis in Bacterial Pathogens: Development of Inhibitors to a Bacterial Amino-Sugar Acetyltransferase from Campylobacter jejuni.
J Med Chem
; 60(5): 2099-2118, 2017 03 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-28182413
11.
Novel 2-aminopyrimidine carbamates as potent and orally active inhibitors of Lck: synthesis, SAR, and in vivo antiinflammatory activity.
J Med Chem
; 49(16): 4981-91, 2006 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-16884310
12.
Discovery of a potent, selective, and orally bioavailable pyridinyl-pyrimidine phthalazine aurora kinase inhibitor.
J Med Chem
; 53(17): 6368-77, 2010 Sep 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-20684549
13.
A quantitative analysis of kinase inhibitor selectivity.
Nat Biotechnol
; 26(1): 127-32, 2008 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-18183025