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1.
Discovery of 6,7-dihydro-5H-pyrrolo[3,4-d] pyrimidine derivatives as a new class of ATR inhibitors.
Bioorg Med Chem Lett
; 63: 128651, 2022 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-35245663
2.
One-pot synthesis of branched oligosaccharides by use of galacto- and mannopyranosyl thioglycoside diols as key glycosylating agents.
Org Biomol Chem
; 11(23): 3903-17, 2013 Jun 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-23657837
3.
Discovery of a potent and highly selective inhibitor of ataxia telangiectasia mutated and Rad3-Related (ATR) kinase: Structural activity relationship and antitumor activity both in vitro and in vivo.
Eur J Med Chem
; 232: 114187, 2022 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-35183872
4.
Discovery of a novel and potent inhibitor with differential species-specific effects against NLRP3 and AIM2 inflammasome-dependent pyroptosis.
Eur J Med Chem
; 232: 114194, 2022 Mar 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-35183871
5.
Non-classical ferroptosis inhibition by a small molecule targeting PHB2.
Nat Commun
; 13(1): 7473, 2022 12 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-36463308
6.
Structural Optimization and Structure-Activity Relationship Studies of 6,6-Dimethyl-4-(phenylamino)-6H-pyrimido[5,4-b][1,4]oxazin-7(8H)-one Derivatives as A New Class of Potent Inhibitors of Pan-Trk and Their Drug-Resistant Mutants.
J Med Chem
; 65(3): 2035-2058, 2022 02 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-35080890
7.
Tuning effect of silyl protecting groups on the glycosylation reactivity of arabinofuranosyl thioglycosides.
Org Lett
; 15(11): 2834-7, 2013 Jun 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-23682928
8.
ß-Arabinofuranosylation using 5-O-(2-quinolinecarbonyl) substituted ethyl thioglycoside donors.
Org Lett
; 15(15): 3974-7, 2013 Aug 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-23879464
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