Detalles de la búsqueda
1.
Cross-view contrastive representation learning approach to predicting DTIs via integrating multi-source information.
Methods
; 218: 176-188, 2023 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37586602
2.
Binding Free Energy Calculation Based on the Fragment Molecular Orbital Method and Its Application in Designing Novel SHP-2 Allosteric Inhibitors.
Int J Mol Sci
; 25(1)2024 Jan 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-38203841
3.
A simple monoselective C-H oxygenation approach for the synthesis of ursane triterpenoids.
Org Biomol Chem
; 21(7): 1395-1398, 2023 02 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-36688572
4.
Design, synthesis and biological evaluation of pteridine-7(8H)-one derivatives as potent and selective CDK4/6 inhibitors.
Bioorg Med Chem Lett
; 76: 128991, 2022 11 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-36130661
5.
Discovery of pyrrolo[1,2-a]quinoxalin-4(5H)-one derivatives as novel non-covalent Bruton's tyrosine kinase (BTK) inhibitors.
Bioorg Chem
; 126: 105860, 2022 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-35661525
6.
Discovery of pyrido[3,4-b]indol-1-one derivatives as novel non-covalent Bruton's tyrosine kinase (BTK) inhibitors.
Bioorg Chem
; 119: 105541, 2022 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-34910982
7.
Design, Synthesis, and Structure-Activity Relationship Study of Potent MAPK11 Inhibitors.
Molecules
; 27(1)2021 Dec 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-35011435
8.
Discovery and optimization of 2-aminopyridine derivatives as novel and selective JAK2 inhibitors.
Bioorg Med Chem Lett
; 30(8): 127048, 2020 04 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-32122740
9.
Design, synthesis and biological evaluation of potent EGFR kinase inhibitors against 19D/T790M/C797S mutation.
Bioorg Med Chem Lett
; 30(16): 127327, 2020 08 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-32631532
10.
Aurora B kinase as a novel molecular target for inhibition the growth of osteosarcoma.
Mol Carcinog
; 58(6): 1056-1067, 2019 06.
Artículo
en Inglés
| MEDLINE | ID: mdl-30790360
11.
Design, synthesis and structure-activity relationship study of aminopyridine derivatives as novel inhibitors of Janus kinase 2.
Bioorg Med Chem Lett
; 29(12): 1507-1513, 2019 06 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-30981578
12.
Discovery and Biological evaluation of pyrimido[4,5-d]pyrimidine-2,4(1H,3H)-dione derivatives as potent Bruton's tyrosine kinase inhibitors.
Bioorg Med Chem
; 27(15): 3390-3395, 2019 08 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31221612
13.
Naringenin inhibits migration of breast cancer cells via inflammatory and apoptosis cell signaling pathways.
Inflammopharmacology
; 27(5): 1021-1036, 2019 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-30941613
14.
68Ga tagged dendrimers for molecular tumor imaging in animals.
Hell J Nucl Med
; 22(1): 78-79, 2019.
Artículo
en Inglés
| MEDLINE | ID: mdl-30968863
15.
Synthesis, Design, and Structureâ»Activity Relationship of the Pyrimidone Derivatives as Novel Selective Inhibitors of Plasmodium falciparum Dihydroorotate Dehydrogenase.
Molecules
; 23(6)2018 May 24.
Artículo
en Inglés
| MEDLINE | ID: mdl-29794978
16.
Development of Degraders of Cyclin-Dependent Kinases 4 and 6 Based on Rational Drug Design.
J Med Chem
; 2024 Jun 29.
Artículo
en Inglés
| MEDLINE | ID: mdl-38943626
17.
Discovery of Novel Non-Nucleoside Inhibitors Interacting with Dizinc Ions of CD73.
J Med Chem
; 67(11): 9686-9708, 2024 Jun 13.
Artículo
en Inglés
| MEDLINE | ID: mdl-38809692
18.
Discovery of new potent inhibitors for carbonic anhydrase IX by structure-based virtual screening.
Bioorg Med Chem Lett
; 23(12): 3496-9, 2013 Jun 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-23664215
19.
Substituted indolin-2-ones as p90 ribosomal S6 protein kinase 2 (RSK2) inhibitors: Molecular docking simulation and structure-activity relationship analysis.
Bioorg Med Chem
; 21(7): 1724-34, 2013 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-23434140
20.
Synthesis, activity evaluation, and docking analysis of barbituric acid aryl hydrazone derivatives as RSK2 inhibitors.
J Enzyme Inhib Med Chem
; 28(4): 747-52, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-22545939