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1.
Discovery of a potent Gilteritinib-based FLT3-PROTAC degrader for the treatment of Acute myeloid leukemia.
Bioorg Chem
; 149: 107477, 2024 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-38820938
2.
Synthesis of 1,4-Dihydroquinolines and 4H-Chromenes via Organocatalytic Domino Aza/Oxa-Michael/1,6-Addition Reactions of para-Quinone Methides and Ynals.
J Org Chem
; 85(17): 11240-11249, 2020 09 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-32786616
3.
Discovery of cyanopyridine scaffold as novel indoleamine-2,3-dioxygenase 1 (IDO1) inhibitors through virtual screening and preliminary hit optimisation.
J Enzyme Inhib Med Chem
; 34(1): 250-263, 2019 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-30734612
4.
Discovery of a Novel Orally Bioavailable FLT3-PROTAC Degrader for Efficient Treatment of Acute Myeloid Leukemia and Overcoming Resistance of FLT3 Inhibitors.
J Med Chem
; 67(9): 7197-7223, 2024 May 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-38655686
5.
Discovery of (Z)-1-(3-((1H-Pyrrol-2-yl)methylene)-2-oxoindolin-6-yl)-3-(isoxazol-3-yl)urea Derivatives as Novel and Orally Highly Effective CSF-1R Inhibitors for Potential Colorectal Cancer Immunotherapy.
J Med Chem
; 64(23): 17184-17208, 2021 12 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-34735158
6.
One-pot synthesis of indoles and quinolinones from ortho-tosylaminophenyl-substituted para-quinone methides.
RSC Adv
; 10(55): 33455-33460, 2020 Sep 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-35515061
7.
Asymmetric Synthesis of 3,3'-Tetrahydrofuryl Spirooxindoles via Palladium-Catalyzed [3+2] Cycloadditions of Methyleneindolinones with Vinylethylene Carbonates.
Org Lett
; 22(15): 5833-5838, 2020 08 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-32790422
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