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1.
Design and cytotoxic evaluation via apoptotic and antiproliferative activity for novel 11(4-aminophenylamino)neocryptolepine on hepatocellular and colorectal cancer cells.
Apoptosis
; 28(3-4): 653-668, 2023 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-36719468
2.
Synthesis, biological evaluation and molecular modelling of 3-Formyl-6-isopropylchromone derived thiosemicarbazones as α-glucosidase inhibitors.
Bioorg Chem
; 139: 106739, 2023 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-37478545
3.
Synthesis and evaluation of novel xanthene-based thiazoles as potential antidiabetic agents.
Arch Pharm (Weinheim)
; 356(1): e2200356, 2023 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-36220614
4.
Cytotoxic Potential of Novel Quinoline Derivative: 11-(1,4-Bisaminopropylpiperazinyl)5-methyl-5H-indolo[2,3-b]quinoline against Different Cancer Cell Lines via Activation and Deactivation of the Expression of Some Proteins.
Int J Mol Sci
; 24(18)2023 Sep 20.
Artículo
en Inglés
| MEDLINE | ID: mdl-37762637
5.
Discovery and Evaluation of Enantiopure 9H-pyrimido[4,5-b]indoles as Nanomolar GSK-3ß Inhibitors with Improved Metabolic Stability.
Int J Mol Sci
; 21(21)2020 Oct 22.
Artículo
en Inglés
| MEDLINE | ID: mdl-33105671
6.
Fluorescence polarization-based assays for detecting compounds binding to inactive c-Jun N-terminal kinase 3 and p38α mitogen-activated protein kinase.
Anal Biochem
; 503: 28-40, 2016 06 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26954235
7.
An optimized and versatile synthesis to pyridinylimidazole-type p38α mitogen activated protein kinase inhibitors.
Org Biomol Chem
; 13(43): 10699-704, 2015 Nov 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-26351018
8.
Synthesis and in vitro testing of antimalarial activity of non-natural-type neocryptolepines: structureactivity relationship study of 2,11- and 9,11-disubstituted 6-methylindolo[2,3-b]quinolines.
Chem Pharm Bull (Tokyo)
; 61(12): 1282-90, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-24436959
9.
Addressing a Trapped High-Energy Water: Design and Synthesis of Highly Potent Pyrimidoindole-Based Glycogen Synthase Kinase-3ß Inhibitors.
J Med Chem
; 65(2): 1283-1301, 2022 01 27.
Artículo
en Inglés
| MEDLINE | ID: mdl-34213342
10.
Synthesis, Biological Evaluation, and In Silico Studies of Novel Coumarin-Based 4H,5H-pyrano[3,2-c]chromenes as Potent ß-Glucuronidase and Carbonic Anhydrase Inhibitors.
ACS Omega
; 7(32): 28605-28617, 2022 Aug 16.
Artículo
en Inglés
| MEDLINE | ID: mdl-35990487
11.
Structural Optimization of a Pyridinylimidazole Scaffold: Shifting the Selectivity from p38α Mitogen-Activated Protein Kinase to c-Jun N-Terminal Kinase 3.
ACS Omega
; 3(7): 7809-7831, 2018 Jul 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-30087925
12.
Tri- and Tetrasubstituted Pyridinylimidazoles as Covalent Inhibitors of c-Jun N-Terminal Kinase 3.
J Med Chem
; 60(2): 594-607, 2017 01 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-27977190
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