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1.
Identification of benzamides derivatives of norfloxacin as promising microRNA-21 inhibitors via repressing its transcription.
Bioorg Med Chem
; 66: 116803, 2022 07 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-35561631
2.
Alkylsulfonamide-containing quinazoline derivatives as potent and orally bioavailable PI3Ks inhibitors.
Bioorg Med Chem
; 27(20): 114930, 2019 10 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-31176568
3.
The dual luciferase reporter system and RT-qPCR strategies for screening of MicroRNA-21 small-molecule inhibitors.
Biotechnol Appl Biochem
; 66(5): 755-762, 2019 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-31021480
4.
Novel 6-aryl substituted 4-pyrrolidineaminoquinazoline derivatives as potent phosphoinositide 3-kinase delta (PI3Kδ) inhibitors.
Bioorg Med Chem
; 26(8): 2028-2040, 2018 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29534936
5.
Synthesis and evaluation of 2,9-disubstituted 8-phenylthio/phenylsulfinyl-9H-purine as new EGFR inhibitors.
Bioorg Med Chem
; 26(8): 2173-2185, 2018 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-29576272
6.
Introduction of pyrrolidineoxy or piperidineamino group at the 4-position of quinazoline leading to novel quinazoline-based phosphoinositide 3-kinase delta (PI3Kδ) inhibitors.
J Enzyme Inhib Med Chem
; 33(1): 651-656, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29536777
7.
Design and synthesis of novel 6-aryl substituted 4-anilinequinazoline derivatives as potential PI3Kδ inhibitors.
Bioorg Med Chem Lett
; 27(9): 1972-1977, 2017 05 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-28325601
8.
Synthesis and antitumor activity evaluation of 4,6-disubstituted quinazoline derivatives as novel PI3K inhibitors.
Bioorg Med Chem Lett
; 26(18): 4408-4413, 2016 09 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-27544401
9.
Design, synthesis, and evaluation of fluoroquinolone derivatives as microRNA-21 small-molecule inhibitors.
J Pharm Anal
; 12(4): 653-663, 2022 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-36105166
10.
Evolution of higher mesenchymal CD44 expression in the human lineage: A gene linked to cancer malignancy.
Evol Med Public Health
; 10(1): 447-462, 2022.
Artículo
en Inglés
| MEDLINE | ID: mdl-36148042
11.
Discovery of novel 9-heterocyclyl substituted 9H-purines as L858R/T790M/C797S mutant EGFR tyrosine kinase inhibitors.
Eur J Med Chem
; 186: 111888, 2020 Jan 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-31787359
12.
F10, a new camptothecin derivative, was identified as a new orally-bioavailable, potent antitumor agent.
Eur J Med Chem
; 202: 112528, 2020 Sep 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-32650182
13.
Discovery of 2-(aminopyrimidin-5-yl)-4-(morpholin-4-yl)-6- substituted triazine as PI3K and BRAF dual inhibitor.
Future Med Chem
; 10(20): 2445-2455, 2018 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-30325235
14.
Discovery of 2,4,6-trisubstitued pyrido[3,4-d]pyrimidine derivatives as new EGFR-TKIs.
Eur J Med Chem
; 148: 221-237, 2018 Mar 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-29466773
15.
Design,synthesis,and evaluation of fluoroquinolone derivatives as microRNA-21 small-molecule inhibitors / 药物分析学报
Journal of Pharmaceutical Analysis
; (6): 653-663, 2022.
Artículo
en Zh
| WPRIM | ID: wpr-955478
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