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1.
(E)-3-(3,4,5-Trimethoxyphenyl)-1-(pyridin-4-yl)prop-2-en-1-one, a heterocyclic chalcone is a potent and selective CYP1A1 inhibitor and cancer chemopreventive agent.
Bioorg Med Chem Lett
; 27(24): 5409-5414, 2017 12 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-29138024
2.
Identification of Potent and Selective CYP1A1 Inhibitors via Combined Ligand and Structure-Based Virtual Screening and Their in Vitro Validation in Sacchrosomes and Live Human Cells.
J Chem Inf Model
; 57(6): 1309-1320, 2017 06 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-28489395
3.
Biphenyl urea derivatives as selective CYP1B1 inhibitors.
Org Biomol Chem
; 14(38): 8931-8936, 2016 Sep 26.
Artículo
en Inglés
| MEDLINE | ID: mdl-27714268
4.
Identification of karanjin isolated from the Indian beech tree as a potent CYP1 enzyme inhibitor with cellular efficacy via screening of a natural product repository.
Medchemcomm
; 9(2): 371-382, 2018 Feb 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30108931
5.
Quinazoline derivatives as selective CYP1B1 inhibitors.
Eur J Med Chem
; 130: 320-327, 2017 Apr 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-28259840
6.
Discovery and characterization of novel CYP1B1 inhibitors based on heterocyclic chalcones: Overcoming cisplatin resistance in CYP1B1-overexpressing lines.
Eur J Med Chem
; 129: 159-174, 2017 Mar 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-28222316
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