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1.
Furanoflavones pongapin and lanceolatin B blocks the cell cycle and induce senescence in CYP1A1-overexpressing breast cancer cells.
Bioorg Med Chem
; 26(23-24): 6076-6086, 2018 12 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-30448188
2.
Glycyrrhiza glabra extract and quercetin reverses cisplatin resistance in triple-negative MDA-MB-468 breast cancer cells via inhibition of cytochrome P450 1B1 enzyme.
Bioorg Med Chem Lett
; 27(24): 5400-5403, 2017 12 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-29150398
3.
Synthesis and biological evaluation of pyrrole-based chalcones as CYP1 enzyme inhibitors, for possible prevention of cancer and overcoming cisplatin resistance.
Bioorg Med Chem Lett
; 27(16): 3683-3687, 2017 08 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-28711350
4.
(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
5.
CYP enzymes, expressed within live human suspension cells, are superior to widely-used microsomal enzymes in identifying potent CYP1A1/CYP1B1 inhibitors: Identification of quinazolinones as CYP1A1/CYP1B1 inhibitors that efficiently reverse B[a]P toxicity and cisplatin resistance.
Eur J Pharm Sci
; 131: 177-194, 2019 Apr 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-30776468
6.
Biotransformation, Using Recombinant CYP450-Expressing Baker's Yeast Cells, Identifies a Novel CYP2D6.10A122V Variant Which Is a Superior Metabolizer of Codeine to Morphine Than the Wild-Type Enzyme.
ACS Omega
; 3(8): 8903-8912, 2018 Aug 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-31459022
7.
Khellinoflavanone, a Semisynthetic Derivative of Khellin, Overcomes Benzo[a]pyrene Toxicity in Human Normal and Cancer Cells That Express CYP1A1.
ACS Omega
; 3(8): 8553-8566, 2018 Aug 31.
Artículo
en Inglés
| MEDLINE | ID: mdl-31458985
8.
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
9.
Biotransformation of Chrysin to Baicalein: Selective C6-Hydroxylation of 5,7-Dihydroxyflavone Using Whole Yeast Cells Stably Expressing Human CYP1A1 Enzyme.
J Agric Food Chem
; 65(34): 7440-7446, 2017 Aug 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-28782952
10.
Quinazoline derivatives as selective CYP1B1 inhibitors.
Eur J Med Chem
; 130: 320-327, 2017 Apr 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-28259840
11.
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
12.
Corrigendum to "CYP enzymes, expressed within live human suspension cells, are superior to widely-used microsomal enzymes in identifying potent CYP1A1/CYP1B1 inhibitors: Identification of quinazolinones as CYP1A1/CYP1B1 inhibitors that efficiently reverse B[a]P toxicity and cisplatin resistance" [Eur. J. Pharm. Sci. 131 (2019) 177-194].
Eur J Pharm Sci
; 136: 104960, 2019 Aug 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-31230886
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