Detalles de la búsqueda
1.
The hop-derived compounds xanthohumol, isoxanthohumol and 8-prenylnaringenin are tight-binding inhibitors of human aldo-keto reductases 1B1 and 1B10.
J Enzyme Inhib Med Chem
; 33(1): 607-614, 2018 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29532688
2.
Selective Inhibition of Human AKR1B10 by n-Humulone, Adhumulone and Cohumulone Isolated from Humulus lupulus Extract.
Molecules
; 23(11)2018 Nov 21.
Artículo
en Inglés
| MEDLINE | ID: mdl-30469331
3.
Inhibition of human anthracycline reductases by emodin - A possible remedy for anthracycline resistance.
Toxicol Appl Pharmacol
; 293: 21-9, 2016 Feb 15.
Artículo
en Inglés
| MEDLINE | ID: mdl-26773812
4.
Reduction of lipid peroxidation products and advanced glycation end-product precursors by cyanobacterial aldo-keto reductase AKR3G1a founding member of the AKR3G subfamily.
FASEB J
; 29(1): 263-73, 2015 Jan.
Artículo
en Inglés
| MEDLINE | ID: mdl-25376835
5.
Potent inhibition of human carbonyl reductase 1 (CBR1) by the prenylated chalconoid xanthohumol and its related prenylflavonoids isoxanthohumol and 8-prenylnaringenin.
Chem Biol Interact
; 305: 156-162, 2019 May 25.
Artículo
en Inglés
| MEDLINE | ID: mdl-30849340
6.
Curcumin is a tight-binding inhibitor of the most efficient human daunorubicin reductase--Carbonyl reductase 1.
Chem Biol Interact
; 234: 162-8, 2015 Jun 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-25541467
7.
Green tea and one of its constituents, Epigallocatechine-3-gallate, are potent inhibitors of human 11ß-hydroxysteroid dehydrogenase type 1.
PLoS One
; 9(1): e84468, 2014.
Artículo
en Inglés
| MEDLINE | ID: mdl-24404164
Resultados
1 -
7
de 7
1
Próxima >
>>