Author:
Kubo Isao,Kinst-Hori Ikuyo,Ishiguro Kyoko,Chaudhuri Swapan K.,Sanchez Yolanda,Ogura Tetsuya
Subject
Organic Chemistry,Clinical Biochemistry,Drug Discovery,Pharmaceutical Science,Molecular Biology,Molecular Medicine,Biochemistry
Cited by
40 articles.
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1. Reply letter to Dr. Wojtasek regarding: Oxidation of flavonoids by tyrosinase and by o-quinones–comment on "Flavonoids as tyrosinase inhibitors in
in silico
and
in vitro
models: basic framework of SAR using a statistical modelling approach” published by K. Jakimiuk, S. Sari, R. Milewski, C.T. Supuran, D. Söhretoglu, and M. Tomczyk (J Enzyme Inhib Med Chem 2022;37:427-436);Journal of Enzyme Inhibition and Medicinal Chemistry;2023-10-18
2. Oxidation of flavonoids by tyrosinase and by
o
-quinones–comment on "Flavonoids as tyrosinase inhibitors in
in silico
and
in vitro
models: basic framework of SAR using a statistical modelling approach” published by K. Jakimiuk, S. Sari, R. Milewski, C.T. Supuran, D. Şöhretoğlu, and M. Tomczyk (J Enzyme Inhib Med Chem 2022;37:427–436);Journal of Enzyme Inhibition and Medicinal Chemistry;2023-10-16
3. Oxidation of baicalein by tyrosinase and by o-quinones;International Journal of Biological Macromolecules;2023-03
4. Natural products in cosmetics;Natural Products and Bioprospecting;2022-11-28
5. Quercetin is a substrate not an inhibitor of tyrosinase - comments on “Quercetin as a tyrosinase inhibitor: Inhibitory activity, conformational change and mechanism” published by Fan et al. (2017);Food Research International;2022-03