Design, synthesis and biological evaluation of hydroxy substituted amino chalcone compounds for antityrosinase activity in B16 cells
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Molecular Biology,Biochemistry
Reference22 articles.
1. Approaches to Identify Inhibitors of Melanin Biosynthesis via the Quality Control of Tyrosinase
2. Role of Tyrosinase as the Determinant of Pigmentation in Cultured Human Melanocytes
3. Characterization of the interaction between 3-Oxotabersonine and two serum albumins by using spectroscopic techniques
4. Chemical and Instrumental Approaches to Treat Hyperpigmentation
5. Tyrosinase inhibition by isophthalic acid: Kinetics and computational simulation
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1. Coordination chemistry of chalcones and derivatives and their use as corrosion inhibitors: A comprehensive review;Coordination Chemistry Reviews;2024-10
2. Chain branching during the polycondensation of isophthalic aldehyde and 1,1′‐diacetylferrocene by the Claisen–Schmidt reaction;Journal of Polymer Science;2024-05-10
3. Tyrosinase Inhibition by Novel Benzimidazole-thione Schiff Base Derivatives;Letters in Drug Design & Discovery;2022-09
4. Phenolic compounds from Ficus hispida L.f. as tyrosinase and melanin inhibitors: Biological evaluation, molecular docking, and molecular dynamics;Journal of Molecular Structure;2021-11
5. Synthesis, Molecular Docking and Tyrosinase Inhibitory Activity of the Decorated Methoxy Sulfonamide Chalcones: in vitro Inhibitory Effects and the Possible Binding Mode;Sains Malaysiana;2021-09-30
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