Synthesis of novel compounds containing morpholine and 5 (4H)-oxazolone rings as potent tyrosinase inhibitors

H Hamidian, S Azizi - Bioorganic & Medicinal Chemistry, 2015 - Elsevier
In this study, six new compounds containing morpholine and 5 (4 H)-oxazolone rings were
synthesized. Structures of the new compounds using IR, 1 H NMR, mass spectroscopy and …

Evaluation of thiazolidinone derivatives as a new class of mushroom tyrosinase inhibitors

M Rezaei, HT Mohammadi, A Mahdavi… - International journal of …, 2018 - Elsevier
Abstract Tyrosinase (EC 1.14. 18.1) is a key copper-containing metalloenzyme widely
distributed in nature and plays determinant role in melanin biosynthesis. The enzyme …

Synthesis and biological evaluation of novel hydroxybenzaldehyde-based kojic acid analogues as inhibitors of mushroom tyrosinase

W Xie, H Zhang, J He, J Zhang, Q Yu, C Luo… - Bioorganic & Medicinal …, 2017 - Elsevier
Two series of novel kojic acid analogues (4a–j) and (5a–d) were designed and synthesized,
and their mushroom tyrosinase inhibitory activities was evaluated. The result indicated that …

Synthesis of novel compounds as new potent tyrosinase inhibitors

H Hamidian - BioMed Research International, 2013 - Wiley Online Library
In the present paper, we report the synthesis and pharmacological evaluation of a new
series of azo compounds with different groups (1‐naphthol, 2‐naphthol, and N, N …

Design and synthesis of 3, 5-diaryl-4, 5-dihydro-1H-pyrazoles as new tyrosinase inhibitors

Z Zhou, J Zhuo, S Yan, L Ma - Bioorganic & medicinal chemistry, 2013 - Elsevier
In this study, twenty 3, 5-diaryl-4, 5-dihydro-1H-pyrazole derivatives with hydroxyl (s)(1a–1p,
2a–2d) were synthesized and their inhibitory activity on mushroom tyrosinase was …

Evaluation of novel pyrimidine derivatives as a new class of mushroom tyrosinase inhibitor

SS Mirmortazavi, M Farvandi, H Ghafouri… - Drug design …, 2019 - Taylor & Francis
Background and aim Tyrosinase (EC 1.14. 18.1) is responsible for enzymatic browning in
fruits and vegetables. Its inhibitors may be applied to efficiently treat hyperpigmentation and …

Synthesis of novel azo compounds containing 5 (4H)-oxazolone ring as potent tyrosinase inhibitors

H Hamidian, R Tagizadeh, S Fozooni… - Bioorganic & medicinal …, 2013 - Elsevier
Six new azo dyes containing of 5 (4H)-oxazolone ring were prepared by diazotization of 4-
aminohippuric acid and coupling with N, N-dimethylaniline, 1-naphthol and 2-naphthol and …

Design and synthesis of 5-(substituted benzylidene) thiazolidine-2, 4-dione derivatives as novel tyrosinase inhibitors

YM Ha, YJ Park, JA Kim, D Park, JY Park… - European journal of …, 2012 - Elsevier
In continuing our search for novel tyrosinase inhibitors, a series of 5-(substituted
benzylidene) thiazolidine-2, 4-diones were rationally designed and synthesized, and their …

A class of potent tyrosinase inhibitors: alkylidenethiosemicarbazide compounds

J Liu, R Cao, W Yi, C Ma, Y Wan, B Zhou, L Ma… - European journal of …, 2009 - Elsevier
A series of alkylidenethiosemicarbazide compounds were synthesized and their inhibitory
effects on the diphenolase activity of mushroom tyrosinase were evaluated. The results …

Synthesis, molecular docking studies of coumarinyl-pyrazolinyl substituted thiazoles as non-competitive inhibitors of mushroom tyrosinase

A Saeed, PA Mahesar, PA Channar, Q Abbas… - Bioorganic …, 2017 - Elsevier
A series of coumarinyl-pyrazolinyl substituted thiazoles derivatives were synthesized and
their inhibitory effects on the DPPH and mushroom tyrosinase were evaluated. The results …