Design, synthesis, and evaluation of (E)-N-substituted benzylidene–aniline derivatives as tyrosinase inhibitors-Reference-Cited by-同舟云学术

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Design, synthesis, and evaluation of (E)-N-substituted benzylidene–aniline derivatives as tyrosinase inhibitors

Published:2012-11 Issue: Volume:57 Page:383-390
ISSN:0223-5234
Container-title:European Journal of Medicinal Chemistry
language:en
Short-container-title:European Journal of Medicinal Chemistry

Author:

Bae Sung Jin,Ha Young Mi,Park Yun Jung,Park Ji Young,Song Yu Min,Ha Tae Kwun,Chun Pusoon,Moon Hyung Ryong,Chung Hae Young

Funder

Ministry of Education, Science, and Technology

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Pharmacology,General Medicine

Reference35 articles.

1. Genetic Disorders of Pigmentation

2. Electron Transfer and Photoprotective Properties of Melanins in Solution

3. Malignant melanoma in South Wales: changing trends in presentation (1986-98)

4. Chemical and Instrumental Approaches to Treat Hyperpigmentation

5. Tyrosinase exacerbates dopamine toxicity but is not genetically associated with Parkinson's disease

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1. Discovery of (E)-3-(4-chlorophenyl)-N-(5-hydroxypentyl)acrylamide among N-substituted cinnamamide derivatives as a novel cosmetic ingredient for hyperpigmentation;Bioorganic Chemistry;2024-09

2. Design and synthesis of novel dihydropyridine- and benzylideneimine-based tyrosinase inhibitors;Frontiers in Pharmacology;2024-03-26

3. Natural products as tyrosinase inhibitors;The Enzymes;2024

4. In silico and in vitro evaluation of a safety profile of a cosmetic ingredient: 4-methoxychalcone (4-MC);Toxicology in Vitro;2023-12

5. Tyrosinase Inhibitors: A Perspective;Molecules;2023-07-30

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