[HTML][HTML] Recent advances in green synthesized nanoparticles for bactericidal and wound healing applications

SN Nandhini, N Sisubalan, A Vijayan, C Karthikeyan… - Heliyon, 2023 - cell.com
Nanotechnology has become an exciting area of research in diverse fields, such as:
healthcare, food, agriculture, cosmetics, paints, lubricants, fuel additives and other fields …

[HTML][HTML] Heterocyclic compounds as synthetic tyrosinase inhibitors: recent advances

S Vittorio, C Dank, L Ielo - International Journal of Molecular Sciences, 2023 - mdpi.com
Tyrosinase is a copper-containing enzyme which is widely distributed in nature (eg, bacteria,
mammals, fungi) and involved in two consecutive steps of melanin biosynthesis. In humans …

Microwave-assisted green synthesis of silver nanoparticles using crude extracts of Boletus edulis and Coriolus versicolor: Characterization, anticancer, antimicrobial …

Ö Kaplan, NG Tosun, A Özgür, SE Tayhan… - Journal of Drug Delivery …, 2021 - Elsevier
The green synthesis of metal nanoparticles has been promising approach in the field of
nanomedicine due to its low-cost, non-toxic, biocompatible and sustainable features. In …

Design, synthesis, molecular modeling, and biological evaluation of novel kojic acid derivatives containing bioactive heterocycle moiety as inhibitors of tyrosinase and …

M He, M Fan, W Liu, Y Li, G Wang - Food Chemistry, 2021 - Elsevier
Tyrosinase plays an important role in melanin biosynthesis and enzymatic browning of fresh-
cut fruit and vegetables. To discover potent tyrosinase inhibitors and antibrowning agents, a …

Anti-tyrosinase, antioxidant and antibacterial activities of gallic acid-benzylidenehydrazine hybrids and their application in preservation of fresh-cut apples and …

Z Peng, Y Li, L Tan, L Chen, Q Shi, QH Zeng, H Liu… - Food chemistry, 2022 - Elsevier
A series of gallic acid-benzylidenehydrazine hybrids were synthesized and evaluated for
their tyrosinase inhibitory activity. Thereinto, compounds 5d and 5f potently inhibited …

[HTML][HTML] Design and synthesis of novel nitrothiazolacetamide conjugated to different thioquinazolinone derivatives as anti-urease agents

M Sohrabi, M Nazari Montazer, SM Farid, N Tanideh… - Scientific Reports, 2022 - nature.com
The present article describes the design, synthesis, in vitro urease inhibition, and in silico
molecular docking studies of a novel series of nitrothiazolacetamide conjugated to different …

[HTML][HTML] Thioquinoline derivatives conjugated to thiosemicarbazide as potent tyrosinase inhibitors with anti-melanogenesis properties

M Noori, R Sabourian, A Tasharoie, M Safavi, A Iraji… - Scientific Reports, 2023 - nature.com
In the present study, a series of aryl-substituted thioqunoline conjugated to
thiosemicarbazide were rationally designed and synthesized. The formation of target …

Evaluating the effects of disubstituted 3-hydroxy-1H-pyrrol-2 (5H)-one analog as novel tyrosinase inhibitors

N Alizadeh, MH Sayahi, A Iraji, R Yazzaf… - Bioorganic …, 2022 - Elsevier
In the present study, a series of 3-hydroxy-1H-pyrrol-2 (5H)-one derivative were rationally
designed and synthesized. The structure of targeted compounds was confirmed by IR, 1 H …

[HTML][HTML] Design, synthesis, and biological evaluation of symmetrical azine derivatives as novel tyrosinase inhibitors

S Karimian, F Kazemi, M Attarroshan, M Gholampour… - BMC chemistry, 2021 - Springer
A series of symmetrical azine derivatives containing different substituted benzyl moieties
were designed, synthesized, and evaluated for their inhibitory activity against tyrosinase …

Catechol-mimicking transition-state analogues as non-oxidizable inhibitors of tyrosinases

M Beaumet, LM Lazinski, M Maresca… - European Journal of …, 2023 - Elsevier
Tyrosinases are copper-containing metalloenzymes involved in several processes in both
mammals, insects, bacteria, fungi and plants. Their phenol oxidation properties are …