Synthesis and biological evaluation of a novel series of bis-salicylaldehydes as mushroom tyrosinase inhibitors
摘要:
A series of novel bis-salicylaldehydes were synthesised and evaluated as tyrosinase inhibitors using a tyrosinase-dependent L-DOPA oxidation assay. The bis-salicylaldehydes exhibited greater inhibitory activity than salicylaldehyde. Our data suggests that these novel compounds may serve as a structural template for the design and development of novel tyrosinase inhibitors. (C) 2010 Elsevier Ltd. All rights reserved.
Brahmbhatt, D. I.; Jayabalan, L.; Hirani, B. R., Indian Journal of Chemistry - Section B Organic and Medicinal Chemistry, 1998, vol. 37, # 7, p. 683 - 685
作者:Brahmbhatt, D. I.、Jayabalan, L.、Hirani, B. R.、Singh, Shashibala
Synthesis and biological evaluation of a novel series of bis-salicylaldehydes as mushroom tyrosinase inhibitors
作者:Giovanna Delogu、Gianni Podda、Marcella Corda、Maria Benedetta Fadda、Antonella Fais、Benedetta Era
DOI:10.1016/j.bmcl.2010.08.018
日期:2010.10
A series of novel bis-salicylaldehydes were synthesised and evaluated as tyrosinase inhibitors using a tyrosinase-dependent L-DOPA oxidation assay. The bis-salicylaldehydes exhibited greater inhibitory activity than salicylaldehyde. Our data suggests that these novel compounds may serve as a structural template for the design and development of novel tyrosinase inhibitors. (C) 2010 Elsevier Ltd. All rights reserved.
Metal-free synthesis of calixsalen-type cavitands for the recognition of fluoride ion
作者:Arpita Desai、Dharti Rana
DOI:10.1080/00397911.2017.1398331
日期:2018.2.1
synthesized using metal-free synthesis from simple and inexpensive materials, such as ethylenediamine and 5,5′-methylene-bis-salicylaldehyde derivatives. The cavitand 1 containing salen functionality recognizes fluoride ion. Fluoride ions switch on fluorescence on binding with the cavitand 1. Substitution on bis-salicylaldehyde part of calixsalen-type cavitand shows change in recognition behavior. On