1048973-61-0Relevant articles and documents
On the importance of antiparallel π-π Interactions in the solid state of isatin-based hydrazides
Ahmed, Muhammad Naeem,Arif, Maryam,Jabeen, Farah,Khan, Haroon Ahmed,Yasin, Khawaja Ansar,Tahir, Muhammad Nawaz,Franconetti, Antonio,Frontera, Antonio
, p. 8122 - 8131 (2019)
The condensation of N-propyl isatin (1) with different carboxylic acid hydrazides (RCONHNH2 (2-6), R = arene) via sonication was used to synthesize five new hydrazones (7-11). Fully characterized molecular structures were further studied by sin
Design and synthesis of a novel series of N-alkyl isatin acylhydrazone derivatives that act as selective cannabinoid receptor 2 agonists for the treatment of neuropathic pain
Diaz, Philippe,Xu, Jijun,Astruc-Diaz, Fanny,Pan, Hao-Min,Brown, David L.,Naguib, Mohamed
experimental part, p. 4932 - 4947 (2009/07/11)
There is growing interest in using cannabinoid receptor 2 (CB2) agonists for the treatment of neuropathic pain. We have synthesized a novel series of N-alkyl isatin acylhydrazone derivatives and have identified and characterized several of them as novel analogues with high functional activity and selectivity at human CB2 receptors using [35S]GTP-γ-S assays. Binding affinities at human CB2 and CB1 were determined for compounds 28, 33, 40, 48, and 58. Structure-activity relationship studies of this novel series led to optimization of our lead compound, compound 33 (MDA19). Compound 33 possessed potent antiallodynic effects in a rat model of neuropathic pain but did not affect rat locomotor activity. More potent and more CB2-receptor-selective compounds, including compounds 37, 40, and 48, were also discovered.