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Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholi...

Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholi...

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_31910701

Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholinesterase and butyrylcholinesterase reactivators

About this item

Full title

Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholinesterase and butyrylcholinesterase reactivators

Publisher

England: Taylor & Francis

Journal title

Journal of enzyme inhibition and medicinal chemistry, 2020-01, Vol.35 (1), p.478-488

Language

English

Formats

Publication information

Publisher

England: Taylor & Francis

More information

Scope and Contents

Contents

The series of symmetrical and unsymmetrical isoquinolinium-5-carbaldoximes was designed and prepared for cholinesterase reactivation purposes. The novel compounds were evaluated for intrinsic acetylcholinesterase (AChE) or butyrylcholinesterase (BChE) inhibition, when the majority of novel compounds resulted with high inhibition of both enzymes and...

Alternative Titles

Full title

Synthesis, in vitro screening and molecular docking of isoquinolinium-5-carbaldoximes as acetylcholinesterase and butyrylcholinesterase reactivators

Identifiers

Primary Identifiers

Record Identifier

TN_cdi_pubmed_primary_31910701

Permalink

https://devfeature-collection.sl.nsw.gov.au/record/TN_cdi_pubmed_primary_31910701

Other Identifiers

ISSN

1475-6366,1475-6374

E-ISSN

1475-6374

DOI

10.1080/14756366.2019.1710501

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