Any feedback?
Please rate this page
(search_result.php)
(0/150)

BRENDA support

Refine search

Search Application

show results
Don't show organism specific information (fast!)
Search organism in taxonomic tree (slow, choose "exact" as search mode, e.g. "mammalia" for rat,human,monkey,...)
(Not possible to combine with the first option)
Refine your search

Search term:

Results 1 - 10 of 64 > >>
EC Number Application Commentary Reference
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4analysis both (R)-(-)- and (S)-(+)-1-(1-[11C]methyl-1H-pyrrol-2-yl)-2-phenyl-2-(1-pyrrolidinyl)ethanone are very promising tracers for positron emission tomography of the MAO-A enzyme in brain. The carbon-11-labeling reaction is fairly simple and robust. Yields of more than 1 GBq are routinely obtained and with high specific activity of the final product. The metabolism of (R)-(-)- and (S)-(+)-1-(1-[11C]methyl-1H-pyrrol-2-yl)-2-phenyl-2-(1-pyrrolidinyl)ethanone is relatively slow in plasma of living pigs, in contrast to [11C]harmine, which is difficult to detect in plasma at times after 10 min. Parametric maps of [11C](R)-(-)- and (S)-(+)-1-(1-[11C]methyl-1H-pyrrol-2-yl)-2-phenyl-2-(1-pyrrolidinyl)ethanone binding are qualitatively very comparable to those of [11C]harmine 688271
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4analysis kinetic assay for detection of MAO-A inhibitors in plant extracts using recombinant MAO-A expressed as GST-fusion protein in yesat 656957
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4analysis on-line immobilized enzyme reactors can be used for the on-line screening of substances for MAO-A and substrate/inhibitor properties 656361
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4analysis on-line immobilized enzyme reactors can be used for the on-line screening of substrances for MAO-A and substrate/inhibitor properties 656361
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4drug development active monoamine oxidase inhibitors represent suitable leads for the development of drugs for neurodegenerative and neuropsychiatric disorders such as Parkinson's disease and depression. Monoamine oxidase inhibitors are also of interest for the treatment of prostate cancer, certain types of cardiomyopathies and Alzheimer's disease 764555
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4drug development dual-target-directed drugs, compounds that inhibit MAO-B and antagonize A2A receptors, may have value in the management of Parkinson's disease, overview 705940
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4drug development indole and benzofuran derivatives are promising reversible MAO-B inhibitors with a possible role in the treatment of neurodegenerative diseases such as Parkinson’s disease 711911
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4drug development MAO-A is a target for a series of therapeutically valuable drugs. Thus, selective MAO-A inhibitors are used as antidepressants 702639
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4drug development MAO-B is a target for a series of therapeutically valuable drugs. Thus, selective MAO-B inhibitors are used in the treatment of Parkinson’s disease 702639
Show all pathways known for 1.4.3.4Display the word mapDisplay the reaction diagram Show all sequences 1.4.3.4medicine a significant association is found between the G-allele of 941G/T in MAO-A and attention deficit hyperactivity disorder (ADHD) 685838
Results 1 - 10 of 64 > >>